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Perrigo
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  • At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewWe are excited to recruit a Regulatory Affairs Professional to join the Non-Medicinal Lifecycle Management team. In this role, you will play an important role in supporting Perrigo's non medicinal portfolio including cosmetics, VMS, general products and other non-medicinal classifications such as medical devices across the product lifecycle. You will contribute to the development and execution of regulatory strategies, helping to deliver high-quality regulatory outcomes across a diverse and dynamic portfolio. You will be responsible for managing lifecycle management activities, including the preparation, maintenance and delivery of regulatory documentation, product information files, technical files, notifications, registrations and supporting records in line with global requirements and business priorities. You will identify regulatory risks, support mitigation activities, and ensure timely, compliant regulatory filings and documentation updates that help maintain supply continuity, consumer safety and market access. Working both independently and collaboratively, you will manage priorities across multiple activities and projects, ensuring effective delivery and alignment with departmental objectives. You will develop strong partnerships with colleagues across Regulatory Affairs and the wider business to support successful execution of lifecycle initiatives. Working closely with cross-functional stakeholders, including Quality, Safety, Supply Chain and R&D, you will provide regulatory input to change management activities and business initiatives. You will help translate regulatory requirements into practical actions that support product maintenance, compliance and portfolio optimisation. You will also contribute to the continuous improvement of Regulatory Affairs processes and ways of working, helping to drive greater efficiency, consistency and effectiveness across lifecycle activities. Through your role, you will support Perrigo's ability to meet evolving regulatory requirements while maintaining high standards of compliance and quality. This role offers the opportunity to make a meaningful contribution within the Regulatory Affairs organisation, supporting product availability and regulatory performance while further developing your regulatory expertise, business knowledge and professional capabilities in a dynamic global environment. Scope of the RoleEnsures regulatory compliance of assigned products through independent ownership of lifecycle regulatory activities across multiple products and markets. Takes ownership of post-market lifecycle changes, regulatory filings, documentation updates and regulatory issues of moderate to significant complexity, translating requirements into practical, risk-based execution. Contributes to both executional and strategic aspects of lifecycle projects and begins to lead workstreams within the LCM remit. Independently manages a range of complex product lifecycle changes, regulatory filings, notifications, registrations and documentation updates across products and markets. Works mostly independently end-to-end, seeking alignment for high-risk decisions and providing risk-based recommendations within delegated authority. Leads workstreams and begins project leadership; impact spans multiple products or markets with material delivery and compliance implications. As part of this role you may have the opportunity to work on other classifications in the non-medicinal area such as medical devices where needed based on business requirements. Lifecycle Strategy & Change Assessment Independently assess and manage a range of complex post-market lifecycle changes, working with cross-functional teams and authorities where needed to identify data requirements and update regulatory documentation and product files. Determine regulatory pathway or classification for complex changes within scope and provide clear rationale and risk-based recommendations. Maintain regulatory intelligence and proactively manage the impact of regulatory changes, informing relevant stakeholders of developments affecting the existing portfolio. Submission Delivery & Compliance Execution Establish, maintain, review, approve, and update product information files, technical files, regulatory records and supporting documentation in compliance with applicable legislation. Manage central notifications, registration filings, renewals, documentation updates or related regulatory procedures across products; prepare files, answer RFIs, and manage timelines. Develop and approve updated master labels and support implementation readiness and traceability to approvals. Support audits and CAPA reporting or follow-up as necessary and mitigate risks to avoid supply disruption. Stakeholder Leadership & Improvement Represent Regulatory in project teams and cross-functional forums and manage stakeholder communication on requirements, risks, and proposals. Support Cluster RA authority communication and respond to queries as necessary for lifecycle topics. Identify, suggest, and execute improvements to processes and ways of working within and across functions to improve quality and predictability of lifecycle delivery. Ensure robust handover and transition of product information files, technical documentation, regulatory decisions, and implementation requirements at launch and through post-market lifecycle changes. Experience RequiredTypically 3–5 years in Regulatory Affairs; relevant scientific or technical degree preferred. Ability to represent Regulatory in project teams and lead defined workstreams with increasing independence. Practical experience across lifecycle submissions, dossier maintenance, and cross-functional issue resolution. BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewWe are excited to recruit a Senior Professional Regulatory Affairs - Non-Medicinal Lifecycle Management, you will play a key role in leading the Biocides portfolio delivering Perrigo’s regulatory strategy across the product lifecycle. You will support the development and execution of regulatory strategies, ensuring the consistent delivery of high-quality regulatory outcomes across a diverse and complex portfolio. You will be responsible for managing lifecycle management activities, overseeing the preparation, submission, and maintenance of regulatory dossier/files in line with global requirements and business priorities. You will proactively identify risks, support mitigation planning, and ensure timely, compliant submissions that help maintain supply continuity, consumer safety, and market access. You will provide clear direction, support capability development, and foster a culture of accountability and continuous improvement. You will manage priorities across multiple activities, ensuring effective execution and alignment with departmental and organisational goals. Working closely with cross-functional stakeholders—including Quality, Safety, Supply Chain, and R&D—you will contribute regulatory expertise to change management and business initiatives. You will help translate regulatory requirements into practical, actionable plans that support product maintenance, compliance, and portfolio optimisation. You will also contribute to the continuous improvement of Regulatory Affairs processes and ways of working, helping to drive efficiency, consistency, and scalability across lifecycle activities. Through your role, you will support Perrigo’s ability to meet evolving regulatory requirements while maintaining high standards of compliance and quality. This role offers the opportunity to make a meaningful impact within the Regulatory Affairs organisation—supporting product availability and regulatory performance while developing your leadership and technical expertise in a dynamic, global environment. Scope of the RoleLeads complex, high-impact biocidal product lifecycle regulatory projects and workstreams across multiple products, markets, or legal bases, supporting the maintenance of registrations, authorisations, compliance and market access. Provides strategic regulatory leadership for significant biocides lifecycle activities, remediation, and compliance risks, ensuring delivery protects regulatory compliance, product availability and supply continuity. Acts as a recognised subject matter expert, mentors others, and drives governance and continuous improvement within the LCM team. Leads complex biocides lifecycle activities such as product authorisation maintenance, active substance and biocidal product compliance, artwork changes, renewals, notifications, formulation changes, supplier changes, manufacturing site changes, packaging changes, classification updates, safety or efficacy-related changes, remediation, or other high-risk lifecycle activities. Operates with high autonomy and is accountable for recommendations and technical direction on complex topics within delegated authority. Acts as senior individual contributor and mentor, leading cross-functional governance with impact across multiple products or portfolio workstreams. While the primary focus of this role is Biocides, you may need to flex your capabilities to support adjacent non-medicinal classifications, such as medical devices, where needed based on business requirements. Strategic Lifecycle Leadership Lead assessment and management of complex and high-risk biocides lifecycle changes across markets, defining data needs, submission strategy, and biocidal product dossier, authorisation file, technical documentation and supporting data package updates. Provide strategic oversight of biocidal product dossiers, authorisation files, technical documentation, supporting data packages and inspection readiness; set and coach high standards for right-first-time quality. Lead complex lifecycle submissions across products and markets, including variations, renewals, remediation, escalated RFIs, and deficiency responses. Approve or recommend change approach and submission strategy within delegated remit and escalate major compliance or supply risks through governance. Risk, Governance & Compliance Anticipate and mitigate significant regulatory risks and lead issue resolution for compliance gaps or supply disruption threats. Lead cross-functional risk reviews, remediation planning, and governance forums with Quality, Supply, Safety, R&D, Manufacturing, RegOps, and Cluster RA. Drive cross-functional improvements to lifecycle processes and systems, define implementation steps, and embed standard work. Leadership & Influence Act as regulatory lead for complex interactions with competent authorities, national authorities and relevant biocides regulatory bodies, coordinating consistent evidence-based responses. Coach and quality review the work of more junior colleagues and embed Good Documentation Practice within the team. Influence senior stakeholders and cross-functional teams without formal authority to achieve aligned decisions and timely delivery. Experience RequiredTypically 5–8+ years in Regulatory Affairs with proven experience leading complex regulatory projects and authority interactions; global biocides, non-medicinal regulated product, EU/UK BPR, national authorisation, renewal and product maintenance experience preferred; relevant scientific or technical degree preferred. Sustained performance in complex lifecycle roles or similar experience considered. Demonstrated capability in strategic lifecycle thinking, governance, and coaching others.  BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewWe are excited to recruit an Associate Professional, Regulatory Affairs within our Medical Device Lifecycle Management team. In this role,you will play an important role in supporting Perrigo's medical device portfolio throughout the product lifecycle. You will contribute to regulatory activities that help maintain ongoing conformity, technical documentation compliance, product availability and market access across multiple regions and markets. You will support lifecycle management activities including technical documentation updates, change assessments, regulatory notifications, registrations/listings and maintenance of regulatory records in accordance with applicable medical device requirements, approved procedures and business priorities. Working alongside experienced regulatory professionals, you will help ensure documentation remains current, traceable and inspection-ready, and that regulatory deliverables are completed to agreed timelines. You will manage a range of defined regulatory activities and support change control, product maintenance, labelling updates, technical file remediation and ongoing compliance obligations. You will help identify potential regulatory issues, support risk mitigation activities and contribute to the successful delivery of medical device lifecycle objectives. Working closely with cross-functional stakeholders including Quality, Safety, Supply Chain, Manufacturing, R&D, Packaging/Artwork, you will provide regulatory support for product and process changes and assist in translating medical device regulatory requirements into practical actions that support compliance and business needs. You will contribute to the continuous improvement of Medical Device Regulatory Affairs processes, systems and ways of working, helping to improve efficiency, consistency, data quality and inspection readiness across lifecycle activities. Through your role, you will build regulatory expertise in medical devices while supporting Perrigo's commitment to maintaining high standards of compliance, consumer safety and product quality. This role offers an excellent opportunity to develop a strong foundation in Medical Device Regulatory Affairs, gain experience across the product lifecycle and build both technical and professional capabilities within a dynamic global environment. Scope of the RoleSupports ongoing conformity and compliance of medical device products through defined lifecycle regulatory activities across assigned products and markets. Delivers routine to moderately complex lifecycle changes, technical documentation updates, regulatory notifications and registration/listing maintenance activities with increasing independence, ensuring compliant and timely execution. Builds practical expertise across medical device classifications, markets, regulatory pathways and ways of working while remaining agile to shifting business priorities.Focused on executional aspects of medical device lifecycle regulatory work and owns defined deliverables under guidance. Assesses and supports routine to moderately complex product, process, labelling and supplier-related changes; prepares and maintains technical documentation, regulatory records, registrations/listings, notifications and conformity-related documentation. Works with guidance and review, contributes within project teams, and has impact on defined products, markets, or deliverables. Lifecycle Compliance & Document Management Support the accuracy and compliance of medical device registrations, listings and regulatory records for assigned products and markets. Prepare and update technical documentation, technical files and supporting regulatory records with senior review and according to Good Documentation Practice. Support labelling, Instructions for Use, packaging and artwork reviews to ensure alignment with approved claims, device requirements and market-specific obligations. Support regulatory notifications, registrations/listings and maintenance trackers to ensure lifecycle status and compliance obligations remain visible and current. Lifecycle Changes and Regulatory Deliverables Assess and support routine to moderately complex medical device lifecycle changes under guidance, gathering data and updating technical documentation and regulatory records. Draft components for regulatory notifications, registration/listing updates, technical documentation updates and authority or notified body responses; support timeline tracking and follow-up. Recommend options for routine change impact assessment, regulatory pathway or documentation approach within delegated scope and escalate uncertainty or higher-risk topics. Support implementation tracking following regulatory clearance, notification, listing update or approved documentation change to help avoid compliance gaps and supply disruption. Risk, Intelligence & Cross-Functional Delivery Draft responses to health authority, competent authority or notified body queries and support document reviews under guidance. Support regulatory intelligence impact assessments for medical device requirements and inform stakeholders as directed. Support audits, inspections, CAPA documentation and follow-up under supervision. Partner with Quality, Safety, R&D, Supply Chain, Manufacturing, Packaging/Artwork, Regulatory Operations and local or cluster Regulatory Affairs teams to implement approved changes and maintain ongoing conformity and market compliance. Experience RequiredTypically 2–4 years in Medical Device Regulatory Affairs, Quality, technical documentation or a related regulatory field; scientific, engineering or technical degree preferred. Ability to participate effectively in cross-functional project teams and manage defined deliverables with accuracy and discipline. Practical capability in technical documentation preparation, regulatory record maintenance, timeline tracking and structured issue escalation. BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewWe re excited to recruit a Manager as Medicines Lead for Lifecycle Management. You will play a key role in delivering Perrigo’s regulatory strategy across the medicines product lifecycle. You will lead the development and execution of post-approval regulatory strategies, ensuring the consistent delivery of high-quality regulatory outcomes across a diverse and complex medicines portfolio. You will be responsible for managing lifecycle management activities, overseeing the preparation, submission, and maintenance of regulatory dossiers and Marketing Authorisations in line with global requirements and business priorities. You will proactively identify risks, support mitigation planning, and ensure timely, compliant submissions that help maintain supply continuity, consumer and patient safety, and market access. Leading a team of multi-regional regulatory professionals, you will provide clear direction, support capability development, and foster a culture of accountability and continuous improvement. You will manage priorities across multiple activities, ensuring effective execution and alignment with departmental and organisational goals. Working closely with cross-functional stakeholders—including Quality, Safety, Supply Chain, and R&D—you will contribute regulatory expertise to change management and business initiatives. You will help translate regulatory requirements into practical, actionable plans that support product maintenance, compliance, and portfolio optimisation. You will also contribute to the continuous improvement of Regulatory Affairs processes and ways of working, helping to drive efficiency, consistency, and scalability across lifecycle activities. Through your role, you will support Perrigo’s ability to meet evolving regulatory requirements while maintaining high standards of compliance and quality. This role offers the opportunity to make a meaningful impact within the Regulatory Affairs organisation—supporting product availability and regulatory performance while developing your leadership and technical expertise in a dynamic, global environment. Scope of the RoleLeads Lifecycle Management Regulatory Affairs for the assigned portfolio and is accountable for post-launch regulatory strategy, compliance performance, and delivery outcomes. Sets direction, priorities, and governance to ensure compliant and timely execution of post-approval activities while balancing business needs, consumer or patient protection, and supply continuity. Leads, develops, and performance-manages a team and shapes capability while driving a consistent One Regulatory Voice across the organisation.Owns governance and decision-making for post-approval changes across the medicines portfolio, including variations, renewals, PV-related regulatory commitments and reporting, maintenance and supply-driven changes, and regulatory intelligence-driven changes. Establishes robust change control management with Quality, Supply Chain, and R&D and oversees impact assessments, submission strategy, implementation tracking, dossier integrity, inspection readiness, and metrics. Acts as final decision-maker within delegated authorities for lifecycle change strategy, prioritisation, resourcing, and governance, escalating enterprise policy or high-risk precedent decisions as required.Lifecycle Strategy, Governance & Delivery Own post-launch regulatory strategy and compliance for the medicines portfolio, including variations, renewals, PV-related regulatory commitments and reporting, maintenance and supply-driven changes, and regulatory intelligence-driven changes. Establish robust change control with Quality, Supply Chain, and R&D, ensuring impact assessments, submission strategy, implementation tracking, and inspection readiness are effective and sustainable. Partner with Pharmacovigilance and Medical/Safety teams on safety-driven variations, product information updates, risk minimisation measures, PV-related regulatory commitments, and reporting requirements. Ensure timely, compliant execution of lifecycle submissions and commitments; monitor performance and remove barriers to delivery. Risk, Authority Engagement & Portfolio Planning Monitor and interpret regulatory trends and legislation; provide timely impact assessments and lead mitigation planning and CAPA governance to protect compliance and avoid supply disruption. Lead authority interactions and escalations for lifecycle topics and represent Perrigo in local or cluster forums and trade associations where required. Provide portfolio planning input for major changes, site transfers, cost optimisation, and portfolio optimisation or discontinuation decisions, ensuring regulatory feasibility and timelines are understood. Leadership, Capability & Operational Excellence Lead and develop the team; set objectives, coach performance, build succession, and shape capability. Drive harmonisation of SOPs and templates, oversee RIMS and workflow data quality, and use metrics to improve cycle times and accountability in partnership with RegOps. Lead governance forums, escalation pathways, and cross-functional alignment so dossiers, decisions, and implementation requirements transition cleanly across Category, Cluster, and LCM interfaces. Experience RequiredTypically 8–10+ years in Regulatory Affairs with strong medicines lifecycle or post-launch compliance expertise, including knowledge of global medicines regulatory frameworks, post-approval variation requirements, CTD/eCTD dossier requirements, and lifecycle maintenance of Marketing Authorisations; relevant scientific or technical degree preferred. Demonstrated people leadership, authority engagement, and experience managing competing priorities across a portfolio. Experience working cross-functionally in a matrixed organization and providing strong regulatory writing and stakeholder management. BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • Financial Accountant  

    - London
    At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewThe Financial Accountant will play an important role in supporting the delivery of accurate and timely financial information across the North Europe Cluster. This is a varied and developing role, offering exposure to core accounting processes, internal controls, financial reporting, and the wider operations of a multinational finance environment.  As the business evolves, the role will continue to grow and adapt in line with changing priorities and areas of focus, providing opportunities to broaden knowledge, build confidence, and contribute to improvements across finance. The position will involve working with a wide range of departments, countries, teams, and stakeholders, requiring flexibility, curiosity, strong communication skills, and the ability to build effective working relationships with different personalities and ways of working.Scope of the RoleFinancial Reporting & Close Support Support the monthly close process, including preparation and review of Profit & Loss and Balance Sheet outputs. Work closely with PBS during pre-close and close cycles, helping to ensure data completeness, timely issue resolution, and accurate reporting. Prepare and review accruals and prepayments, ensuring calculations are accurate, supported, and aligned to business activity. Support review of monthly results by investigating variances, explaining movements in key balances, and preparing commentary for review by the Financial Controller. Balance Sheet Management & Analysis Prepare and maintain balance sheet reconciliations, ensuring accounts are fully supported, accurate, and cleared on a timely basis. Review and analyse balance sheet movements, identifying unusual items and escalating potential risks or opportunities to the Financial Controller. Support the tracking and review of contingencies, provisions, and accruals, ensuring appropriate documentation and timely follow-up. Support fixed asset accounting activities, including monitoring Assets Under Construction, ensuring timely capitalisation and depreciation, and assisting with impairment review preparation. Controls, SOX & Governance Execute, evidence, and document SOX controls, ensuring adherence to internal control requirements and company timelines. Support the maintenance of strong financial governance by following company policies, procedures, and approval requirements. Identify control issues, process gaps, or compliance risks and escalate appropriately with suggested actions where possible. Statutory, Tax & Regulatory Support Support the preparation of statutory reporting and filings, building knowledge of local reporting requirements while ensuring accuracy and timely completion. Assist with tax and regulatory reporting requirements by preparing supporting schedules, reconciliations, and analysis where required. Provide support for internal and external audits, including data preparation, query resolution, and follow-up of audit actions. Stakeholder Collaboration & Business Support Work with colleagues across Finance, PBS, Tax, Legal, Supply Chain, Commercial, and other business functions to support accurate reporting, issue resolution, and delivery of finance priorities. Build effective working relationships across countries and teams, adapting communication style to different stakeholders, cultures, and ways of working. Support the Financial Controller with ad hoc analysis, queries, and business requests as priorities evolve. Contribute to clear communication between local markets, shared service teams, and functional experts to help ensure alignment and timely resolution of open items. Projects, Process Improvement & Learning Support finance projects and process improvement initiatives, helping to simplify ways of working and strengthen reporting accuracy. Take ownership of personal development by building technical accounting knowledge, systems capability, and understanding of company policies. Develop confidence in using ERP systems, finance tools, and data to support analysis, reporting, and decision-making. Seek feedback and apply learning to improve accuracy, efficiency, and contribution to the team Experience RequiredTechnical & Professional Good understanding of accounting principles, applied to reconciliations, accruals, prepayments, reporting and analysis. Strong numerical and analytical skills, with the ability to investigate variances and explain movements clearly Good attention to detail, with a focus on accuracy, completeness, and timely delivery. Willingness to develop technical accounting knowledge and build confidence within a finance environment. Experience & Qualifications Degree or equivalent experience in Finance, Accounting, Business, or a related field. Studying towards, or interested in pursuing, a professional qualification such as ACA, ACCA, or CIMA. Previous experience in a finance, accounting, shared services, apprenticeship, or placement role would be advantageous. Systems & Tools Good Excel skills, including formulas, data organisation, lookups, pivot tables, and Power Query. Experience using ERP or finance systems, such as SAP, Oracle, or similar, would be advantageous. Comfortable working with data and learning new systems, reporting tools, and finance processes. Personal Attributes Curious and proactive, with a willingness to ask questions, learn and take ownership. Proactive, positive and solution-oriented, contributing to continuous improvement across processes and ways of working. Able to communicate clearly with stakeholders at all levels, across finance and non-finance teams. Flexible and adaptable, able to manage priorities and work at pace in a busy finance environment. Collaborative approach, building effective working relationships across different departments, countries, teams and ways of working. BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • FP&A Finance Analyst  

    - London
    At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewWorking across the full North region, this role is primarily responsible for leading commercial reporting across brands, categories, countries, and currencies. The role provides full P&L visibility and insight by bringing together data from multiple reporting systems, including Power Query, Power BI, Workday Adaptive, SAP, and CFIN. The role requires the development of strong systems knowledge and the ability to become a key expert for internal data resources. It also requires the ability to work at pace, demonstrating strong time management, planning, and prioritisation skills to ensure deadlines are consistently met and outputs are delivered to a high standard. Scope of the RoleMonthly Forecasting (IBP) Partner with Demand Planning to ensure forecast volumes are well understood, commercially validated, and accurately interfaced between financial systems. Support local country reporting and North Cluster consolidations, ensuring key assumptions are correctly loaded into Adaptive each cycle to enable accurate forecasting and clear performance tracking. Work closely with Finance Operations teams to understand movements in cost of goods, freight, and related supply chain costs, translating these impacts into clear commercial insight for the business. Prepare robust statistical and financial analysis to assess the impact of pricing strategy changes on the regional P&L, highlighting key drivers, risks, and opportunities. Collaborate with the Marketing team to improve forecast accuracy for advertising and promotional spend, supporting the team with tracking, explaining, and reporting changes in spend across the forecast cycle. Build strong, trusted relationships with the Commercial Finance team in London, wider Finance teams in Dublin, Belgium, and the USA, and the broader Commercial business, ensuring effective collaboration across markets and functions. Prepare insightful category-level financial commentary, connecting performance trends to relevant market data to validate key assumptions. Ensure outputs from the IBP cycle are supported by robust commercial and financial assumptions, with a clearly joined-up IBP plan across volume, sales, margin, and cost drivers. Annual Budgeting Support the annual budget cycle from a commercial finance perspective, ensuring the plan is built on robust, clearly documented assumptions across volume, price, mix, margin, cost of goods, freight, advertising, and promotional spend. Work alongside the wider Finance community to understand how volume changes impact cost prices, gross margin, freight, and supply chain assumptions, ensuring movements are clearly explained and reflected accurately in the budget. Partner with commercial planning teams, including RGM, CSI, Marketing, and Sales, to ensure budget inputs are aligned to category strategies, customer plans, pricing decisions, promotional activity, and market expectations. Prepare detailed deep-dive analysis during the planning cycle to challenge and validate key assumptions, identifying material movements, risks, opportunities, and areas requiring further business input. Collaborate with commercial business leads to ensure the final budget reflects a joined-up view across countries, brands, categories, and currencies, with clear visibility of the key drivers underpinning the North Cluster plan. System Expert Own the regional numbers presented in Adaptive, ensuring a clear understanding of what has changed, why it has changed, and how key movements impact the commercial forecast and reporting outputs. Build deep knowledge of the system to identify opportunities for process improvement and use this expertise to support and train the wider team. Support the business with ad hoc reporting requirements, ensuring internal reporting tools are regularly reconciled to SAP and Power BI to maintain accurate, complete, and consistent reporting to corporate stakeholders. Experience RequiredPrevious experience in FP&A within a fast-paced, commercially focused environment, with a strong understanding of financial planning, forecasting, and performance reporting. Strong analytical capability, with a proven ability to interpret and interrogate complex data, perform detailed reconciliations, identify key drivers, and constructively challenge assumptions where results do not align with expectations. Confident working across multiple financial and reporting systems, including SAP, Adaptive, Power BI, Power Query, and Visual Fabriq, with the ability to connect data sources and support accurate reporting outputs. Able to communicate clearly and effectively with senior and junior stakeholders across finance and non-finance teams, translating financial insight into practical business understanding. Proactive, positive, and solution-oriented, with a willingness to take ownership, learn quickly, and contribute to continuous improvement across processes, reporting, and ways of working. BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • Financial Accountant  

    - Greater London
    At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewThe Financial Accountant will play an important role in supporting the delivery of accurate and timely financial information across the North Europe Cluster. This is a varied and developing role, offering exposure to core accounting processes, internal controls, financial reporting, and the wider operations of a multinational finance environment.  As the business evolves, the role will continue to grow and adapt in line with changing priorities and areas of focus, providing opportunities to broaden knowledge, build confidence, and contribute to improvements across finance. The position will involve working with a wide range of departments, countries, teams, and stakeholders, requiring flexibility, curiosity, strong communication skills, and the ability to build effective working relationships with different personalities and ways of working.Scope of the RoleFinancial Reporting & Close Support Support the monthly close process, including preparation and review of Profit & Loss and Balance Sheet outputs. Work closely with PBS during pre-close and close cycles, helping to ensure data completeness, timely issue resolution, and accurate reporting. Prepare and review accruals and prepayments, ensuring calculations are accurate, supported, and aligned to business activity. Support review of monthly results by investigating variances, explaining movements in key balances, and preparing commentary for review by the Financial Controller. Balance Sheet Management & Analysis Prepare and maintain balance sheet reconciliations, ensuring accounts are fully supported, accurate, and cleared on a timely basis. Review and analyse balance sheet movements, identifying unusual items and escalating potential risks or opportunities to the Financial Controller. Support the tracking and review of contingencies, provisions, and accruals, ensuring appropriate documentation and timely follow-up. Support fixed asset accounting activities, including monitoring Assets Under Construction, ensuring timely capitalisation and depreciation, and assisting with impairment review preparation. Controls, SOX & Governance Execute, evidence, and document SOX controls, ensuring adherence to internal control requirements and company timelines. Support the maintenance of strong financial governance by following company policies, procedures, and approval requirements. Identify control issues, process gaps, or compliance risks and escalate appropriately with suggested actions where possible. Statutory, Tax & Regulatory Support Support the preparation of statutory reporting and filings, building knowledge of local reporting requirements while ensuring accuracy and timely completion. Assist with tax and regulatory reporting requirements by preparing supporting schedules, reconciliations, and analysis where required. Provide support for internal and external audits, including data preparation, query resolution, and follow-up of audit actions. Stakeholder Collaboration & Business Support Work with colleagues across Finance, PBS, Tax, Legal, Supply Chain, Commercial, and other business functions to support accurate reporting, issue resolution, and delivery of finance priorities. Build effective working relationships across countries and teams, adapting communication style to different stakeholders, cultures, and ways of working. Support the Financial Controller with ad hoc analysis, queries, and business requests as priorities evolve. Contribute to clear communication between local markets, shared service teams, and functional experts to help ensure alignment and timely resolution of open items. Projects, Process Improvement & Learning Support finance projects and process improvement initiatives, helping to simplify ways of working and strengthen reporting accuracy. Take ownership of personal development by building technical accounting knowledge, systems capability, and understanding of company policies. Develop confidence in using ERP systems, finance tools, and data to support analysis, reporting, and decision-making. Seek feedback and apply learning to improve accuracy, efficiency, and contribution to the team Experience RequiredTechnical & Professional Good understanding of accounting principles, applied to reconciliations, accruals, prepayments, reporting and analysis. Strong numerical and analytical skills, with the ability to investigate variances and explain movements clearly Good attention to detail, with a focus on accuracy, completeness, and timely delivery. Willingness to develop technical accounting knowledge and build confidence within a finance environment. Experience & Qualifications Degree or equivalent experience in Finance, Accounting, Business, or a related field. Studying towards, or interested in pursuing, a professional qualification such as ACA, ACCA, or CIMA. Previous experience in a finance, accounting, shared services, apprenticeship, or placement role would be advantageous. Systems & Tools Good Excel skills, including formulas, data organisation, lookups, pivot tables, and Power Query. Experience using ERP or finance systems, such as SAP, Oracle, or similar, would be advantageous. Comfortable working with data and learning new systems, reporting tools, and finance processes. Personal Attributes Curious and proactive, with a willingness to ask questions, learn and take ownership. Proactive, positive and solution-oriented, contributing to continuous improvement across processes and ways of working. Able to communicate clearly with stakeholders at all levels, across finance and non-finance teams. Flexible and adaptable, able to manage priorities and work at pace in a busy finance environment. Collaborative approach, building effective working relationships across different departments, countries, teams and ways of working. BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • Associate Director - Regulatory Affairs Operations  

    - Greater London
    At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewWe are excited to recuit a new Associate Director - Regulatory Affairs Operations to join Perrigo Scientific Office. As the Operations lead, you will play a key role in delivering Perrigo’s enterprise regulatory systems, publishing digitialisation/data, process, and metrics across the product lifecycle. You will lead the development and execution of regulatory strategies for regulatory operating models, systems programs and transformation into digitialisation environment as part of the function's day to day activities. You will ensure the consistent delivery of high-quality regulatory outcomes across a diverse and complex portfolio of classifications and markets. Working closely with all RA teams and cross-functional stakeholders—including Quality, IT, Supply Operations, R&D—you will contribute regulatory expertise to change management and business initiatives. You will also contribute to the continuous improvement of Regulatory Affairs processes and ways of working, helping to drive efficiency, consistency, and scalability across lifecycle activities. Through your role, you will support Perrigo’s ability to meet evolving regulatory requirements while maintaining high standards of compliance and quality.This role offers the opportunity to make a meaningful impact within the Regulatory Affairs organisatio - supporting product availability and regulatory performance while developing your leadership and technical expertise in a dynamic, global environment.Scope of the RoleOwn enterprise governance and decision-making including regulatory platforms, publishing/submission standards, data governance, document and records management, workflow design, metrics, and operational support for lifecycle submissions, commitments, and major business changeDefine and maintain global operating model/interfaces across LCM, Category, Cluster, Quality, Supply Chain, R&D, IT  to ensure data integrity, compliant execution, efficient implementation of regulatory change, and clear accountabilityFinal decision-maker within delegated authorities for strategy, capability roadmap, standards, process design, system priorities, investment recommendations, and operational governance, escalating enterprise policy, significant risk, or precedent-setting decisions as requiredProvide team direction, support development, foster culture of accountability/continuous improvementManage priorities across multiple activities, ensure effective execution and alignment with department/ organisation goalsManage central publishing of CTD dossiers in line with business priorities across the full product lifecycle.Develop regulatory system programs and roadmapsDevelop and maintain operating model ensuring consistent approach Enterprise Regulatory Operations Strategy, Governance & DeliveryOwn enterprise Regulatory Operations strategy and roadmap for systems, publishing, document management, regulatory data, workflow controls, and service delivery supporting the full product lifecycleLead on design, implementation, and governance of global processes and platforms to ensure compliant, efficient, and scalable execution of submissions, post-approval activity, authority commitments, and regulatory changeEstablish clear governance, prioritisation, and performance management for activities, ensuring delivery risks are visible, resolved, and escalated appropriatelyProvide strategic leadership to Regulatory Affairs leadership teams on operational readiness, organisational scalability, and the regulatory implications of business transformation, portfolio change, and market expansion.Digital Data & Compliance LeadershipDefine and lead the enterprise roadmap for regulatory systems, structured data, reporting, and automation to support evolving external requirements, stronger insight generation, and efficient regulatory executionMonitor and interpret evolving external regulatory data and submission requirements, including SPOR, IDMP, IRIS, and related regional standards; translate these into business impacts, capability needs, and implementation plansSet and enforce data governance, control standards, quality expectations, and inspection-readiness requirements for regulatory information, ensuring traceability, consistency, and sustainable compliance across the organisationLead vendor, platform, and process optimisation decisions that improve user adoption, data quality, submission quality, cycle times, and organisational visibility through meaningful metrics and dashboardsLeadership, Capability & Operational ExcellenceLead/develop organisation set vision and objectives, coach senior leads, build succession and shape capability in operations, systems, publishing, data governance,digital transformationDrive harmonisation of SOPs, templates, roles, governance forums, and ways of working, and embed a culture of accountability, continuous improvement, and operational excellenceLead cross-functional governance, escalation pathways, and business change initiatives so operational requirements, regulatory decisions, and implementation needs transition cleanly across Category, Cluster, and LCM interfaces and with external partners where relevantExperience RequiredRelevant senior level experience in Regulatory Affairs with significant leadership experience in Regulatory Operations, regulatory systems, publishing, regulatory data management, or adjacent operational leadership roles, and relevant scientific or technical degree preferred.Demonstrated leadership of managers and/or complex matrixed teams, with experience setting enterprise strategy, influencing senior stakeholders, and leading transformation across functions, geographies, and product classifications.Strong experience with regulatory systems, structured data standards, operational compliance requirements, and business case development, with the ability to translate complex requirements into scalable operating models and investment priorities.Demonstrated areas of expertise:Enterprise Regulatory Leadership: Sets enterprise direction and ensures a consistent, future-ready Regulatory Operations approach aligned to One Regulatory Voice and business priorities.Organisational Leadership: Builds and leads high-performing teams and leaders through coaching, talent development, succession planning, and clear accountability.Strategic Execution: Translates strategy into operating models, governance, investment choices, capability roadmaps, and measurable outcomes and drives continuous improvement.Decision-Making & Accountability: Makes risk-based decisions balancing compliance, data integrity, speed, efficiency, inspection readiness, and business continuity.Stakeholder Partnership: Acts as a strategic partner to senior leaders and leads cross-functional alignment and escalations on systems, data, process, and operating model change.Risk & Compliance Ownership: Accountable for enterprise compliance outcomes in Regulatory Operations, including data quality, submission standards, records integrity, audit and inspection readiness, and prevention of execution risk.External Awareness & Influence: Monitors regulatory operations trends and represents the organisation in relevant external associations, consultations, vendor partnerships, or industry forums where appropriate.BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • Shopper & Customer Activation Executive  

    - Greater London
    At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewWe are excited to be recruiting for a permanent Shopper & Customer Activation Executive to join our Commercial Strategy & Execution team based in central London. In this role, you will be responsible for driving shopper-focused activation strategies and ensuring successful execution of branded and own-label initiatives across Perrigo’s self-care categories.This position is ideal for a creative, but process-orientated, ambitious professional eager to make a real impact at the point of purchase.At Perrigo, our Shopper Marketing function is a critical part of the Commercial Strategy & Execution team.Your job will be to make leading self-care products such as Galpharm, Solpadeine, NiQuitin, Bronchostop, ellaOne, and Compeed visible and accessible to consumers.The role will have great exposure to leadership with strong progression opportunities across our commercial functions.Scope of the RoleShopper & Category Expertise: Serve as the go-to expert for shopper activation at Perrigo, translating brand and category growth strategies into actionable shopper marketing plans.Agency Management: Manage day to day relationship with our shopper marketing agency to deliver projects. Make recommendations for process improvements, efficiencies and innovative solutions.Performance Tracking: Monitor and analyse POS for continuous improvement sharing insights and opportunities to optimise ROI and market share growth.Monthly Business Cycle: Play a key role in monthly meetings, feeding shopper activation plans into internal forums, and supporting Sales teams with compelling activation proposals, which meet brand objectives and retailer priorities.Retailer engagement: Launch annual shopper marketing toolkits and support sales teams at customer strategy days with tailored activation plans.Cross-Functional Collaboration: Partner with commercial strategy,  RGM, Sales, Marketing and Supply Chain to deliver integrated activation plans.Experience RequiredMinimum of 3 years in FMCG or Consumer Healthcare, with previous experience in shopper marketing, marketing or commercial strategy.Proven ability to manage budgets and deliver measurable ROI through effective activation.Strong analytical skills and ability to translate insights into actionable plans.Excellent stakeholder management and communication skills, with experience influencing across functions and with retailers.University degree or equivalent experience required.London-based with hybrid working and occasional travel (approx. 5–10%). BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less
  • At Perrigo, we are driven by our mission to Makes Lives Better Through... Read More
    At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care.Description OverviewWe are excited to recruit an Associate Professional, Regulatory Affairs within our Medical Device Lifecycle Management team. In this role,you will play an important role in supporting Perrigo's medical device portfolio throughout the product lifecycle. You will contribute to regulatory activities that help maintain ongoing conformity, technical documentation compliance, product availability and market access across multiple regions and markets. You will support lifecycle management activities including technical documentation updates, change assessments, regulatory notifications, registrations/listings and maintenance of regulatory records in accordance with applicable medical device requirements, approved procedures and business priorities. Working alongside experienced regulatory professionals, you will help ensure documentation remains current, traceable and inspection-ready, and that regulatory deliverables are completed to agreed timelines. You will manage a range of defined regulatory activities and support change control, product maintenance, labelling updates, technical file remediation and ongoing compliance obligations. You will help identify potential regulatory issues, support risk mitigation activities and contribute to the successful delivery of medical device lifecycle objectives. Working closely with cross-functional stakeholders including Quality, Safety, Supply Chain, Manufacturing, R&D, Packaging/Artwork, you will provide regulatory support for product and process changes and assist in translating medical device regulatory requirements into practical actions that support compliance and business needs. You will contribute to the continuous improvement of Medical Device Regulatory Affairs processes, systems and ways of working, helping to improve efficiency, consistency, data quality and inspection readiness across lifecycle activities. Through your role, you will build regulatory expertise in medical devices while supporting Perrigo's commitment to maintaining high standards of compliance, consumer safety and product quality. This role offers an excellent opportunity to develop a strong foundation in Medical Device Regulatory Affairs, gain experience across the product lifecycle and build both technical and professional capabilities within a dynamic global environment. Scope of the RoleSupports ongoing conformity and compliance of medical device products through defined lifecycle regulatory activities across assigned products and markets. Delivers routine to moderately complex lifecycle changes, technical documentation updates, regulatory notifications and registration/listing maintenance activities with increasing independence, ensuring compliant and timely execution. Builds practical expertise across medical device classifications, markets, regulatory pathways and ways of working while remaining agile to shifting business priorities.Focused on executional aspects of medical device lifecycle regulatory work and owns defined deliverables under guidance. Assesses and supports routine to moderately complex product, process, labelling and supplier-related changes; prepares and maintains technical documentation, regulatory records, registrations/listings, notifications and conformity-related documentation. Works with guidance and review, contributes within project teams, and has impact on defined products, markets, or deliverables. Lifecycle Compliance & Document Management Support the accuracy and compliance of medical device registrations, listings and regulatory records for assigned products and markets. Prepare and update technical documentation, technical files and supporting regulatory records with senior review and according to Good Documentation Practice. Support labelling, Instructions for Use, packaging and artwork reviews to ensure alignment with approved claims, device requirements and market-specific obligations. Support regulatory notifications, registrations/listings and maintenance trackers to ensure lifecycle status and compliance obligations remain visible and current. Lifecycle Changes and Regulatory Deliverables Assess and support routine to moderately complex medical device lifecycle changes under guidance, gathering data and updating technical documentation and regulatory records. Draft components for regulatory notifications, registration/listing updates, technical documentation updates and authority or notified body responses; support timeline tracking and follow-up. Recommend options for routine change impact assessment, regulatory pathway or documentation approach within delegated scope and escalate uncertainty or higher-risk topics. Support implementation tracking following regulatory clearance, notification, listing update or approved documentation change to help avoid compliance gaps and supply disruption. Risk, Intelligence & Cross-Functional Delivery Draft responses to health authority, competent authority or notified body queries and support document reviews under guidance. Support regulatory intelligence impact assessments for medical device requirements and inform stakeholders as directed. Support audits, inspections, CAPA documentation and follow-up under supervision. Partner with Quality, Safety, R&D, Supply Chain, Manufacturing, Packaging/Artwork, Regulatory Operations and local or cluster Regulatory Affairs teams to implement approved changes and maintain ongoing conformity and market compliance. Experience RequiredTypically 2–4 years in Medical Device Regulatory Affairs, Quality, technical documentation or a related regulatory field; scientific, engineering or technical degree preferred. Ability to participate effectively in cross-functional project teams and manage defined deliverables with accuracy and discipline. Practical capability in technical documentation preparation, regulatory record maintenance, timeline tracking and structured issue escalation. BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Find out more about Total Rewards at Perrigo. Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo Read Less

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany