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Hologic Inc.
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  • Product Development Engineer  

    - Cambridge
    Product Development EngineerRole location: Cambridge, UK Discover a ca... Read More
    Product Development EngineerRole location: Cambridge, UK Discover a career with real meaning. One that offers the opportunity to showcase your talents, achieve measurable success and gain immense satisfaction by shaping the future of cancer care.  At Endomag, a Hologic company, we’re redefining cancer treatment and empowering clinicians worldwide with innovative medical solutions.  We’re now looking for a talented Product Development Engineer to join our dynamic team in Cambridge —someone who thrives on solving complex challenges, driving excellence, and making an impact that truly matters. As Product Development Engineer at Endomag, a Hologic company, you will play a critical role in our development programs with a focus on hands on mechanical design and development of components, instruments, sub-assemblies and disposable devices within our Breast Surgery product portfolio. You will define requirements, design and prototype solutions, and lead verification/validation activities within a regulated environment (ISO 13485). You will collaborate closely with a network of third-party suppliers, contract development organisations, consultants and internal cross functional teams to deliver innovative, compliant and manufacturable products.  KEY RESPONSIBILITIES Own mechanical design of product and sub-assemblies from concept through detailed design, prototyping and verification/validation, ensuring safety, performance and manufacturability Perform mechanical architecture, materials selection, tolerance analysis (GD&T). Design for manufacture, assembly and serviceability; generate CAD models and drawings Project manage work streams: build and track plans, risks and budgets, drive decisions, report status, ensure delivery to ISO 13485 design controls Lead relationships with external partners (suppliers, consultants, contract manufacturers) Ensure robust risk management (ISO 14971) and compliance with relevant standards Collaborate closely with cross-functional teams including Product Engineering, Quality, Marketing, Regulatory Affairs, and our Implantables Team. Prepare and maintain detailed documentation for all design and development activities including design specifications, test protocols and compliance reports.   KNOWLEDGE, SKILLS & EXPERIENCE Educational background in Mechanical Design, Materials Engineering, (or a related field) or equivalent experience in mechanical product development within regulated industries Knowledge of CAD (e.g. SolidWorks), GD&T, materials and plastics selection, tolerance stack-ups, DFM/DFA Project management skills—able to plan, prioritise, and keep teams on track and experience leading external suppliers/contractors Experience with design verification and validation, and working through product development phases Working knowledge of ISO 13485, ISO 14971, ISO 10993, IEC 62366 Excellent problem-solving and communication skills and a collaborative team spirit Eager to learn, with a drive for continuous improvement Ready to Make an Impact? Read Less
  • Country Business Manager  

    Hologic is a global leader in women’s health, committed to earlier det... Read More
    Hologic is a global leader in women’s health, committed to earlier detection, more accurate diagnosis, and less invasive treatment. Our Breast & Skeletal Health portfolio includes innovative imaging and interventional solutions that help clinicians detect breast cancer earlier and manage skeletal health more effectively.The UK & Ireland are strategically important markets with strong brand recognition, a high installed base and significant untapped potential – particularly as the market accelerates adoption of advanced imaging technologies. What to Expect Lead and develop your team Direct and support regional sales managers, sales representatives and applications specialists. Hire, train, and coach to build a consistently high‑performing, engaged team. Implement shared goals and clear performance metrics; embed a growth mindset and strong team values. Own commercial strategy and execution Establish and refine go‑to‑market strategies across the UK & Ireland portfolio. Translate market insights into account and territory plans that drive sustainable growth. Lead the planning and execution of new product introductions, working closely with marketing and other functions. Drive technology adoption and recurring revenue models Manage the P&L and drive performance Own the P&L, using data to make sound decisions on pricing, resource allocation and investment. Use robust sales methodologies to manage pipeline, forecast accurately, and improve productivity. Continuously seek ways to improve and enhance performance and profitability. Build partnerships and influence stakeholders Develop transparent, collaborative relationships with distributors, key customers and external stakeholders. Work cross‑functionally with marketing, finance, operations, service, and other divisions to maximise revenue opportunities. Represent the UK & Ireland business within regional and global forums, contributing insights on market trends, competition and emerging opportunities. What We Expect You are a proven commercial leader in Medical Technology (ideally women’s health or diagnostic/imaging) who: Experience & Knowledge Has substantial experience in the MedTech commercial sector, with a clear track record of outperforming market and competitor trends. Has owned and managed a business or BU P&L, using financial insight to drive better decisions. Has led sizeable, dispersed teams, not just small local units. Knows how to shift organisations from conservative to growth mindsets, recurring revenue / service / SaaS models. Has driven technology adoption in markets where new solutions are introduced frequently. Has implemented or enhanced systems and processes that improved ways of working and results. Has completed significant leadership development and understands different leadership styles and when to use them. Leadership & Coaching Builds high‑performing teams and can demonstrate consistent improvement in engagement and results. Is a strong coach who can talk specifically about developing individuals and how that lifted team performance. Sets shared goals and key metrics that keep teams focused on delivering above expectations. Can navigate blockers and resistance, especially in periods of change. What’s In It For You? A mission‑driven role in a company that is genuinely improving outcomes for women. End‑to‑end ownership of a critical business in a key market, with real autonomy to shape strategy and team. Visibility at UK leadership and regional level, in a growing, ambitious global organisation  #LI-HE1 Read Less
  • Technical Documentation Specialist - 12 months FTC  

    - Cambridge
    Technical Documentation Specialist – 12 months FTCRole location: Cambr... Read More
    Technical Documentation Specialist – 12 months FTCRole location: Cambridge, UK (hybrid working) Discover a career with real meaning. One that offers the opportunity to showcase your talents, achieve measurable success and gain immense satisfaction by shaping the future of cancer care.  At Endomag, a Hologic company, we’re redefining cancer treatment and empowering clinicians worldwide with innovative medical solutions.  We’re now looking for a Technical Documentation Specialist to join our dynamic team in Cambridge on a 12 months fixed term contract. As a Technical Documentation Specialist, you will play a pivotal role in ensuring the accuracy, consistency and compliance of technical documentation for our products. You will collaborate with multi-disciplinary engineers, clinical trial managers, regulatory affairs specialists and quality assurance experts to create and maintain audit-ready documentation. Your efforts will directly support to deliver innovative, high-quality medical technologies that transform cancer care and improve patient outcomes worldwide. KEY RESPONSIBILITIES Oversee the creation and maintenance of technical documentation for Endomag’s products, including user needs, design inputs, design outputs, verification and validation testing plans and reports, engineering drawings and manufacturing specifications Lead Cross-Functional Collaboration: act as the primary liaison between R&D, Regulatory Affairs, Clinical Affairs, Product Engineering and Quality Assurance, ensuring seamless integration of their inputs into the technical documentation Champion Good Documentation Practices: adopt a meticulous approach to creating and editing content, driving efforts to improve documentation practices and ensure consistency and audit readiness Support Regulatory Compliance: review technical documents to ensure compliance with Endomag’s Quality Management System, FDA, MDR regulations, and applicable international standards (e.g., ISO 13485, ISO 14971) Participate in Regulatory Submissions and Audits: facilitate reviews by internal and external auditors, interact with regulatory agencies as needed, and lead efforts to implement Corrective and Preventive Actions (CAPAs)  KNOWLEDGE, SKILLS & EXPERIENCE Educational background in engineering or a scientific field Experience in creating and editing technical reports and documentation Exceptional attention to detail and high levels of accuracy Demonstrated ability to take ownership of initiatives, deliver results and drive continuous improvement Excellent content creation and editing skills Excellent written and verbal communication skills, with the ability to communicate effectively with cross-functional teams and regulatory agencies. Good organizational and time management skills to handle conflicting priorities and meet tight deadlines Experience in design assurance, quality or technical documentation roles in the medical device industry or other regulated industries, e.g. automotive, aerospace is highly desirable Ready to Make an Impact? Read Less
  • Senior Project and Programme Manager - 12 months FTC  

    - Manchester
    Senior Project and Program Manager - 12 months FTCRole location: Remot... Read More
    Senior Project and Program Manager - 12 months FTCRole location: Remote (UK based) At Hologic, our purpose is to enable healthier lives everywhere, every day. We are driven by a passion to become the global champion for women’s health, delivering on our promise to bring The Science of Sure to life. As a member of our International Commercial PMO Centre of Expertise, you will be at the heart of strategic innovation—leading projects that make a meaningful impact across our Diagnostics, Breast and Skeletal Health & Gyno Surgical Solutions. We are looking for people with solid experience of Project Management and understanding of best practices to skillfully lead the delivery of a range of strategic commercial projects - for example New Product Introductions / Go To Market, Sustaining and Operational projects. Your excellent communication and stakeholder management skills will support effective cross functional collaboration across Hologic, working with Global and International teams from Marketing, Commercial, Operations, R&D, Clinical Applications, Regulatory and Technical groups. Reporting to the Head of Commercial PMO International, you will support continuous improvement efforts in the operations of the PMO CoE, helping to strengthen delivery capabilities and return value to the business. KEY RESPONSIBILITIES Strategic Project Leadership: Drive delivery of high-impact commercial initiatives—including New Product Introductions (NPI), Go-To-Market launches, sustaining and operational projects—across multiple international divisions. Cross-Functional Collaboration: Build strong, honest partnerships with global and regional teams (Marketing, Commercial, R&D, Regulatory, Operations, Supply Chain, IT, Clinical Applications) fostering effective teamwork and communication. Portfolio & Programme Management: Establish and manage core teams and steering committees, create project charters, and ensure robust project planning, risk management, and proactive problem-solving. Stakeholder Engagement: Present insights, performance metrics, and recommendations to diverse audiences, influencing decision-making at all levels—including PMO leadership and senior stakeholders. Continuous Improvement: Champion best practices and change management within the PMO CoE, coaching team members, introducing new tools, and driving a culture of excellence and collaboration. Reporting & Governance: Develop dashboards and reports to support transparency, integrating updates into portfolio management processes and tools. Financial & Contract Oversight: Forecast, manage project budgets, and report on financials to support strategic decision-making and value delivery. KNOWLEDGE, SKILLS & EXPERIENCE To excel in this role, you will thrive in a fast-paced, matrixed environment, enjoy building strong partnerships, and have a passion for delivering world-class commercial programmes. Your expertise will help shape the future of healthcare innovation at Hologic. Project Management Experience ideally within Medical Devices, Diagnostics, or Commercial functions. Proven track record of driving NPIs and complex, multi-stakeholder projects. Familiarity with stage gate processes and project lifecycle management. Qualifications: PMP Certification (or equivalent) required. Educational background in Science, Engineering, Marketing, or Business preferred. Commercial Acumen: Experience working with commercial functions and external suppliers; understanding of market regulations, product launches, and international portfolio management. Technical Skills: Proficiency with Microsoft Suite (including MS Project), PMO enterprise tools (e.g., Planview), and data-driven reporting. Exceptional communication, stakeholder management and relationship-building skills. Ability to influence in matrixed organizations, both regionally and globally. Continuous Improvement Mindset: proactive, adaptable, and committed to introducing best practices and driving process improvements. Ready to Make an Impact? If you’re excited by the opportunity to lead transformative programmes in a purpose-driven organization—and have the skills and drive to succeed—we’d love to hear from you. #mid-seniorlevel #LI-KP1 Read Less
  • Applications Specialist  

    Join Hologic as an Applications Specialist – GSS (Gynecology & Surgica... Read More
    Join Hologic as an Applications Specialist – GSS (Gynecology & Surgical Solutions), Central South UK Are you ready to drive advancements in gynecology and surgical care? At Hologic, we are passionate about empowering healthier lives through innovation, with a dedicated focus on women’s health and clinical certainty. Our state-of-the-art Gynecology & Surgical Solutions (GSS) portfolio is transforming diagnostics, treatment pathways, and patient care, and we’re looking for a talented Applications Specialist to help us lead the way across the Central South region of the UK. As an Applications Specialist for GSS, you will be instrumental in delivering exceptional clinical support and training to our customers across Central South. You will empower gynecologists, surgeons, theatre teams, and wider clinical staff to achieve optimal results with our advanced technologies, such as our hysteroscopic solutions and related surgical devices. From initial installation and first cases through to ongoing education, you will ensure our customers are confident and successful in using Hologic’s solutions to improve patient outcomes. Working in close collaboration with Sales, Field Service Engineering, Marketing, Technical Solutions, and Customer Service, you will be a trusted clinical partner, representing Hologic’s commitment to excellence in women’s health. What To Expect: Clinical Applications Support:
    Provide expert, field-based support to customers using Hologic’s GSS portfolio, ensuring best practice, procedural efficiency, and high clinical standards in gynecology and surgical settings. Training & Education:
    Deliver engaging and informative training for new and existing users (consultants, registrars, nurses, ODPs, and theatre staff), enhancing their expertise and confidence in the use of Hologic’s gynecology and surgical technologies. Case Support & Proctoring:
    Support live cases in theatres and procedure rooms, assisting with product setup, workflow optimisation, and practical tips to help clinicians achieve consistent, high-quality outcomes. Pre-Site & Site Assessment:
    Guide customers through pre-installation evaluations, theatre set-up, and on-site assessments to ensure seamless adoption and integration of Hologic systems into clinical pathways. Clinical Troubleshooting:
    Offer hands-on assistance and problem-solving for application-specific questions and challenges in gynecological and surgical environments, working in partnership with Technical and Service teams where needed. Collaboration:
    Work cross-functionally with Sales and Service teams to address clinical needs, support evaluations and trials, and help drive customer satisfaction and long-term adoption. Conferences & Study Days:
    Represent Hologic at study days, workshops, conferences, and trade shows focused on gynecology, minimally invasive surgery, and women’s health, providing clinical expertise and product demonstrations. Documentation & Reporting:
    Maintain accurate records of training sessions, case support, and customer interactions using Hologic’s CRM systems. Travel:
    Regular travel across the Central South UK region (and occasionally more widely within the UK and Ireland) according to business needs. What We Expect: Education:
    Bachelor’s degree in a healthcare or life sciences-related field (e.g., Nursing, Operating Department Practice, Biomedical Science, Midwifery) or equivalent clinical experience in gynecology, theatres, or women’s health. Clinical Experience:
    Experience in gynecology, operating theatres, minimally invasive surgery, or women’s health environments is highly desirable. A strong interest in developing deep clinical and product knowledge within Hologic’s GSS portfolio is essential.  Technical Proficiency:
    Familiarity with Microsoft Office Suite; experience with CRM systems (e.g., Salesforce) and ERP tools (e.g., Oracle) is a plus. Regulatory Awareness:
    Understanding of UK clinical, governance, and regulatory requirements related to medical devices, operating theatres, and training. Language Skills:
    Fluent in English, both written and spoken. Skills & Behaviours: Excellent communication and interpersonal skills to effectively support, educate, and influence clinical users at all levels. Strong analytical and troubleshooting abilities in fast-paced clinical environments. Customer-focused, proactive, and detail-oriented, with a strong sense of ownership and accountability. Collaborative team player who thrives in a dynamic, field-based role with frequent interactions across functions. Holds a current UK driver’s license and has the right to work in the UK. Adaptable, resilient, and eager to learn and grow within gynecology and surgical applications. Hologic’s Purpose: We enable healthier lives, everywhere, every day.
    Our Passion: Become global champions for women’s health.
    Our Promise: The Science of Sure. If you’re committed to advancing gynecological and surgical care and passionate about supporting healthcare professionals, we invite you to apply and join our team in the Central South UK region. Ready to make an impact? Read Less

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