One of my clients are a leading and rapidly growing pharmaceutical company who are recruiting for enthusiastic and passionate Production Technician.
Rotating Day Shift: Monday to Friday on rotating shifts of 7am-3pm and 10am-6pm. You will be responsible for the production of sterile products and operation of production equipment on a state-of-the-art manufacturing facility.
This role will offer you Opportunity to move into your first role within the biopharmaceutical/life science industry Opportunity to work in a fast-paced GMP site A dedicated training program to progress your skills on a state-of-the-art manufacturing facility Opportunity to work at the forefront of science £25,600 annual salary (Over £27,000 annually with shift bonus)
You will be responsible for Production of pharmaceutical products and the preparation and use of operational equipment in a timely manner Support the preparation of sterile products, labelling, packaging and dispatch Following SOPs in terms of Procedures, Policies, Rules, Regulations Generating documentation for risk assessments and ensuring GMP compliance Maintaining production areas to the required standards Environmental monitoring Validation of equipment
You will bring the following Knowledge of GMP working environment Experience working within production / manufacturing GCSEs
If you would like to learn more about this exciting opportunity or to recommend a valued professional from your network, please apply to this advertisement or reach out on:
Laboratory and Facilities Coordinator – 12 month FTC – Central London
BioTalent are happy to be supporting an oncology-focused biotechnology company that are looking to recruit a Laboratory and Facilities Coordinator on a 12 month fixed term contract.
This is a perfect opportunity for a Lab Technician/Junior Scientist who is looking to take a step up into a full lab operations based role. Please note, this position will not involve any research activities.
You will be responsible for:
Support Laboratory Operations: Assist technical staff and scientists in maintaining a safe and efficient lab environment. Equipment Maintenance Coordination: Collaborate with engineers to ensure timely maintenance and repairs. Inventory Management: Monitor, order, and maintain stock levels of chemicals, reagents, consumables, and office supplies. Supplier Liaison: Coordinate with suppliers for laboratory equipment procurement. General Laboratory Upkeep: Oversee glassware maintenance, waste disposal, and equipment cleaning. Asset Management: Oversee and maintain an up-to-date asset register. Laboratory Safety Compliance: Ensure lab staff adhere to company safety policies and procedures. Health & Safety Support: Assist the Head of Operations in maintaining health and safety standards and policies.
You will bring the following:
lab operations background. Hands-on experience with ordering, shipping, etc. Ability to work under minimal supervision on tasks/ and to support scientists and team members.
Please apply to this advert or reach out on the following:
Lead Qualified Person (QP) – Multi-Site Pharmaceutical Organisation (UK-Wide)
We are seeking an experienced Lead Qualified Person to join a leading pharmaceutical organisation, overseeing a team of QPs across multiple UK sites. This is a senior leadership role, ensuring the highest standards of GMP compliance, product release, and regulatory alignment across the organisation’s operations.
Key Responsibilities:
Strategic QP Leadership: Oversee and provide guidance to a team of Qualified Persons across multiple UK sites, ensuring consistent quality and regulatory compliance. Batch Certification & Product Release: Lead the QP function in certifying and releasing medicinal products in accordance with EU GMP and MHRA requirements. Regulatory & Compliance Oversight: Ensure all sites maintain full compliance with MHRA, EU GMP, and GDP regulations, supporting regulatory inspections and audits. Process Improvement & Risk Management: Identify and mitigate quality risks, implement Corrective and Preventive Actions (CAPAs), and drive continuous improvement across the QP function. Training & Development: Mentor and develop the QP team, ensuring ongoing training, competency, and professional development. Stakeholder Collaboration: Work closely with senior management, manufacturing, quality, and regulatory teams to align QA and QP activities with business objectives.
What We’re Looking For:
Eligibility to act as a Qualified Person. Proven experience in a senior QP role, ideally leading QPs. Strong knowledge of GMp, MHRA regulations, and pharmaceutical quality systems. Must have exposure to releasing sterile/aseptic dosage forms. Demonstrated leadership skills with the ability to manage, mentor, and develop a high-performing team. Experience in audits, inspections, and batch release for a variety of pharmaceutical products.
This is a unique opportunity to take on a senior QP leadership role within a well-established pharmaceutical organisation. If you are a strategic leader with a passion for quality excellence and compliance, we would love to hear from you!
Head of Quality Assurance – Multi-Site Pharmaceutical Organisation (UK-Wide)
We are seeking an experienced Head of Quality Assurance to join a leading pharmaceutical organisation, overseeing Quality Assurance (QA) operations across five UK sites. This is a pivotal role for a strategic and hands-on leader who will drive compliance, continuous improvement, and regulatory excellence across multiple locations.
Key Responsibilities:
Quality Leadership: Develop and implement a unified QA strategy across all sites, ensuring consistent compliance with MHRA, GMP, GDP, and ISO standards. Regulatory Compliance: Oversee internal audits, external inspections, and regulatory submissions, ensuring adherence to UK and international pharmaceutical regulations. Site Oversight: Provide QA leadership and support to five sites, working closely with site QA teams to maintain operational excellence. CAPA & Risk Management: Identify quality risks, drive Corrective and Preventive Actions (CAPAs), and implement continuous improvement initiatives. Training & Development: Lead and mentor QA teams across multiple locations, fostering a culture of quality and compliance. Stakeholder Engagement: Collaborate with senior management, operations, and regulatory bodies to uphold the highest standards of quality and safety.
What We’re Looking For:
Extensive experience in Quality Assurance leadership within the pharmaceutical industry. Strong understanding of GMP, GDP, MHRA regulations, and international quality standards. Experience with aseptic/sterile dosage forms QP eligibility advantageous but not a deal breaker. Proven track record of managing QA operations across multiple sites. Expertise in audits, inspections, CAPA management, and risk assessment. Ability to lead, influence, and engage cross-functional teams.
This is a fantastic opportunity to play a key leadership role in shaping the quality strategy of a well-established pharmaceutical company. If you thrive in a multi-site environment and have a passion for driving excellence in quality, we would love to hear from you!
Job Title: Data Governance Manager Location: London- Hybrid 3 days a week Job Type: Contract
BioTalent is delighted to be partnered with a medical research charity based in London. We are on the hunt for a Data Governance Manager to join the team on a contract basis.
What You’ll Do: Develop & Implement robust data governance frameworks, policies, and standards to ensure compliance, integrity, and security. Advise Senior Leadership on data governance strategies and regulatory requirements (e.g., GDPR, ISO27001). Lead Data Strategy Initiatives to align with business objectives, drive operational efficiency, and improve decision-making. Collaborate with Stakeholders across technology, legal, risk management, data science, and business units. Ensure Data Quality & Compliance by setting up governance KPIs, classification, retention, and master data management processes. Leverage Technology & Tools like Power Automate and Work to cleanse and enhance data.
What We’re Looking For: Proven expertise in Data Governance & Data Strategy Development, ideally in a complex organisation. Strong knowledge of UK & EU data regulations (including GDPR). Experience with data governance tools (e.g., Collibra, Informatica, Alation). Excellent stakeholder management & communication skills – ability to influence without authority. A problem-solver & innovator, driving data governance excellence across an organisation. Relevant qualifications in Computer Science, Information Systems, or Data Management (DAMA CDMP, CIPP certification preferred).
Qualifications: Degree in Computer Science, Information Systems, Data Management or a related field. Certifications in data governance or data management (e.g. DAMA Certified Data. Management Professional (CDMP), Certified Information Privacy Professional (CIPP)). Experience in data governance within the medical research, healthcare, or public sector is an advantage.
If you are keen to find out more about this Data Governance Manager role, please reach out.
BioTalent Ltd is acting as an employment agency for this opportunity
