Senior Chemistry Analyst in Runcorn

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

As a Senior Chemistry Analyst you will provide technical and scientific expertise within the Quality department. You will support material and product analysis to ensure quality products are supplied to customers on time and in full, helping the department achieve its objectives. You will also support the QC department by maintaining robust documentation, procedures and quality processes to ensure customer service targets are consistently met.

Key Responsibilities

• Review documentation and testing data for components, raw materials, bulk product, CIP samples, water systems, and finished product using the correct procedures in compliance with cGLP, cGMP, Health & Safety, SOPs, environmental and regulatory requirements.
• Provide training and support for analysts within the QC department.
• Assist with method transfer processes and qualification studies, ensuring timely completion in line with project plans.
• Generate, update and implement documentation including SOPs, analytical documents, quality reports, monthly measures and Product Quality Reviews (PQRs).
• Contribute to the review, improvement and introduction of laboratory processes to support continuous improvement initiatives.
• Support the completion of LIRs, deviations and CAPAs through the Veeva system and support rolling reviews to ensure compliance targets are maintained.
• Communicate effectively within Quality Control and across other departments to ensure continuity of activities.
• Plan, design and coordinate laboratory-based projects.
• Update visual management boards with information reflecting departmental measures and KPIs.
• Support laboratory resource and manpower planning.
• Lead and manage relevant customer complaints within agreed timelines and in accordance with company procedures.

Your Skills and Experience

Do You Have?

• A Degree in Chemistry or another relevant scientific discipline.
• Proven experience in analytical chemistry, ideally within a pharmaceutical or GMP-regulated environment.
• Knowledge of cGMP, GLP, regulatory requirements and Health & Safety standards.
• Experience operating analytical laboratory instrumentation such as HPLC, FT-IR, UV-Vis, TOC and DSC.
• Project management experience within a laboratory environment.
• Experience working to regulatory standards within the pharmaceutical industry.

Are You?

• A strong communicator and team player.
• A proactive problem solver with a root-cause mindset.
• Highly organised with strong planning skills.
• Able to make sound decisions and exercise good judgement.
• Committed to quality, compliance and integrity.
• Comfortable working in a fast-paced laboratory environment.

If so, we would like to hear from you.

How We’ll Take Care of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.

When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.