Our Team, Your Impact
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

How We’ll Take Care of You
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. Twist, our one-stop shop for career development platform, gives you access to learning programs, short-term projects and opportunities for internal growth.

Already Working @Teva?
Apply through our internal career site on Twist.

Teva Pharmaceuticals is committed to equal opportunity in employment 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.