We Are Teva
Our Team, Your Impact
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
Already Working @Teva?
Teva’s Equal Employment Opportunity Commitment
Senior Chemistry Analyst employer: Teva Pharmaceutical
At Teva, we pride ourselves on being a leading biopharmaceutical company that fosters a high-performing and inclusive culture. As an Associate Director – Category Manager Devices, you will enjoy generous benefits, flexible working arrangements, and ample opportunities for career development through our Twist platform, all while contributing to meaningful health solutions worldwide. Join us in a collaborative environment where your expertise will drive impactful procurement strategies and enhance supplier relationships.