Senior Chemistry Analyst: GMP Quality & Analytics Leader

Teva Pharmaceutical; Runcorn; On-site; GBP 42,000 - 52,000; Full time

Job summary

Teva is seeking a Senior Chemistry Analyst to provide technical expertise in the Quality department and to support material and product analysis to ensure timely, compliant delivery of high-quality medicines.

You will help maintain robust documentation, SOPs and quality processes while supporting the QC team and cross‑department collaboration in a fast-paced pharmaceutical environment in the United Kingdom.

Qualifications

• 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.

Responsibilities

• Review documentation and testing data for components, raw materials, bulk product, CIP samples, water systems, and finished product using 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 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.

Skills

Degree in Chemistry

Analytical chemistry experience

cGMP/GLP knowledge

HPLC

FT-IR

UV-Vis

TOC

DSC

Project management

Regulatory compliance

Education

BSc in Chemistry

Tools

HPLC

FT-IR

UV-Vis

TOC

DSC

Job description

Teva is seeking a Senior Chemistry Analyst to provide technical expertise in the Quality department and to support material and product analysis to ensure timely, compliant delivery of high-quality medicines.

You will help maintain robust documentation, SOPs and quality processes while supporting the QC team and cross‑department collaboration in a fast-paced pharmaceutical environment in the United Kingdom.