Senior Chemistry Analyst

Teva Pharmaceuticals ,
Runcorn, Cheshire
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Senior Chemistry Analyst Date: Jun 2, 2020 Location: Runcorn, GB, WA7 3FA Company: Teva Pharmaceuticals Company Info Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth! Job Description We are recruiting a Senior Chemistry Analyst on a Full Time, Permanent basis to carry out Material and Product analysis and to supply quality products to the customer on time and in full. Key Responsibilities: + To test and analyse components/raw materials/bulk/CIP samples/water systems and finished product using the correct procedures in compliance with cGLP, cGMP, Health and + safety, SOPs and environmental and regulatory requirements. + To deliver high customer service level to customers by testing components/raw materials/bulk and finished product in an efficient and timely manner. + To process, maintain and archive all QC documentation, right first time, i.e. correct and in full, in order to achieve customer service and GMP. + To establish performance/development goals. Maintain training records accurately ensuring compliance with regulatory and business standards. + To monitor and purchase laboratory consumables ensuring availability for timely testing of all samples. + To ensure performance of instrument maintenance and calibration checks. + To assist with the method transfer process ensuring timely completion in line with manufacturing plans. + To assist with qualification studies on existing and new methods. Knowledge, Skills and Experience + Pharmaceutical experience operating to regulatory standards is desirable. + Good knowledge of Laboratory instrumentation (such as FT-IR, UV-Vis, HPLC, TOC and DSC). + A good communicator and team worker with the ability to deliver high performance standards relating to Quality, Safety, cost and customer service. + Attention to detail Qualifications + Degree within a relevant science discipline. Function Quality Sub Function Manufacturing Quality Control Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. 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. EOE including disability/veteran

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