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Group Leader Quality Control
Date: Aug 9, 2022
Location: Gwalior, IN, 477117
Company: Teva Pharmaceuticals
Who are we?
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
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24 × 7 audit readiness.
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Participation in internal, external, regulatory audits and conducting self- audits.
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Maintaining a set of procedures supporting to the quality control system (GLP and GMP techniques implementation).
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Professional / regulatory training to be arranged for the team as requirement. Ensure 100% participation of desired team in training’s against CAPA’s.
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Maintaining a system of methods and specifications for all materials and products.
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Managing the laboratory teams and determining work priorities. Manpower planning.
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Ensuring the investigation on LIR, OOS, OOT & boarder line results. Involving in the OOS and deviations from QA, Production, warehouse and other like departments. Lab investigations must be closed within time frame.
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Signing on approved column in analytical log books, laboratory control card and in LIMS. Signing on the COA of finished products (hard copies as well as approval in LIMS) in non-availability of Head – QC.
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Handling of customers queries. Supporting to DMF’S wrt required documents from QC.
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Implementing quality system with respect to regulatory, ICH, CGMP, pharmacopeia and ISO requirement.
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Preparation and review of specification of RM/FP/STP/SOP.
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Ensure the maintain and calibration of all QC instruments
Qualifications
MSC/ Bpharm/ BSC with 10+yrs of relevant Experience
Function
Quality
Sub Function
Manufacturing Quality Control
Reports To
Assoc Dir 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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
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
