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Private Jobs / Private Sector
Teva Pharmaceuticals Hiring for Quality Control Analyst I at Gwalior, India Full Time
Quality Control Analyst I
Date: Apr 5, 2023
Location:
Gwalior, India, 477117
Company: Teva Pharmaceuticals
Job Id: 47054
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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Participation in internal, external, regulatory audits.
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Ensure 100% participation in training’s against CAPA’s.
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Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge.
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Supporting to share required documents from QC to RA/ other requirement.
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Determining team priorities in accordance with the plant’s needs, while coordinating with the teamleader /Manger.
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Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory.
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Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms.
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Perform analytical test according to the monograph and SOP.
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Responsible for calibration and verification of instruments.
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Maintaining of reserved samples room and chambers / autoclaves / incubators.
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Help in preparation of documents related to department (like STP’s, SOP’s and etc.)
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Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis.
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Must be ensured sampled, approved and rejected labels timely as required.
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Responsible to maintain the stock record of chemicals and reconciliation of standards.
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Responsible to maintain safety CAPA.
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Responsible to maintain 5-S in QC.
Qualifications
B.Sc/M.Sc with minimum 4 yrs of experience with API Industry
Function
Quality
Sub Function
Manufacturing Quality Control
Reports To
Mgr 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