Job as Executive – Quality Control in Pfizer

Founded in 1849, Pfizer is the world’s premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.

Post: Executive –  Quality Control

Job Description:
The Incumbent as a member of the Quality Control Team is responsible for sampling, analysis, Testing, line clearance, release, related documentation and other related Quality Control functions in respect of RM/PM/Finished goods/ in process /Validation and stability samples.
Job Responsibilities
1. To sample the Incoming RM/Packaging material.
2. To conduct analysis and testing of RM/PM/FG/actives and intermediates with the help of analytical instruments and techniques.
3. To calibrates/verifies analytical instruments/balances
4. To Trouble shots analytical instruments
5. To coordinates and follows up with engineering dept for timely availability of their services to attend breakdowns. Interruptions and scheduling of maintenance.
6. To inspect Packaging lines and issues Line clearances
7. To review and update raw material and packaging material specifications
8. To prepare testing specifications.
9. To prepare, review and update working standards.
10. To maintain calibration records of instruments.
11. To prepare trend analysis of finished products.
12. To generates PR for the Consumables/glass wares /chemicals and other laboratory aids /spares required for the dept.
13. To perform Chemical assays and standardizations of reagents.
14. To prepare SOPs, reviews for biannual review. Prepare Training outlines.
15. To maintain and control inventory of Reagents. Chemicals/glass wares.
16. To conduct stability studies of reagents.
17. Prepares analytical reports and certificates of analysis.
18. To investigate laboratory errors/LIRs
19. To validate instruments, equipments, processes, analytical methods.
20. To prepare and evaluate stability data
21. To prepare stability protocols
22. To validates stability indicating methods

Candidate Profile:
Education: BSc Chemistry / Msc Chemistry
Experience: 3 to 7 years of experience in Quality Control Department of a solid dosage forms manufacturing pharmaceutical company.
ALL INTERNAL CANDIDATES MUST HAVE AN APPROVAL FROM THIER MANAGER, PRIOR TO APPLICATION.

Additional Information:
Experience: 3-7 Years
Location: Goa
Education: B.Sc, M.Sc
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area: QC
Job ID: 969331

LAST DATE: 17th Aug, 2012

TO APPLY CLICK HERE AND PUT JOB ID. AND SELECT REGION: ASIA PACIFIC; COUNTRY: INDIA;

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