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Teva Pharmaceutical opening for Quality Senior Specialist 

Teva Pharmaceutical opening for Quality Senior Specialist 

Post : Quality Sr Specialist

Job Description 
• To ensure compliance to GMP systems on shop floor
• To ensure all the master Batch Manufacturing Records (BMR), Batch Packing Records (/BPR) are in compliance with Dossier/Quality procedures
• To review the master BMR/BPR`s
• To review executed batch manufacturing and packing records & perform IPQA activities
• To perform the issuance activity of BMR and BPR
• To perform the spot audits on shop floor
• To participate in resolving of product complaints
• Support in review & execution of qualification/requalification protocols of process equipment/ instruments/ utilities system
• Preparation and training of SOP’s, cGMP, Hygiene
• To ensure compliance to documentation control policy
• To ensure compliance to the requirements of site procedures on Data integrity in GxP data handling
• To prepare and review of Hold time protocols and reports
• To prepare and review of Product Quality Review
• Management of Retention samples

Additional Information
Qualification : B.Pharm/M. pharm
Experience : 2 to 4 years
Location : Goa
Industry Type : Pharma
Functional Area : Quality
End Date : 20th September, 2020

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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