Teva Pharmaceuticals Hiring Quality Sr Specialist B.Pharm/M. Pharm Apply Now
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
Qualifications
B.Pharm/M. Pharm 2 to 4 years
Function Quality
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