Quality Assurance Manager

Quality Assurance Manager

1 Nos.
76967
Full Time
10.0 Year(s) To 13.0 Year(s)
8.00 LPA TO 14.00 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
B.Pharma - Pharmacy; M.Pharma - Pharmacy
Job Description:

Role & responsibilities

1. Handling Deviations / Change Control / CAPA / Incidence Reports / Training Records.

2. Handling MFR / BMR / BPR preparation and Review

3. Handling preparation of SOPs / Protocols / QMS.

4. Handling Documentation Control.

5.. Handling of SMF /VMP / Qualification

6. Should be able to handle audit compliance and market complaints as an when required

7.Responsible for the all quality assurance related activities.

8..Monitoring and tracking of QA activities as per defined schedule and company requirements.

9.Preparation of annual training summary report.

10.Review of qualification, validation and calibration records.

11.To perform Cleaning verification / validation as and when required

12. Experience in supporting to RA Dept is an added advantage.

13.Able to handle Art Work Review , Change Control , Deviations , Incidences , Vendor Approval , FAT / SAT , Dispensing activities. Able to lead a team of 04 Persons. Shall be able to prepare protocols of Validations.

 

 



Company Profile

company is a technology driven pharmaceutical company with interest in development, manufacturing & marketing of formulations. Our Client specialize in the manufacturing of general therapeutic & antibiotic drugs in tablets, capsules, oral liquid & dry powder sachets.

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