Titan Laboratories Job Openings for QA - Documentation / Validations
Officer to Executive -QA Documentation, Validation- Mahad(Male)
Experience: 1 to 6 yrs
Job Location: Mahad
No. of Openings: 16
Qualification: B.Pharm
Job description:
To ensure cGMP compliance with regulatory and QMS requirements.
Preparation and Review of Annual Product Quality Review.
Handling of Deviation in Track wise including Preparation, Review and Compliance of deviation
investigation Report as well as completion of deviation flow in Track wise.
Review and active participation in investigation of Market Complaints in area of operation.
To Perform and Monitoring IPQA Activities in Various area of operation in Solid Oral Dosage form.
To Perform Sampling In-Process, Finished Product for Exhibit, Validation and commercial Product.
To Review and compliance of Batch Manufacturing Record and Batch Packaging for Commercial and
Exhibit batches.
To Perform Calibration of Various IPQA instrument and review of Calibration Record.
Handling of Team and to impart training to team members related to SOP in area of operation.
To ensure updation of area as per audit agenda and keep team up to date as per audit agenda.
Statistical Evaluation and Continuous Process Verification (CPV) of Products using Minitab.
Preparation and Review of Risk Assessment for continuous process verification for all new product and
legacy products.
Initial Assessment, Review and Trending of oversight observation in Area of Operation.
Kindly send your resumes on recruitment@titanpharma.com & jyoti.g@titanpharma.com
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