To follow the GMP, Saftey norms and adhere to company policy.
Documents issuance and submission from of all departments.
Master documents handling and its distribution.
Verify the GMP compliance during plant round, if any abnormalities intimate to QA head and respective department Head.
Participate in sampling activities of intermediated and finished goods.
Participate in Dispatch activities of finished goods and intermediates.
Audit preparation and ensure the Audit readiness for regulatory as well as customer audits.
General indent to be done as per requirement.
Handling of QMS documents.
Maintain the doc cell and keep all documents in proper sequence.
Additional responsibilities to be performed when ever assigned by QA head.
Ensuring all the analytical test reports before releasing the batch.
Participate in process validation, cleaning validation and other equipment qualifications.
Attending various training related to Safety, cGMP and On job.
|Experience||2 - 4 Years|
|Salary||2 Lac To 2 Lac 50 Thousand P.A.|
|Industry||Pharma / R&D / Biotech|
|Key Skills||Analytical Chemistry QTP-Quick Test Professional QC - Quality Control Quality Control Quality Control Executive Pharmacy QC chemist QA Pharmaceutical Production Pharmacy|
|Contact Person||SAFFRON CONSULTANCY SERVICES|
|Address||Registered Office :602, Patel Park ,Opposite Tadwadi BRTS stand.|