Cipla Hiring for Junior Team Member - QC

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Cipla Hiring Junior Team Member QC Rangpo Sikkim QC documentation specifications SOPs policy operating documents predefined quality parameters pharmacopeia cGMP.

Cipla – Junior Team Member QC

Company: Cipla | Role: Junior Team Member QC | Location: Rangpo Sikkim | Experience: 1-3 years QC pharmaceutical organization regulatory standards compliance
Job Purpose: Prepare update review specifications SOPs policy operating documents analysis materials alignment quality parameters compliance standards pharmacopeia cGMP requirements
Key Accountability 1: Prepare SOPs specifications non-routine documentation timely availability support analysis Prepare revise corporate SOPs general analytical methods coordinating site QC QA Review applicable pharmacopeia guidelines updates Review instrument calibration data w.r.t operating documents
Key Accountability 2: Review latest pharmacopeial updates supplements amendments evaluating updates required document compliance current pharmacopeia consent regulatory Review new revised monograph current pharmacopeia Review latest updates monitor timely implementation avoid non-conformances Intimate stakeholders initiate complete activities before effective date pharmacopeia Escalate non-conformances timely avoid delays operation
Key Accountability 3: Document all activities valid procedure online standard approved formats correct accurate authentic Maintain system integrity updating documentations deviations CipDox Maintain online documentation timely entries supporting documents Prepare new documents update existing GMP requirement
Key Accountability 4: Issue documents applicable units maintaining record issuance record bound book current version available unit Issue applicable bound books units maintaining log current format available record data entries Maintain correct updated record issuance documents bound books
Key Accountability 5: Execute harmonization simplification process documents reduce complexities standardized procedures Evaluate prepare documents standardization across all units site Coordinate CFTs check requirements existing procedures simplify process Provide suggestions ideas exploring new possibilities work simplification
Dimensions: Units supported 4 Avg documentation per months 10 Achieve finalization NLT 80% documents within timeline 100% implementation pharmacopoeial updation after supporting data
Interactions: CDC QC QA RA approval documents Daily ADL R&D data deficiency response IPD new projects
Apply Online: https://careers.cipla.com/job/Rangpo-Junior-Team-Member-QC-Sikk/1366211466/