Explore career opportunities at Shivalik Rasayan Limited.
Current Openings
Responsible for batch manufacturing, documentation, and cGMP compliance in API production.
Job Description
Execute production batches as per approved batch manufacturing records.
Maintain cGMP documentation and ensure safety compliance.
Coordinate with QA and engineering for smooth plant operations.
Maintain cGMP documentation and ensure safety compliance.
Coordinate with QA and engineering for smooth plant operations.
Requirements
B.Sc/M.Sc in Chemistry or related field.
Experience in API or pharmaceutical manufacturing.
Good knowledge of cGMP and plant SOPs.
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Experience in API or pharmaceutical manufacturing.
Good knowledge of cGMP and plant SOPs.
Support QA systems, audits, batch record review, and regulatory compliance activities.
Job Description
Review batch manufacturing and analytical records.
Support internal and external audits.
Assist in CAPA, change control, and deviation management.
Support internal and external audits.
Assist in CAPA, change control, and deviation management.
Requirements
B.Pharm/M.Sc with QA experience in pharma/API industry.
Knowledge of USFDA/EU GMP requirements.
Strong documentation and communication skills.
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Knowledge of USFDA/EU GMP requirements.
Strong documentation and communication skills.