Biologics Research Laboratory Quality Assurance

Role Overview: As an Officer / Executive / Sr. Executive in the Biologics Research Laboratory Quality Assurance at Nerul (Navi Mumbai), your primary responsibility will be to ensure the quality and compliance of processes in the biotechnology, biochemistry, microbiology, chemistry, and pharmacy domains. You will be expected to validate processes such as fermentation and purification using chromatography techniques, conduct line clearances, manage document issuance and retrievals, monitor in-process quality assurance, report deviations and non-compliances, review batch records and clean utilities, coordinate internal audits, perform cleaning validations, CIP and SIP validations, handle failure investigations, review in-process data, and qualify process equipment. Key Responsibilities: - Validate processes like fermentation and purification using chromatography techniques - Conduct line clearances, issuance, and retrievals of documents - Monitor IPQA of processes and report deviations and non-compliances - Review batch records, clean utilities, and coordinate internal audits - Perform cleaning validations, CIP, and SIP validations - Conduct failure investigations, review in-process data, and qualify process equipment Qualifications Required: - Graduate or Post Graduate in Biotechnology, Biochemistry, Microbiology, Chemistry, or Pharmacy - Experience of at least 2 years in a similar role - Knowledge of GMP standards Please send your resumes to kajal.bhanushali@usv.in if you are interested in this opportunity. Role Overview: As an Officer / Executive / Sr. Executive in the Biologics Research Laboratory Quality Assurance at Nerul (Navi Mumbai), your primary responsibility will be to ensure the quality and compliance of processes in the biotechnology, biochemistry, microbiology, chemistry, and pharmacy domains. You will be expected to validate processes such as fermentation and purification using chromatography techniques, conduct line clearances, manage document issuance and retrievals, monitor in-process quality assurance, report deviations and non-compliances, review batch records and clean utilities, coordinate internal audits, perform cleaning validations, CIP and SIP validations, handle failure investigations, review in-process data, and qualify process equipment. Key Responsibilities: - Validate processes like fermentation and purification using chromatography techniques - Conduct line clearances, issuance, and retrievals of documents - Monitor IPQA of processes and report deviations and non-compliances - Review batch records, clean utilities, and coordinate internal audits - Perform cleaning validations, CIP, and SIP validations - Conduct failure investigations, review in-process data, and qualify process equipment Qualifications Required: - Graduate or Post Graduate in Biotechnology, Biochemistry, Microbiology, Chemistry, or Pharmacy - Experience of at least 2 years in a similar role - Knowledge of GMP standards Please send your resumes to kajal.bhanushali@usv.in if you are interested in this opportunity.