Asst Manager - Documentation(Investigations) - Production- API - Bidar
SAI Life Sciences · Bidar · onsite · Posted 37d ago
Undisclosed8–13 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
- Drafting and Review of Investigation Reports in co-ordination with cross functional departments like Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D, QC and AR&D etc.
- Preparation of Quality Risk Assessment and its Impact Assessment Reports as or when required.
- Handling of documents related to Quality Management System (QMS) like Change controls, Deviations, Planned changes, CAPAs etc., as per requirement in co-ordination with cross functional departments like Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D, QC, AR&D etc.
- Follow the cGMP compliance by following the SOPs and approved procedures.
- Responsible for any activities assigned by HOD or Senior Management.
Sourced from naukri
Skills
ootAPI ManufacturingoosBulk DrugsInvestigationQMSproductionDocumentation
About SAI Life Sciences
SAI Life Sciences
Clinical Research
3.8k+
employees
1999
27 years old
Hyderabad
India
About
SAI Life Sciences collaborates with pharmaceutical and biotech firms to expedite the development and manufacturing of complex molecules in the healthcare industry.
Industries
Clinical ResearchBiotech & Life sciences
Employee ratings
1,496 reviews
3.9/ 5
Culture
3.7
Career growth
3.2
Work-life
3.7
Employees rate it well for
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