Shilpa Biologicals Walk-in Interview 2025.Shilpa Biologicals Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..
Vacancy details:
Important Details :
Job Description: Greeting from Shilpa Biologicals !!!
Key Responsibilities:
1. Quality Management System (QMS) Oversight: Review, track, and manage QMS documents, ensuring timely completion, updates, and closure while maintaining compliance with GMP/GDP standards.
2. Standard Operating Procedures (SOPs): Prepare, review, and approve SOPs, protocols, and reports, as well as manage change controls and related documentation throughout manufacturing and packaging processes.
3. Deviation and Investigation Management: Review deviations and investigations, track corrective actions (CAPA), and manage documentation related to market complaints, including trend analysis and root cause identification.
4. Audit Support: Prepare for and assist in internal, external, and vendor audits, including documentation management, audit report preparation, and addressing observations or non-conformances.
5. Quality Risk Management: Support quality risk management activities, participate in investigations with relevant departments and Subject Matter Experts (SMEs), and contribute to process improvements by identifying opportunities for new procedures or initiatives.
6. Monitoring and Reporting: Monitor GMP/GDP compliance across the facility, prepare QMS trend reports by analyzing quality metric data, and escalate any non-compliance concerns.
Employee Benefits – Medical Insurance, Accidental Insurance, Relocation Allowances, Two Saturday’s Off, Canteen and Transportation Facility.
Interested candidates are invited to send their updated resumes to hrd_bio@shilpabio.com
Join us at Shilpa Biologicals to be a part of a dynamic environment committed to innovation and excellence in the pharmaceutical sector!
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