Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. The group has state-of-the-art vertically integrated manufacturing facilities for APIs and Formulations, spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim.
Job Title – Dy. Manager – Manufacturing Excellence and Investigator
No.of.Openings – 2
Experience – 5 – 10 Years
Location – Panjim/Panaji
Job Description:
A. Manufacturing Excellence (1 Position) :
- Responsible for manufacturing excellence initiatives at plant level.
- Responsible for taking initiatives in improvement of all aspects of working processes and methodologies.
- Predictive analytics improvement of operational parameters like Yield, cycle time, equipment efficiency, Process Cycle Efficiency, CPP trending etc.
- Leading the OEE (Overall Equipment Efficiency) program for the formulation plants to diagnose and identify opportunities to improve OEE.
- Architect for Lean Six Sigma framework.
- Having experience in Process capability Improvement, DMAIC/8D methodology, Statistical analysis and other Operational Excellence tools. Should be acquainted with application like Minitab , Visio and Quality Companion.
- Must have worked in regulated plants having approvals of US FDA, MHRA. etc.
- Hands-on experience in handling and implementing cGMP (Current Good Manufacturing Practice) practices and Good Documentation Practices.
- Technically competent on all aspects of Tablet /capsule manufacturing with FDA approval.
B. Investigator/Trouble shooting (1 Position)
- Relevant experience of IPQA Activities / QMS/
- Assessment of change controls relating to risk management and gap analysis.
- Preparation and review of Failure Investigation Reports against Quality Impacting deviations, Out-of-Specifications and major Non-Conformances.
- Market Complaints and Regulatory Audit observations / Identification of scope for implementation of Preventive Action to mitigate or reduce risk of recurrence in oral solid dosage/ Injectable Manufacturing facilities.
- Must have worked in regulated plants having approvals of US FDA, MHRA. etc.
- Hands-on experience in handling and implementing cGMP (Current Good Manufacturing Practice) practices and Good Documentation Practices.
Desired Profile:
- UG – B.Pharma – Pharmacy
- PG – M.Pharma – Pharmacy