SUN PHARMA
Location
Vadodara | India
Job description
JOB RESPONSIBILITIES
: Person should have Strong understanding of GMP requirements, exposure to Regulatory Inspection, and knowledge of international GMP requirements Person should have experience in investigations related to complaint, product rejection, non-conformances, recalls, deviations, audits, regulatory inspections, QC etc. Person should have handled change management, quality risk management and Corrective Action and Preventive Action System throughout the Product Lifecycle Person should have experience in implementation and maintenance of effective QMS Essential Job Functions: · Establish road map for the remediation activities · Assure timely resolution of issues/risks on remediation projects · Facilitate preparation for Executive Steering Committee reviews · Identify and list key activities for implementation, assign activity owners and target completion dates · Act as the point of contact and communicate remediation status adequately to all team members · Review the completed remediation actions for their adequacy and ensure it meets the agreed commitment · Ensuring that key stakeholders are informed on relevant risks and implementing remediation plans · Candidate needs to be dynamic with good communication and leadership qualities · Performs all work in line with Sun Pharma values of Humility, Integrity, Passion and Innovation. Performs all work in accordance with all established regulatory and compliance and safety requirement Educational Qualification : M.Sc / B.Pharm / M.Pharm Location : Baroda Experience : 15 to 20 YrsJob tags
Salary
