The JAMP group is a proud Canadian owned company with its international headquarters located in Boucherville, 20 minutes from downtown Montreal, Quebec, Canada. The JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma Generics, Orimed branded products, our Wampole and Laboratoire Suisse natural health supplements and our Cosmetic Import beauty and personal care products. The JAMP Pharma Group has also made a major investment in biosimilars which is one of the fastest growing markets in the pharmaceutical industry.
Post : Senior Executive / Assistant Manager (Quality Assurance - Investigations)
Key Responsibilities
• Initiates investigations as needed, collects data, determines the source of the problem using tools such as the Ishikawa diagram, the “5 whys” and/or the DMAIC approach, performs the risk assessment, determines the CAPAs, concludes the investigation and determines the disposition of the impacted lots.
• Plans and leads meetings with various stakeholders when required.
• Maintains up-to-date monitoring of investigations and CAPAs.
• Ensures that justified extension requests are made before the investigation deadline and that the investigations and CAPAs are closed within the required timeframe.
• Acts as a guardian of metrics by carrying out periodic follow-ups regarding investigations and CAPAs opened with internal and external partners.
• Develops and maintains key performance indicators (KPIs) for the investigations and CAPA sector to monitor their effectiveness and compliance.
• Ensures compliance across multiple stages, including compliance with the various stages of investigations and CAPAs, in accordance with applicable SOPs.
• Provides support for internal and regulatory inspections, as needed.
• Collaborates closely with other departments to understand, expedite, and quickly finalize investigations.
• Reviews proofs for drug submissions (Drug Identification Number - DIN), natural health product launches (Natural Product Number - NPN) intended for the
• Canadian market as well as for commercial products in accordance with regulatory requirements. Initiates and evaluates change controls as needed.
• Advises stakeholders on requirements related to printed materials and actively participates in resolving issues related to printed product materials.
• Collaborates closely with the Regulatory Affairs department. Promotes Good Manufacturing Practices (GMP).
Additional Information
Department : Quality Assurance - Investigations
Experience : 4 - 8 years
Qualification : B.Pharma / M.Pharma
Location : Ahmedabad
End Date : 5th May 2025
Send profile at sjani@jamppharma.com or Apply Online
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