• Full Time
  • Windsor

Pancap Pharma

Pancap Pharma Inc. is a leader in specialty contract manufacturing of pharmaceutical dosage forms. The company began its contract manufacturing operations in January of 1994 and since then has translated experience into quality production for a wide range of clients. We are currently opening a new facility in Windsor, Ontario. From concept to full package delivery, we have the experience and commitment to meet the needs of even the most unique clients. We offer a wide range of manufacturing and support capabilities including capsule fabrication, compounding of non-sterile liquids, packaging, labelling, regulatory affairs, testing and quality assurance. The products we manufacture are then shipped around the world. Quality is the cornerstone upon which Pancap has built its foundation. Our Quality Assurance System was developed in order to ensure the production of safe and effective products in compliance with the current Good Manufacturing Practice (cGMP) regulations, industry standards and our client’s specifications/marketing requirements. Candidate should possess a high degree of initiative and is a team player with excellent communication abilities. You are comfortable in a pharmaceutical manufacturing environment while your attention to detail, comprehensive understanding of GMP, GLP guidelines and strong organizational skills with the ability to drive projects to completion. Primary Duties & Responsibilities: Manage the GMP Documentation, Change Controls, OVR, OOS, OAL, MVR CAPA Management manages/tracks site CAPA program and ensures all departments are meeting obligations for CAPA based on deviation, complaints, audits, change controls SOP Management oversees site GMP related SOPs and ensures that they are meeting current corporate and regulatory requirements Complaints Provides QA support for complaint investigation Manage the preparation/review and day to day activities of the APR (Annual Product Review) Activities Monitors and Reviews Facility Purified Water, Air Flows and Environmental Reports Audits & Trends PM (Preventative Maintenance) Program Maintenance of Quality Agreements with Suppliers, Customers, Contractors Participate in Client Audits and Regulatory Inspections Responsible for monitoring and timely requisition of laboratory supplies Perform other duties as assigned Manage calibration and maintenance of data loggers system EXPERIENCE AND QUALIFICATIONS: University/College Degree in Science 2-5 years Quality Assurance Experience in a Pharmaceutical environment Technical writing in a Pharmaceutical Industry is an asset Knowledge of laboratory testing equipment such as UV, IR, Titrators would be an asset Advanced word processing skills in Microsoft Word, Excel, PowerPoint Excellent oral and written English communication skills Deadline oriented with a flexibility to work in a multitasking environment Pancap Pharma would like to thank everyone for their interest; however, only qualified candidates will be contacted. Job Type: Full-time Schedule: 8 hour shift Work remotely: No

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