We are currently looking to fill 4 Quality Control positions for our clients. We have two opportunities in the Greater Toronto Area and two in the Ottawa, Canada area. We do not charge you a fee for connecting you with the companies that are looking to hire. This is an opportunity to get in on the ground floor of a new market in Canada that will explode. The Medical Cannabis market created by the Canadian Government is expected to grow to 1.4 billion in the next ten years, you can be a leader in that market by joining a winning team. You must be able to pass a RCMP security check and be able to work in Canada. Job Title: QA Manager Summary: The position of QA Manager includes, but is not limited to, working cooperatively with the President, the Chief Scientific Officer and other department heads, to ensure compliance with all aspects of GMP regulations as required by Health Canada, the US FDA, and corporate contractual obligations. Responsibilities and Duties: Ensure compliance with GMP regulations as required by Health Canada, the US FDA, or other jurisdictions in order to obtain GMP status (e.g. the Establishment License). Participate in internal GMP and third party Audits. Participate in analytical investigations of out-of-specification, examine results, change control requests when necessary, generate deviation reports, root cause determination, and provide recommendation for corrective actions. Act as authority for all interaction with Health Canada, external agencies and contracts for quality assurance and regulatory compliance related activities and documentation. Act as authority on validation of IQ/OQ/PQ, which include test methods, machines, operation process, cleaning, etc. Act as authority on release, rejection, customer complaint management and potential recall of all products sold by the company; ensure that customers are satisfactorily dealt with in a timely manner. Make decisions on release or rejection of materials based on sound judgment and compliance to regulatory requirements, reports and specifications. Write, review and revise SOPs, quality policies and procedures, customer methods to ensure continuous compliance with GMP and regulatory compliance as well as customer requirements. Review and approve method transfer and validation protocols and reports. Provide assistance and technical support for equipment or process optimization, validation, calibration, qualification or certification. Contact customers and internal departments to respond to their inquiries and resolve QA issues. Handle export and import document applications. Provide GMP and SOP training for staff. As required, coordinate the Safety Unit Officer and the Chief Scientific Officer for staff training on WHMIS. Participate in other tasks that may be assigned by the President & CEO. Qualifications: - Advanced knowledge of GMP and the US FDA regulations for manufacturing/packaging pharmaceutical or nutraceutical products. - Familiarity with the regulatory requirements of foreign jurisdictions would be considered an asset. - Able to work as a team and possess soft skills such as personnel integrity, and interpersonal skills. - Proven ability to supervise personnel and excellent verbal/written communication skills. Please contact Georges at 613-294-2324 or email [email protected]
Posted on: Wed, 16 Jul 2014 19:13:15 +0000
Trending Topics
Recently Viewed Topics
© 2015