QA Manager - Canada - Jobs in Mispec

Job Description

Experiencing together a unique human adventureAnimal health is key to the health of the planet. Working at Virbac means taking part in a unique human adventure in which the engagement of each individual contributes to its evolution. Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between managers and employees are as many perspectives of motivation for our teams. We also offer them a work environment conducive to exploring new territories and balancing their professional and personal lives. Finally, fostering their engagement to animal health also means listening to them and helping them to acquire new skills, preparing them for the challenges of tomorrow and encouraging them to contribute to an ever more responsible approach to our business.Area of responsibility 1: Ensure Quality Systems are managed and sustained.Main activitiesThis position is directly responsible for leading all Quality Assurance functions for Virbac Canada.This person shall develop and sustain the functional Quality Assurance systems processes structure, including electronic systems managing documents, change controls, CAPA, deviations, APQRs, stability review, training, recalls, product release, and internal and external audits, to ensure ongoing GMP compliance is maintained.This position is a working manager position that will be required to be actively engaged in problem solving, daily executions and project management.Identifies and presents evidence of quality and compliance risks to Virbac North America QA Management and General Manager of Canada as they appear.Expected results: Defined QA operating structure to ensure oversight of all assigned responsibilitiesArea of responsibility 2: Develop and managed the product and material disposition and release systemMain activitiesQualified Person designee performing batch release.Develop and sustain a GMP system with Quality review of all finished good releases.Perform Quality Assurance activities relating to Third Party Manufacturing / WarehousingExpected results: A functioning disposition system supported by SOPs and personnel that meets all regulatory requirementsArea of responsibility 3: Regulatory Compliance and InspectionsMain activitiesResponsible for leading and achieving successful outcomes of Health Canada inspections, inspections by other GMP regulatory authorities, and GMP customer audits.Maintain a current knowledge of applicable governmental regulations and their application to similar industries.Provide required documentation to support regulatory body requests (inspection responses, incomplete letters, review questions and investigation progress).Expected results: Successful outcomes of inspections and auditsArea of responsibility 4: PerformanceMain activitiesUnderstand all internal/external audit findings and industry trends and apply improvements as necessary at the manufacturing facility to facilitate continual improvement and sustainable systems in GMPs.Review and manage QA operations to look for opportunities for improving throughput and efficiencies positively impacting product release timing. Use data to look for areas of improvement.A thorough understanding of the gaps within the operational system and define steps for improvementFocus on standardizing all operations in the interest of improving the operating compliance and performance standards.Expected results: The Quality Assurance group contributes effectively to the goals of Virbac CanadaArea of responsibility 5: Team ManagementMain activitiesManage activities of direct reports by that fulfill the group #39;s roles, and provides both primary and secondary responsibilities for all activitiesCreating individual development programs based on individual needsWorking collaboratively with all internal/external business partners and key stakeholders to assess project deliverables or project challenges to provide input on solutions utilizing strong interpersonal, influencing, and negotiating skills.Expected results: Ensures project objectives are communicated to proper levels of the organization. Additionally ensure all escalated issues are resolved to ensure timely completion of the project. Create formal documented development program for direct reportsRequirements (Diploma and experience)Must hold a Canadian University degree, or a degree recognized as equivalent by the Canadian accreditation body, in a science related field. Bachelor #39;s degree in Biology, Chemistry, Engineering or related field and experienceGenerally 7+ years pharmaceutical quality, with a preference for Veterinary Pharma experience and 12+ years in the pharmaceutical industryMust meet the requirements for being the Senior Person in Charge (SPIC) and/or Responsible Person in Charge (RPIC) per Health Canada #39;s Precursor Control Regulations.SkillsDemonstrated skill in effective team building, communicating with other departments, customers, employees at all levels of the organization.Demonstrated ability to manage projects and influence individuals outside of reporting structure.Demonstrated experience in managing peopleVirbac provides numerous career opportunities, thanks to the diversity of its jobs and their international dimension.Joining Virbac means joining dynamic teams ambitious for success.Add Your Talent to Ours!