Quality Assurance Training, Lead

BIOVECTRA, now a part of Agilent, is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients specializing in clinical-to-commercial scale production for microbial fermentation, synthetic small molecules including ADC, HPAPI, plasmid DNA, mRNA, LNP and sterile filling capabilities. With over 650 employees at both the Windsor, NS and Charlottetown, PEI sites, BIOVECTRA supports over 100 clients, including over 20 top pharma and biotech companies.Agilent is currently searching for a Quality Assurance Training, Lead. This role will focus on designing and implementing quality assurance (QA) training programs that align with safety, regulatory standards, and business goals. It involves enhancing staff competency by identifying skill gaps and creating targeted learning plans. Ensuring training programs align with applicable regulatory requirements including Health Canada GUI-0001, 21 CFR 211.25, ICH Q10, and applicable GMP standardsThe responsibilities will includePartnering with functional areas to conduct ongoing needs analysis, training effectiveness checks, and trend results, as appropriateKnowledge of Health Canada, FDA, and ICH Q10 regulatory expectations for personnel training and qualificationExperience with LMS or equivalent electronic training management systemServing as the primary training system representative during regulatory inspectionsPartnering with global training and quality leadership to ensure alignment of site training practices with enterprise-wide standards and governance frameworksCoordinating training program execution across multiple BioVectra sites (PEI and Windsor)Establishing and maintaining a trainer qualification programPartnering with functional areas to develop training materials and knowledge assessments for area SOP’s review knowledge assessmentsLiaising with functional departments to draft, implement, approve, and revise training materialsFacilitating/Supporting instructor led training courses, including annual cGMP Training, as appropriateThis role has the option of working onsite at our Windsor, NS or Charlottetown, PEI facilityQualificationsRequiredPost-Secondary EducationPrior experience in a GMP-regulated qualityFour years of relevant experience and/or training and management of teams within a biotech or pharmaceutical environmentExceptional facilitation and presentation skillsExperience with Quality systemsDesiredTrain the Trainer CertifiedAPI facility experienceRise Articulate platform knowledgeLMS experienceKnowledge of metrics/trendingAdditional DetailsThis job has a full time weekly schedule.The full-time equivalent pay range for this position is $81,022.00 - $126,596.00/yr CAD plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.Travel Required10% of the TimeShiftDayDurationNo End DateJob FunctionQuality/Regulatory