{"id":4322356,"url":"https://alion.io/job/catalent-quality-assurance-supervisor-2","title":"Quality Assurance Supervisor","company":{"id":1785256,"name":"Catalent","domain":"catalent.com","url":"https://alion.io/company/catalent-com","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":null},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Strathroy, Canada"],"countries":["CA"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":65000,"max":81000,"currency":"CAD","period":"year","gross":null,"usd_annual":56791},"salary_estimate":null,"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-10-26T00:00:00Z","employer_posted_date":"2026-10-26","last_verified_at":"2026-11-14T21:03:54Z","board_verified":true,"closed_at":null,"days_open":19,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":19},"description":"Quality Assurance Supervisor\nAbout Site\nStrathroy, Ontario is one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries. We have a broad range of integrated formulation, manufacturing, analytical and packaging services to offer full-service turnkey solutions.\nPosition Summary\nWe have an opportunity for a Quality Assurance Supervisor to join our team. In this role, you will oversee daily priorities for the Quality Assurance team and ensure compliance with cGMP standards throughout the production process. You will be responsible for quality assurance activities, batch release, and maintaining archiving programs. This position plays a key role in supporting quality systems and continuous improvement initiatives.\nShift: Monday -Friday, 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch\nLocation: Strathroy, ON\n100% Onsite\nThe Role\nCommunicate daily work plans and priorities with the Quality team to meet product release timelines and expectations.\n\nCollaborate with functional areas to resolve quality issues and ensure product compliance with cGMP, SOPs, and standards.\n\nLead, coordinate, and participate in investigations and corrective actions for deviations and documentation issues, ensuring timely closure.\n\nWork closely with operations to support the quality management system and provide guidance on cGMP and SOP compliance during production and packaging.\n\nEnsure all manufacturing batch documents for finished products are properly maintained and controlled.\n\nReview and approve quality documents, including Master Batch Production Records, specifications, directives, reports, and SOPs.\n\nLiaise with customer QA contacts regarding quality issues and agreements.\n\nProvide leadership, motivation, and training for employees, monitoring performance in line with company policies.\n\nPerform other duties as required.\n\nThe Candidate\nMinimum Requirements\nBachelor’s degree in science, engineering (chemistry, biochemistry), or a related field required.\n\n3+ years of experience in QA/QC or a related field required., with at least 1 year of supervisory experience preferred.\n\nWhile performing the responsibilities of the job, the employee is required to talk and hear. The employee is often required to sit and use their hands and fingers to handle or feel and to manipulate keys on a keyboard. Use of manual dexterity is required. The employee is occasionally required to stand, walk, reach with arms and hands, bend or twist, and to stoop, kneel, crouch or crawl. Vision abilities required by this job include close vision. There is also the potential exposure to chemicals.\n\nDemonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.\n\nPreferred Skills & Background\nExperience working in manufacturing, pharmaceutical, and/or GMP facilities preferred.\n\nUnderstanding of overall business needs and objectives.\n\nExpertise in tools to meet current and advancing cGMP requirements.\n\nExcellent verbal and written communication skills.\n\nAbility to multi-task and prioritize effectively.\n\nAbility to respond quickly to a changing regulatory environment.\n\nCandidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency as determined by the Alliance of Credential Evaluation Services of Canada (ACESC) such as WES.\n\nCurrently, Catalent participates in the Ontario Immigrant Nominee Program (OINP) on a limited basis.\n\nPay\nThe final salary offered to a successful candidate may vary within this range $65,000 - $81,000, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a global employer, and this salary range does not reflect positions that work in other countries.\nWhy You Should Join Catalent\nComprehensive benefit package including health, dental, vision, and life insurance.\n\nGroup retirement savings with employer contributions.\n\nEmployee reward and recognition programs.\n\nOpportunities for professional and personal development, including tuition reimbursement.\n\nCatalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.\npersonal initiative. dynamic pace. meaningful work.\nVisit Catalent Careers to explore career opportunities.\nCatalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.\nIf you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.\nNotice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. 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