Analytical Analyst (Strathroy)

Position Summary Work Schedule: Monday-Friday 8:00 AM – 4:30 PM; potential to transition to 12‑hour shifts in the future. This position is 100% on‑site at the Adair site. The newly launched manufacturing facility on Adair Blvd marks a pivotal expansion of Catalent’s Zydis® technology, a globally renowned fast‑dissolve oral dosage form that has transformed the lives of millions of patients worldwide. This is your opportunity to join a dedicated team at the forefront of pharmaceutical manufacturing. At Adair, you’ll play a vital role in the startup of a site built for innovation and excellence, from installation and qualification to regulatory approval and commercial manufacturing. Reporting to the Quality Control Supervisor, the Analytical Analyst is responsible for coordinating and performing laboratory activities/projects including analysis of raw materials, finished product, and stability samples using instrumental and wet chemistry methods. The Role Perform Finished Product QC release testing and testing of raw materials using techniques such as balances, pH meter, UV, Karl Fisher, FT‑IR, TLS, dissolution, HPLC (including degradation analysis), and coulometric Karl Fisher; troubleshoot basic instrumentation issues. Calibrate and maintain instruments according to relevant SOPs; maintain adequate levels of laboratory supplies. Maintain laboratory setting in a safe and clean manner: laboratory/equipment cleaning, glassware washing, storing of supplies, etc. Train, advise, and assist laboratory personnel as required (methods, procedures, tests, etc.). Work extended hours, weekends as needed, especially when problems occur or deadlines must be met. Consistently perform all tasks with a safety‑first mindset by following established policies and procedures, applying the STAR (Stop, Think, Assess, Respond) method, and ensuring full compliance with Environmental, Health, and Safety regulations while proactively leading safety improvements. Carry out work in a manner that protects the environment and supports Catalent’s environmental policies and sustainability goals. Perform other duties as required. The Candidate Bachelor’s degree in science, chemistry, or related field is required. 2+ years of experience as a lab analyst is preferred; experience working in a pharmaceutical and/or GMP facility is preferred. Formal laboratory investigation report writing, validation report writing, and experience with Empower software. Strong analytical and problem‑solving skills to identify and resolve quality issues, optimize quality systems and processes, and drive continuous improvement. Candidates with non‑Canadian credentials must provide an evaluation confirming the Canadian equivalency of the credentials as determined by the Alliance of Credential Evaluation Services of Canada (ACESC). This position does not qualify for sponsorship. While performing job duties, the employee must communicate effectively, sit for extended periods, use manual dexterity to operate a computer and office equipment; occasional standing, walking, reaching, bending, stooping, kneeling, or crouching may be required. Close vision is required. The role may involve exposure to hazardous chemicals; employees are expected to follow all applicable safety procedures. Pay Salary range: $49,000 – $60,000. Final salary offered will depend on factors such as experience, industry background, skill set, education, and business needs. Benefits Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance) Group Retirement Savings – Registered Pension Plan (RPP) with employer contributions Paid Time Off Programs Opportunities for professional and personal development & growth, including tuition reimbursement Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law. #J-18808-Ljbffr Apply on Kit Job: kitjob.ca/job/2oya1l