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Compounder - Rotating shifts

Job in Brampton, Ontario, Canada
Listing for: SUN PHARMA
Full Time position
Listed on 2026-10-13
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing
  • Pharmaceutical
    Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 50500 CAD Yearly CAD 50500.00 YEAR
Job Description & How to Apply Below
Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients.

As part of our mission to Reach People and Touch Lives, we deliver Innovative Medicines, Generics and Consumer Healthcare products that improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, we improve access to effective, affordable treatments that promote better health and well-being.

Reaching People. Touching Lives.

Job Purpose
Responsible for the cleaning, setting up and operation of manufacturing equipment as part of the process of compounding pharmaceutical creams, ointments, gels and liquids.

Duties And Responsibilities
Complete G.M.P. documents, such as the Batch Record, cleaning & sanitizing logs, housekeeping logs and other documents / log records pertaining to manufacturing
Follow safety rules/regulations and report any workplace injuries or accidents. Assist when required to improve equipment safety related procedures. Wash and sanitize compounding rooms and vessels
Compounding batches as per SOP’s and Master Formulas. Report discrepancies and deviations in a timely manner to compounding lead hand or supervisor
Dispense raw materials when required
Perform accurate inventory transactions using SAP
Maintain a clean and organized working environment. Familiar with 5S processes and Lean Manufacturing Concepts
Participate and assist with continuous improvement projects and processes
Work safely and accurately with a focus on completing tasks and documentation right first time
Complete all GMP Documentation correctly and in a timely manner
Complete all training assignments and maintain personal training records
Participate in and/or lead Non-Conformance Investigations
Complete Corrective and Preventive Actions (CAPA’s)
Initiate, and follow through with actions required to close Change Controls
Participate in Internal, Customer and Regulatory Audits.
Assist with the training of new compounders
Perform start-up and shutdown procedures for all vessels
Minor repairs to the facility and equipment where applicable
Perform verification checks for equipment (scales, mixers, pH meters) used in manufacturing as per predefined time periods
May be required to assist Validation or Pharmaceutical Technology staff with new formulations and scale ups
May be required to assist with investigations where necessary
Notify compounding lead hand and mechanic in a timely manner if equipment parts and compounding consumables are low in quantity
Other duties as assigned.

Additional Responsibility (Only Applicable To Customer Facing Roles)
Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day

Qualifications
University degree with 1-2 years of technical training experience or equivalent experience.
Post-Secondary education in scientific discipline is preferred or a minimum of 5 years’ experience in a pharmaceutical environment
Must possess the ability to function effectively in a team environment
Must be able to actively listen and receive coaching and applicable training
FL licence preferred
Excellent math skills
Proficient in MS Word, Excel, PowerPoint and Lotus Notes. Must be comfortable with use of tablets and trainable on associated programs (MES, SAP)
Excellent verbal communication skills for interacting with personnel on a daily basis
Previous experience in a pharmaceutical manufacturing environment
Issues that may arise that have a GMP impact are evaluated at the time of occurrence in conjunction with the supervisor and QA.

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