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Compounder

Job in Brampton, Ontario, Canada
Listing for: Sun Pharmaceutical Industries, Inc.
Full Time position
Listed on 2026-08-20
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 51000 CAD Yearly CAD 51000.00 YEAR
Job Description & How to Apply Below
Driven by abold pursuit of science and fueled byan 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, weimprove 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

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.

Working conditions

Overtime will be required to address priority items. This may be additional time during the work week and / or on weekends with last minute notice

Shift work required which may include weekends

Use of G.M.P garments and Safety Equipment (PPE) as required

Physical requirements

Physically fit, able to lift at least 25 kgs

Stand for long periods of time

Bending and  squatting  throughout the work day

Direct reports
NA

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