Pharma Compounder: GMP Manufacturing Technician

Sun Pharmaceutical Industries, Inc.

Brampton

Hybrid

CAD 51,000 - 63,000

Full time

14 days+

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Benefits offered by this job

Medical coverage

Dental and vision

RRSP savings plan

Paid time off

Job summary

Sun Pharmaceuticals Industries, Inc. in Brampton, Canada seeks an on-site compounder to operate and set up manufacturing equipment for creams, ointments, gels, and liquids. You will complete GMP documents, maintain records, and ensure safe, accurate production with SAP/MES support.

The role requires 1–2 years of technical training or pharma experience, strong teamwork, and good communication. Overtime, weekend shifts, and PPE use are expected; base pay ranges from CAD 50.5k to CAD 63k with bonus

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
Excellent verbal communication skills for interacting with personnel on a daily basis
FL licence preferred
Proficient in MS Word, Excel, PowerPoint and Lotus Notes. Must be comfortable with use of tablets and trainable on MES, SAP

Responsibilities

Complete GMP 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.