Work Location: 3505 Laird Road Mississauga
Department: Manufacturing
Reports to: Pharmaceutical Solution Manufacturing Supervisor
Work Model: On-site
Status: Permanent Full-time
Closing date: December 17 2025
Duties and Responsibilities:
- Operate aseptic filling equipment to ensure accurate and sterile filling of products.
- Perform routine cleaning and sanitization of equipment and work area to maintain a cleanroom environment.
- Conduct in-process checks and environmental monitoring.
- Troubleshoot and resolve technical issues with aseptic filling equipment.
- Record and maintain accurate documentation of the production process including batch records and logbooks.
- Follow safety protocols to prevent contamination and ensure the safety of all personnel in the aseptic environment
- Assist with inventory managements / vendor relations / order placements.
- Perform process troubleshooting and root cause analysis specific to buffer solution manufacturing and aseptic filling addressing deviations and ensuring continuous improvement.
- Participate in validation and qualification activities for manufacturing processes equipment and facilities in accordance with regulatory requirements and company guidelines.
- Assist in developing and execution of validation protocols including Installation Qualification (IQ) Operational Qualification (OQ) and Performance Qualification (PQ).
- Identify opportunities for process optimization innovation and cost reduction.
- Must be able to work in a sterile controlled cleanroom environment.
- Performs all other job-related duties as assigned.
Qualifications :
- Undergraduate degree in chemical process engineering pharmaceutical Sciences Microbiology Biotechnology chemistry biochemistry or related field.
- Minimum of 2-3 years of experience in aseptic filling sterile manufacturing or a related role in a laboratory or pharmaceutical manufacturing.
- Experience with cleanroom gowning and aseptic techniques.
- Strong interpersonal and communication skills with the ability to work independently and collaborate effectively with cross functional teams.
- Excellent analytical and problem-solving skills with a keen attention to detail.
- Knowledge of aseptic processing GMP and regulatory compliance (FDA EMA).
- Proficiency in statistical analysis and experimental design (e.g. Design of Experiments) is beneficial but not mandatory.
- Ability to work in a sterile controlled cleanroom environment. Comfortable with standing for extended periods.
- Ability to lift and carry materials up to 20 lbs and handle sensitive equipment.
Remote Work :
No
Employment Type :
Full-time
Work Location: 3505 Laird Road MississaugaDepartment: ManufacturingReports to: Pharmaceutical Solution Manufacturing SupervisorWork Model: On-siteStatus: Permanent Full-timeClosing date: December 17 2025Duties and Responsibilities: Operate aseptic filling equipment to ensure accurate and sterile fil...
Work Location: 3505 Laird Road Mississauga
Department: Manufacturing
Reports to: Pharmaceutical Solution Manufacturing Supervisor
Work Model: On-site
Status: Permanent Full-time
Closing date: December 17 2025
Duties and Responsibilities:
- Operate aseptic filling equipment to ensure accurate and sterile filling of products.
- Perform routine cleaning and sanitization of equipment and work area to maintain a cleanroom environment.
- Conduct in-process checks and environmental monitoring.
- Troubleshoot and resolve technical issues with aseptic filling equipment.
- Record and maintain accurate documentation of the production process including batch records and logbooks.
- Follow safety protocols to prevent contamination and ensure the safety of all personnel in the aseptic environment
- Assist with inventory managements / vendor relations / order placements.
- Perform process troubleshooting and root cause analysis specific to buffer solution manufacturing and aseptic filling addressing deviations and ensuring continuous improvement.
- Participate in validation and qualification activities for manufacturing processes equipment and facilities in accordance with regulatory requirements and company guidelines.
- Assist in developing and execution of validation protocols including Installation Qualification (IQ) Operational Qualification (OQ) and Performance Qualification (PQ).
- Identify opportunities for process optimization innovation and cost reduction.
- Must be able to work in a sterile controlled cleanroom environment.
- Performs all other job-related duties as assigned.
Qualifications :
- Undergraduate degree in chemical process engineering pharmaceutical Sciences Microbiology Biotechnology chemistry biochemistry or related field.
- Minimum of 2-3 years of experience in aseptic filling sterile manufacturing or a related role in a laboratory or pharmaceutical manufacturing.
- Experience with cleanroom gowning and aseptic techniques.
- Strong interpersonal and communication skills with the ability to work independently and collaborate effectively with cross functional teams.
- Excellent analytical and problem-solving skills with a keen attention to detail.
- Knowledge of aseptic processing GMP and regulatory compliance (FDA EMA).
- Proficiency in statistical analysis and experimental design (e.g. Design of Experiments) is beneficial but not mandatory.
- Ability to work in a sterile controlled cleanroom environment. Comfortable with standing for extended periods.
- Ability to lift and carry materials up to 20 lbs and handle sensitive equipment.
Remote Work :
No
Employment Type :
Full-time
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