Coordinator, Sterile Validation
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- Richmond Hill, ON
- 65.790-87.720 $ par an
- Permanent
- Temps-plein
- Ensure all sterile validation activities are performed in compliance with corporate policies, FDA, HPFBI, EC, and ICH's guidelines including but not limited to the following:
- Thermal (Moist / Dry Heat) and Gaseous (VHP / ETO) Validation
- Irradiation (Gamma / E-Beam) of Primary Packaging Components
- Container Closure Integrity
- Sterilizing Filter Validation
- Airflow Visualization Studies (Smoke Studies)
- Filter Validation Studies
- Generate and coordinate the execution of all sterile validation protocols.
- Complete summary reports for Sterilization Validation
- Assess impact of proposed changes to validated production equipment / production processes, evaluate and execute requalification and revalidation when there is significant change in either product or its manufacturing process and for ongoing validation maintenance.
- Preparation of Sterilization Process Validation and other reports for regulatory submissions, including, responses to deficiencies, comparability protocols, new submissions and supplements.
- Operate and maintain equipment/instruments.
- Assist in the calibration of equipment/instruments as required.
- Initiate change controls and update SOPs in the area of expertise.
- Communicate with suppliers to obtain required technical information.
- Provide technical guidance and subject matter expertise to sterile operations and investigations.
- Review validation documentation for compliance with cGMP and SOPs.
- Works in a safe manner collaborating as a team member to achieve all outcomes.
- Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
- Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
- All other relevant duties as assigned.
- Education
- Minimum B.Sc in Biology / Microbiology / Applied Pharmaceutical Sciences, Engineering or related discipline.
- Knowledge, Skills and Abilities
- Proficiency in Written and Verbal English communication.
- Knowledge of Excel, Word, other Microsoft office programs, and validation software
- Experience
- Minimum 3-5 years of experience in a GMP production environment, sterile manufacturing or validation experience is an asset.
We are looking for top talent. If your qualifications differ from those listed above, the scope of work and final agreed-upon salary may be adjusted to reflect your individual qualifications.
The Apotex Total Rewards package goes beyond base salary. Apotex offers bonus programs based on your position in the organization, you can excel based on our pay-for-performance philosophy. With comprehensive benefits, a pension plan to help you save for retirement and learning and development opportunities, we provide a comprehensive package for your personal and professional development.Apotex will use artificial intelligence to screen, select and/or assess your application for this job.This job posting is for a role that is currently available and vacant at Apotex.