Biopharmaceutical Commissioning Engineer
5 days ago
We are seeking a highly skilled Biopharmaceutical Commissioning Engineer to join our team at MMR Consulting Inc. As a key member of our engineering team, you will be responsible for the commissioning, qualification, and start-up of various equipment and facilities in the biopharmaceutical industry.
Key Responsibilities:- Provide technical guidance on commissioning, qualification, and start-up of equipment and facilities.
- Lead the development of key qualification deliverables during the project lifecycle.
- Coordinate meetings with cross-functional departments to drive project progress and facilitate decisions.
- Engage other departments for design reviews and decisions.
- Travel may be required for meetings with clients, equipment fabrication vendors, or Factory Acceptance Testing (FATs).
- 12+ years of experience in commissioning, qualification, or validation of various systems within the pharmaceutical/biotech industry.
- Minimum 6+ years of direct C&Q experience with upstream or downstream bioprocess equipment/systems.
- Excellent written and spoken English, including preparation of technical documents.
- Knowledge of cGMP operations, including SOPs, Change Controls, and Validation.
- Experience with developing and executing validation projects, including Risk-Based Commissioning & Qualification approaches.
- A dynamic and growing team in the pharmaceutical and biotechnology industries.
- Opportunities for professional growth and development.
- A collaborative and inclusive work environment.
At MMR Consulting Inc, we are committed to creating an inclusive environment for all employees. We celebrate diversity and are an equal opportunity employer. If you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.
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