We're partnered with one of the top innovators in the biotech industry. Since its founding in 2010, it has been at the forefront of a healthcare revolution, utilizing cutting-edge mRNA technology to create groundbreaking vaccines and therapeutics. It has made significant strides in its growth, now operating in over six countries with a headcount exceeding 5,000.
Looking for an experienced CQV Engineer to support commissioning, qualification, and validation (CQV) activities for a cutting-edge drug product (DP) or drug substance (DS) manufacturing equipment. This role focuses on new filling and packaging equipment at a state-of-the-art facility in Massachusetts.
Key Responsibilities:
- Provide CQV support for commissioning activities related to Optima filling and packaging systems.
- Execute and document protocols for equipment qualification and process validation.
- Collaborate with cross-functional teams to ensure project milestones are met efficiently and in compliance with GMP standards.
Experience Required:
- Proven experience in CQV activities within the pharmaceutical or biotechnology industries.
- Hands-on expertise with filling and packaging equipment, preferably Optima systems.
- Strong knowledge of GMP regulations and guidelines related to commissioning and validation processes.
This is an exciting opportunity to contribute to a high-impact project in a fast-paced, innovative environment. If this interests you, don't hesitate to reach out to understand more.
*W2 Contract ONLY NO C2C*
