Job Summary
The C&Q Engineer I supports commissioning and qualification activities for pharmaceutical manufacturing systems. Working with cross-functional partners, this entry-level engineer helps ensure that equipment and systems meet applicable GMP requirements and regulatory expectations. The position is intended for recent graduates with 0–2 years of experience and offers an opportunity to contribute to compliant manufacturing operations.
Responsibilities
- Assist with preparing commissioning and qualification protocols for pharmaceutical manufacturing systems.
- Support protocol execution and document results accurately.
- Help maintain validation deliverables and related documentation.
- Collaborate with cross-functional teams to support GMP compliance and adherence to regulatory standards.
Qualifications
- Bachelor’s degree in Engineering or a related technical field.
- 0–2 years of experience; recent graduates are encouraged to apply.
- Strong technical aptitude and the ability to work with engineering and validation documentation.
- Effective communication skills for coordinating with cross-functional teams.
