C&Q Engineer (Pharma) (USA)
Date Posted: November 5, 2024
Job Description
We are seeking a skilled C&Q Engineer to join our team for pharmaceutical projects around New Jersey. The ideal candidate will lead commissioning, qualification, and validation activities to ensure compliance with industry standards, ensuring the efficient and compliant operation of equipment and systems within the pharmaceutical sector.
Key Responsibilities
- Lead C&Q activities for pharmaceutical manufacturing and packaging systems
- Develop and execute commissioning, qualification, and validation protocols (FAT, SAT, IQ, OQ, PQ)
- Coordinate with cross-functional teams to ensure timely completion of validation and commissioning tasks
- Ensure compliance with cGMP, FDA, and other regulatory standards
- Prepare and review C&Q documentation, including reports, test scripts, and procedures
- Troubleshoot and resolve issues during the commissioning and qualification process
- Provide guidance and training to junior engineers and other team members
- Support project teams in maintaining project timelines and compliance
Required Qualifications and Skills
- Bachelor’s degree in Engineering (Mechanical, Electrical, or Chemical preferred)
- 3-5 years of C&Q experience in pharmaceutical or biotech environments
- Strong knowledge of pharmaceutical validation and commissioning processes (FAT, SAT, IQ, OQ, PQ)
- Familiarity with cGMP, FDA, and other regulatory requirements
- Excellent problem-solving and troubleshooting skills
- Strong technical documentation and report-writing abilities
- Ability to work independently and in cross-functional teams
- Willingness to travel to project sites within New Jersey
If you are keen to grow your career with this job, apply with us and send us your resume now. All shortlisted candidates will be contacted shortly.
Reference no.: 122-4948-2918-NW
Registration no.: 968446516E
