What are the responsibilities and job description for the CQV Engineer position at PharmEng Technology?
Job Description
Job Description
Position : CQV Engineer
Company Overview :
PharmEng Technology is a leading global provider of engineering and consulting services to the pharmaceutical and biotechnology industries. We specialize in providing innovative solutions to our clients to help them achieve their goals in drug development, manufacturing, and compliance.
Job Summary :
We are seeking a highly motivated and experienced CQV Engineer to join our team in Holly Springs, North Carolina. The CQV Engineer will be responsible for leading commissioning, qualification, and validation activities for new and existing pharmaceutical facilities and equipment.
Key Responsibilities :
- Develop and execute commissioning, qualification, and validation protocols for new and existing pharmaceutical facilities and equipment.
- Conduct risk assessments and gap analyses to identify potential compliance issues and develop strategies to mitigate them.
- Lead and manage CQV project teams, including coordinating with internal and external stakeholders.
- Ensure compliance with all relevant regulations and guidelines, including FDA, EMA, and ICH.
- Generate and maintain CQV documentation, including protocols, reports, and standard operating procedures (SOPs).
- Troubleshoot and resolve technical issues related to CQV activities.
- Train and mentor junior CQV engineers and technicians.
- Participate in client meetings and provide regular updates on project progress.
- Continuously improve CQV processes and procedures to ensure efficiency and effectiveness.
Qualifications :
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a self-motivated and dedicated CQV Engineer looking for a challenging and rewarding career, we encourage you to apply for this position.
Join our team and be a part of shaping the future of the pharmaceutical industry!
