Title: CQV Engineer
Long term Contract Role
Location: Pennington, NJ
Description:
We are seeking experienced CQV (Commissioning, Qualification, and Validation) Engineers with a strong pharmaceutical background to join our team in Pennington, NJ. The ideal candidate must be ready to work fully onsite and possess deep expertise in CQV processes, specifically within the pharmaceutical industry. This role will involve ensuring that all systems and equipment are properly commissioned, qualified, and validated according to industry standards and regulatory requirements.
Key Responsibilities:
Conduct commissioning, qualification, and validation activities for pharmaceutical manufacturing equipment and systems.
Develop and execute protocols for IQ/OQ/PQ (Installation Qualification, Operational Qualification, and Performance Qualification).
Collaborate with cross-functional teams, including Engineering, Quality, and Manufacturing, to ensure compliance with GMP and regulatory standards.
Document all CQV activities, including deviations and corrective actions, in accordance with company and regulatory guidelines.
Support the implementation and validation of new systems, equipment, and processes.
Participate in risk assessments and ensure proper mitigation strategies are in place.
Provide technical support during audits and inspections.
Requirements:
Proven experience as a CQV Engineer in the pharmaceutical industry.
Strong knowledge of GMP, FDA regulations, and industry standards.
Ability to work effectively in a team-oriented environment.
Excellent documentation and communication skills.
- Willingness to work fully onsite.
Thanks
Ritika Aithmian
Lead Recruiter
D : +1 617-848-2313 (P)| +1 984-262-2736
Ritika.aithmian@mastechdigital.com
