What are the responsibilities and job description for the CQV Engineer position at Global Compliance Partners?
Position Overview
We are seeking a CQV Engineer to support on-site execution activities in Walkersville, Maryland. The ideal candidate will have hands-on experience in commissioning, qualification, and validation of manufacturing, laboratory, and quality control equipment, preferably with performing airflow visualization testing in a classified environment.
Responsibilities
- Support commissioning and qualification of GMP manufacturing equipment, facilities, and utilities.
- Execute IQ/OQ protocols and document results in accordance with GMP requirements.
- Assist with field verification, equipment walkdowns, and system readiness assessments.
- Support airflow visualization (smoke study) activities as needed.
- Document deviations, discrepancies, and corrective actions.
- Maintain accurate qualification documentation in accordance with GDP standards.
- Collaborate with Engineering, Quality, Validation, and Manufacturing teams.
Qualifications
- Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
- 1–5 years of CQV experience in pharmaceutical or biotechnology manufacturing.
- amiliarity with GMP requirements and IQ/OQ execution.
- Strong technical documentation and communication skills.
- Ability to work onsite in Walkersville, MD.