CQV Engineers - Future Opportunities

TSO- CQV Future Opportunities

DPS Group Global is seeking experienced CQV Engineers interested in future opportunities to support pharmaceutical clients on upcoming projects. DPS provides global consulting engineering and construction management serving high-tech industries around the world. Our exceptional talent helps our clients meet capital project and operational goals. DPS culture values honest, dynamic, adaptable, and human relationships. We focus on integrated solutions and repeat business to drive our overall success in creating lasting partnerships with our clients. The CQV Engineer will be responsible for projects in commissioning/ qualification/ validation as they relate to the pharmaceutical, biomanufacturing, biotech, and other regulated industries. The selected candidates will have strong experience interacting with project teams to complete specific validation deliverables including validation documents for equipment, instruments, facilities, utilities, and protocols. Ideal candidates will be open to travel/relocation to client sites in North Carolina or other client locations on the East coast. Life Science industry experience is a must-have.

Category:
Quality
Location:
North Carolina
Years of Experience Req.:
5
Date Posted:
10/06/2021
Days Remaining:
48
Employment Type:
Full-time
Education Level Req.:
Bachelors

Key responsibilities:

  • Provide direction, input, review and approval of engineering studies, FAT, IQ, OQ, and PQ validation protocols and reports for facilities, equipment, systems and utilities to ensure thoroughness, accuracy and compliance with company policies.
  • Manages, schedules, executes and tracks multiple project activities of moderate complexity with multidisciplinary departments to ensure timely completion of deliverables.
  • Conducts deviation investigations, such as validation failures, complaints and hold investigations. Identifies appropriate corrective actions.
  • Perform, evaluate and analyz665292.695765e validation protocols and associated data for compliance with FDA and ISO guidelines.
  • Start-up C&Q experience of process and utility systems.

 

Education & experience:

  • B.S. Degree in Engineering or scientific discipline with 5+ years validation experience in the
  • pharmaceutical or medical device industry performing the tasks listed above.
  • Experience with sterile fill and groninger filling machines strongly preferred.
  • Knowledge of cGMP practices and standards required.
  • Experience in developing and executing processes, equipment, and cleaning validation protocols.

 

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