CQV Engineer I: Field Start-Up & Validation Lead

MMR Consulting; Seattle (WA); On-site; USD 80,000 - 115,000; Full time

Job summary

MMRConsulting is seeking a Jr. CQV Engineer to join a team of engineers responsible for the validation of upstream/downstream bioprocess systems and equipment in the biopharmaceutical industry.

The ideal candidate will lead teams of intermediate and junior engineers and work at client facilities in the Greater Denver/Boulder region. The role requires strong CQV knowledge, ability to travel, and commitment to safety standards in GMP environments.

Qualifications

• 2-4 years of experience in commissioning, qualification, or validation of pharmaceutical/biotech systems.
• Previous experience in pharma/biotech with knowledge of cGMP operations.
• Validation experiences such as cleaning validation, thermal validation, mixing studies, process validation, computer systems validation.

Responsibilities

• Provide technical guidance in commissioning, qualification and start-up of cGMP process equipment, utilities and facilities.
• Lead development of qualification deliverables (DQ, FAT, SAT, IQ, OQ, PQ) during the project lifecycle.
• Perform field execution of qualification test cases and protocols.
• Support development of Project Validation Plans (PVPs) to ensure the action plan is applicable and relevant.
• Lead qualification processes to ensure timely completion and adherence to specifications.
• Coordinate meetings with cross-functional departments to drive project progress.

Job description

MMRConsulting is seeking a Jr. CQV Engineer to join a team of engineers responsible for the validation of upstream/downstream bioprocess systems and equipment in the biopharmaceutical industry.

The ideal candidate will lead teams of intermediate and junior engineers and work at client facilities in the Greater Denver/Boulder region. The role requires strong CQV knowledge, ability to travel, and commitment to safety standards in GMP environments.