Senior CQV Engineer — Lead Biopharma Commissioning

MMR Consulting; Boulder (CO); On-site; USD 90,000 - 115,000; Full time

Job summary

A consulting firm in the pharmaceutical industry is seeking a Sr. CQV Engineer to lead validation projects in Boulder, Colorado. The ideal candidate will have over 12 years of experience in commissioning and qualification within the pharmaceutical/biotech sectors. This role involves managing project deliverables, guiding teams, and ensuring compliance with cGMP standards. Candidates should possess strong leadership skills, along with an engineering degree. Compensation ranges from $90,000 to $115,000 based on experience.

Qualifications

• 12+ years of experience in commissioning, qualification or validation in pharma/biotech.
• Experience with cleaning and thermal validation, process validation is an asset.
• Ability to lead teams and manage priorities.

Responsibilities

• Provide technical guidance in commissioning and qualification of process equipment.
• Lead development of qualification deliverables like DQ, FAT, SAT, IQ, OQ.
• Coordinate with cross-functional departments for project progress.

Skills

Leadership skills

Knowledge of cGMP operations

Project management skills

Education

Engineering degree in Mechanical, Electrical or Chemical

Tools

Process control systems (PCS, SCADA)

Biotech process equipment

Job description

A consulting firm in the pharmaceutical industry is seeking a Sr. CQV Engineer to lead validation projects in Boulder, Colorado. The ideal candidate will have over 12 years of experience in commissioning and qualification within the pharmaceutical/biotech sectors. This role involves managing project deliverables, guiding teams, and ensuring compliance with cGMP standards. Candidates should possess strong leadership skills, along with an engineering degree. Compensation ranges from $90,000 to $115,000 based on experience.