CQV Consultant - Biopharma Commissioning & Validation

Brevitas; Boston (MA); On-site; USD 75,000 - 95,000; Full time

Job summary

A leading consulting firm is seeking a motivated US - CQV Consultant in Boston, MA. The role involves writing critical CQV documents, reviewing protocols for compliance, and leading efforts in biopharmaceutical manufacturing. Candidates should hold a Bachelor's in Engineering with 3-4 years of relevant experience in the Pharmaceutical or Biotech industries. This opportunity requires travel and offers a chance to contribute to impactful projects with a strong focus on quality and compliance.

Qualifications

• 3-4+ years of experience in Pharmaceutical, Biotech, or QA.
• Experience with VMP, FQ, IQ, OQ and PQ protocols for GMP Utilities.
• Must have experience with qualifying clean utilities and HVAC Systems.

Responsibilities

• Write C/Q/V documents including Master Plans and SOPs.
• Review protocols and reports for compliance.
• Lead CQV efforts in biopharmaceutical manufacturing.

Skills

Pharmaceutical industry knowledge

Validation expertise

Technical writing skills

Strong communication

Education

Bachelor's Degree in Engineering

Tools

MS Office

Job description

A leading consulting firm is seeking a motivated US - CQV Consultant in Boston, MA. The role involves writing critical CQV documents, reviewing protocols for compliance, and leading efforts in biopharmaceutical manufacturing. Candidates should hold a Bachelor's in Engineering with 3-4 years of relevant experience in the Pharmaceutical or Biotech industries. This opportunity requires travel and offers a chance to contribute to impactful projects with a strong focus on quality and compliance.