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CQV Engineer

Job in Columbus, Franklin County, Ohio, 43224, USA
Listing for: PSC Biotech
Full Time position
Listed on 2026-05-18
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Process Engineer, Pharma Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Position

Experienced CQV Engineer

Responsibilities
  • Develop and execute commissioning, qualification, and validation protocols for required equipment and systems.
  • Prepare and maintain comprehensive documentation, including validation protocols, plans, reports, and standard operating procedures.
  • Identify and assess risks associated with CQV activities and develop effective mitigation strategies.
  • Troubleshoot and resolve issues related to equipment and process performance.
  • Collaborate with cross‑functional teams to ensure alignment on CQV activities and project timelines.
  • Ensure compliance with regulatory requirements (FDA, EMA, etc.) and industry standards (GMP, GAMP, etc.).
  • Additional responsibilities as required to drive successful validation project deliverables.
Requirements
  • Bachelor’s degree in Engineering, Life Sciences, or a related field.
  • 5 years minimum of equipment commissioning, qualification, and validation engineering experience in the pharmaceutical and/or biotech industries.
  • Strong knowledge of regulatory requirements and industry standards.
  • Experience with validation lifecycle management and risk‑based approaches.
  • Excellent analytical and technical problem solving skills.
  • Strong technical writing skills and understanding of full lifecycle documentation (protocols, reports, procedures, risk assessments, specifications and requirements, etc.).
  • Effective communication and interpersonal skills.
  • Proactive with strong organization, time management, and project management abilities.
  • Excellent attention to detail with commitment to quality and compliance.
  • Willingness to travel as needed for project assignments and client engagements, and ability to adapt to different locations, cultures, and work environments.
  • Must be authorized to work in the US.
  • No C2C at this time.
Equal Employment Opportunity

PSC Biotech is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs.

Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.

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