CQV Consultant

CQV Consultant Valpro - 4.5 Oceanside, CA Job Details Full-time | Contract 7 hours ago Benefits Paid holidays Paid time off 401(k) matching Qualifications Cross-functional collaboration Cross-functional communication Full Job Description Valpro has several available opportunities supporting our world-class client sites or partner organizations. Whether you are an independent consultant or a potential employee looking for your next project, learn more about what we have to offer. View our open positions below. CQV Consultant - Upstream / Downstream / CIP / PSE /

Clean Utilities Location:

Holly Springs (100% Onsite)

Type:

Long-Term Contract Start Date:

ASAP Overview We are seeking experienced CQV Consultants to support a major biopharmaceutical manufacturing project in Holly Springs, NC. This is a long-term onsite opportunity supporting commissioning, qualification, and validation activities across multiple process and utility systems in a GMP manufacturing environment. We are specifically looking for strong "A+" level consultants with hands-on pharmaceutical or biotech project experience supporting large-scale manufacturing operations. We are hiring CQV professionals with experience in one or more of the following areas: Upstream Processing Downstream Processing CIP (Clean-in-Place) Systems PSE (Process Support Equipment) Clean Utilities Key Responsibilities Execute CQV lifecycle activities including commissioning, IQ/OQ, and field verification Support startup and qualification of GMP manufacturing equipment and utility systems Author, review, and execute validation documentation and protocols Coordinate with engineering, operations, quality, automation, and project teams Support deviation investigations, change controls, and CAPA activities Ensure compliance with GMP, FDA, and regulatory requirements Participate in walkdowns, system turnover, and punch-list resolution Maintain accurate documentation in accordance with data integrity and quality standards Qualifications Prior CQV experience in pharmaceutical, biotech, or GMP-regulated manufacturing environments Strong knowledge of commissioning and qualification processes Experience supporting one or more of the following: Upstream, Downstream, CIP, PSE, or Clean Utilities systems Familiarity with GMP documentation practices and regulatory requirements Ability to work onsite in Holly Springs, NC on a full-time basis Strong communication and cross-functional collaboration skills Preferred Experience Large-scale biologics or vaccine manufacturing projects Startup or greenfield facility experience Experience with DeltaV, MES, or automated process systems Knowledge of clean utilities including WFI, clean steam, compressed gases, and purified water systems Valpro offers flexible career options that includes benefits such as paid time off, paid holidays, medical, 401K match, and other unique incentives. When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net or @valspec.net. Any other domains are impersonations and should be ignored. Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time. Any third-party unsolicited resume submission(s) will immediately become the property of Valpro. Valpro will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established. Valpro is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.