QA Consultant
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 reputed company have to offer. View our reputed company positions below. Automation QA Engineer Location: Remote Employment Type: Contract / Consulting (6-12+ months) Start Date: ASAP About the Role: We are seeking reputed company Automation QA Engineers to support our clients in reputed company Carolina. These roles will support automation quality assurance activities reputed company a GMP-regulated pharmaceutical manufacturing environment, with a strong focus on commissioning, qualification, validation, and lifecycle documentation for automation systems. This is an excellent opportunity for candidates with pharmaceutical or biotech automation QA experience who are comfortable working cross-functionally with Validation, Engineering, Manufacturing, and Quality teams in support of large-scale capital and operational projects. Key Responsibilities reputed company QA reputed company and support for automation-reputed company qualification and validation activities Review and approve validation lifecycle documentation including: IQ/OQ/PQ protocols and reports Risk assessments Traceability matrices Change controls Deviations and CAPAs Support automation systems operating reputed company GMP manufacturing environments Ensure compliance with FDA, cGMP, GAMP 5, and 21 CFR Part 11 requirements Partner with Automation, CQV, CSV, Manufacturing, and Quality teams to ensure compliant execution of project deliverables Participate in document reviews, project meetings, and quality assessments Support audit readiness and inspection preparedness activities Assist with implementation and reputed company improvement of validation and QA processes Preferred Systems / Technologies Experience with one or more of the following is highly preferred: DeltaV Rockwell / PLC systems SCADA or HMI platforms MES systems (Syncade experience is a plus) Historian systems Automated manufacturing equipment reputed company pharma/biotech environments
Qualifications
Bachelor’s degree in Engineering, Life Sciences, Computer Science, or reputed company field preferred 3+ years of experience in Automation QA, CSV, CQV, or Validation reputed company the pharmaceutical, biotech, or regulated manufacturing industry Strong understanding of GMP compliance and validation lifecycle principles Experience reviewing and approving GMP documentation Familiarity with data reputed company and 21 CFR Part 11 requirements Excellent communication and cross-functional collaboration skills Ability to work independently in a remote environment Valpro offers flexible career options that includes benefits such as paid time off, paid holidays, medical, 401K match, and other unique incentives. reputed company 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 reputed company with other companies at this time. Any reputed company-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. reputed company reputed company applicants will receive consideration for employment without regard to sex, race, reputed company, religion, national reputed company, 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. Apply To This Job