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 what we have to offer. View our open positions below.

Automation QA Engineer

Location: Remote
Employment Type: Contract / Consulting (6-12+ months)
Start Date: ASAP

About the Role: We are seeking experienced Automation QA Engineers to support our clients in North Carolina. These roles will support automation quality assurance activities within 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

Provide QA oversight and support for automation-related 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 within 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 continuous 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 within pharma/biotech environments

 Qualifications

Bachelor’s degree in Engineering, Life Sciences, Computer Science, or related field preferred

3+ years of experience in Automation QA, CSV, CQV, or Validation within 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 integrity 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.

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.