Senior DeltaV Automation Engineer Valpro - 4.5 Oceanside, CA Job Details Contract 1 day ago Benefits Paid holidays Paid time off 401(k) matching Qualifications Chemical process control design Engineering development testing Testing (project management phases) GMP Piping and instrumentation diagrams (P&IDs) Pharmaceutical company experience Manufacturing Control systems Cross-functional communication Providing code feedback Pharmaceutical manufacturing facility experience 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. Senior DeltaV Automation Engineer Contract | Pharmaceutical Manufacturing | Midwest Region Position Summary Valpro is seeking a Senior DeltaV Automation Engineer for a long-term contract supporting a major pharmaceutical manufacturing automation project. This role will provide technical ownership of DeltaV automation for an assigned process area, including functional specifications, control strategies, software development, testing, FAT, and implementation.

Anticipated Start:

Early 2027 |

Expected Duration:

Through Q4 2027, with potential extension Responsibilities Lead DeltaV automation activities for an assigned pharmaceutical process area. Develop and review functional specifications, control strategies, phases, and recipes. Review P&IDs and define required DeltaV software changes. Provide technical oversight of software development and code reviews. Support software testing, FAT, defect resolution, and change verification. Coordinate with process engineering, automation, validation, and system integration teams. Identify technical risks and resolve automation issues. Required Qualifications Bachelor's degree in Engineering or equivalent relevant experience. Strong Emerson DeltaV and DeltaV Batch experience. Pharmaceutical manufacturing experience. Working knowledge of

ISA-88 / S88.

GMP and validation experience. Experience with functional specifications, P&IDs, control strategies, phases, and recipes. Experience with DeltaV software/code reviews, testing, and FAT. Strong communication and multidisciplinary collaboration skills. Preferred Qualifications 8+ years of pharmaceutical automation experience. API or bulk pharmaceutical manufacturing experience. Experience with reactors, columns, filters, or filter dryers. Experience developing S88 models from P&IDs. Experience with Parameter and Recipe Specifications. 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.