Validation Engineer

Job Description

Job Description

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.

Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.

Validation Engineer – MES (Emerson Syncade)

Location: Remote
Assignment Length: 6 Months
Division: Automation & Digital Manufacturing Solutions

We're seeking a driven and detail-oriented Validation Engineer with expertise in computer software validation (CSV) for manufacturing execution systems—specifically Emerson Syncade MES. This role is ideal for someone passionate about ensuring digital systems in life sciences manufacturing meet the highest standards of compliance, reliability, and performance. This role is a contract position, but we are able to employ both W2 or 1099 professionals. There are full-time benefits available.

You'll be part of a collaborative team that supports digital transformation initiatives across regulated manufacturing environments. Whether you're looking for a long-term opportunity or a consulting engagement, we welcome professionals who thrive in dynamic, fast-paced settings.

• Support validation activities for Emerson Syncade MES implementations and upgrades.
• Develop and execute validation deliverables including risk assessments, protocols (IQ/OQ/PQ), and summary reports.
• Collaborate with cross-functional teams to align validation strategies with project goals and regulatory expectations.
• Ensure compliance with industry standards such as GAMP 5, 21 CFR Part 11, and ASTM E2500.
• Participate in audits and inspections, providing documentation and subject matter expertise as needed.
• Contribute to continuous improvement of validation processes and documentation practices.

• Minimum 3 years of experience in computer system validation within GMP-regulated environments.
• Hands-on experience with Emerson Syncade MES is strongly preferred.
• Familiarity with automation systems, MES, and data integration platforms.
• Solid understanding of the system development life cycle (SDLC) and validation lifecycle.
• Strong communication skills and the ability to work effectively with clients and internal teams.
• A proactive mindset with a focus on quality, compliance, and operational excellence.

You'll be part of a forward-thinking team that values innovation, integrity, and impact. We offer opportunities to work on cutting-edge projects that shape the future of digital manufacturing in the life sciences sector.

Valspec offers a standout culture, fantastic work environment, and has very competitive benefits to include premium medical, 401K match, tuition reimbursement, 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 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 Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.

Valspec 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.