Validation Engineer

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.

VALIDATION ENGINEER

We are looking for a talented Validation Engineer to join our teams in Greater Philadelphia, Southern California, Upstate New York, and Maryland, for special projects involving the Emerson DeltaV distributed control system.

As a Validation Engineer, you will play a pivotal role in ensuring the successful validation of the Emerson DeltaV distributed control system for our special project. Your experience in the system development life cycle of automated computer systems within biopharmaceutical environments is critical to the project's success. This is a consulting role, offering an exciting opportunity to work with a dynamic team on a time-sensitive project.

Responsibilities

• Emerson DeltaV Validation: Support the validation efforts for the Emerson DeltaV distributed control system, ensuring compliance with industry standards and regulatory requirements.
• System Development Life Cycle: Apply your expertise in the system development life cycle to design, plan, execute, and document validation activities.
• Documentation: Create and maintain validation protocols, test scripts, and other relevant documentation.
• Change Control: Manage change control processes related to system validation, including assessing and mitigating the impact of changes.
• Collaboration: Work closely with cross-functional teams to ensure the successful integration of the Emerson DeltaV system into our biopharmaceutical environment.
• Adaptability: Quickly adapt to changing project priorities and provide solutions to challenges as they arise.
• Compliance: Ensure that all validation activities align with regulatory guidelines and industry best practices.

Qualifications

• Bachelor's degree in Chemical, Electrical, Computer, Management Information Systems, Biomedical, or Mechanical Engineering.
• Proven experience in the validation of automated computer systems within biopharmaceutical environments.
• Familiarity with the Emerson DeltaV distributed control system is highly desirable.
• Strong understanding of industry regulations, including GxP, 21 CFR Part 11, and ISPE GAMP.
• Excellent problem-solving skills and ability to work effectively in a team.
• Exceptional communication and documentation skills.

Consulting Role Details

• Duration: 8-12 months.
• Competitive compensation package.

Valpro offers flexible career options that includes benefits such as paid time off, paid holidays, medical, 401K match, and other unique incentives.

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.