Recent College Graduate Validation Engineer

About the role

Valspec is a global provider of system validation and lifecycle services for the Life Sciences industry. Established in 1999, the company delivers commissioning and qualification of computerized systems to help clients meet capital project and lifecycle maintenance goals, ensuring life‑changing drugs are available and production is efficient.

The position is an entry‑level Equipment Validation Engineer supporting Commissioning, Qualification, and Validation (CQV) activities for GMP manufacturing and utility equipment at client sites. The role offers structured training, mentorship, and exposure to GMP equipment systems, regulatory compliance, and real‑world validation execution in a client‑facing environment.

Responsibilities

• Support CQV activities for GMP manufacturing and utility equipment, including autoclaves, CIP/SIP systems, bioreactors, incubators, freezers and refrigerators, centrifuges, washers, controlled temperature units, environmental chambers, HVAC systems, clean steam generators, WFI systems, process tanks, and utility systems (compressed air, nitrogen, etc.).
• Assist in the development, execution, and documentation of validation deliverables such as User Requirements Specifications (URS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and qualification summary reports.
• Execute protocol testing under the guidance of senior CQV engineers and accurately document results.
• Participate in commissioning activities and help troubleshoot equipment issues during startup and qualification.
• Support equipment risk assessments and impact analyses as part of validation planning.
• Collaborate with Engineering, Automation, Manufacturing, and Quality teams to support project execution.
• Maintain compliance with cGMP, FDA, and internal quality standards.
• Communicate test results, observations, and issues clearly to project team members.

Skills & Qualifications

• Bachelor’s degree in engineering, Life Sciences, or a related technical discipline (recent graduates encouraged to apply).
• 0–2 years of experience in a regulated manufacturing or validation environment (internship, co‑op, or academic project experience acceptable).
• Interest in pharmaceutical, biotechnology, or life sciences manufacturing.
• Basic understanding of GMP concepts and validation principles preferred.
• Exposure to IQ, OQ, and PQ activities is a plus but not required.
• Familiarity with manufacturing equipment, utilities, or automated systems is beneficial.
• Strong attention to detail, technical writing ability, and willingness to learn.
• Ability to work on‑site and collaborate effectively in a team‑based environment.

Why Join Valspec?

• Employee Stock Ownership Plan (ESOP) – every team member has a stake in the company’s success.
• Highly competitive benefits package, including premium medical coverage, 401(k) with company match, tuition reimbursement, unique performance incentives, and more.
• Collaborative culture with a strong sense of ownership and opportunities to work on interesting projects for top‑notch clients.

Candidates must be legally eligible to work in the United States without company sponsorship. Valspec is an Equal Opportunity Employer and a Drug‑Free Workplace.