Staff Validation Engineer at PerfVal Labs, Inc.

McPherson, Kansas, United States -

Full Time

Start Date

Immediate

Expiry Date

31 Jul, 26

Salary

0.0

Posted On

02 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Validation, Commissioning, Qualification, FDA regulations, cGMP principles, Technical documentation, Risk assessment, Thermal mapping, Computer systems validation, Process validation, Problem solving, Communication, Attention to detail, Project management

Industry

Pharmaceutical Manufacturing

Description

Staff Validation Engineer – Entry Level McPherson, Kansas Start Your Engineering Career Where It Actually Matters Most engineering jobs ask you to specialize early and stay in your lane. This one is different. At Performance Validation, you'll work directly in FDA-regulated facilities — pharmaceutical plants, medical device manufacturers, biotech labs — making sure the systems and processes that produce life-saving products actually work the way they're supposed to. It's hands-on, technically demanding, and genuinely important work. We hire engineers straight out of college and teach them everything. If you're sharp, curious, and ready to grow fast, we'll invest heavily in making you an expert. What We Do Performance Validation is a 100% employee-owned consulting firm with over 30 years of experience providing Commissioning, Qualification, and Validation (CQV) services to the life sciences industry. Our engineers work on-site with pharmaceutical, biotech, and medical device clients across the U.S. and internationally, helping them meet rigorous FDA and industry standards. We have teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina. What You'll Do From day one, you'll be embedded in project teams alongside experienced engineers, learning by doing on real client engagements. Over time, you'll take on increasing responsibility across the full validation lifecycle: * Travel to client facilities and perform hands-on qualification and verification activities, including Installation, Operational, and Performance Qualifications (IQ/OQ/PQ) * Develop technical documentation including User Requirements, Risk Assessments, Test Protocols, and Summary Reports under the guidance of senior engineers * Learn to apply FDA regulations (including 21 CFR Parts 11, 210/211, and 820) and cGMP principles to real-world client systems and processes * Perform system walk-downs in manufacturing environments — this is field work, and may involve stairs, ladders, confined spaces, and moderate lifting * Support identification and resolution of test failures and non-conformances * Build expertise in a technical discipline such as thermal mapping, computer systems validation, or process validation — depending on your interests and the needs of your team * This role involves travel to client sites, typically several days per month, with more intensive travel during active project phases. What We're Looking For We don't expect you to know validation. We expect you to be the kind of person who can learn it — and thrive in a client-facing, project-based environment. That means: * A Bachelor's degree in Engineering, Life Sciences, or a related technical field (or equivalent military training) * Genuine curiosity and a drive to understand how things work * High attention to detail — in this industry, documentation errors have real consequences * Strong written and verbal communication skills; you'll be interacting with client engineers, quality managers, and site personnel from day one * Professionalism and dependability; consulting means representing PV on client sites, not just in our offices * Willingness and enthusiasm to travel * Comfort working independently once you've been trained, and the judgment to ask for help when you need it * Preferred engineering disciplines include Biomedical, Chemical, and Mechanical Engineering, though we've built great careers with graduates from a wide range of technical backgrounds. What We Offer Being 100% employee-owned isn't a footnote — it means that when PV does well, you do well. Our compensation and benefits reflect that: * Competitive base salary * Biannual profit sharing — you share directly in the company's success * Employee Stock Ownership Program (ESOP) — you build equity in the company over time, at no cost to you * 401(k) with company match * Medical, dental, and vision coverage * Disability and life insurance * Paid vacation and holidays * Cellphone stipend And we invest in your development: * Structured mentorship from senior engineers on every project team * Internal and external training programs, including industry certifications * A clear path to advancement through our defined career levels * Exposure to diverse industries, clients, and technical disciplines across our national footprint Why PV We're a mid-sized firm with a long track record and a genuine culture of ownership — in every sense of the word. Our engineers aren't siloed into one product or one facility. You'll see the inside of facilities most engineers never encounter, build expertise that's valued across the life sciences industry, and do it alongside people who have chosen to build their careers here. We also know that consulting requires give and take. We ask a lot of our engineers, and we work hard to make it worth it. Qualified candidates must be legally authorized to work in the United States. Performance Validation does not anticipate providing visa sponsorship for this position.

Responsibilities

You will perform hands-on qualification and verification activities at client facilities, including IQ/OQ/PQ protocols. Additionally, you will develop technical documentation and support the resolution of test failures while adhering to FDA and cGMP standards.