Validation Engineer

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.

Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success.

The Experience

With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.

We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.

At PSC Biotech®, it’s about more than just a job—it’s about your career and your future.

Your Role

We are looking for motivated validation engineers to join our team! PSC Biotech is actively engaging Validation Engineers to support ongoing and upcoming client projects across the life sciences industry. This application is not tied to one specific role—instead, it allows qualified professionals to be considered for 6‑month consulting assignments aligned with their experience, technical strengths, and location preferences.

We support pharmaceutical, biotechnology, medical device, and laboratory environments and welcome validation engineers at varying levels of experience who are interested in project‑based consulting work! Assignments may vary based on business needs, project scope, and individual experience.

We are particularly interested in candidates with experience in one or more of the following life sciences environments:

• cGMP / GxP Regulated Manufacturing
• Medical Device (FDA / ISO-regulated)
• GLP Laboratory Operations
  
  

Responsibilities

• Support commissioning, qualification, and validation (CQV) activities for equipment, systems, utilities, facilities, laboratories, or processes.
• Author, review, and execute validation documentation such as URS, risk assessments, IQ/OQ/PQ, protocols, and summary reports.
• Ensure compliance with applicable FDA and global regulatory requirements (e.g., cGMP, GxP, ISO, 21 CFR Part 11, data integrity).
• Collaborate with client stakeholders, engineering teams, quality groups, and vendors to deliver compliant outcomes.
• Support audits, inspections, and ongoing validation maintenance activities.
• Adapt quickly to new environments and project scopes typical of consulting engagements.
  
  

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or a related field (or equivalent industry experience).
• Experience in validation within pharmaceutical, biotechnology, medical device, or laboratory environments.
• Working knowledge of cGMP / GxP, GLP, or medical device regulations.
• Experience authoring and executing validation and qualification documentation.
• Ability to work in a client-facing, project‑based environment.
• Strong documentation, communication, and organizational skills.
• Preferred ability to travel and relocate for client-facing projects.
• Must be authorized to work in the U.S.
• No C2C at this time.
  
  

Benefits

Offering a full suite of benefits, PSC Biotech™ is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.

• Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
• Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more.
• 401(k) and 401(k) matching
• PTO, Sick Time, and Paid Holidays
• Education Assistance
• Pet Insurance
• Discounted rate at Anytime Fitness
• Financial Perks and Discounts
  
  

Equal Opportunity Employment Statement

PSC Biotech is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.