Cleaning Validation Engineer

PSC Biotech•Dallas, TX

About The Position

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 hiring a motivated Cleaning Validation Engineer to join our team! The Cleaning Validation Engineer supports site validation activities within a GMP‑regulated pharmaceutical or biotechnology manufacturing environment. This role assists with routine validation tasks and provides hands‑on support for cleaning validation activities for assigned process trains.

Requirements

Bachelor’s degree in engineering, life sciences, or a related technical discipline.
3-5 years experience supporting cleaning validation activities in a GMP‑regulated pharmaceutical or biotechnology environment.
Working knowledge of validation lifecycle principles, including execution, documentation, and requalification activities.
Experience drafting or supporting validation protocols and reports.
Ability to work under direction while managing assigned validation tasks and timelines.
Strong written and verbal communication skills.
Ability to work flexible hours with some overtime and weekend shifts required.
Must be authorized to work in the U.S.
No C2C at this time.

Responsibilities

Assist with routine validation activities, including periodic reviews and requalification efforts, as required.
Support cleaning validation activities for assigned process train.
Execute cleaning validation activities in accordance with approved protocols and regulatory requirements.
Draft and support the review of cleaning validation protocols and final reports.
Participate in project‑related meetings and provide validation updates as needed.
Support documentation activities to ensure compliance with site procedures and GMP expectations.