Jobs and Careers

Senior Validation Engineer

Los Angeles, United Statesfull_timeVerifiedPosted 1 Dec 2025

💰 $130,000/yr($100,000/yr – $130,000/yr)

About the role

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 BiotechÂ® 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 BiotechÂ®, it’s about more than just a job—it’s about your career and your future. Your Role We are hiring an experienced Senior Validation Engineer. In this role you will be responsible for drafting, executing, and reviewing validation protocols with adherence to quality and compliance standards. A strong candidate will demonstrate exceptional attention to detail, rigorous documentation practices, and effective collaboration across cross-functional teams

Execute validation protocols for equipment, systems, and processes in compliance with regulatory and internal quality standards

Prepare and maintain validation documentation including protocols, reports, and standard operating procedures (SOPs)

Collect and analyze data during qualification activities to support validation conclusions

Identify and document deviations and assist in resolution and corrective actions

Ensure validation activities are completed according to established schedules and project timelines

Collaborate with cross-functional teams including quality, engineering, and operations to align on validation deliverables

Maintain audit-ready documentation and support internal and external inspections

Support change control assessments and evaluate the impact of changes on validated systems

Participate in continuous improvement initiatives to enhance validation processes and documentation practices

Ensure adherence to cGMP, FDA, EMA, and other applicable regulatory requirements

Requirements

7+ years of hands-on experience in validation roles across pharmaceutical and biopharmaceutical environments

Strong commitment to quality assurance and precision in execution

Extensive knowledge of validation processes and lifecycle management

Thorough understanding of global regulatory frameworks

Proficient in navigating quality systems

Effective communication and interpersonal skills.

Proactive with strong organization, time management, and project management abilities.

Excellent attention to detail with commitment to quality and compliance.

Preferred experience in Validation Lifecycle Management Platforms and QMS's

At PSC Biotech, many of our projects and clients are located in various regions around the country. Therefore, we value candidates who are willing and able to travel as needed for project assignments and client engagements. The ability to adapt to different locations, cultures, and work environments are essential, as it allows our team members to collaborate effectively with clients and colleagues na