Analytical Systems Specialist

Ventura, United States | Posted on 03/09/2026

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 an experienced Analytical Systems Specialist to join our team! The Analytical Systems Specialist supports manufacturing and laboratory operations within a GMP-regulated environment by ensuring analytical systems are compliant, reliable, and fit for intended use. This role partners closely with business process owners, Quality, Manufacturing, and Facilities & Engineering to support the full lifecycle of analytical systems, including implementation, upgrades, data integrity oversight, and continuous improvement initiatives.

This role contributes to cross-functional projects involving analytical technologies, data review and trending, documentation, and regulatory compliance, while maintaining strict adherence to safety, quality, and cleanroom requirements.

• Support analytical system lifecycle activities, including implementation, commissioning, qualification, upgrades, and ongoing system performance within a GMP manufacturing and laboratory environment.
• Partner with business process owners and cross-functional stakeholders to ensure analytical systems remain compliant with global regulatory expectations and aligned with operational needs.
• Perform analytical data review and verification within validated systems, including assessment of invalid results, trend analysis, and data integrity oversight.
• Develop and support Testing Result Assessments (TRAs), including evaluation of method trending data.
• Collaborate with Quality and subject matter experts to support root cause investigations and the identification and implementation of corrective and preventive actions.
• Author, review, and revise GMP documentation such as SOPs, forms, and system-related documentation to ensure alignment with current operations.
• Support change control activities, including process impact assessments, system upgrades, and introduction of new analytical technologies.
• Participate in audit trail reviews, data integrity assessments, and review of computerized system validation documentation.
• Contribute to compendial and regulatory impact assessments related to analytical testing in support of global regulatory requirements.
• Apply technical, scientific, and operational knowledge to support troubleshooting efforts and continuous improvement initiatives.
• Participate in operations meetings, communicate findings effectively, and support cross-functional decision-making.
• Work on-site as required to support manufacturing schedules, including flexible shifts, while complying with cleanroom gowning, safety, and GMP requirements.

• Degree in Engineering, Life Sciences, or a related discipline.
• 6+ years relevant experience supporting GMP manufacturing, laboratory operations, analytical systems, engineering, process development, or technical support…