Equipment Validation Engineer

Los Angeles, United States | Posted on 10/27/2025

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, incompliance 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 areproud of the roles we have fulfilled to help our clients achieve success.

With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together to form something truly special. When you makethe 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 andlearn.

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

We are hiring motivated and hands-on engineers with direct experience in commissioning, qualifying, and validating pharmaceutical manufacturing facilities, utilities, and large-scale process equipment. This role is critical to ensuring the successful startup and compliance of complex systems used in regulated environments. You will be responsible for developing and executing validation protocols, troubleshooting equipment, and generating comprehensive lifecycle documentation.

• Develop and execute commissioning, qualification, and validation protocols (IQ/OQ/PQ) for cleanroom environments and large process equipment.
• Write and review technical documentation including specifications (URS, FS, DS), SOPs, risk assessments, and final reports.
• Collaborate with cross-functional teams to ensure validation activities align with project timelines and regulatory expectations.
• Conduct impact, gap, and risk assessments to identify potential issues and implement mitigation strategies.
• Analyze test data and acceptance criteria to ensure accuracy and compliance.
• Operate and troubleshoot equipment during startup and validation phases to assess performance and recommend modifications.
• Ensure all validation activities meet current industry standards and regulatory requirements (cGMP, FDA, etc.).
• Additional responsibilities as needed to support project deliverables.

• Bachelor’s degree in Engineering or a related technical field.
• 2 – 7 years of hands-on experience commissioning, qualifying, and validating process equipment within the pharmaceutical manufacturing industry.
• Experience qualifying cleanroom facilities.
• Experience in large process equipment in pharmaceutical manufacturing (vessels, centrifuges, filter presses and CIP skids).
• Experienced writing and generating technical validation documentation including final summary reports, IQ/OQ/PQ protocols, specifications (URS, FS, DS), operating procedures, etc.
• Proven knowledge of regulatory requirements and industry standards (cGMP, FDA, etc.).
• Strong understanding of risk-based validation approach.
• Excellent analytical, problem-solving, and communication skills.
• Ability to manage multiple projects and work both independently and collaboratively.
• Ability to work extended hours.
• 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 is essential, as it allows our team members to collaborate effectively with clients and colleagues nationally.
• Must be authorized to work in the US.
• No C2C at this time.

Adhering to the requirements of California's law on salary…