Senior Process 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.

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.

We are seeking a Senior Process Engineer to support the design, improvement, and implementation of manufacturing processes and equipment within biotechnology production environments. In this role, you will contribute to process development, scale‑up, technology transfer, equipment integration, and ongoing operational support. You will work closely with cross‑functional teams to ensure that processes are reliable, efficient, compliant, and aligned with business and production goals.

• Support the design, optimization, and implementation of bioprocessing operations and manufacturing systems.
• Execute and support activities on filling/packaging lines, including process monitoring, issue troubleshooting, and performance optimization.
• Analyze process performance and identify opportunities to improve consistency, efficiency, and product quality.
• Collaborate with Manufacturing, Engineering, Quality, Validation, and R&D to enable efficient process transfer and operational readiness.
• Develop and maintain engineering documentation, including process descriptions, flow diagrams, specifications, and technical reports.
• Assist with equipment selection, procurement, installation, commissioning, and lifecycle management.
• Troubleshoot process or equipment issues to minimize downtime and maintain compliance.
• Ensure all processes align with applicable regulatory and quality standards, including cGMP expectations.
• Participate in continuous improvement activities focused on safety, productivity, and process robustness.
• Write and execute technical reports, including process evaluations, deviations, investigations, and equipment‑related documentation.
• Perform additional engineering‑related duties as assigned.

• Bachelor’s degree in Engineering or a related scientific/technical field.
• 10+ years of experience in process engineering or related roles within the biotech, biopharmaceutical, or pharmaceutical manufacturing sector.
• Advanced knowledge of filling line operations.
• Strong understanding of bioprocessing concepts and manufacturing operations in regulated environments.
• Familiarity with engineering documentation, process analysis, and equipment implementation.
• Working knowledge of regulatory and quality frameworks such as cGMP and related guidelines.
• Experience with process equipment, automation concepts, or manufacturing support.
• Strong technical writing skills—ability to write and execute reports, protocols, and documentation.
• Strong problem‑solving, communication, and project coordination skills.
• Ability to work independently and collaboratively within cross‑functional teams.
• High attention to detail and commitment to safety, quality, and compliance.
• Willingness to travel as needed to support client sites and project assignments nationwide.
• Must be authorized to work in the U.S.
• No C2C at…