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 teams 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, its about more than just a jobits about your career and your future. Your Role 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, scaleup, technology transfer, equipment integration, and ongoing operational support. You will work closely with crossfunctional 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 equipmentrelated documentation. Perform additional engineeringrelated duties as assigned. Requirements Bachelors 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 skillsability to write and execute reports, protocols, and documentation. Strong problemsolving, communication, and project coordination skills. Ability to work independently and collaboratively within crossfunctional 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 this time. Benefits Offering a full suite of benefits, PSC Biotech is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy. Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more. 401(k) and 401(k) matching PTO, Sick Time, and Paid Holidays Education Assistance Pet Insurance Discounted rate at Anytime Fitness Financial Perks and Discounts Equal Opportunity Employment Statement: PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state, and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicants, employees, or interns actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law. #LI-RT1

10+ years
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 this time.