Process Engineer II

RoslinCT US; Hopkinton (MA); On-site; USD 90,000 - 120,000; Full time

Job summary

RoslinCT US is seeking a Process Engineer II to develop and execute technology transfer plans for partner programs. You will collaborate with Manufacturing, Quality, Facilities and Operations to optimize processes and ensure compliance as products move from clinical development to commercialization.

You bring hands-on experience with aseptic manufacturing, cell culture, and cell therapy instrumentation, plus independence in experimental design, data analysis, and troubleshooting.

Qualifications

• Bachelor’s degree in Biological, Biomedical or Chemical Engineering with 3–5 years of relevant process and/or analytical experience in cell therapy.
• Hands-on experience with aseptic manufacturing processes, cell culture, and cell therapy instrumentation.
• Experience with cell therapy equipment support and troubleshooting.
• Demonstrated independence in experimental design, execution, data analysis, and troubleshooting.

Responsibilities

• Support New Product Introduction for products entering the RoslinCT facility.
• Collaborate with Operations, Quality Control, and Quality Assurance as well as external clients and suppliers to execute technology transfer, equipment setup and qualification, engineering and training runs, and process validation as applicable.
• Draft and design GMP Batch Records and SOPs to support partner programs and right-first-time execution by Manufacturing.
• Support GMP production with process or equipment troubleshooting, deviation investigations, and CAPAs, as needed.
• Execute feasibility testing of new or alternative technologies and engage with key stakeholders to ensure technology development alignment with RoslinCT and client program requirements.
• Collaborate with partners to experimentally determine key process and product monitoring and control attributes, analyze results and draft technical reports.
• Perform test runs and development studies as needed to support client and RoslinCT initiatives.
• Compile comprehensive data packages, operating procedures, and technical documentation to support technology transfer and process improvement.
• Be proactive in identifying opportunities to add value to processes and cross-functional teams.

Skills

Aseptic manufacturing

Cell culture

Experimental design

Data analysis

Troubleshooting

Process transfer

Documentation

Cross-functional collaboration

Quality systems

Education

Bachelor's degree in Biological, Biomedical or Chemical Engineering

Tools

Microsoft Excel

Statistical software

Job description

WHO WE ARE

RoslinCT is a world-leading cell therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.

THE ROSLINCT WAY

Here at RoslinCT, our team can contribute to the development and delivery of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.

ACCELERATING YOUR FUTURE

The Process Engineer II,as a key member of the MS&T team, willdevelop and execute technology transfer plans for RoslinCT’s partner programs, including collaborating with key stakeholders in Manufacturing, Quality, Facilities, and Operations departments. As a technical subject matter expert, the position will also support routine production with troubleshooting, technical assessments of deviations, and product disposition evaluations. The Process Engineer will play a key role in optimizing manufacturing processes, ensuring compliance, and continuously improving quality, efficiency, and reliability while supporting products through clinical development to commercialization.

HOW YOU WILL MAKE AN IMPACT

• Support the New Product Introduction for products entering the RoslinCT facility
• Partner with colleagues in Operations, Quality Control, and Quality Assurance as well as external clients and suppliers to execute technology transfer, equipment setup and qualification, engineering and training runs, and process validation as applicable
• Draft and design GMP Batch Records and SOPs to support partner programs and right-first-time execution by Manufacturing
• Support GMP production with process or equipment troubleshooting, deviation investigations, and CAPAs, as needed

• Execute feasibility testing of new or alternative technologies and engage with key stakeholders to ensure technology development alignment with RoslinCT and client program requirements
• Collaborate with partners to experimentally determine key process and product monitoring and control attributes, analyze results and draft technical reports.
• Perform test runs and development studies as needed to support client and RoslinCT initiatives
• Compile comprehensive data packages, operating procedures, and technical documentation to support technology transfer and process improvement
• Be proactive in identifying opportunities to add value to processes and cross-functional teams

WHAT YOU WILL BRING

• Bachelor’s degree. in Biological, Biomedical or Chemical Engineering (or similar) with 3-5 years of relevant process and/or analytical experience within the Cell and Gene Therapy industry
• Hands-on experience with aseptic manufacturing processes, cell culture, and cell therapy instrumentation

• Experience with cell therapy equipment support and troubleshooting
• Demonstrated independence in experimental design, execution, data analysis, and troubleshooting

Preferred Qualifications

• Advanced degree or additional certifications in science, engineering, or cGMP operations
• Experience with bioreactor cell culture
• Experience with cell selection, cell washing, lentiviral transduction, and cryopreservation
• Experience with Microsoft Excel and statistical programs for data analysis and visualization
• Excellent technical writing and oral communication skills
• Driven and works well independently and within cross-functional teams

*May serve in an “on call” rotation to respond remotely to urgent issues (~1 week per month)

Final compensation will be based on a variety of factors, including education, experience, technical expertise, specialized skill sets, market demand, internal equity, and business needs.

At RoslinCT, we offer more than just competitive pay. Our comprehensive Total Rewards package is designed to support your health, financial well-being, and professional development throughout your career. Benefits include medical, dental, and vision insurance, educational assistance, a 401(k) program, and a variety of additional resources to help you thrive both personally and professionally.

OUR COMMITMENT

All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.

RoslinCT is proud to be an equal opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.