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Senior Process Engineer

Roslin CT US Holdings,LLC
Posted 2 days ago, valid for 2 days
Location

Hopkinton, MA 01748, US

Salary

$80,000 - $110,000 per year

Contract type

Full Time

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Sonic Summary

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  • RoslinCT is seeking a Senior Process Engineer with 5-10 years of relevant experience in the Cell and Gene Therapy industry to join their MS&T team.
  • The role involves developing technology transfer plans, optimizing manufacturing processes, and collaborating with various departments to ensure compliance and quality.
  • Candidates should possess a Bachelor’s degree in Biological, Biomedical, or Chemical Engineering and have hands-on experience with aseptic manufacturing processes and cell therapy instrumentation.
  • The position offers a competitive salary, which is commensurate with experience, along with an attractive benefits package and a flexible work environment.
  • RoslinCT is committed to fostering a diverse and inclusive workplace, encouraging applicants from all backgrounds to apply.

WHO WE ARE 

We are a 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. We work both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.

THE ROSLINCT WAY 

Here at RoslinCT, our team contributes to the development 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 Senior Process Engineer, as a key member of the MS&T team, will develop 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  

  • Lead 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 5-10 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 
  • Proficiency with Quality Systems including but not limited to Deviations, CAPAs, and Change Controls
  • Demonstrated independence in experimental design, execution, data analysis, and troubleshooting 
  • Excellent technical writing and oral communication skills 
  • Experience with Microsoft Excel and statistical programs for data analysis and visualization 



 Preferred Qualifications

  • Advanced degree or additional certifications in science, engineering, or cGMP operations 
  • Expertise in bioreactor cell culture
  • Expertise in cell selection, cell washing, lentiviral transduction, and cryopreservation 
  • Knowledge of aseptic media fills, process validation and comparability.
  • Experience performing Risk Assessments (e.g. FMEAs).
  • Experience supporting both clinical and commercial cell therapy programs.
  • Experience in hands-on training curriculum development for cell therapy manufacturing personnel.
  • 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) 


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.






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