Process Engineer (I, II, III) - Cellares
View Company Profile- Job Title
- Process Engineer (I, II, III)
- Job Location
- Bridgewater, NJ
- Job Description
- Position SummaryWe are seeking an innovative and highly motivated Process Engineer on our MSAT team who will contribute significantly to establishing our IDMO Smart Factories.This position is focused on supporting the development and implementation of automated cell therapy manufacturing processes. You will work closely with the Process Engineering Lead and other cross-functional teams to execute, develop, design, optimize, and validate processes to ensure efficient, high-quality, scalable manufacturing solutions.This is a multidisciplinary role & this individual will interface across many parts of the company (with customers, scientists, researchers, and engineers) to develop the best solutions possible. Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows.Responsibilities
- Design and implement operational workflows to streamline manufacturing and reduce errors
- Participate in the execution of manufacturing study campaigns, working closely with cross-functional teams to ensure successful execution
- Assist in the design, execution, and analysis of process development studies to optimize cell therapy manufacturing processes
- Support the development and implementation of automated manufacturing processes using the Cellares platform
- Prepare and maintain technical documentation, including study protocols, reports, and standard operating procedures (SOPs)
- Collect and analyze process data to identify trends, troubleshoot issues, and recommend improvements
- Provide technical support during technology transfer, process validation, and routine manufacturing
- Collaborate with cross-functional teams, including Quality, Supply Chain, Manufacturing, and Analytical Sciences, to ensure successful process development and implementation
- Identify opportunities for process improvements and participate in continuous improvement initiatives to enhance manufacturing efficiency and product quality
Requirements- Bachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, or a related field
- 0-4 years of experience in bioprocess engineering, cell therapy GMP manufacturing, or a related field
- Prior experience with automated manufacturing processes is a plus
- Knowledge of cell therapy manufacturing processes, including cell culture, separation, and purification
- Familiarity with bioprocessing equipment and automation systems
- Proficiency in data analysis tools (e.g., Excel, statistical software)
- Experience writing, reviewing and approving GMP documentation
- Experience troubleshooting complex technical issues
- Strong problem-solving skills with a hands-on approach
- Excellent communication and teamwork abilities
- Detail-oriented with strong organizational skills
- Ability to work in a fast-paced, dynamic environment
- Willingness to learn and adapt to new technologies and processes
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Cellares Company Size
Between 100 - 500 employees
Cellares Founded Year
2019
Cellares Total Amount Raised
$355,000,000
Cellares Funding Rounds
View funding detailsSeries C
$255,000,000 USD
Series B
$82,000,000 USD
Series A
$18,000,000 USD