Process Engineer

Candidate will be responsible for the technology transfer and commercial support of biologics drug substance processes across the network, including both t

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he manufacturing network and/or Contract Manufacturing Organizations. You will work as a member of a team of engineers and scientists, as you use engineering principles to implement manufacturing process in a cGMP environment.

 

– Provide solutions to a variety of technical problems of moderate scope and complexity to enable Technology Transfer of various clinical and commercial molecules.

– Under general supervision will evaluate, select and apply standard engineering techniques and procedures. Assistance given for unusual problems.

– Perform assignments that have clear and specific objectives and require investigation of limited number of variables.

– Initiate and complete routine technical tasks associated with Technology Transfer.

– Routinely monitor manufacturing processes for performance indicators and operations. Suggest problem resolution and provide troubleshooting mentorship.

– Apply engineering principles and statistical analysis, including design of experiments, in-order to address processing issues and evaluate opportunities for process improvements

– Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for processes and/or system modifications.

– Communicate and collaborate with technical and management staff within Manufacturing, Process Development, and Quality departments.

– Support non-standard shift organization and extended hours, as per business needs.

 

Preferred Qualifications:

– Education background in Chemical Engineering, Bioengineering or Biotechnology

– 2+ years of experience in a Process Development/Process Engineering environment, with specific experience in the implementation and support of biopharmaceutical manufacturing processes.

– Experience in process scale-up and technology transfer from laboratory to pilot and/or manufacturing scale

– Experience working with commercial manufacturer of biologics using single-use technology

– Basic understanding cGMP requirements; Experience related to upstream and/or downstream biologics process development technology transfer, scale-up and ongoing manufacturing of biologics (cGMP). This includes technical support for nonconformance investigations and other commercial support activities

– Experience in working with design and optimization of pharmaceutical processing unit operations including cell expansion, harvest, clarification, Protein A, IEX, SEC, TFF, UFDF, and sterile filtration among others for a variety of biological molecules. Experience working with data and digital tools preferred.

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