Process Engineer III, Manufacturing Sciences

Work Schedule

Environmental Conditions

Job Description

How will you make an impact

We are searching for a Process Engineer 3 with education and experience in biopharmaceutical processing or a related field. This member of our team provides technological input in the development validation and transfer of manufacturing processes. A Process Engineer 3 routinely supports the Process Engineering team as technical owners of customer programs in a manufacturing environment and will be highly involved and act as a subject matter expert in defining and shaping Thermo Fisher Scientifics own technology role will collaborate internally with supervisors and technicians in the Operations department Quality Assurance fellow Engineers and scientists in Process Development and with the client as a Process Engineer program lead. These activities are conducted in projects and involve teamwork with experts across functional groups to ensure project success.

What will you do

• Draft review and approve Standard Operation Procedures and Job Aids and consult internally to ensure scientifically sound and robust procedures.
• Collaborate with the process development to develop standardized methodologies and learn/explore new methodologies for conducting unit operations at the manufacturing scale including cell culture harvest and purification.
• Contribute to Internal and Customer meetings based upon sound evidence guided by minimal supervision.
• Manages internal projects and tasks and lead client projects and manage timelines with minimal support from supervision.
• Actively identify error proofing opportunities and initiate and drive engineering initiatives to improve practices and procedures with minimal supervision.
• Provide scientific expertise for GMP deviations by assessing reviewing and approving the impact of major deviations on both the product quality and the validation of the process.
• Lead changes to equipment and process design proactively and with minimal supervision.
• Draft review and approve Manufacturing Batch Records Performance Qualifications Process Validation protocols process flow diagrams automation methods and Bill of Materials ensuring the process is technically accurate and designed for Manufacturing.
• Draft review and approve Process control documents campaign summary report and process validation reports
• Reviews analyzes and trends process data without supervision
• Provide technical feedback on documents created by other departments such as Tech Transfer Protocols and SOPs.
• Troubleshoot technical challenges on the manufacturing floor as needed for a 24/7 manufacturing facility.
• Support our MSAT team with additional tasks to improve the site ensure patient safety and deliver for our customers.
• Provides development and training for Process Engineers/Scientists.

How will you get here

Education

• Bachelors degree required in a scientific field preferably an engineering field.
• 5 years of experience in GMP regulated Biologics / Pharma Industry or equivalent experience (or masters degree in a scientific field 3 years experience or Ph.D.).

Experience

• 5 years of experience in GMP regulated Biologics / Pharma Industry or equivalent experience (or masters degree in a scientific field 3 years experience or Ph.D.).
• Follow Environmental Health and Safety policies and procedures and ensure a safe and healthy workplace environment.
• Ability to self-motivate prioritize work and time.
• Demonstrates a foundation in general scientific practices principles and concepts.
• Writes and communicates effectively.
• Ability to work both independently and as part of a team.
• Knowledge of current Good Manufacturing Practices and US/EU regulations.
• Intermediate knowledge of statistical methods used for Pharmaceutical Process Analysis is a plus.
• Proficient in Microsoft Word and Excel.
• Ability to stand for prolonged periods of time and gown into manufacturing areas.