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Job Requirements of Process Engineer III (Engineering):
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Employment Type:
Full-Time
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Location:
St. Louis, MO (Onsite)
Do you meet the requirements for this job?
Process Engineer III (Engineering)
Job ID: 25-62060
Pay Range: $50 - $75/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Key Responsibilities:
- The successful candidate will work with a group of scientists and engineers responsible for support of commercial mammalian cell culture processes in the external manufacturing MSAT group.
- This group support commercial operations across a diverse network of manufacturing facilities and external partners.
- Key responsibilities may differ among employees with same job title and may change over time in accordance with business needs.
- Provide technical support and routine process monitoring for commercial products manufactured at CMOs.
- Provides person-in-plant observations of manufacturing operations at CMOs and communicates observations to the product team.
- Reviews manufacturing processes, deviations, and/or development and production data.
- Reviews manufacturing batch records, protocols, and control strategies.
- Provide technical support and data analysis for investigations and deviation resolution.
- Recommends changes or additional experiments to improve quality, productivity, recovery, and overall efficiency.
- Interacts with colleagues and external partners from various functions, such as Engineering, Manufacturing, and Quality departments
- Oversees and reports on overall manufacturing progress.
Key Requirements and Technology Experience:
- Key skills; Process Engineer, biologics processes, biologics development, process validation. Root cause analysis and/or risk assessment, GMP.
- Prior experience in a technical role supporting a GMP, MSAT, or commercial processes,
- Experience with equipment qualification
- Bachelor’s degree in engineering or science with 5 years of experience
- Master’s degree in engineering or science with 3 years of experience
- Experience in biologics development, bioprocess engineering, technology transfer, and / or commercial manufacturing operations
- Experience with Good Manufacturing Practices and supporting a commercial facility
- Experience in cell culture and/or downstream purification (direct lab experience a plus)
- Experience with equipment qualification and process validation
- Familiarity with formal root cause analysis and/or risk assessment
- Experience working with statistical analysis software and investigative data analysis
- Experience with project leadership
- Experience communicating with cross functional teams
- Strong technical writing and communication skills
- Proficient in Microsoft Word, Excel, and PowerPoint
- Ability to gown and gain entry to manufacturing areas
- Ability to travel (up to 20% of time)
- Role is primarily remote, they will not report onsite daily.
- Possibility for travel to Framingham, MA and reimbursement would be provided • Possibility of extension.
- Candidates must be local to the St. Louis, MO area and willing to visit local CMO. (Location is ?5 mins from the airport)
- No other team members are local, manager sits in Framingham, MA
- Free parking onsite, coordinator with CMO
- Direct (hands-on) lab experience in biologics development would be good experience.
- Technical supporting role of commercial biologics processes.
- This would include activities like root cause investigation, process validation, lifecycle manage, and/or process trending. All of this would be done in alignment with GMP practices.
- Process validation & Root cause analysis and/or risk assessment experience
- Bachelor’s degree in engineering or science with 5 years of experience in Process Engineer or related role at Pharm/ Biotech Company OR master’s degree in engineering or science with 3 years’ experience in Process Engineer or related role at Pharm/ Biotech Company
- PhD candidates welcome if min of 3 years of experience as mentioned above Nice to Have
- Prior experience in a technical role supporting a GMP, MSAT or commercial processes,
- Experience with equipment qualification
Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
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