Summary**
This position will support and assist in manufacturing pharmaceutical products for commercial and clinical supplies. Key duties include scale-up and transfer of oral solid dosage formulations/processes to the production facility, designing and recommending equipment purchases, and writing and executing equipment specification and commissioning protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control systems) to reduce waste and increase process reliability. Assure the resolution of deviations, corrective actions, action items from Change Control systems, and any audit non-compliance items. Perform process and equipment evaluation (FMEA, etc) to identify risks and weaknesses in new and current processes. Develop and implement SOPs in support of new and upgraded processes. Champion projects as they move into and through the manufacturing areas. Provide regular updates to leadership on project status and issues.
**Essential Functions**
- Troubleshoot and maintain manufacturing systems, processes, and equipment.
- Support the development or transfer of manufacturing and cleaning processes for the manufacturing area.
- "Hands-on" ability to install and troubleshoot instrumentation and equipment.
- Author high-quality technical protocols/reports (engineering studies, summary reports, equipment specifications, change controls, and investigations)
- Specify and size manufacturing systems, equipment, and process equipment.
**Competencies**
- Excellent communication and documentation skills
- Excellent organizational skills
- Ability to self-manage and prioritize workload.
- Ability to react quickly to understand and solve problems.
- Excellent troubleshooting skills
- Fosters collaborative relationships within and across groups through influencing and negotiation skills
- Positive attitude
**Process Engineer I**
**Basic Qualifications:**
- BS degree in Engineering or technical discipline.
- 0-2 year of manufacturing experience or technical experience.
**Preferred Qualification:**
- 0-2 years of OSD pharmaceutical experience or 5 years of pharmaceutical engineering experience.
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- Experience with OSD equipment procurement.
- Thorough knowledge of cGMP, OSHA, EPA and FDA facility requirements and regulations.
- Thorough knowledge of OSD operations, statistics, equipment design, process control, and process scale-up.
- Knowledge of OSD pharmaceutical process and equipment validations.
- Experience in statistical analysis: sample sizing, ANOVA, regression analysis, control charts, etc
**Process Engineer II**
**Basic Qualifications:**
- BS degree in Engineering or technical discipline.
- 2-5 year of manufacturing experience or technical experience.
**Preferred Qualification:**
- 2-5 years of OSD pharmaceutical experience or 5 years of pharmaceutical engineering experience.
- Experience with OSD equipment procurement.
- Thorough knowledge of cGMP, OSHA, EPA and FDA facility requirements and regulations.
- Thorough knowledge of OSD operations, statistics, equipment design, process control, and process scale-up.
- Knowledge of OSD pharmaceutical process and equipment validations.
- Experience in statistical analysis: sample sizing, ANOVA, regression analysis, control charts, etc
**Lead Engineer I**
**Basic Qualifications:**
BS degree in Engineering or technical discipline.
5+ year of man
This position will support and assist in manufacturing pharmaceutical products for commercial and clinical supplies. Key duties include scale-up and transfer of oral solid dosage formulations/processes to the production facility, designing and recommending equipment purchases, and writing and executing equipment specification and commissioning protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control systems) to reduce waste and increase process reliability. Assure the resolution of deviations, corrective actions, action items from Change Control systems, and any audit non-compliance items. Perform process and equipment evaluation (FMEA, etc) to identify risks and weaknesses in new and current processes. Develop and implement SOPs in support of new and upgraded processes. Champion projects as they move into and through the manufacturing areas. Provide regular updates to leadership on project status and issues.
**Essential Functions**
- Troubleshoot and maintain manufacturing systems, processes, and equipment.
- Support the development or transfer of manufacturing and cleaning processes for the manufacturing area.
- "Hands-on" ability to install and troubleshoot instrumentation and equipment.
- Author high-quality technical protocols/reports (engineering studies, summary reports, equipment specifications, change controls, and investigations)
- Specify and size manufacturing systems, equipment, and process equipment.
**Competencies**
- Excellent communication and documentation skills
- Excellent organizational skills
- Ability to self-manage and prioritize workload.
- Ability to react quickly to understand and solve problems.
- Excellent troubleshooting skills
- Fosters collaborative relationships within and across groups through influencing and negotiation skills
- Positive attitude
**Process Engineer I**
**Basic Qualifications:**
- BS degree in Engineering or technical discipline.
- 0-2 year of manufacturing experience or technical experience.
**Preferred Qualification:**
- 0-2 years of OSD pharmaceutical experience or 5 years of pharmaceutical engineering experience.
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```
- Experience with OSD equipment procurement.
- Thorough knowledge of cGMP, OSHA, EPA and FDA facility requirements and regulations.
- Thorough knowledge of OSD operations, statistics, equipment design, process control, and process scale-up.
- Knowledge of OSD pharmaceutical process and equipment validations.
- Experience in statistical analysis: sample sizing, ANOVA, regression analysis, control charts, etc
**Process Engineer II**
**Basic Qualifications:**
- BS degree in Engineering or technical discipline.
- 2-5 year of manufacturing experience or technical experience.
**Preferred Qualification:**
- 2-5 years of OSD pharmaceutical experience or 5 years of pharmaceutical engineering experience.
- Experience with OSD equipment procurement.
- Thorough knowledge of cGMP, OSHA, EPA and FDA facility requirements and regulations.
- Thorough knowledge of OSD operations, statistics, equipment design, process control, and process scale-up.
- Knowledge of OSD pharmaceutical process and equipment validations.
- Experience in statistical analysis: sample sizing, ANOVA, regression analysis, control charts, etc
**Lead Engineer I**
**Basic Qualifications:**
BS degree in Engineering or technical discipline.
5+ year of man
Job ID: 482073838
Originally Posted on: 6/20/2025
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