Process Engineer Pharmaceuticals I
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Job Location:
Durham County, NC - USA
Monthly Salary:
Not Disclosed
Posted on:
8 days ago
Vacancies:
1 Vacancy
Job Summary
Process Engineer Pharmaceuticals I Job Summary
Location: Research Triangle Park NC Duration: 234 Days Contract Bill Rate: $56.99/hr
Role Overview:
The Process Engineer Pharmaceuticals I is a laboratory-based contract position supporting hands-on manufacturing and process development activities for AAV gene therapy research and late-stage clinical programs. The role focuses on executing upstream and downstream bioprocess operations supporting experimental studies and ensuring data integrity and manufacturing readiness. This is an execution-driven role with no people management responsibilities ideal for those seeking direct involvement in laboratory and manufacturing environments.
Skills Required:
- BS or MS in Biotechnology Chemistry Biochemistry Chemical/Biochemical Engineering or similar
- Minimum 2 years (BS) or 0 years (MS) of relevant experience in lab research biologics manufacturing or process development
- Hands-on experience with upstream/downstream bioprocess operations
- Strong protocol adherence; ability to follow scheduled deliverables
- On-site work in a fast-paced laboratory setting
Skills Preferred:
- Exposure to cGMP environments or manufacturing-support labs
- Experience with scale-up/scale-down or process characterization experiments
- Familiarity with DOE concepts and JMP/statistical tools
- Proficiency in Microsoft Word Excel and PowerPoint
- Attention to detail and data accuracy
Key Responsibilities:
- Execute routine and defined rAAV manufacturing and laboratory tasks per established protocols and records
- Perform upstream and downstream operations (cell culture vector production purification)
- Support process development and experimental studies at small and pilot scales
- Document activities results and data in compliance with departmental SOPs and data integrity standards
- Assist with batch record completion data compilation and review
- Communicate progress and results to project stakeholders
- Support manufacturing investigations and troubleshooting including confirmatory experiments and data collection
- Contribute to technical protocols experimental reports and summary presentations
- Maintain laboratory readiness: equipment setup/maintenance consumables management and clean workspace
- Follow all safety quality and documentation procedures
:
Recruiter Insights:
- Competitive contract rate with exposure to cutting-edge gene therapy manufacturing
- Opportunity to work in a highly collaborative laboratory-focused environment
- No management or program ownership demands; focus on scientific execution
- Preferred skills (e.g. cGMP DOE JMP) enhance candidate value but are not mandatory
Candidate Insights:
- Role offers hands-on involvement in impactful gene therapy research and clinical manufacturing
- Excellent for those seeking to deepen laboratory process development and manufacturing experience
- Opportunity to collaborate closely with industry experts in a state-of-the-art facility
- Strong emphasis on protocol execution data accuracy and professional growth in biologics manufacturing
Impact & Expectations:
This position is critical to the timely and accurate execution of laboratory and manufacturing studies for gene therapy programs. Success is measured by the ability to deliver high-quality experimental and manufacturing outcomes maintain rigorous documentation and support the team in achieving research and clinical milestones. The role is suited for candidates who excel in execution thrive in dynamic lab settings and are committed to quality and data integrity.
Location: Research Triangle Park NC Duration: 234 Days Contract Bill Rate: $56.99/hr
Role Overview:
The Process Engineer Pharmaceuticals I is a laboratory-based contract position supporting hands-on manufacturing and process development activities for AAV gene therapy research and late-stage clinical programs. The role focuses on executing upstream and downstream bioprocess operations supporting experimental studies and ensuring data integrity and manufacturing readiness. This is an execution-driven role with no people management responsibilities ideal for those seeking direct involvement in laboratory and manufacturing environments.
Skills Required:
- BS or MS in Biotechnology Chemistry Biochemistry Chemical/Biochemical Engineering or similar
- Minimum 2 years (BS) or 0 years (MS) of relevant experience in lab research biologics manufacturing or process development
- Hands-on experience with upstream/downstream bioprocess operations
- Strong protocol adherence; ability to follow scheduled deliverables
- On-site work in a fast-paced laboratory setting
Skills Preferred:
- Exposure to cGMP environments or manufacturing-support labs
- Experience with scale-up/scale-down or process characterization experiments
- Familiarity with DOE concepts and JMP/statistical tools
- Proficiency in Microsoft Word Excel and PowerPoint
- Attention to detail and data accuracy
Key Responsibilities:
- Execute routine and defined rAAV manufacturing and laboratory tasks per established protocols and records
- Perform upstream and downstream operations (cell culture vector production purification)
- Support process development and experimental studies at small and pilot scales
- Document activities results and data in compliance with departmental SOPs and data integrity standards
- Assist with batch record completion data compilation and review
- Communicate progress and results to project stakeholders
- Support manufacturing investigations and troubleshooting including confirmatory experiments and data collection
- Contribute to technical protocols experimental reports and summary presentations
- Maintain laboratory readiness: equipment setup/maintenance consumables management and clean workspace
- Follow all safety quality and documentation procedures
:
Recruiter Insights:
- Competitive contract rate with exposure to cutting-edge gene therapy manufacturing
- Opportunity to work in a highly collaborative laboratory-focused environment
- No management or program ownership demands; focus on scientific execution
- Preferred skills (e.g. cGMP DOE JMP) enhance candidate value but are not mandatory
Candidate Insights:
- Role offers hands-on involvement in impactful gene therapy research and clinical manufacturing
- Excellent for those seeking to deepen laboratory process development and manufacturing experience
- Opportunity to collaborate closely with industry experts in a state-of-the-art facility
- Strong emphasis on protocol execution data accuracy and professional growth in biologics manufacturing
Impact & Expectations:
This position is critical to the timely and accurate execution of laboratory and manufacturing studies for gene therapy programs. Success is measured by the ability to deliver high-quality experimental and manufacturing outcomes maintain rigorous documentation and support the team in achieving research and clinical milestones. The role is suited for candidates who excel in execution thrive in dynamic lab settings and are committed to quality and data integrity.
