We’re currently hiring for a Purification Manufacturing Technician I role at a new biopharmaceutical manufacturing facility in Hopewell, NJ (100% on-site).
This is a 6 Month Contract
General Description: The Purification Manufacturing Technician I / II position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations.
1) Facility Start-Up: Focused on cell culture related activities required to design, build, commission, and license first biopharmaceutical plant in the United States.
Essential functions of the job include but not limited to:
A. Design review
B. Equipment selection, procurement and testing
C. Protocol development and execution
D. Acceptance testing and equipment/automation debugging
E. Technical training
2) Hands-On cGMP Operations: Focused on execution of cGMP manufacturing activities required to deliver the production plan reliably and compliantly.
Essential functions of the job include but not limited to:
A) Follow cGMP procedures to support manufacturing execution and automated recipes.
B) Clean-In-Place (CIP) & Steam-In-Place (SIP).
C) Buffer preparation & transfers / filtration
D) Operational and cleaning of chromatography and filtration systems.
E) Equipment & process troubleshooting.
F) Deviation identification, reporting and closure.
G) cGMP procedure development and optimization.
- Additional Skills/Attributes Required:Evidence of good verbal and written communication.
- Ability to work in fast paced dynamic environment with competing priorities.
- Demonstrated ability to collaborate within and between diverse groups.
- Proactive identification and implementation of continuous improvement opportunities.
- Able to receive and incorporate feedback – passion for ongoing professional development a plus.
- Aptitude for learning moderately complex technical systems
