What are the responsibilities and job description for the Upstream Scientist, TS/MS position at Eliassen Group?
Description
Onsite in Lebanon, IN
Our client seeks an Upstream Scientist to support gene therapy manufacturing within a new facility, spanning clinical and commercial production. The role will provide technical expertise for upstream process development, implementation, and technology transfer in a GMP environment. The scientist will contribute to documentation, Operational Readiness Plan milestones, and cross-functional startup activities. The position reports to the Senior Scientist of Advanced Therapies.
Due to client requirements, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance.
Rate: $55.00 to $80.00/hr. w2
Responsibilities
Onsite in Lebanon, IN
Our client seeks an Upstream Scientist to support gene therapy manufacturing within a new facility, spanning clinical and commercial production. The role will provide technical expertise for upstream process development, implementation, and technology transfer in a GMP environment. The scientist will contribute to documentation, Operational Readiness Plan milestones, and cross-functional startup activities. The position reports to the Senior Scientist of Advanced Therapies.
Due to client requirements, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance.
Rate: $55.00 to $80.00/hr. w2
Responsibilities
- Provide technical support for upstream TS/MS technology transfer activities.
- Support the development, implementation, and optimization of gene therapy manufacturing processes.
- Prepare, review, and contribute to technical documentation including protocols, reports, and regulatory filings.
- Collaborate cross-functionally to ensure successful process transfer and startup activities.
- Support completion of Operational Readiness Plan milestones and associated project deliverables.
- Ensure all activities comply with applicable regulatory and quality standards.
- Demonstrated experience in upstream bioprocessing in gene therapy or biologics manufacturing.
- Hands-on experience with technology transfer and process scale-up.
- Strong technical writing and documentation skills.
- Familiarity with GMP manufacturing environments and regulatory requirements.
- Ability to work effectively in cross-functional teams within a fast-paced startup environment.
- Bachelor’s, Master’s, or PhD in Biochemistry, Chemical Engineering, Biotechnology, or a related scientific discipline.
Salary : $55 - $80