Downstream Purification Scientist, MSAT, New Mfg. Facility
Lebanon, IN
Category: Manufacturing
Industry: Life Sciences
Reference ID: JN -072026-108021
Date Posted: 07/22/2026
Shortcut: http://careers.eliassen.com/jkUgcJ
Description:
On-site in Lebanon, IN
Our client seeks a Downstream Purification Scientist to provide technical leadership and execution support for downstream purification activities associated with gene therapy drug substance manufacturing. The role supports technology transfer, process implementation, manufacturing readiness, and documentation for clinical and commercial production. The position supports documentation activities and frontline manufacturing operations and reports to the Head of Advanced Therapies at the site.
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: $65.00 to $75.00/hr. w2
Responsibilities:
- Provide technical support for downstream MSAT technology transfer activities.
- Lead and facilitate discussions related to process lock, process optimization, and unit operation finalization.
- Prepare, review, and provide technical input to manufacturing and technical documentation.
- Author, review, and approve Master Batch Records (MBRs) and Electronic Batch Records (EBRs).
- Track MBR/EBR development status, progress, and turnaround timelines.
- Support Operational Readiness Plan deliverables for the manufacturing site.
- Serve as the downstream purification representative during internal, global, and external partner meetings.
- Support manufacturing floor activities and provide technical troubleshooting as needed.
- Identify technical issues, process deviations, and project risks, escalating concerns appropriately to management.
- Provide timely communication regarding critical manufacturing or project issues.
- Support continuous improvement initiatives while ensuring compliance with cGMP requirements.
Experience Requirements:
- Previous MSAT experience supporting downstream purification processes for gene therapy or mAb/large molecule manufacturing.
- Experience within pharmaceutical manufacturing and GMP-regulated environments.
- Experience supporting commercial manufacturing processes and developing Master Batch Records.
- Working knowledge of cGMP data integrity principles, including ALCOA+ requirements.
- Demonstrated project management skills with the ability to manage priorities and meet timelines.
- Strong technical writing, communication, and documentation skills.
Education Requirements:
- Bachelor's, Master's, or Ph.D. in Chemical Engineering, Biochemistry, Biology, or Biotechnology.
Skills, experience, and other compensable factors will be considered when determining pay rate. The pay range provided in this posting reflects a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.
W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre-tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick time if required by law in the worked-in state/locality.
If anyone reaches out to you about an open position connected with Eliassen Group, please ensure that you are working directly with us by confirming the following:
· When you work with Eliassen Group, all email communication will come from an Eliassen.com address, never Gmail, Yahoo, etc.
· Eliassen Group will never ask you for personal information (home address, bank account, or check routing number) until you have worked with someone clearly associated with Eliassen Group.
If you have any indication of fraudulent activity, please contact fraud@eliassen.com.
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Eliassen Group is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. Eliassen Group’s Affirmative Action Plan (AAP) is available for inspection by any employee or applicant for employment upon request, during normal business hours of Monday through Friday, 8:30am to 5:30pm EST. Interested persons should contact Phaedra Wells at pwells@eliassen.com for assistance. It is unlawful in Massachusetts and Maryland to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Applicants with disabilities that believe they require an accommodation or assistance with a position, please email our HR team at hradmin@eliassen.com. This email inbox is designed exclusively to assist job seekers whose disability prevents them from being able to apply online. Emails sent for other purposes will not receive a response.
Please be advised that a number of fraudulent job postings have been released under the Eliassen Group brand.
Unfortunately, fraudulent job postings can happen. If anyone reaches out to you about an open position connected with Eliassen Group, never provide personal or financial information to anyone who is not clearly associated with Eliassen Group
If anyone seemingly from Eliassen Group has ever requested this personal information in the past or does so in the future, please contact fraud@eliassen.com.
Please ensure that you are working directly with us by confirming the following:
- When you work with Eliassen Group, all email communication will come from an Eliassen.com address, never Gmail, Yahoo, etc.
- Eliassen Group will never ask you for personal information (home address, bank account, or check routing number) until you have worked with someone clearly associated with Eliassen Group, as indicated above