Job Description

The role responsibilities include, but are not limited to, the following:

• Applies a variety of GMP analytical methodologies to support the development of processes to manufacture cell therapy and monoclonal antibody therapeutics.
• Performs process development experiments, data processing, and presents results to internal departments and in technical reports and laboratory notebooks.
• Communicates scientific findings, provides status updates on assigned tasks in one-on-one discussions and within the project team and department meetings.
• Contributes to the functions of the laboratory including ordering, organization, chemical and equipment monitoring, and maintenance.

Qualifications

• Bachelor’s or Master’s degree in chemistry, biology or related degree concentration
• 1-3 years of relevant experience.
• Strong understanding of GMP requirements and process development methodology.
• Experience with protein chromatography, viral filtration, tangential flow filtration, cell culture.
• Previous experience operating AKTA, HPLC, counter-flow centrifuges and cell counting instrumentation.
• Good oral and written communication skills and the ability to review SOPs and author technical reports.

Additional Information

• Position is full-time, first shift, Monday-Friday.

• Pay range: $67,000 – $77,0000

Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.