Process Scientist
Millipore Corporation

Work Location: St. Louis, Missouri
Shift: No
Department: LS-SC-POKPGA Team 3 Group 2
Recruiter: Beverly Dellisola

This information is for internals only. Please do not share outside of the organization.

Your Role:

Working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma in St. Louis, MO, the Process Scientist role will serve as an individual contributor in the Process and Analytical Development organization. The role will involve working in a lab setting on process optimization for external customers in the field of Antibody Drug Conjugates (ADC). The role will involve problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations.

Responsibilities:

• Document and communicate experimental results utilizing strong customer-facing skills
• Deliver data in a timely manner, ensure documents are compliant with transfer to GMP, make go / no-go decisions based on data
• Independent management of daily activities, lead project initiatives, lead process improvement initiatives
• Serve as mentor to less experienced scientists, become an emerging subject matter expert with ability to troubleshoot issues as they arise

Who You Are:

Minimum Qualifications:

• Bachelor's Degree in Biochemistry, Chemistry, Biology, Chemical Engineering, or other Life Science Discipline with 3+ years of industry experience

OR

• Master's Degree in Biochemistry, Chemistry, Biology, Chemical Engineering, or other Life Science Discipline with 1+ years of industry experience

OR

• PhD in Biochemistry, Chemistry, Biology, Chemical Engineering, or other Life Science Discipline

Preferred Qualifications:

• Protein purification and/or Protein Conjugation Chemistry experience
• Understanding of Design of Experiments (DoE) methodology
• Prior experience working with customers and matrix teams
• Working knowledge of Microsoft Office suite and digital documentation (modern data acquisition systems and electronic notebooks)
• Experience in process development and transfer to GMP

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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