Senior Analytical Scientist

Work Location:

St. Louis, Missouri

Shift: No
Department: LS-SC-UYKPA Cherokee STL PAD Team 7
Recruiter:
Kathy Lewison

In this role you will be involved with problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing.

• Serve as a subject matter expert in analytical development, perform troubleshooting / provide efficient and innovative solutions, and support transfer of analytical methods to GMP QC labs.
• Utilize customer‑facing skills, document experimental results, communicate results to all stakeholders, author method development and qualification documents, contribute to information for customer proposals.
• Serve as a project lead and ensure project deliverables are on quality and on time, develop multiple technical approach plans as needed to solve problems and mitigate risk, ensures process and methods are in place for efficient GMP start.
• Lead project teams, influence exemplary work in other team members, lead process improvement initiatives, scout for new technologies / emerging trends, proactively consider the impact of quality, regulatory, manufacturing, and safety requirements when planning project activities.

• Bachelor’s Degree in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 6+ years of research experience.
• Master’s Degree in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 2+ years of research experience.
• PhD in in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 1+ years of research experience.

• Experience with protein characterization via ELISA, SPR, Isoelectric Focusing, CE‑based methods, UV‑Vis, and/or chromatography (HPLC/GC/IC/UPLC/SEC/HILIC).
• Experience with advanced laboratory techniques; theory and practice to enable the development of novel approaches to solve complex process and analytical problems on fast‑paced projects with changing priorities.
• Knowledge of small molecule or bio‑therapeutics drug development process.
• Experience with antibody‑drug conjugation.
• Knowledge in Biochemistry or Organic Chemistry.
• Experience in automation in an analytical setting and instrument maintenance and troubleshooting.
• Knowledge of Microsoft Word, Excel, and PowerPoint.
• Experience with advanced data acquisition and/or statistical software systems.
• Ability to coordinate information exchange and manage data generated by contract testing labs.

Pay Range for this position: $68,700/yr - $132,700 yr. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job‑related factors. Position may be eligible for sales or performance‑based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.

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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.