Senior Analytical Scientist

Millipore Corporation; St. Louis (MO); On-site; USD 76,000 - 114,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Retirement contributions

Job summary

Millipore Corporation is seeking a Sr. Analytical Scientist in St. Louis, MO. You will solve problems, manage timelines, and contribute to documentation for method qualification and transfer into GMP manufacturing.

Responsibilities include leading analytical development, troubleshooting, authoring development documents, and guiding cross-functional teams to ensure on-time, high-quality project delivery in a fast-paced GMP environment.

Qualifications

• Bachelor's degree in chemistry, biochemistry, biomedical engineering, chemical engineering or other life science or engineering discipline and 6+ years of research in an industrial or post-graduate setting.
• Master's degree in chemistry, biochemistry, biomedical engineering, chemical engineering or other life science or engineering discipline and 2+ years of research in an industrial or post-graduate setting.
• PhD in chemistry, biochemistry, biomedical engineering, chemical engineering or other life science or engineering discipline and 1+ years of research in an industrial or post-graduate setting.

Responsibilities

• 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, ensure 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.

Skills

Analytical development

Troubleshooting

Project leadership

Documentation

Cross-functional communication

Regulatory awareness

Data analysis

Quality mindset

Education

Bachelor's degree in Chemistry or Life Science with 6+ years of research

Master's degree in Chemistry or related field with 2+ years of research

PhD in Chemistry or related field with 1+ years of research

Tools

ELISA

SPR

HPLC

Isoelectric focusing

UV-Vis

Chromatography

Job description

Work Location: St. Louis, MissouriShift: NoDepartment: LS-SC-UYKPEA Cherokee STL PAD Team 6 Group 1Recruiter: Michelle Cole

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

Key responsibilities include the following:

• 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, ensure 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

Minimum Qualifications

• Bachelor's degree in chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 6+ years of research in an industrial or post-graduate setting
• Master's degree in chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 2+ years of research in an industrial or post-graduate setting
• PhD in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 1+ years of research in an industrial or post-graduate setting

Preferred Qualifications

• 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 analytical settings 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 and Benefits

Pay Range for this position: $75,700 - $113,500 annually

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.

For more information.

Equal Employment Opportunity

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.