Senior Analytical Scientist

The businesses of Merck KGaA, Darmstadt, Germany; St. Louis (MO); On-site; USD 70,000 - 100,000; Full time

Job summary

A leading company in the Life Sciences sector is seeking a Senior Analytical Scientist in St. Louis to lead analytical method development efforts for external clients. The role prioritizes process improvement and requires strong troubleshooting and communication skills. Candidates should hold an advanced degree in a related scientific discipline and possess substantial research experience, with a focus on antibody drug conjugates.

Qualifications

• Minimum 6+ years of research experience for bachelor's degree.
• 2+ years of research experience for master's degree.
• 1+ years of research experience for PhD.

Responsibilities

• Serve as a subject matter expert in process and analytical development.
• Document experimental results and communicate with stakeholders.
• Lead project teams and ensure project deliverables are on quality and time.

Skills

Troubleshooting

Time Management

Attention to Detail

Communication Skills

Analytical Skills

Education

Bachelor’s Degree in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline

Master’s Degree in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline

PhD in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Statistical Software

Job description

Work Location: St. Louis, Missouri
Shift: No
Department: LS-SC-POKPE Cherokee STL PAD Team 6
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 Senior Analytical Scientist will serve as an individual contributor in the Process and Analytical Development organization. The role will involve working in a lab setting on analytical method development for external customers in the field of Antibody Drug Conjugates (ADC). 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.

Responsibilities:

• Serve as a subject matter expert in process and analytical development, perform troubleshooting / provide efficient and innovative solutions, and support transfer to GMP manufacturing
• 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

Who You Are:

Minimum Qualifications:

• Bachelor’s Degree in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 6+ years of research experience

OR

• Master’s Degree in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 2+ years of research experience

OR

• PhD in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 1+ years of research experience

Preferred Qualifications:

• Demonstrated skills in general and 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
• Current knowledge of small molecule or bio-therapeutics drug development process. Experience with antibody-drug conjugation
• Extensive hands-on experience and in-depth knowledge of the following bio/analytical technologies including: chromatography (HPLC/GC/IC/UPLC/SEC/HILIC/), protein characterization, protein functional assays and/or USP methodologies
• Robust expertise in biochemistry or organic chemistry
• Demonstrated success in contributing to the advancement of projects, project teams, and process improvements
• Excellent time management, attention to detail and strong communication skills (both written and verbal) with the abilityto efficiently communicate concepts to both specialist and general audiences
• Automation (medium to high-throughput) experience in an analytical setting and instrument maintenance / troubleshooting
• Working knowledge of Microsoft Word, Excel, and PowerPoint, as well as experience with advanced data acquisition and/or statistical software systems
• Ability to coordinate information exchange and manage data generated by contract testing labs

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.