Senior Associate Scientist

Pfizer; St. Louis (MO); On-site; USD 69,000 - 114,000; Full time

Benefits offered by this job

401(k) plan with matching

Paid time off and holidays

Health benefits

Job summary

Pfizer in Chesterfield, MO is seeking a Senior Associate Scientist in Analytical R&D to develop and apply analytical methods for biotherapeutics and vaccines. You will work on method development, transfer, verification, and qualification to support process and formulation development in a regulated setting.

The role requires a bachelor's or master's in chemistry/biochemistry/biology with 3+ years (or 0-2 with master's) and experience with laboratory analytics, data documentation, and

Qualifications

• Bachelor's or Master's degree with related experience as specified.
• Laboratory experience in analytical techniques.
• Ability to follow procedures.
• Desirable: Quality Systems and Good Documentation Practices.
• Knowledge of drug development processes for biologics.
• Experience with AI tools to support problem solving and productivity.

Responsibilities

• Develop analytical methodologies to support process development of biotherapeutics and vaccines.
• Proficiency with HPLC, colorimetric, and electrophoresis assays.
• Record, archive, and report data per guidelines.
• Collaborate effectively with peers and leaders in a multi-disciplinary team.
• Thrive in a fast-paced environment with strong attention to detail and organization.
• Document analytical results in technical reports.

Skills

Analytical methods

Documentation

Team collaboration

AI tools literacy

Education

Bachelor's degree in Chemistry/Biochemistry/Biology

Master's degree in Chemistry/Biochemistry/Biology

Tools

ChatGPT

Microsoft Copilot

Job description

Use Your Power for Purpose At Pfizer, our purpose is to deliver breakthroughs that change patients' lives. As a Senior Associate Scientist, you will be at the forefront of this mission, working within our Research & Development division. Your role will be pivotal in translating advanced science and technologies into therapies and vaccines that matter most. By leveraging cutting-edge design and process development capabilities, you will help accelerate the delivery of best-in-class medicines to patients globally, ultimately improving their lives.

ROLE SUMMARY

The qualified candidate will join the Analytical R&D organization to enable development of biological therapeutics and vaccines in Chesterfield, MO. They will be responsible for applying analytical methods in the assessment of product quality, detection of impurities, and characterization. This group performs testing in the R&D and/or regulated settings in support of clinical drug and vaccine candidates. The group performs method development, transfer, verification, and qualification in support of process and formulation development for biotherapeutics and vaccines.

ROLE RESPONSIBILITIES

• Developing, troubleshooting, and utilizing analytical methodologies to support process development of biotherapeutics, vaccines and oligonucleotides.
• Becoming proficient in a breadth of analytical methodologies including HPLC, colorimetric, and electrophoresis assays.
• The colleague must work within corporate guidelines and must appropriately record, archive, and report all data.
• The colleague must also be able to interact effectively with peers and leaders as part of a multi-disciplinary team.
• The candidate must thrive in a fast-paced environment.
• Attention to detail, strong organizational skills, the ability to multitask and effective interpersonal and communication skills are required.
• Documentation of analytical results in technical reports is required.

QUALIFICATIONS

• Minimum: Bachelor's degree in Chemistry, Biochemistry, Biology, or a related field, with 3+ years of relevant experience; or Master's degree in Chemistry, Biochemistry, Biology, or a related field, with 0-2 years of relevant experience.
• Laboratory experience in a variety of analytical laboratory techniques.
• Ability to follow established procedures under minimal supervision.
• Desirable: Experience with Quality Systems and Good Documentation Practices.
• Some knowledge of drug development process for progression of biological candidates.
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.
• Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use.

OTHER ATTRIBUTES DESIRABLE

• Excellent documentation skills
• Self-motivated and highly effective in a team-based environment
• Effective oral and written communication skills
• Experience in analysis of large molecules
• Experience with laboratory data systems such as Laboratory Information Management Systems

PHYSICAL/MENTAL REQUIREMENTS

Position requires occasional light lifting and periods of standing, sitting or walking.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

None

Work Location Assignment: On Premise

On Premise

COMPENSATION & BENEFITS

The annual base salary for this position ranges from $68,600.00 to $114,300.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 7.5% of the base salary.

We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage.

Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States. Relocation assistance may be available based on business needs and/or eligibility. Candidates must be authorized to be employed in the U.S. by any employer. U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States. Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [e-mail].

RESEARCH AND DEVELOPMENT

Research and Development Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We are looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.