Principal Scientist, Pharmaceutical Research & Development

ROLE SUMMARY

This scientific leadership role sits within Pfizer’s Biotherapeutics Pharmaceutical Sciences organization and is part of the Pharmaceutical Research & Development (PhRD) department. As Principal Scientist, you will lead formulation development and physico-chemical characterization efforts for Pfizer’s biotherapeutics portfolio, which includes antibody-drug conjugates (ADCs), nucleic acid delivery systems, monoclonal antibodies, antibody constructs, proteins, and vaccines.

Initially focused on supporting the ADC portfolio, this role requires working in a dynamic, interdisciplinary environment to advance preclinical, clinical, and commercial development programs. You will be responsible for scale-up and technology transfer activities, ensuring robust and scalable formulation strategies that meet regulatory and manufacturing requirements.

The ideal candidate will contribute to regulatory documentation by generating source materials for formulation selection and characterization. Success in this role demands exceptional time management, strong communication skills, and meticulous attention to detail. A broad understanding of analytical methodologies, biophysical characterization techniques, and formulation design principles is essential, along with experience in process development and drug delivery technologies.

ROLE RESPONSIBILITIES

You will be responsible for conducting experiments to support the development, evaluation, and characterization of formulations, processes, components, and delivery technologies for a wide range of therapeutic modalities. These include, but are not limited to, candidate molecules derived from mammalian and microbial fermentation, peptides, antibody-drug conjugates (ADCs), and targeted delivery strategies.

This role requires close collaboration with cross-functional teams to advance project goals. You will demonstrate technical awareness across various aspects of drug discovery and development, and lead technical project teams that apply characterization and stability data to design dosage forms that meet both clinical and commercial requirements.

You are expected to show a strong drive for learning new techniques, a deep scientific commitment, and the ability to make impactful contributions within the Pharmaceutical Research and Development (PhRD) team and broader project teams.

Responsibilities include:

• Design, execute, and analyze experiments for existing and novel modalities. Define the appropriate parenteral dosage form, formulation, process design, scale up approaches, identify critical parameters, and define the design space
• Support development of novel characterization techniques to characterize formulations to support process development and formulation design.
• Lead experiments to confirm robust process performance across the control space. Compile experimental and analytical results, perform data interpretation, summarize, and report on data with conclusions and recommended next steps
• Provide technical representation and subject matter expertise (SME) in cross functional project teams
• Provides leadership and mentorship to matrixed program team colleagues
• Collect and share relevant academic literature, leverage external consultants/SMEs, and establish new collaborations with internal groups. Optimize current processes to ensure robust manufacturing of Pfizer’s biotherapeutic portfolio
• Interface extensively in a matrixed environment with process and analytical development teams for process investigation support, assess new analytical technologies, support on-going process characterization and post-approval changes.
• Maintain accountability for project success and results delivery.
• Communicate research and development findings internally and externally.

QUALIFICATIONS

• Master of Science degree with 9 or more years of industrial experience; or B.S. with 12 or more years of industrial experience in Pharmacy, Pharmaceutics, Analytical Chemistry, Biophysics, Biomedical Eng, Chemical Eng, Biochemistry, Biotechnology, Virology, Biology or equivalent scientific field.
• Solid foundation in formulation, analytical, chemistry, material science, and/or nano-particle technologies.
• Experience in formulation development, pharmaceutics, pharmacy or drug product manufacturing or scale-up of biotherapeutics modalities.
• Experience with various biophysical and light scattering techniques (DLS, NTA, Coulter Counter, etc.).
• Experience with regulatory filings and submissions.
• Effective communication skills and the ability to write detailed technical reports.
• Exceptional organizational, communication, and critical thinking skills, and the ability to thrive in an interdependent and idea-rich environment.
• Strong work ethic and attention to detail.

PREFERRED QUALIFICATIONS

• PhD with 4 or more years industrial experience in biotherapeutics formulation and process development.
• Expert understanding and leadership of technical areas necessary for biotherapeutic molecule formulation development.
• Experience in designing parenteral dosage forms for biotherapeutics modalities including protein based, conjugates, vaccines or nanoparticle delivery systems.
• Experience in antibody drug conjugate development
• Excellent leadership skills.
• Experience in scale-up and technology transfer of aseptic processes to pilot/commercial scale manufacturing facilities.
• Solid understanding of thermodynamics and kinetics.
• Working knowledge of GLP/GMP requirements.
• Experience in authoring regulatory submissions (IND, IMPD, BLA, MAA).
• Solid understanding of QbD concept in design, execution, and interpretation of formulation and process development experiments.
• Ability to demonstrate autonomy in representing functional area.

ADDITIONAL INFORMATION

Relocation support available.

Work Location Assignment: On premise.

Last date to apply: September 2nd, 2025

The annual base salary for this position ranges from $102,900.00 to $171,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program. 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. Learn more at Pfizer Candidate Site – U.S. Benefits nearmejobs.eu (uscandidates.mypfizerbenefits.com). 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.

Sunshine Act

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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.

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Research and Development

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