Senior Associate Scientist

Use Your Power for Purpose

At Pfizer our purpose is to deliver breakthroughs that change patients lives. As a Senior Associate Scientist Biology you will be at the forefront of our mission contributing to the development of innovative therapies and vaccines that have the potential to transform patient care. Reporting to the Research & Development division you will leverage advanced science and cutting-edge technologies to make a tangible impact on global health. Your work will be instrumental in ensuring drug safety and efficacy supporting clinical trials and accelerating the delivery of top-tier medicines to patients worldwide.

What You Will Achieve

In this role you will be part of Pharmaceutical Research and Development supporting Pfizers biotherapeutics portfolio contributing to the development of parenteral formulations for antibodydrug conjugates (ADCs) and monoclonal antibodies (mAbs) with potential to work on proteins and other biologics.

You will perform formulation development and analytical characterization of candidate molecules and formulations using a range of biophysical and biochemical techniques. You will also support drug product manufacturing process development and be responsible for data compilation presentations and technical report writing.

A strong foundation in scientific principles and best practices will enable you to meet critical deadlines and deliver highquality work. As a technical contributor you will assess assigned tasks and make informed decisions through the direct application of your expertise. Your dedication will help Pfizer reach new milestones and ultimately improve the lives of patients worldwide.

How You Will Achieve It

The responsibilities of theSenior Associate Scientistposition include but are not limited to:

• Support development of parenteral formulations and manufacturing processes for ADCs and mAbs.

• Characterize candidate molecules and formulations to establish stability profiles using a broad range of biophysical and biochemical techniques (e.g. U/HPLC imaged capillary electrophoresis (iCE) capillary gel electrophoresis (CGE) spectroscopy).

• Assist with scale-up of drug product processes (fluid handling sterilizing filtration lyophilization) from bench to pilot scale and support technology transfer to manufacturing facilities.

• Collaborate within team and crossfunctionally to advance formulation optimization and candidate progression.

• Summarize data prepare presentations and author technical reports to communicate results.

Here Is What You Need(Minimum Requirements)

• Bachelors degree (BA/BS) in Biochemistry Chemical or Biochemical Engineering Pharmacy Chemistry Biology or a related discipline withat least 2 years of relevant experience or a Masters degree in a relevant discipline with 0 years of experience.

• Handson laboratory experience with a variety of analytical techniques which may include UPLC (SEC IEX) capillary gel electrophoresis (CGE) imaged capillary electrophoresis (iCE) and spectroscopic methods.

• Excellent problemsolving and criticalthinking skills used to solve scientific problems using experimental techniques with contemporaneous recording of experimental details and data in an electronic laboratory notebook (ELN).

• Ability to effectively communicate (oral and written) and collaborate with experience working within multidisciplinary project teams

• Strong attention to detail and a high level of accuracy in scientific work and documentation

• Strong organizational and timemanagement skills.

• Proficiency with general computer software including word processing spreadsheets and presentation tools.

Bonus Points If You Have(Preferred Requirements)

• Experience in formulation and process development for lyophilized ADC and/or mAb drug product

• Hands-on experience with analytical techniques such as SEUPLC RPUPLC Karl Fischer titration differential scanning calorimetry (DSC) freeze-drying microscopy (FDM) dynamic light scattering (DLS) etc.

• Knowledge of current U.S. and global regulatory requirements including FDA and ICH guidance.

• Experience using common AIenabled tools including generative technologies such as ChatGPT or Microsoft Copilot to support problem solving and enhance productivity.

PHYSICAL/MENTAL REQUIREMENTS

This is an on-site lab-based position and incumbent must be able to perform all lab-based duties.

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

Some travel expected to support work across other Pfizer sites or CMO/CDMO network.

Additional Information:

• Work Location Assignment:On Premise
• Last Day to Apply: May 15 2026

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.