Sr. Associate Scientist- Formulation Development

Why Patients Need You

Pfizers purpose is to deliver breakthroughs that change patients lives. Research and Development is at the heart of fulfilling Pfizers purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences ensuring drug safety and efficacy or supporting clinical trials you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

What You Will Achieve

This position will be part of Drug Product Design and Development (DPDD) within the Pharmaceutical Research and Development (PhRD) department. The incumbent will participate in the development of parenteral formulation for biologics modalities such as monoclonal antibodies peptide-based therapeutics antibody drug conjugates proteins and vaccines. This position will be responsible for performing analytical characterization of candidate molecules by using various biophysical and biochemical characterization techniques. Furthermore this position will assist in developing processes for drug product manufacturing responsible for data compilation data presentations and report writing.

Your strong foundation in general scientific practice its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge.

It is your dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

The responsibilities of Senior Associate Scientist position include but are not limited to:

• Participate in developing parenteral formulations for biotherapeutic modalities such as monoclonal antibodies peptide-based therapeutics antibody drug conjugates proteins and vaccines. This position will be responsible to assist in developing manufacturing processes (under general supervision).

• Perform rapid comprehensive characterization of candidate molecules to determine the stability profile and applying this information to develop an appropriate dosage form to meet clinical needs. This will be achieved by applying various biophysical and biochemical techniques such as UPLC (SE-UPLC IEX RP-UPLC) SDS-PAGE LC-MS Capillary Gel electrophoresis (CGE) imaged Capillary Electrophoresis (iCE) Spectroscopy techniques such as UV and Fluorescence spectroscopy Circular Dichroism and FTIR.

• The incumbent will assist in the development and scale-up of drug product processes from bench top to pilot scale and as required technology transfer to commercial plants. Examples of drug product processes are fluid transport sterilizing filtration and lyophilization.

• The Senior Associate Scientist must be able to interact effectively with a multi-disciplinary team of scientists for formulation optimization and overall candidate progression.

• This position will be responsible for preparing data summary presentation compiling data and authoring technical reports.

• Effective communication skills are desirable for interactions with laboratory scientists project managers and colleagues from numerous functions serving on multi-disciplinary project teams.

Qualifications

• B.S. in Biochemistry Chemical/Biochemical Engineering Pharmacy Chemistry Biology or equivalent with a minimum of 2 years relevant industry experience.

• Ability to follow established procedures independently is required.

• Working knowledge of SE-UPLC RP-UPLC LC-MS peptide mapping UPLC (IEX) SDS-PAGE Capillary Gel electrophoresis (CGE) imaged Capillary Electrophoresis (iCE) spectroscopy techniques.

• In addition experience with biotherapeutics analytical methods such as UPLC (IEX) SDS-PAGE Capillary Gel electrophoresis (CGE) imaged Capillary Electrophoresis (iCE) spectroscopy techniques

• Demonstrated scientific documentation skills

Preferred Qualifications

• M.S. Degree in above and 0-2 years of experience preferred.

• Experience with drug development of biologics and vaccines.

• 2-4 years of hands-on lab experience in analytical techniques.

• Excellent documentation skills.

• Self-motivated and highly effective in a team-based environment.

• Effective written and oral communication skills.

• Familiarity with GMP requirements.

• Familiarity with parenteral manufacturing requirements container/closure integrity and clinical and commercial unit operations.

• Practical knowledge of lyophilization and lyophilization cycle development

PHYSICAL/MENTAL REQUIREMENTS

Lab-based position requiring standing and working a lab and operating analytical and formulation instruments and equipment.

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

Occasional travel required to support project work or training.

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.