Scientist​/Engineer

What You Will Do

• Execute processes at lab and pilot scales, including development, characterization, scale‑up, tech transfer to commercial manufacturing, simulation, modeling, troubleshooting, and new technology implementation.
• Operate recovery and purification unit operations such as preparative chromatography, Tangential Flow Filtration (TFF), and Normal Flow Filtration (NFF) at lab, pilot, and, when required, commercial scales.
• Lead or contribute to cross‑functional projects, coordinating multiple technical projects simultaneously with clear organization and communication.

• Apply technical expertise to moderately complex projects involving development, scale‑up, characterization of processes, equipment, and control strategies, as well as technology transfer to GMP facilities.
• Execute, analyze, document, and communicate results from experimental studies at all scales; interpret data and recommend process optimizations to improve yields and facilitate smooth transitions from development to implementation.
• Troubleshoot and resolve process issues, diagnosing technical problems and determining short‑ and long‑term solutions.
• Work independently and within teams, coordinating priorities and delivering results on schedule.

• Education:
  
  BA/BS with at least 6 years of experience or MBA/MS with at least 4 years of experience; degree in Chemical/Biochemical Engineering, Biochemistry, or related biotechnology discipline.
• Technical
  
  Competencies:
  
  Knowledge and skills in purification of biologics through industrial or academic experience; demonstrated experience operating, monitoring, and controlling purification processes including chromatography, TFF, and NFF.
• Behavioral
  
  Competencies:
  
  Self‑starter, motivated, ability to work independently or as part of a team; integrity and adherence to Pfizer values, policies, and cGMP; commitment to safety and regulatory compliance; application of discipline principles for scientific judgment.

• Directly reports to the Sr. Manager / Manager of Purification in the MSAT organization.
• Interacts primarily with Purification group members and cross‑functional teams within MSAT, including Pharmaceutical Science, Technical Operations, Manufacturing, Supply Chain, Warehouse, and Quality organizations.
• Participates on cross‑functional and matrixed teams; may lead some teams with coaching from supervisor.

Occasionally required to work off‑shift, overtime, weekends, and/or holidays to meet business or stakeholder needs.

Physical:
The role may involve lifting up to 50 lb, standing in the lab for extended periods, and walking between labs and facilities.

Mental:
Requires ability to perform mathematical calculations and complex data analysis.

Annual base salary ranges from $82,700.00 to $. Eligible for a bonus target of 10.0% of base salary through Pfizer’s Global Performance Plan. Benefits include a 401(k) plan with matching contributions, paid vacation, holidays, personal days, paid caregiver/parental leave, and medical, prescription drug, dental and vision coverage.

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 expression, national origin, disability, or veteran status. Pfizer complies with all applicable nondiscrimination laws and employment eligibility verification requirements. This position requires permanent work authorization in the United States.

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws. This includes public disclosures of your name, address, and type of payments received. If you are a licensed physician and incur recruiting expenses that Pfizer pays or reimburses, those costs may be reported under the Sunshine Act.