Use Your Power for Purpose
Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them.
What You Will Achieve
The Quality Control Raw Materials group is seeking a highly motivated candidate to support GMP analytical testing activities for raw materials at the Andover site. The work includes various instrumental techniques including HPLC, GC, IR, UV, as well as wet chemical methods. The candidate will also be expected to support additional QC Analytical testing activities as needed. This position requires working collaboratively with the QC raw materials team and active participating in scheduling, visual management, metrics, and continuous improvement activities. The successful candidate will be team oriented, have a passion for excellence, act with integrity, demonstrate equity and inclusivity, seek continuous improvement opportunities, and actively participate in site recognition programs.
How You Will Achieve It
In this role you will:
Perform analytical testing of raw material samples.
Record and maintain all related data and records in compliance with cGMP and quality procedures.
Identify basic technical issues, atypical or out-of-specifications test results, instrument malfunctions and methodology problems, and participate in investigations for resolution and correction.
Participate in continuous improvement culture within laboratories. Utilize continuous improvement tools.
Participate and use 5S, standard work, and visual management tools and processes.
Perform work consistent with Pfizer Values of Courage, Excellence, Equity, and Joy.
Here Is What You Need (Minimum Requirements)
B.S./B.A. in Biology, Chemistry, or related scientific discipline.
Experience working in QC testing laboratory in GMP environment in pharmaceutical industry.
Proficiency with computer systems (Microsoft Office applications, LIMS, etc.).
Strong oral and written communication skills.
Candidate must be self-motivated and be able to adapt to rapidly changing project priorities.
Bonus Points If You Have (Preferred Requirements)
Testing of compendial and non-compendial raw materials using GC, HPLC, FTIR, pH, titrations, UV, and wet chemical techniques.
Experience following USP/EP/JP compendia preferred.
Experience with six sigma, lean, and continuous improvement tools desired.
Experience with electronic laboratory information management systems such as LIMS preferred.
Physical/Mental Requirements
Normal lifting, sitting, standing, and walking requirements to facilitate testing in a laboratory environment.
Non-Standard Work Schedule, Travel or Environment Requirements
Position is first shift Monday through Friday. Some off hour (night/weekend/holiday) support may be required to support staff and operations.
Other Job Details:
Last day to apply: June 30th, 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.

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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Quality Assurance and Control