Associate Scientist, Microbiology (2nd Shift)
- United States - Massachusetts - Andover
Why Patients Need You
Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s 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
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality.
The qualified candidate will join the Analytical R&D Microbiology organization to enable development of biological therapeutics in Andover, MA. The qualified candidate will be responsible for applying GMP microbiological methods (bioburden, LAL, PCR, etc.) in the assessment of product quality and detection of impurities. This group also performs micro method qualifications and Environmental Monitoring (EM) of Drug Substance and Drug Product facilities.
How You Will Achieve It
The qualified colleague is responsible for utilizing established microbiological methodologies to support GMP in-process, release, and stability testing of clinical supplies.
The individual is responsible for becoming proficient in aseptic lab technique and facility gowning for EM, bioburden and LAL testing, microbial identifications, and qPCR.
The colleague must work within corporate guidelines and must appropriately record, archive and report all data as this is a cGMP compliant laboratory.
The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team.
The candidate must thrive in a fast-paced environment. Attention to detail, strong organizational skills, the ability to multitask and effective interpersonal, influencing skills and communication skills are required.
Qualifications
Must-Have
BA/BS in microbiology, biochemistry, biology or related field with 0-2 years of experience in Biotech/pharmaceutical GMP laboratory.
Ability to follow established procedures under minimal supervision.
Experience with Quality Systems in a GMP environment.
Some knowledge of drug development process for progression of biological candidates.
Nice-to-Have
Excellent documentation skills
Self-motivated and highly effective in a team-based environment
Effective oral and written communication skills
Experience with laboratory data systems such as Laboratory Information Management Systems (LIMS)
PHYSICAL/MENTAL REQUIREMENTS
Occasional lifting, sitting, standing, walking, bending. Time spent at a computer.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
2nd Shift 1-9pm M-F
PHYSICAL/MENTAL REQUIREMENTS
Lifting, sitting, standing, walking, bending and occasional computer time.
Work Location Assignment: On Premise
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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Research and Development