Andover, Massachusetts, USA
1 day ago
Associate Scientist
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

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 to support GMP in-process, release, and stability testing of clinical supplies. This group also performs micro method qualifications and Environmental Monitoring (EM) of Drug Substance and Drug Product facilities.

The individual is responsible for becoming proficient in aseptic lab technique and facility gowning for EM in various GMP facilities (Cell Banking, Drug Substance, Drug Product) as well as facility water collection & testing, facility gas system collection & testing. Other assays may include bioburden, endotoxin, microbial identifications, media qualification, qPCR (e.g. MMV), and sterility testing.  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

Required:  BA or BS in biology, microbiology, or related field with o to 2 years of experience

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)/Electronic Laboratory Notebook (ELN)

Nice to Have

1- year Biotech/pharmaceutical GMP laboratory experience.

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. 

  

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

This is a first shift position, Tues-Sat (Mondays off).

Other Job Details
 Job Location: On premise


The annual base salary for this position ranges from $54,700.00 to $91,100.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

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.

Research and Development

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