Quality Control Raw Materials Sampling Associate

Posted Yesterday
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Andover, MA, USA
In-Office
60K-100K Annually
Entry level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Performs GMP raw material sampling, sanitization, analytical testing, and data recording in warehouse and ISO-classified sampling areas. Conducts appearance, gas, and Raman spectroscopy testing, maintains compliant records, prioritizes assignments, supports manufacturing operations, and contributes to continuous improvement. Requires laboratory, cGMP, computer system, and raw material sampling knowledge, with physical work involving frequent walking, lifting, and material movement.
Summary Generated by Built In
Use Your Power for Purpose
The Quality Control Analytical group is seeking a highly motivated candidate to support GMP sampling and analytical testing of raw materials at the Andover site. The candidate will perform sampling, testing, and support activities for raw materials, attend meetings, and participate in continuous improvement activities
What You Will Achieve
In this role, you will:
  • Perform Raw Material Sampling in the GMP warehouse to support clinical and commercial manufacturing operations
  • Perform Daily Sanitization of ISO classified Sampling Areas
  • Perform and Review Appearance, Gas, and Raman Spectroscopy testing on Raw Materials.
  • Participate in continuous improvement culture within sampling areas. Identify opportunities for improvements and utilize site continuous improvement tools.
  • Plan and prioritize assignments to meet department and site goals
  • Record and maintain all related data and records in compliance with cGMP and quality procedures.
  • Perform work in a manner consistent with company safety policies and procedures.
  • Participate in company culture based programs.
  • Perform additional tasks as needed in the QC Analytical Department

Here Is What You Need (Minimum Requirements)
  • Bachelor's degree with any years of experience, or an associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience
  • Experience performing QC analytical testing and following procedures in a GMP laboratory
  • Strong understanding of cGMP regulations
  • Proficiency with computer systems (Microsoft Office applications, LIMS, etc.)

Bonus Points If You Have (Preferred Requirements)
  • QC laboratory experience includes Raman Spectroscopy testing
  • Experience with sampling raw materials for GMP operations
  • Experience with GMP industry standards as applied to raw materials
  • Experience with Labware LIMS PREFERRED QUALIFICATIONS

PHYSICAL/MENTAL REQUIREMENTS
Lifting up to 50-100 pounds daily. 5 to 8 hours walking, lifting, moving materials in the warehouse. Position is first shift Monday through Friday. Some off hour (night/weekend/holiday) support may be required to support staff and operations.
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:
  • Work Location Assignment: On Premise
  • Last Day To Apply: November 12th

The annual base salary for this position ranges from $60,200.00 to $100,400.00. 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.
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
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.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected] . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control

Skills Required

  • Bachelor’s degree with any years of experience; or associate’s degree with 4 years of relevant experience; or high school diploma or equivalent with 6 years of relevant experience
  • Experience performing QC analytical testing and following procedures in a GMP laboratory
  • Strong understanding of cGMP regulations
  • Proficiency with computer systems, including Microsoft Office applications and LIMS
  • QC laboratory experience including Raman Spectroscopy testing
  • Experience sampling raw materials for GMP operations
  • Experience with GMP industry standards applied to raw materials
  • Experience with Labware LIMS

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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Typical time on-site: 2.5 days a week
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