Quality Control Raw Materials Sampling Associate

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.

 

 

 

 

 

 

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