Quality Control Raw Materials Sampling Associate - Andover, MA

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps.
Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

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.