Quality Control Raw Materials

Randstad USA; Norwood (MA); On-site; USD 46,838 - 47,802; Full time

Job summary

A leading staffing and workforce solutions provider in Norwood, Massachusetts is seeking an Associate I, Quality Control to ensure the highest standards of raw materials in their manufacturing site. This on-site role requires a Bachelor’s degree and a collaborative spirit to work within a dynamic team. Responsibilities include sampling, inspection, and maintaining compliance with GxP regulations. Ideal candidates should possess strong attention to detail and a proactive attitude towards quality assurance. Apply now to contribute to life-changing medicines!

Qualifications

• 0-1 years of experience with a BS, or 2+ years in a GMP Quality Control laboratory setting.
• Desire to learn and master GxP regulations and SOP-driven workflows.
• Ability to work effectively within a cross-functional team.

Responsibilities

• Perform sampling and inspection of raw materials and consumables.
• Coordinate sample logistics between internal and external labs.
• Log data into LIMS and maintain meticulous cGMP documentation.
• Operate within cleanroom environments using aseptic techniques.
• Support quality systems including deviations, CAPAs, and investigations.
• Maintain lab supplies and uphold a safe, collaborative work culture.

Skills

GMP Quality Control

Collaboration

Compliance Mindset

Education

Bachelor’s degree in a relevant scientific discipline

Tools

LIMS

Job description

Associate I, Quality Control (Raw Materials)

Location: Norwood, MA (On-site) Shift: Monday – Friday, First Shift (8:00 AM – 5:00 PM)

Base Pay Range: $34.00/hr – $34.70/hr

Are you ready to launch your career in the cutting‑edge world of mRNA technology? We are seeking a motivated Associate I, Quality Control to join our team at our state‑of‑the‑art manufacturing site in Norwood. This is a vital individual contributor role focused on the quality, safety, and integrity of raw materials that power life‑changing medicines.

The Impact You’ll Make: You will be on the front lines of Quality Control, ensuring that every material entering our facility meets the highest standards. From hands‑on sampling in cleanroom environments to managing complex data in LIMS, your work ensures our manufacturing processes remain seamless and compliant.

Key Responsibilities

• Perform sampling and inspection of raw materials and consumables.
• Coordinate sample logistics between internal and external labs.
• Log data into LIMS and maintain meticulous cGMP documentation.
• Operate within cleanroom environments using aseptic techniques.
• Support quality systems, including deviations, CAPAs, and investigations.
• Maintain lab supplies and uphold a safe, collaborative work culture.

What You’ll Need (Basic Qualifications)

• Education: Bachelor’s degree in a relevant scientific discipline.
• Experience: 0–1 years of experience with a BS, or 2+ years of experience in a GMP Quality Control laboratory setting.
• Compliance Mindset: A strong desire to learn and master GxP regulations and SOP‑driven workflows.
• Collaboration: A positive attitude and the ability to work effectively within a cross‑functional team.

Note: This position is 100% site‑based and is not eligible for remote work.

Apply today to help us innovate, collaborate, and build the future of medicine!

FOR MORE IMMEDIATE CONSIDERATION, email a current resume to [e-mail]

Seniority Level

• Associate

Employment Type

• Contract

Job Function

• Quality Assurance and Manufacturing
• Industries: Pharmaceutical Manufacturing and Biotechnology Research

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