GMP Manufacturing Associate

Randstad USA; Marlborough (MA); On-site; USD 48,000 - 52,000; Full time

Job summary

Randstad, in partnership with our client, is excited to welcome a Manufacturing Associate II to an incredible, dynamic team in Marlborough, MA! If you thrive in a collaborative environment that values innovation, direct mentorship, and hands‑on growth, this is the perfect place to build your future.

As a Manufacturing Associate II, you will play a key role in supporting the production of mRNA medicines for clinical and commercial evaluation.

Qualifications

• 2+ years of experience in a fast-paced, cGMP manufacturing environment.
• Strong written and verbal communication skills.
• Ability to collaborate with peers and leaders while managing multiple tasks with minimal supervision.
• Desire to learn, grow, and contribute to life-changing work.

Responsibilities

• Operate bioprocessing equipment and maintain standard cGMP practices.
• Partner with QA, QC, and Logistics to ensure technical success and rapid product disposition.
• Follow written procedures to document process instructions, data, and equipment operations.
• Monitor operations to ensure quality and environmental standards.
• Assist in deviation investigations and share insights to improve efficiency.
• Maintain safe work habits and cleanroom/gowning standards.

Skills

Communication

Teamwork

Autonomy

Attention to detail

Job description

Are you looking to take the next step in your biomanufacturing career with a supportive, high-growth team where your work directly impacts lives?

Randstad, in partnership with our client, is excited to welcome a Manufacturing Associate II to an incredible, dynamic team in Marlborough, MA! If you thrive in a collaborative environment that values innovation, direct mentorship, and hands‑on growth, this is the perfect place to build your future.

• Location: Marlborough, MA (100% Onsite)
• Pay Rate: $35.00 – $38.00/hr (depending on experience) + 5% Shift Differential
• Position Type: 6-Month Contract
• Available Shift Options:
• Experience Required: 2+ years in a fast-paced cGMP manufacturing environment

Why You’ll Love Working Here

We believe that great work happens when people come together. Working onsite gives you real‑time collaboration, strong connections with your peers, direct access to mentorship, and the opportunity to make a tangible impact every single day. You will join a culture that is bold, relentless, curious, and collaborative, operating within a safe, clean, and welcoming state‑of‑the‑art facility.

What You’ll Do

As a Manufacturing Associate II, you will play a key role in supporting the production of mRNA medicines for clinical and commercial evaluation. You will:

• Operate bioprocessing equipment and maintain standard cGMP manufacturing practices.
• Partner closely with cross‑functional teams in Quality Assurance, Quality Control, and Logistics to ensure technical success and rapid product disposition.
• Follow clear written procedures to accurately document process instructions, data, and equipment operations.
• Monitor process operations to ensure strict adherence to quality specifications and environmental standards.
• Assist in procedural deviation investigations and share insights to continuously improve operational efficiency.
• Practice safe work habits, uphold cleanroom/gowning standards, and maintain a safe, collaborative workspace.

What You’ll Need to Succeed

• Experience: 2+ years of experience working in a fast‑paced, dynamic cGMP manufacturing environment.
• Communication: Strong written and verbal communication skills with great attention to detail.
• Teamwork & Autonomy: Ability to collaborate seamlessly with peers and leaders while managing multiple tasks with minimal supervision.
• Mindset: A desire to learn, grow, and contribute to groundbreaking, life‑changing work!

Ready to Join the Team?

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [e-mail].

Pay offered to a successful candidate will be based on several factors including the candidate’s education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short‑term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.