GMP Bioprocess Operator (mRNA) — 3-Day Weekend

Randstad USA

Marlborough (MA)

On-site

USD 48,000 - 52,000

Full time

12 hours ago
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Benefits offered by this job

3-day weekend
5% shift differential
Drug-free workplace

Job summary

Randstad USA is seeking a Manufacturing Associate II for our Marlborough, MA site. The role involves hands-on bioprocess operations in a cGMP environment, ensuring quality and compliance on a fast-growing mRNA biopharma production line.

You will work with QA/QC, logistics, and process development teams, documenting data and driving continuous improvement using GenAI-enabled tools. This is an on-site opportunity with a 3-day weekend schedule and competitive hourly pay.

Qualifications

  • 2+ years hands-on experience in a fast-paced GMP manufacturing environment.
  • Solid working knowledge of standard bioprocess unit operations and cleanroom practices.
  • Exceptional written, verbal, and organizational skills with attention to detail.
  • Proven ability to execute multi-step tasks independently while collaborating across teams.
  • Proactive, inquisitive mindset aligned with Bold, Relentless, Curious, and Collaborative values.

Responsibilities

  • Operate bioprocess equipment safely and effectively, maintaining process execution and product quality.
  • Uphold cGMP standards and internal SOPs with proper gowning and regulatory adherence.
  • Collaborate with QA, QC, Logistics, Process Development, and Tech Transfer teams.
  • Maintain real-time documentation and contribute to deviation investigations and root-cause analyses.
  • Identify operational efficiencies and leverage GenAI and digital tools to improve workflows.

Skills

GMP manufacturing
Bioprocess operations
Cleanroom practices
Documentation
Cross-functional collaboration

Tools

Generative AI tools

Job description

Randstad USA is seeking a Manufacturing Associate II for our Marlborough, MA site. The role involves hands-on bioprocess operations in a cGMP environment, ensuring quality and compliance on a fast-growing mRNA biopharma production line.

You will work with QA/QC, logistics, and process development teams, documenting data and driving continuous improvement using GenAI-enabled tools. This is an on-site opportunity with a 3-day weekend schedule and competitive hourly pay.

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