Manufacturing Associate (Night Shift)

Randstad USA; Norwood (MA); On-site; USD 56,000 - 84,000; Full time

Benefits offered by this job

Opportunities for professional growth

Learn new skills

Part of a prestigious organization

Job summary

A leading health tech firm in Norwood is looking for a Biotech Manufacturing Associate to play a key role in producing innovative mRNA therapeutics. You will execute complex manufacturing processes while ensuring compliance with Good Manufacturing Practices. A Bachelor’s degree in a relevant field and familiarity with biopharmaceutical standards are required. This position offers opportunities for professional growth in a globally recognized organization committed to changing lives through healthcare.

Qualifications

• Bachelor’s degree completed in a relevant field is mandatory.
• Familiarity with biopharmaceutical manufacturing standards.

Responsibilities

• Execute manufacturing operations using advanced technologies.
• Ensure compliance with current Good Manufacturing Practices (cGMP).
• Document technical and operational observations accurately.
• Follow waste handling procedures to meet environmental regulations.

Skills

Familiarity with cGMP regulations

Biotechnology knowledge

Education

Bachelor’s degree in Biotechnology, Biochemistry, Molecular Biology, or a related field

Job description

Join Our Team as a Biotech Manufacturing Associate!

We are at the forefront of revolutionizing healthcare by leveraging mRNA technology to develop innovative therapies and vaccines with the potential to change lives. Our cutting‑edge manufacturing facility is committed to producing top-quality mRNA‑based products that meet global medical needs.

As a Biotech Manufacturing Associate, you will be instrumental in driving our mission forward by actively contributing to the production of groundbreaking mRNA therapeutics and vaccines.

Key Responsibilities

• Execute manufacturing operations using advanced disposable technologies, automation, and Manufacturing Execution Systems (MES) to produce mRNA products.
• Ensure strict compliance with current Good Manufacturing Practices (cGMP), standard operating procedures, and precise manufacturing documentation.
• Accurately document and communicate technical and operational observations in alignment with Good Documentation Practices (GDP).
• Adhere to waste handling procedures to uphold environmental regulations.

Qualifications

• Bachelor’s degree in Biotechnology, Biochemistry, Molecular Biology, or a related field. (Required)
• Familiarity with cGMP regulations and industry standards in biopharmaceutical manufacturing.

Why Join Us

• Work with supportive management committed to your professional growth and success.
• Gain opportunities to learn new skills and advance your career.
• Be part of a globally recognized, prestigious organization.

Shift: 12Hrs (6pm-6am)

Email: [e-mail] with your resume for a faster response.