Manufacturing Associate (Day Shift)

Randstad USA; Norwood (MA); On-site; USD 36,368 - 51,797; Full time

Benefits offered by this job

Comprehensive benefits package

Opportunities for career growth

Supportive management

Job summary

A leading biopharmaceutical organization in Norwood, Massachusetts is seeking a Biotech Manufacturing Associate to drive the production of innovative mRNA therapeutics and vaccines. The role requires a Bachelor’s degree in a relevant field and familiarity with cGMP regulations. Responsibilities include executing manufacturing operations using advanced technologies and ensuring compliance with documentation procedures. The position offers a competitive pay rate of $32/hr along with various benefits, supporting professional growth in a globally recognized company.

Qualifications

• Bachelor's degree is required in a related field.
• Understanding of cGMP regulations and biopharmaceutical standards.

Responsibilities

• Execute manufacturing operations using advanced technologies.
• Ensure compliance with cGMP and documentation procedures.
• Adhere to waste handling procedures to maintain regulations.

Skills

Familiarity with cGMP regulations

Execution of manufacturing operations

Documentation in alignment with GDP

Education

Bachelor’s degree in Biotechnology, Biochemistry, Molecular Biology, or 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 (6am-6pm)
• Pay: $32/hr. with shift differential pay

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.