Biopharma Cleanroom Technician — 12h Rotating Shift (1-Year)

Randstad USA; Plainville (MA); Presencial; USD 37.000 - 39.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical

Prescription

Dental

Vision

AD&D

Life insurance offerings

Short-term disability

401K plan

Descripción de la vacante

Randstad USA in Plainville, MA is seeking a manufacturing contractor for a 1-year assignment on a rotating 12-hour day shift (7:00 AM – 7:00 PM). You will support biopharmaceutical manufacturing with strict GDP and cGMP adherence.

Responsibilities include executing batch records, maintaining documentation, and ensuring product quality while working in cleanroom environments. High school diploma required; 1 year of related experience preferred.

Formación

• High school diploma or equivalent is required.
• At least 1 year of work experience in manufacturing, operations, production, or a laboratory setting.
• Technical aptitude with biopharmaceutical manufacturing equipment and safety standards.
• Ability to follow strict cleanroom gowning regulations and wear PPE.
• Strong written and verbal communication with precise documentation.
• Willingness to work a rotating 12-hour day shift on-site in Plainville, MA.

Responsabilidades

• Execute work instructions and batch records accurately per GDP and cGMP.
• Spend ~90% of shift in cleanroom suites operating biomanufacturing equipment.
• Inspect in-process and finished products to ensure quality specs.
• Assist with batch record reconciliation, routine maintenance, and inventory tracking.
• Follow aseptic gowning protocols and safety guidelines while supporting CAPA closures.

Conocimientos

Manufacturing experience

Biopharmaceutical equipment knowledge

PPE gowning compliance

Documentation accuracy

Strong written and verbal communicator

Shift work adaptability

Educación

High school diploma or equivalent

Descripción del empleo

Randstad USA in Plainville, MA is seeking a manufacturing contractor for a 1-year assignment on a rotating 12-hour day shift (7:00 AM – 7:00 PM). You will support biopharmaceutical manufacturing with strict GDP and cGMP adherence.

Responsibilities include executing batch records, maintaining documentation, and ensuring product quality while working in cleanroom environments. High school diploma required; 1 year of related experience preferred.