Biopharma Cleanroom Tech - 12-Hour Shifts, 1-Year Contract

Randstad USA

Plainville (MA)

Presencial

USD 37.000 - 39.000

Jornada completa

Hace 5 días
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Ventajas ofrecidas por este puesto de trabajo

Medical insurance
Dental insurance
Vision insurance
401K plan
Short-term disability
Life insurance

Descripción de la vacante

Randstad USA in Plainville, MA is seeking a contracted biopharma manufacturing associate for a 1-year assignment. The role operates on a 12-hour day shift schedule (7:00 AM–7:00 PM) with rotating weeks in a cleanroom environment, performing GDP- and cGMP-compliant manufacturing activities.

Responsibilities include executing batch records and operating biomanufacturing equipment in cleanrooms, inspecting products, reconciling batches, routine maintenance, and inventory tracking with PPE and

Formación

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

Responsabilidades

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

Conocimientos

Attention to detail
Communication skills
PPE compliance

Educación

High school diploma

Herramientas

Biopharma equipment

Descripción del empleo

Randstad USA in Plainville, MA is seeking a contracted biopharma manufacturing associate for a 1-year assignment. The role operates on a 12-hour day shift schedule (7:00 AM–7:00 PM) with rotating weeks in a cleanroom environment, performing GDP- and cGMP-compliant manufacturing activities.

Responsibilities include executing batch records and operating biomanufacturing equipment in cleanrooms, inspecting products, reconciling batches, routine maintenance, and inventory tracking with PPE and

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