Manufacturing Associate - Biotech

Aequor Technologies LLC

  • Vacaville, CA
  • 30+ days ago

    Highlights

    40% Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment.

    Numbers & Facts

    LocationVacaville, CA
    IndustryStaffing/Employment Agencies
    Company Size100 to 499 employees

    Description

    Rate details:
    Day shift (Shift 1): ***/hr
    Night shift (Shift 3): ***/hr
    - Please keep these standard pay rates aligned with the rest of the department.
    - Only submit candidates that are flexible and open to either day or night shift. The hiring team will do their best to adhere to a preference. However, shift details will be confirmed once offer has been extended.

    Shifts and Hours schedule:
    Upstream Day Shift: 6am - 7pm
    Upstream Night Shift: 6pm - 7am
    Downstream Day Shift: 6:30am - 7:30pm
    Downstream Night Shift: 6:30pm - 7:30am
    - These roles follow a 3-4-3 shift pattern

    Role Purpose:
    The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.

    40% Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate
    20% Attain qualification for all assigned tasks and maintain individual training plan
    10% Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
    10% Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
    10% Maintain facility and equipment through routine cleaning and sanitization, support 6S programs
    10% Administrative tasks attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.

    High School Diploma or Equivalent minimum; AS/BS preferred
    Preferred area of study: Science related discipline
    0-3 years experience; some prior experience in a manufacturing setting preferred.
    Proven logic and decision making abilities, critical thinking skills

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