Manufacturing Associate

Katalyst Healthcares & Life Sciences

Manufacturing Associate

Portsmouth, NH
Full Time
Paid
  • Responsibilities

    Job Description

    Job description:
    The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. 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 products and materials.

    Responsibilities:

    • 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.
    • Attain qualification for all assigned tasks and maintain an individual training plan.
    • Perform material movements, transfer raw materials and chemicals into, out of, across the production areas.
    • Maintain facility and equipment through routine cleaning and sanitization, support 6S programs.
    • Must be willing to gown and work in a "clean room " environment.
    • Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.
    • Perform other duties as assigned.

    Requirements:

    • High School Diploma or equivalent experience minimum with an AS/BS preferred
    • Preferred area of study: Science related field, degrees in Genetics are relevant.
    • Prior work experience in a cleanroom, laboratory, or another sterile setting is preferred.
    • Prior experience with Aseptic Techniques and gowning procedures is preferred.
    • Working experience in manufacturing; cGMP setting preferred. The ideal candidate will have experience within the Cell and Gene Therapy field.
    • Able to follow documentation procedures for day-to-day tasks in a regulated industry.
    • Proven logic and decision-making abilities, critical thinking skills.
    • Strong written and verbal communication skills

    Note:

    • Days - 12 hour shifts - days 7am – 7pm.
    • Night shift 7 pm - 7 am, 12hr shift.
  • Qualifications

    Additional Information

    All your information will be kept confidential according to EEO guidelines.

  • Industry
    Hospital and Health Care