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Manufacturing Operator I

Portsmouth, NH

Posted: 01/12/2023 Division: Life Sciences Job Number: JN -012023-16225

Job Description

Manufacturing Operator I

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.

Title: Manufacturing Operator I

Location: Portsmouth, NH

Industry: Pharmaceutical

Hours: Day shift 7 AM - 7 PM: 12hr days rotating schedule, every other weekend

Salary: $22.50/ hourly paid weekly (Benefits Available)

Employment Type: 1 year contract - possible extend

Summary:

The Manufacturing Services Associate I is responsible for supporting all cGMP manufacturing production suites. They support the production groups by ensuring the suites are appropriately stocked with raw materials and consumables, assemble and autoclave assemblies for use, clean soiled parts, perform daily/weekly maintenance on analytical equipment, and complete scheduled cleaning requirements that are not fulfilled by company's contracted cleaning staff. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products and materials.

Duties may include any of the following:

  • Perform 6S and stock each suite daily, clean soiled parts daily.
  • Determine production needs for autoclaved assembles and deliver to suites.
  • Perform daily and weekly maintenance activities on analytical equipment.
  • Perform weekly and monthly cleans of inoculum rooms.
  • Report all activities 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 individual training plan
  • Prepare materials for transport and delivery to manufacturing suites. Perform material movements into, out of, and across the production areas.
  • Maintain facility and equipment through routine cleaning and sanitization.
  • Administrative tasks attending suite shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
  • Perform other duties as assigned.

Education and Experience:

  • 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
  • Proven logic and decision making abilities, critical thinking skills

EOE/ADA

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