Manufacturing Operator

Manufacturing Associate

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 Associate I
Location: Portsmouth, NH
Industry: Pharmaceutical
Hours: Days: 7 AM - 7 PM: 12hr days Every other weekend (rotating schedule including weekends)
Salary: Days: $23.25 hourly paid weekly (Benefits Available)
Employment Type: 1 year contract

Summary:
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 of products and materials.

Duties may include any of the following:

• 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 individual training plan.
• Perform material movements, transfer raw materials, 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.

• High School Diploma or Equivalent minimum AS/BS preferred.
• Preferred area of study: Science related discipline
• 1-3 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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