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
Hours: Night: 6:45AM - 6:45PM: 12hr days 3 days one week and 4 the next.
Salary: $19.90 hourly paid weekly (Benefits Available)
Employment Type: 12 month contract
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 Lonza 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:
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..
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