The Staffing Resource Group, Inc
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Biotechnologist Associate
Posted: 07/09/2024
2024-07-09
2024-10-15
Employment Type:
Contract
Division: Life Sciences
Job Number: JN -072024-19228
State: New Hampshire
Job Description
Biotechnologist Associate
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: Biotechnologist Associate -multiple openings
Location: Portsmouth, NH
Industry: Pharmaceutical
Shift Hours: Two shift options, 12 hour shifts,7AM-7PM or 7PM-7AM
Salary: $23.25/hr. for day shift $27.00/hr. for night shift
Employment Type: Up to one year contract with possible extension or opportunity to go permanent (Benefits Available)
The Biotechnologist 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.
Responsibilities:
EOD/ADA
IND123
#LI-SRG15
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: Biotechnologist Associate -multiple openings
Location: Portsmouth, NH
Industry: Pharmaceutical
Shift Hours: Two shift options, 12 hour shifts,7AM-7PM or 7PM-7AM
Salary: $23.25/hr. for day shift $27.00/hr. for night shift
Employment Type: Up to one year contract with possible extension or opportunity to go permanent (Benefits Available)
The Biotechnologist 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.
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-40% of time
- Attain qualification for all assigned tasks and maintain individual training plan-20% of time
- Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.-10% of time
- Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.-10% of time
- Maintain facility and equipment through routine cleaning and sanitization, support 6S programs. 10% of time
- Administrative tasks attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned. 10% of time
- 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. Pharmaceutical, FDA regulated experience is highly desired.
- Experience within upstream, cell/gene manufacturing within and FDA regulated environment is a plus.
- Proven logic and decision-making abilities, critical thinking skills
EOD/ADA
IND123
#LI-SRG15
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