TekWissen ®
1 day ago Be among the first 25 applicants
Get AI-powered advice on this job and more exclusive features.
TekWissen ® provided pay range
This range is provided by TekWissen ®. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$23.00/hr - $27.50/hr Job Title: Manufacturing Associate Location: Portsmouth, NH, 03801 Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Payrate:$ $23 to $27.50 per hour Overview
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. Our client is a leading global partner to the pharmaceutical, biotech, and nutrition industries, focusing on enabling customers to develop, manufacture, and deliver life-changing therapies. Our client provides integrated solutions across the full product life cycle, from early development and custom manufacturing to commercialization, supported by advanced technologies, strong scientific expertise, and a commitment to quality, sustainability, and innovation. Job Description
The Biotechnologist Associate / 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. 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. Required Skills & Qualifications
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. TekWissen® Group is an equal opportunity employer supporting workforce diversity. Seniority level
Associate Employment type
Contract Job function
Manufacturing
#J-18808-Ljbffr
This range is provided by TekWissen ®. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$23.00/hr - $27.50/hr Job Title: Manufacturing Associate Location: Portsmouth, NH, 03801 Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Payrate:$ $23 to $27.50 per hour Overview
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. Our client is a leading global partner to the pharmaceutical, biotech, and nutrition industries, focusing on enabling customers to develop, manufacture, and deliver life-changing therapies. Our client provides integrated solutions across the full product life cycle, from early development and custom manufacturing to commercialization, supported by advanced technologies, strong scientific expertise, and a commitment to quality, sustainability, and innovation. Job Description
The Biotechnologist Associate / 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. 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. Required Skills & Qualifications
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. TekWissen® Group is an equal opportunity employer supporting workforce diversity. Seniority level
Associate Employment type
Contract Job function
Manufacturing
#J-18808-Ljbffr