ASK Consulting · 3 days ago
Biotechnologist Associate (Night Shift) (273259)
Portsmouth, NH, US
Full-time
Onsite
New Grad, Entry Level
$27/hr - $27/hrASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. They are seeking a Biotechnologist Associate responsible for manufacturing therapeutic proteins under cGMP conditions, executing process recipes, and performing laboratory tasks while training under supervision.
Human ResourcesRecruitingStaffing Agency
No H1B
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
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
Qualification
Required
Must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted
Unable to provide sponsorship
Responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions
Expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes
Perform basic laboratory tasks, including pH, conductivity, sampling
Conduct routine sanitization tasks to maintain facility and equipment
Attain a basic understanding of cGMP compliance while training under close supervision
Demonstrate 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
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
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
Company
ASK Consulting
ASK Consulting provides innovative talent implementation, workforce management, and project solutions to various industries.
Founded in 1995
501-1000 employees
Funding
Current Stage
Late StageLeadership Team
Justin Kidd
Senior Vice President - Strategic Partnerships
Jim Wilson
Founder
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