Biotechnologist Associate

VIVOS Professional Services, LLC; Portsmouth (NH); On-site; USD 52,000 - 90,000; Full time

Job summary

VIVOS Professional Services, LLC in Portsmouth, NH is seeking a Manufacturing Associate for a 12-month contract with possible extension or full-time conversion. The role involves manufacturing therapeutic proteins under cGMP conditions, following SOPs, and training under close supervision.

Set up, operate equipment, monitor CIP/SIP, and maintain documentation in GMP/GDP systems. Fresh grads with a life sciences bachelor’s degree are encouraged to apply; some prior manufacturing experience is

Qualifications

• Bachelor's degree in life sciences.
• Some prior experience in a manufacturing setting preferred.
• Willing to work in a clean room environment.

Responsibilities

• Manufacture therapeutic proteins (API) under cGMP conditions.
• Execute process recipes and follow SOPs while monitoring equipment and processes.
• Perform basic lab tasks including pH, conductivity, sampling and routine sanitization.
• Maintain GMP/GDP documentation and report production in written and electronic systems.
• Set up, operate, and monitor CIP and SIP operations.
• Attain task qualifications and maintain training plans.
• Perform material movements and transfer raw materials.
• Participate in 6S programs and work in a clean room environment.
• Attend shift exchanges and meetings; perform administrative tasks.
• Perform other duties as assigned.

Skills

Aseptic technique

Documentation

Basic lab tasks

Process following SOPs

Education

Bachelor's degree in life sciences

Job description

Duration: 12 months contract with possible extension or full time conversion

Pay Rate Night shift: $29/hr. on W2 (OT every 2nd Week 20 hr. OT with hourly rate of $43/hr. )

Pay Rate Day Shift: $25/hr. on W2 (OT every 2nd Week 20 hr. OT with hourly rate of $37/hr.)

Night shift 7PM-7AM 12 hour shift

Days shift 7AM-7PM 12 hour shift

This role is for fresh grads who have a bachelor's degree in life sciences.

Job Description :

Daily Task :

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.

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 plans.

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 grow and work in a "clean room" environment.

Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.

Perform other duties as assigned.

Qualifications:

bachelor's degree in life sciences.

some prior experience in a manufacturing setting preferred