Biotechnologist Associate

VIVOS Professional Services, LLC; Portsmouth (NH); On-site; USD 34,000 - 59,000; Full time

Job summary

VIVOS Professional Services, LLC is seeking an entry-level Associate to join our life sciences manufacturing team on a 12-month contract with potential full-time conversion.

You will work 12-hour shifts (night or day) with pay rates of $29/hr (night) or $25/hr (day) plus overtime; training in cGMP, SOPs, and aseptic technique is provided, with a focus on producing API under GMP conditions and maintaining strict documentation.

Qualifications

• Bachelor's degree in life sciences.
• Some prior experience in a manufacturing setting preferred.

Responsibilities

• Manufacture therapeutic proteins (API) under cGMP conditions.
• Execute process recipes and follow SOPs.
• Monitor equipment and processes and perform basic lab tasks (pH, conductivity, sampling).
• Maintain GMP/GDP documentation and complete training plans.
• Perform material movements and clean/instrument processes (CIP/SIP).
• Attend shift exchanges, meetings, and participate in projects.

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.)

During one week you would be only working two 12-hour shifts per week. (5 days off that week)

The following week, while you are working 60 hours (five 12-hours shifts), you are getting paid x1.5 (20 hours of overtime every two weeks)

Night shift 6:30PM-6:30AM

Days shift 7AM-7PM

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

Daily Task :

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