Biotechnologist Associate (Manufacturing)

VIVOS Professional Services, LLC; Portsmouth (NH); On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a Biotechnologist Associate to join their manufacturing team. In this role, you will be responsible for the production of therapeutic proteins in a clean room environment, ensuring compliance with cGMP standards. You will execute process recipes, monitor equipment, and perform essential laboratory tasks while maintaining a high standard of cleanliness. This is a fantastic opportunity for those looking to grow their expertise in the pharmaceutical manufacturing sector and contribute to innovative biotechnological advancements. If you are eager to learn and thrive in a collaborative environment, this role is perfect for you.

Qualifications

• Basic understanding of cGMP compliance and aseptic techniques required.
• Ability to perform basic laboratory tasks and operate manufacturing equipment.

Responsibilities

• Responsible for manufacturing therapeutic proteins under cGMP conditions.
• Execute process recipes, monitor equipment, and perform routine sanitization tasks.

Skills

cGMP compliance

aseptic technique

laboratory tasks

equipment operation

Job description

Biotechnologist Associate (Manufacturing)

2 days ago Be among the first 25 applicants

VIVOS Professional Services, LLC provided pay range

This range is provided by VIVOS Professional Services, LLC. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$20.00/hr - $23.00/hr

Portsmouth, NH

Job Responsibilities

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 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.

Seniority level

Associate

Employment type

Contract

Job function

Manufacturing

Industries

Pharmaceutical Manufacturing and Biotechnology Research