Biotechnologist Associate

C&G Consulting Services, Inc; Portsmouth (NH); On-site; USD 40,000 - 70,000; Full time

Job summary

An established industry player seeks a Manufacturing Associate to contribute to the production of therapeutic proteins. In this role, you'll work under cGMP conditions, executing process recipes and performing essential laboratory tasks. You'll gain valuable experience in a clean room environment while ensuring compliance with industry standards. This position offers a unique opportunity to develop skills in biotechnology and pharmaceutical manufacturing, making a significant impact in the production of life-saving therapies. If you're eager to learn and grow in a dynamic setting, this role is perfect for you.

Qualifications

• Basic understanding of cGMP compliance and aseptic techniques.
• Ability to perform laboratory tasks such as pH and conductivity measurements.

Responsibilities

• Set up and monitor production equipment while adhering to GMPs.
• Maintain facility cleanliness and support routine sanitization tasks.

Skills

cGMP compliance

aseptic technique

laboratory tasks

clean room environment

Education

High School Diploma

Associate's Degree in Science

Tools

production equipment

clean-in-place (CIP) systems

steam-in-place (SIP) systems

Job description

Job Description: Manufacturing Associate

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 should attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling products and materials.

Responsibilities include:

1. Setting up, operating, and monitoring production equipment, including clean-in-place (CIP) and steam-in-place (SIP) operations, and reporting production in written and electronic documents in accordance with GMPs and GDPs.
2. Reviewing documentation as appropriate.
3. Attaining qualification for all assigned tasks and maintaining individual training plans.
4. Performing material movements, transferring raw materials and chemicals into, out of, and across production areas.
5. Maintaining facility and equipment through routine cleaning and sanitization, supporting 6S programs.
6. Willingness to gown and work in a clean room environment.

Additional duties include administrative tasks such as attending shift exchanges and meetings, sending/receiving emails, participating in projects, and performing other duties as assigned.

Job Details

• Seniority level: Not Applicable
• Employment type: Contract
• Job function: Manufacturing, Quality Assurance, and Science
• Industries: Biotechnology Research, Pharmaceutical Manufacturing, and Manufacturing

Note: This pay range is provided by C&G Consulting Services, Inc. Your actual pay will be based on your skills and experience. Talk with your recruiter to learn more.