Biotechnologist Associate/Manufacturing Technician

Net2Source Inc.; Portsmouth (NH); On-site; USD 60,000 - 80,000; Full time

Job summary

Join a forward-thinking company as a Biotechnologist Associate, where you will play a crucial role in manufacturing therapeutic proteins. This entry-level position offers a unique opportunity to work in a clean room environment, ensuring compliance with cGMP standards. You will execute process recipes, monitor equipment, and conduct essential lab tasks, contributing to groundbreaking advancements in biotechnology. With shifts that accommodate work-life balance, this role is perfect for those eager to start their career in pharmaceutical manufacturing. If you have a background in science or relevant courses, we encourage you to apply and be part of a team dedicated to innovation and quality.

Qualifications

• Basic understanding of cGMP compliance and aseptic techniques.
• Experience in manufacturing and lab tasks like pH and conductivity.

Responsibilities

• Manufacturing therapeutic proteins under cGMP conditions.
• Executing process recipes and monitoring equipment.

Skills

cGMP compliance

aseptic techniques

basic lab tasks

process recipes execution

documentation skills

Education

Background in science

Manufacturing experience

Relevant courses

Job description

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This range is provided by Net2Source Inc.. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$23.00/hr - $27.00/hr

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Job Description:

Job Title: Biotechnologist Associate/Manufacturing Technician

Job Location: Portsmouth NH 03801

Duration: 12 months (possibility of extension)

Shift: Night Shift 7pm - 7am OR Day Shift 7am - 7pm (3 days on, 2 days off and 2 days on, 3 days off)

Job Description: The Manufacturing Associate is responsible for manufacturing therapeutic proteins (API) under cGMP conditions. Responsibilities include executing process recipes, following SOPs, monitoring equipment and processes, performing basic lab tasks (pH, conductivity, sampling), and conducting routine sanitization to maintain facility and equipment. The role requires a basic understanding of cGMP compliance, aseptic techniques, equipment setup and operation, and documentation in accordance with GMPs and GDPs. Candidates will perform material transfers, maintain facility cleanliness, support 6S programs, and work in a clean room environment. Administrative duties include shift exchange, meetings, emails, and participating in projects. Additional duties may be assigned.

Candidates with backgrounds in science, manufacturing experience, or relevant courses are encouraged to apply.

Seniority level

• Entry level

Employment type

• Contract

Job function

• Manufacturing and Production
• Industries: Pharmaceutical Manufacturing, Manufacturing, Biotechnology Research

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