Biotechnologist Associate

Katalyst CRO; Portsmouth (NH); On-site; USD 40,000 - 70,000; Full time

Job summary

An innovative company is seeking entry-level candidates for exciting roles in drug safety and clinical research. This position involves manufacturing therapeutic proteins in a clean room environment, ensuring compliance with cGMP regulations, and executing essential laboratory tasks. As part of a dynamic team, you will gain valuable experience in the pharmaceutical industry, working closely with university hospitals and pharmaceutical companies. If you're passionate about healthcare and eager to start your career in clinical trials, this opportunity is perfect for you!

Qualifications

• Basic understanding of cGMP and laboratory practices.
• Willingness to work in a clean room environment.

Responsibilities

• Manufacturing therapeutic proteins under cGMP conditions.
• Executing process recipes and performing laboratory tasks.
• Maintaining equipment and facility cleanliness.

Skills

cGMP compliance

aseptic technique

laboratory tasks

equipment monitoring

documentation procedures

Education

Bachelor's degree in Life Sciences

Relevant certifications

Tools

Laboratory equipment

Documentation software

Job description

Company Description

• Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
• We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description

Roles & 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.
• Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.
• Perform other duties as assigned.

Additional Information

All your information will be kept confidential according to EEO guidelines.