Biotechnologist Associate

HireTalent; Portsmouth (NH); On-site; USD 60,000 - 80,000; Full time

Job summary

Ein innovatives Unternehmen sucht einen Biotechnologen, der in der Herstellung therapeutischer Proteine unter strengen cGMP-Bedingungen tätig ist. In dieser spannenden Rolle sind Sie verantwortlich für die Ausführung von Prozessrezepten, die Überwachung von Produktionsabläufen und die Durchführung grundlegender Labortätigkeiten. Sie arbeiten in einem sauberen Raum und müssen bereit sein, sich an strenge Hygiene- und Sicherheitsprotokolle zu halten. Diese Position bietet die Möglichkeit, praktische Erfahrungen in einem dynamischen Umfeld zu sammeln und sich in der Biotechnologiebranche weiterzuentwickeln. Wenn Sie eine Leidenschaft für Wissenschaft und Technik haben, könnte dies die perfekte Gelegenheit für Sie sein.

Qualifications

• Grundkenntnisse der cGMP-Compliance sind erforderlich.
• Fähigkeit, SOPs und Richtlinien zu befolgen.

Responsibilities

• Herstellung therapeutischer Proteine unter cGMP-Bedingungen.
• Überwachung von Produktionsprozessen und Dokumentation.

Skills

Aseptische Techniken

GMP Compliance

Laboratory Skills

Dokumentationsfähigkeiten

Mechanische Fähigkeiten

Computer Skills

Education

Wissenschaftlicher Abschluss

Tools

Reinigungs- und Sanitärgeräte

Job description

Job Title: Biotechnologist Associate

Job Duration: 12 months
Job Location: Portsmouth, NH
Shift time: 7:00 pm - 7:00 am

Summary:

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.

1. 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.
2. Attain qualification for all assigned tasks and maintain individual training plan.
3. Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
4. Maintain facility and equipment through routine cleaning and sanitization, support 6S programs. Must be willing to gown and work in a 'clean room' environment.
5. Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.
6. Perform other duties as assigned.

Preferred Backgrounds:

Candidates with the following backgrounds have had success in manufacturing at *** combined with a scientific degree, manufacturing experience or courses/interests in science:

• Food service
• Cooks (can follow recipes)
• Pharmacy techs
• Mechanical aptitude
• Robotics
• Computer skills (this is ever more important as our suites are more automated)
• EMTs
• Tech Support
• Anything in which they need to follow SOPs, Guidelines, industry regulations
• Sig Sauer employees
• Security guards
• Nurses/nurse aides