cGMP Operator Produktion (m/w/d)

JR Germany; Frankfurt; Vor Ort; EUR 40.000 - 65.000; Vollzeit

Zusammenfassung

An established industry player is seeking a cGMP Operator to join their dynamic team in Frankfurt. This role involves preparing and processing synthetic oligonucleotides while ensuring compliance with GMP standards. You will operate advanced synthesis and HPLC systems, contributing to the production of innovative active ingredients for modern medicines. With a focus on creating a harmonious work environment, the company offers flexible working hours and opportunities for professional development. If you're passionate about biotechnology and eager to make an impact, this is the perfect opportunity for you.

Leistungen

Attractive Compensation

Mobility Benefits

Development Opportunities

Flexible Working Hours

Qualifikationen

• Completed training in production or chemistry-related fields.
• Experience in the chemical or pharmaceutical industry is a plus.

Aufgaben

• Prepare and process synthetic oligonucleotides in a lab setting.
• Operate synthesis machines and monitor production equipment.

Kenntnisse

GMP Compliance

Chemical Processing

Laboratory Skills

Fluent German

Basic English

Ausbildung

Bachelor's Degree in Chemistry/Biotechnology

Training as Production Specialist

Chemical Technician Training

Tools

HPLC Systems

Synthesis Machines

Ultrafiltration Equipment

Freeze-Drying Equipment

Jobbeschreibung

Join us in moving the elements of life.

BioSpring is a globally leading manufacturer of synthetic nucleic acids for use in therapy, diagnostics, research, and development.

We are a medium-sized, owner-managed biotechnology company headquartered in Frankfurt am Main.

cGMP Operator Production (all genders)

Job Description

1. You will be responsible for preparing, manufacturing, and processing synthetic oligonucleotides in laboratory and pilot plant scale.
2. You will operate and monitor state-of-the-art synthesis machines, HPLC systems, ultrafiltration, and freeze-drying equipment, working with the Large Scale team after thorough training.
3. You will work independently in cleanrooms within the downstream process, ensuring GMP compliance through careful work and documentation.
4. You will acquire fundamental GMP knowledge to apply in the production of innovative active ingredients for modern medicines.

Qualifications

1. You have successfully completed training as a production specialist, chemical technician, chemical laboratory technician, or a bachelor's degree in chemistry/biotechnology or related fields.
2. Ideally, you have some professional experience in the chemical or pharmaceutical industry and familiarity with GMP guidelines.
3. No GMP experience? No problem! You will participate in GMP training and be integrated into the team to ensure product quality.
4. You have fluent German skills and, ideally, good English skills.
5. You are willing to work in shifts from 6:00 AM to 10:00 PM, with flexible and regulated working hours. Feel free to discuss this during the interview.

What We Offer

We provide a harmonious, dynamic, and multicultural work environment in an exciting industry. All our work areas are modern and high-tech, offering engaging tasks and opportunities to influence processes.

Our package includes attractive compensation, mobility benefits, development opportunities, and a secure position in a growth-oriented company with flexible working hours.

Application Process

Interested in moving the building blocks of life with us? Apply now with reference number YF-21104 via our applicant portal.

Get a visual insight into our team through our video: BioSpring - The Nucleic Acid Company

Questions? Contact us at:

BioSpring GmbH | Human Resources | Paul Lietz
Alt Fechenheim 34 | 60386 Frankfurt am Main | www.biospring.de