Erreiche deine beruflichen Ziele als Chemist / Radiochemist for Project Work in Radiopharmacy (m/f/d) bei ABX advanced biochemical compounds GmbH in Radeberg

ABX advanced biochemical compounds GmbH

Our profile

ABX is a young, fast-growing chemical and pharmaceutical company based in Saxony, Germany. We are the global market leader in the production of precursors and kits for PET diagnostics. These are mainly used in the detection of tumours by positron emission tomography (PET).

ABX currently employs over 360 people. Due to our strong market position we have a continuous profitable growth. Since 2007 we have been part of a large Japanese pharmaceutical group.

For the implementation of projects and the optimisation of new and existing products according to GMP requirements (GMP = Good Pharmaceutical Manufacturing Practice), we are looking for a chemist / radiochemist (m/f/d) in the Radiopharmacy department.

We offer

A modern working environment in the pharmaceutical industry
A long-term and secure job in an expanding, future-oriented and internationally oriented company
Full-time employment with an initial fixed-term contract with the express wish of a long-term cooperation
Flexible working hours
Job ticket / travel allowance / company bicycle
Proximity to public transport (Radeberg railway station) and very good and fast connections to Dresden and the surrounding regions
Free drinks and company events (summer party, Christmas party, departmental hiking days ...)
Allowance for fitness and sports activities

Qualification

Successful completion of a Bachelor's or Master's degree; preferably in one of the subjects: Chemistry, biotechnology, pharmacy, physics or similar natural science subjects
Initial experience in handling radioactive compounds and knowledge of the GMP environment
Experience with sterile production and/or aseptic filling advantageous
Very good written and spoken German and English
High level of motivation, communication skills and initiative
Distinct accuracy, reliability, ability to work in a team and under pressure
Cooperative leadership style and ability to work in a team

Task

Establishment of new manufacturing processes and process optimisation
Preparation of the associated documentation taking into account the currently valid laws, regulations and GMP regulations
Maintaining the qualified and validated state of the production environment
Participation in the preparation and adaptation of approval documents
Support of project partners and clients

If you are interested in shaping the future of our company, we look forward to receiving your application documents by e-mail in pdf format, including information on your salary expectations and the earliest possible start date.

Ms Stephanie Ziesche will be happy to answer any technical queries you may have, and Ms Conny Kobus will be happy to answer any questions about the application process.