Technical Assistant (m/w/d)

Оccupation: Laboratory assistant

AbbVie's mission is to discover innovative drugs that solve serious health problems today and address the medical challenges of tomorrow. We strive to exert a remarkable influence on human life in a wide range of therapeutic key areas: immunology, oncology, neuroscience, ophthalmology, virology, women's health and gastroenterology, as well as products and services from the entire AbbVie portfolio in the field of allergan aesthetics. For more information about AbbVie please visit us at www.abbvie.com.

Move big together - as

Chemical laboratory / Pharmakant / Chemical / PTA / CTA / BTA for the production of parenteral clinical trials (all genders) (full-time, unlimited)

REF: R00132743

We are looking for active support for our motivated and committed team in the development and production of parenteral medicinal forms. Our department is working on innovative processes and products for clinical trials and ensures smooth transfer from development to clinical trials. Our tasks and batch sizes adapt to the respective research and development projects. Our focus is on preparation and preparation as well as the aseptic filling of liquids in vials and syringes on our filling lines with RABS and isolator technology. These activities and many exciting projects await you with us. We look forward to your application.

Self-employed and GMP-compliant preparation of parenteral test preparations in compliance with GMP rules, occupational safety regulations and legal requirements for pharmaceutical production independent development, implementation and evaluation of processes and processes used in the production of parenteral test preparations, such as: steam sterilization, H2 O2 decontamination, aseptic work in clean room class C (e.g. batch of bulk solutions), aseptic work in clean room class A/B on RABS and insulator (e.g. fillings on automatic and semi-automatic fillings) Self-fulfilment of all occurring laboratory activities by instruction, e.g. in-process control and documentation of the results in compliance with applicable GMP guidelines and operational regulations Self-creation and processing, verification of GMP-compliant documents (e.g. work instructions, operating instructions, batch documentation) Takeover of special roles, e.g. project responsibility, optimization of production processes, takeover of equipment and system responsibilities or support of investment projects including production of the corresponding documentation Independent coordination of maintenance and training Ensure occupational safety and environmental protection in accordance with statutory and operational regulations

Completed training as a chemical laboratory, pharmaceutical, chemical, PTA, CTA, BTA or comparable scientific technical training At least 2-3 years of professional experience required in aseptic production (working in clean room class C/B), very good knowledge of hygiene work and relevant experience with GMP guidelines required Embossed team capacity, conscientiousness, reliability, high operational readiness and flexibility in handling frequently changing projects Motivation to learn new things and willingness to adapt to frequently changing requirements and to master new challenges Good knowledge of how to use MS Office

with a diverse working environment where you can do something with an open corporate culture with an attractive remuneration with an intensive onboarding including a mentor *in with flexible working models for a healthy...

Joblocations:

67061 Ludwigshafen am Rhein, AbbVie-Allee 1, RHEINLAND_PFALZ, GERMANY