Key Responsibilities:

Your responsibilities include, but are not limited to:

• Provide support in the coordination and production of biopharmaceuticals (Assembly and Packaging) as well as in GMP processes.
• Preparation of production supporting documents, as well as for internal and regulatory inspections.
• Ensure real time shop floor support and the completion of production operations on time, in accordance with the documentation and in compliance with GMP rules.
• Collaboration and management of improvement projects in the production environment.
• Preparation / execution of training for production personnel regarding industrial hygiene, GMP and safety.
• Execution of performance qualifications on assembly and packaging lines.
• Handling of deviations, complaints and implementation / coordination of defined actions as well as implementation of approved change requests.
• Creation and handling of packaging material specifications.
• Communication with suppliers regarding testing material and supplier complaint handling

Role Requirements:

• Completed studies in the field of Process Engineering, Biotechnology, Biology, Pharmaceutical Technology, Technical Chemistry, Pharmacy (or comparable studies), min. Bachelor's degree.
• GMP knowledge.
• Proficiency in English and German (spoken & written).
• Desirable Requirements:
• First experience in the pharmaceutical industry, preferably manufacturing of large molecules or development.

Why Novartis?
Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: http://www.novartis.com/about/strategy/people-and-culture

You’ll receive:

You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. http://www.novartis.com/careers/benefits-rewards
In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 58.199,96 year (on a full-time basis). In most cases, the actual salary will be higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies.
We are open for part-time and job-sharing models and support flexible and remote working where possible.

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Adjustments for Applicants with Disabilities:
If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to disabilities.austria@novartis.com and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance at all stages of the application process. Austrian law provides candidates the opportunity to involve the local disability representative, Behindertenvertrauensperson (BVP), in the application process. If you would like to request this, please let us know in advance as a note on your CV.

Join our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: http://talentnetwork.novartis.com/network