Senior Specialist QC Systems & Data (m/f/d)

Be part of a vital chain and contribute to our common goal of improving the lives of people. Octapharma is one of the world's largest manufacturers of drugs based on human proteins and develops and produces drugs from human plasma and human cell lines. We are a privately run company where the warmth of a family atmosphere meets the strength of a global organization.

The Octapharma production company Deutschland mbH (OPGD) in Springe near Hannover is one of five state-of-the-art production sites. There we produce with our around 850 employees: a finished product and intermediate products for further processing.

In your role as Senior Specialist (m/w/d) QC Systems & Data, you are involved in developing and ensuring the integration of electronic systems into the routine processes of quality control. This position is sought in full time with 38.5 hours per week and indefinitely.

Create the future of new health solutions with us and improve the lives of people.

Support for local conceptual and operational development and integration of electronic QC systems Ensuring the integration of electronic systems into the routine processes of quality control Review, definition and continuous updating of master data of electronic QC systems Creation/Programming and Validation of Reports for Electronic QC Systems (e.g. Power BI, SAP Crystal Reporte etc.) Key User/Adminstrator of Electronic QC Systems (e.g. NRT-DB, octaCMMS, LIMS) Reporting, processing and remedying technical problems Planning and implementation of user training for electronic QC systems

Completed scientific (technical) studies (B.Sc.) or completed vocational training (CTA, or comparable) with professional training 1-2 years of professional experience in the GMP environment Knowledge of relevant standards & laws (in particular EP, USP) Very good mathematical understanding Very good IT user knowledge (in particular MS Office, LIMS / Database Experience) Your department where you do something The area of quality carries the overall responsibility for the quality control and safety of our medicines with the aim of ensuring the safety of our patients. The area is divided into four departments: Quality Assurance, Quality in Operation, Quality Control and Assessment & Release. The Quality Control with around 80 employees is primarily responsible for sampling, specifications and testing as well as organizational, documentation and approval procedures.

You help to save lives - every day is important, because we make life-saving drugs Social benefits - employer-funded occupational pensions, long-term account, Hansefit, Benefit portal with advantageous offers, bicycle leasing, external health coaching and regular company celebrations Expertise development – We offer various internal and external employee and executive training, trainee programs and digital solutions Miscellaneous - With us you can start the short Friday earlier in the weekend