We are Teva
We are Teva – a leading, innovative biopharmaceutical company with a strong generics business. Whether it's innovation in neuroscience and immunology or the global delivery of high-quality medicines, our goal is to meet the needs of patients today and in the future. With us, you'll become part of a high-performing and inclusive company culture that values fresh thinking and collaboration. You'll have room for personal growth, the flexibility to balance work and life, and the opportunity to work together to improve health worldwide.
A day in quality control - as a Quality Analyst qualification
In your new role as "Quality Analyst Qualification," you will be part of the Analytical Instrument Qualification (AIQ) team within Quality Control at Teva Biotech GmbH.
A key aspect of your responsibilities will be the planning, coordination, monitoring, and execution of qualifications and validations of analytical systems used in various departments (USP, DSP, Engineering, IT, and QC). This will be done in close collaboration with the responsible personnel from the different departments to demonstrate and maintain the qualified status of the systems.
You will provide support in addressing questions, leading and overseeing the planning and execution of system qualifications, taking into account applicable laws, guidelines, and cGMP-relevant aspects. This also includes independently creating and reviewing cGMP-relevant documentation for the system qualification of individual systems.
Furthermore, you will independently conduct tests on existing and new analytical systems in accordance with applicable regulations. This includes, among other things, the monitoring and qualification of the Quality Control cooling and freezing systems.
Continuous communication and close collaboration with the relevant departments at Teva Biotech regarding individual projects and life cycle topics related to analytical systems are central to all tasks.
Your responsibilities also include creating cGMP-relevant documents (standard operating procedures), processing quality assurance procedures (change requests, deviations, CAPAs, laboratory tests), and managing the systems administratively in SAP.
Who are we looking for?
You are
- a well-organized and flexible team player (m/f/d) with experience in the qualification of analytical systems in the pharmaceutical environment
- A responsible and goal-oriented individual with an understanding of the processes in a quality control laboratory under cGMP conditions.
- Committed, a team player, but also independent in your work style
- solution-oriented, eager to learn, and communicative
- an open personality who likes to contribute and develop ideas
You have
- a completed degree in natural sciences such as chemistry, biotechnology, food/process engineering or a comparable field with relevant specializations
- Professional experience in a pharmaceutical environment, ideally in the field of qualification of analytical systems
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