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Calibration and Compliance Specialist GMP

Gi Life Sciences Stein

Employment type
Full-time
Workload
100%
Location
Basel
Company
Gi Life Sciences Stein, 4001 Basel
First posted
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Background

The Synthetic Molecules Technical Development (PTDC) department combines comprehensive expertise in the areas of Drug Substance (DS), Drug Product (DP), Analytical Sciences, as well as Manufacturing Science & Technology. In close cooperation with Research, Early Development, and Global Technical Development, PTDC contributes significantly to developing effective medicines from synthetic molecules.

The Plant Support & Compliance (PTDC-T) team ensures calibration, infrastructure, operational safety, and technical projects for the Drug Substance and Drug Product areas. In doing so, the team makes a decisive contribution to reliable plant operation and compliance with regulatory requirements in the GMP environment.

Your Tasks

  • Execution of calibrations on manufacturing plants, analytical devices, and monitoring systems in the areas of Drug Substance (DS) and Logistic Solutions (PS)
  • GMP-compliant documentation of all calibration activities
  • Planning and coordination of calibration measures in close cooperation with internal stakeholders and external service providers
  • Management of the testing equipment inventory, including new intake, certification, and decommissioning
  • Maintenance and updating of calibration master data in BMRAM, SAP, and SAP S/4HANA
  • Creation, revision, and maintenance of calibration instructions as well as Standard Operating Procedures (SOPs)
  • Support with Changes, Deviations, as well as Corrective and Preventive Actions (CAPA)
  • Further development and ensuring of calibration support for development and commercial production areas

Your Profile

Technical Qualifications

  • Completed vocational training in the technical or pharmaceutical field, for example as:
  • Chemistry or pharmaceutical technologist
  • Pharmaceutical technician
  • Chemical technician
  • Automation technician
  • or comparable qualification
  • At least three years of professional experience in a GMP-regulated environment, preferably in production and/or development
  • Sound knowledge of cGMP requirements and their practical application
  • Strong technical understanding of chemical manufacturing plants as well as their automation systems
  • Ideally experience in the calibration of measuring and process instruments
  • Knowledge in the manufacture of non-sterile active ingredients is an advantage
  • Experience with SAP, SAP S/4HANA or comparable systems desirable
  • Very good German language skills as well as good English language skills in spoken and written form

Personal Competencies

  • Independent, responsible, and structured way of working
  • High level of initiative, integrity, and reliability
  • Strong teamwork skills as well as high social competence
  • Solution-oriented thinking and action with a focus on quality and customer satisfaction
  • Ability to critically question processes and drive continuous improvements
  • Fact-based decision-making and consistent implementation of measures
  • Openness towards digital technologies and willingness for continuous further training
  • Courage to actively address challenges and constructively contribute different perspectives

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Posted 1 week ago

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