Your responsibilities
- Process external deviations and OOX results initiated by external partners (CMO, CL, Service Providers) in compliance with regulations and BI internal procedures
- Enter information about external deviations / OOX results in the database
- Assess external deviations and coordinate the investigation and CAPA in alignment with the Team Member Quality as needed
- Coordinate deviation / investigation related activities and present the results to the key personnel at BI
- Support and advice functional departments during processing of deviations, investigations and CAPAs
- Represent the interface between functional departments, pharmaceutical key personnel as well as subject matter experts and external partners
- Contribute to the optimization and development of the process and the supporting IT system for Deviation/Investigation / CAPA Management
- Present deviations during inspections
- Generate KPIs, overviews and trend reports related to external deviations
- Supports the qualification process of external service and material suppliers by contributing to the creation and maintenance of Quality Assurance Agreements and collection of documents and performing data entry in the corresponding electronic database
Your profile
- Bachelor or Master degree with focus on natural science (e.g. Pharmaceutics, Chemisty, Biology or Biotechnology) or Professional Training with several years of experience in the pharmaceutical industry in a GMP regulated area (e.g. Quality Assurance)
- Several years of experience in the pharmaceutical industry in a GMP regulated area
- Knowledge and hands-on experience gained in GMP regulated environments in pharmaceutical development or production or quality control or quality assurance for several years
- Experience in development and manufacture of pharmaceuticals, biopharmaceuticals or ATMPs would be beneficial.
- Knowledge of international regulatory guidelines (US, EU, ICH) and quality standards for human pharmaceuticals including respective development activities and data handling.
- Knowledge of quality and risk management tools would be beneficial
- Well organized and structured working approach
- Good communication and presentation skills
- Fluency in written and spoken English and German
- Proficient in the use of personal computers
Your benefits
- Working in an international company
About Hays
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
Staffing process for a permanent or temporary position
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We will review your application documents and carry out a detailed analysis of your professional qualification.
Your contact at Hays
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