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As aQuality Analystyou will be responsible for the development, implementation and review of quality system documentation.
Please note: This opportunity is for a definite period of 2 years (maternity cover).
- Management of supplier qualification
- Management of Regulatory compliance
- Support and maintenance of related Key Performance Indicators
- Achieving, controlling and maintaining consistent quality of products- Ensure implementation of preventive & corrective actions (CAPA)- Monitor and escalate deviations, out of specifications (OOS), CAPA and Change Control management
- Organize and maintain various databases
- Deal with requests from other departments
• University degree in Chemistry, Pharmacy or Microbiology University
• Good interpersonal skills, ability to work with all levels of personnel and management
• Good problem solving and risk assessment abilities
• Good organizational and in time management skills
• Analytical thinking, attention to detail, communication skills, proactivity, result orientation
• Proven flexibility and ability to deal with multiple and changing priorities
• Knowledge about Microsoft office word and excel is a must and ability to learn and become proficient with appropriate software
• Minimum 2 year experience on Quality Unit in Pharma Industry (it could be an advantage)
• GMP Guidelines knowledge
• Oral and written fluency in English
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