המקום בו המומחים והחברות הטובות ביותר נפגשים
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
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
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