QA Systems Professional - Project Based 1 year
Sanofi -
Cairo, EgyptPosted 4 years ago120People have clicked1 open position
Job Details
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Job Description
1- Annual GxP Training Plan management:
- Creation of annual GxP training.
- Follow up of training implementation on monthly basis.
2- Global Quality Documents Gap analysis
- Following up the performance of gap analysis for any updated global quality documents and implementation of any raised actions from this gap analysis
- Perform gap analysis for the assigned documents.
3- Non-Production areas shop floor activities.
- To follow GMP compliance of activities done in Utilities (HVAC & Water stations) Participating in investigation of relevant deviations and follow up of its CAPA.
- To follow changes control system in the area of responsibility
4- Annual Utilities Review:
- Prepare AUR plan and follow up the plan implementation.
- Collecting data from various departments concerned with AUR.
- Reviewing & checking the collected data. Follow up all possible corrections if any with concerned responsible person.
5- Artwork:
- Approval of artworks of different products on Vista system to ensure its compliance with the registered artwork at the
- Approval of suppliers proofreading to ensure its compliance with the approved artwork.
- Review and Approval of specifications for the artwork of different products on Geode+.
- Investigation of any deviation related to the secondary packaging material raised from quality control or production to achieve the site KPI.
6- HSE & Energy.
- Ensures HSE approval on any SOP that requires certain HSE precautions.
- Ensures HSE approval on any change.
- Follow the laboratory safety procedures Commitment to the appropriate PPE use.
- Follow the approved HSE policy and requirements.
- Following the statutory legislation concerning Health, Safety and environmental law.
7- Respect of company values, code of ethics & social charter.
8- Perform other duties as assigned.
9- Key “MUST HAVE” competencies, skills & experiences
Job Requirements
- QA Experience from 0 to 1 years ( in Sanofi or other companies )
- Scientific background
- Successful performance records
- Good communication & Presentation skills.
- Problem solving skills.
- Report writing skills.
- Ability to co-ordinate several inter-departmental activities.
- Good command of MS Word, Excel & Power Point.
10- “Desirable” / compromise experience
- Good Manufacturing Practices (GMP) & Good Documentation Practices (GDP).