Κωδ:QA/QP SPV
Quality Assurance Supervisor/Qualified Person
101-250
Φαρμακευτικές & Κλάδος Υγείας
πριν 18 μέρες
Ημ. ανάρτησηςπριν 18 μέρες
Με κάποια εμπειρίαΕπίπεδο εμπειρίας
Με κάποια εμπειρίαΠλήρης απασχόλησηΤύπος απασχόλησης
Πλήρης απασχόλησηΦαρμακευτικά / ΥγείαΚατηγορία θέσης
Φαρμακευτικά / ΥγείαThe Greek Pharmaceutical Industry Medicair S.A., operating at the Industrial area of Schimatari, Viotia, is seeking for:
Quality Assurance Supervisor/Qualified Person
The position reports directly to the QA Manager. The QA supervisor will be responsible for the proper functioning of his/her area of responsibility and will have among others ,the following responsibilities:
Qualified Person
- Batch certification / batch record review-release / serialization
- QP declaration / API
QA Supervisor
- Reporting to QA Manager of quality system responsibilities assigned.
- Evaluation and monitoring of suppliers and updating of relevant lists.
- Qualification of API producers
- Qualification of excipients (formalized risk assessment)
- Participation in internal audits as an assistant auditor.
- Preparation of Product Quality Reviews and plan.
- Preparation of quality-related SOPs or other written procedures within area of responsibility.
- Supervising of quality system documentation policy (master list of documents, revision due dates etc)
- Implementation of CAPA plan related to QA department within area of responsibility.
- Monitoring and implementation of Validation Master Plan
- Coordination of the calibration of operations instruments and areas’ qualification.
- Coordination and participation in quality investigations (deviations, complaints)
- Coordination of the on-time closing of the CAPA plan
- Participation in external audits (front or back office)
- Supervising validation processes
Necessary qualifications:
- Graduate of a University in the fields of Chemistry or Pharmacy or Chemical Engineering or Biology, etc. (specialty that allows appointment as a Qualified Person of EOF). Post graduate degree will be considered as a positive qualification.
- Necessary experience at least 2 years in the production and/or control of pharmaceuticals
- Necessary experience in the same position or QA officer position or equivalent
- Very good knowledge of English, written and oral. Knowledge of an additional language will be considered as a positive qualification.
- Ability to communicate and collaborate
- Teamwork and hard work
- Organizational skills
The Company offers:
- Competitive salary
- Friendly working environment
- Career Opportunities and skills development
ΠΕΡΙΛΗΨΗ ΘΕΣΗΣ
Quality Assurance Supervisor/Qualified Person
Σχηματάρι
πριν 18 μέρες
Με κάποια εμπειρία
Πλήρης απασχόληση