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Quality Specialist - Multiple
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Engineering
Projektbeschreibung
ROLE - QUALITY SPECIALIST X 2
LOCATION - CO. TIPPERARY, IRELAND
TYPE - UNTIL THE END OF 2016
SUMMARY:
One of our key clients, a global Pharmaceutical leader, supply active pharmaceutical ingredients to subsidiaries worldwide, develop late stage clinical API and develop innovative methods for the formulation of new products through the new Formulation R&D and Manufacturing Facility.
They are in need of a Quality Specialist reporting directly to the Quality Lead for the area, working within the Quality department supporting both the API and Formulation aspects.
KEY RESPONSIBILITIES:
Responsible for all aspects of Quality Assurance including:
- Internal auditing
- Ensuring compliance with regulatory requirements
- Review of pre and post-processing documentation and annual process reviews
- Review of validation and qualification documentation
- GMP and compliance training and will also be involved in leading quality improvement projects.
KEY REQUIREMENTS:
- Bachelors or Master's degree in a Science or Engineering discipline.
- Demonstrated leadership and teamwork skills, excellent analytical and problem solving abilities, proven written and verbal communications skills
- Experience is desirable in one or more of the following areas in the pharmaceutical/chemical industry.
- Quality function
- Laboratory Analytical function
- Product development
- Technical services
LOCATION - CO. TIPPERARY, IRELAND
TYPE - UNTIL THE END OF 2016
SUMMARY:
One of our key clients, a global Pharmaceutical leader, supply active pharmaceutical ingredients to subsidiaries worldwide, develop late stage clinical API and develop innovative methods for the formulation of new products through the new Formulation R&D and Manufacturing Facility.
They are in need of a Quality Specialist reporting directly to the Quality Lead for the area, working within the Quality department supporting both the API and Formulation aspects.
KEY RESPONSIBILITIES:
Responsible for all aspects of Quality Assurance including:
- Internal auditing
- Ensuring compliance with regulatory requirements
- Review of pre and post-processing documentation and annual process reviews
- Review of validation and qualification documentation
- GMP and compliance training and will also be involved in leading quality improvement projects.
KEY REQUIREMENTS:
- Bachelors or Master's degree in a Science or Engineering discipline.
- Demonstrated leadership and teamwork skills, excellent analytical and problem solving abilities, proven written and verbal communications skills
- Experience is desirable in one or more of the following areas in the pharmaceutical/chemical industry.
- Quality function
- Laboratory Analytical function
- Product development
- Technical services
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik