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Quality Assurance Consultant | Contract | Belgium
Eingestellt von Templeton and Partners
Gesuchte Skills: Support, Consultant
Projektbeschreibung
QUALITY ASSURANCE CONSULTANT
PHARMACEUTICAL SECTOR
BELGIUM
CONTRACT - 6 MONTHS +
COMPETITIVE DAILY RATE
JOB DESCRIPTION:
- Support the development and implementation of effective Quality Systems, including but not limited to internal audit, NC and CAPA
- ISO requirements are met
- Support implementations of procedures
- Manage the developments, deployment and implementation of effective policies, requirements and strategies for Quality Systems
- Ensure the development of a comprehensive risk management plan
- Ensure effective and consistent application of Quality Assurance tools and techniques..
- Ensure compliance with company policies and procedures.
- Provide guidance and recommendations involving the implementation of regulatory
MANDATORY SKILLS:
- Analytical capabilities
- Someone who can support and do the technical work; audit will only be needed at a later stage.
Standards & ISO:
- European Guideline on Good Distribution Practice of medicinal products for human use (2013/c 343/01)
- ISO 13485:2003 - Medical devices - Quality Management Systems -
- Medical Device Directive 93/42/EEC (MDD)
PHARMACEUTICAL SECTOR
BELGIUM
CONTRACT - 6 MONTHS +
COMPETITIVE DAILY RATE
JOB DESCRIPTION:
- Support the development and implementation of effective Quality Systems, including but not limited to internal audit, NC and CAPA
- ISO requirements are met
- Support implementations of procedures
- Manage the developments, deployment and implementation of effective policies, requirements and strategies for Quality Systems
- Ensure the development of a comprehensive risk management plan
- Ensure effective and consistent application of Quality Assurance tools and techniques..
- Ensure compliance with company policies and procedures.
- Provide guidance and recommendations involving the implementation of regulatory
MANDATORY SKILLS:
- Analytical capabilities
- Someone who can support and do the technical work; audit will only be needed at a later stage.
Standards & ISO:
- European Guideline on Good Distribution Practice of medicinal products for human use (2013/c 343/01)
- ISO 13485:2003 - Medical devices - Quality Management Systems -
- Medical Device Directive 93/42/EEC (MDD)
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Organisation/Management, Sonstiges