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- Process Owner for document archival system on site.
- Maintain QA oversight of documents archived on-site and off-site
- Provide QA consultation and troubleshoot on document archival related issues.
- Ensure that all deviations / change controls are closed or assessed for impact on archival system
- Review / Author of SOPs related to document archival
- Perform annual system review for effectiveness and implement actions accordingly
- Process owner for GMP training system on site, as assigned
- Maintain QA oversight of documents archived on-site and off-site
- Maintain QA oversight of the processes for Training and perform governance checks on executed Training Change Request (TCR)
- Support management of electronic tracking system (PIER, myLearning).
- Manage site training metrics reporting.
- Provide QA consultation on GMP training related issues
- Minimum University Degree in a Science or Engineering discipline
- Minimum 3 years' experience within the pharmaceutical industry
- Experience in pharmaceutical industry in GMP regulated areas is preferred.
- User experience with SAP will be preferred.
- Good knowledge of quality management systems
- An extensive understanding of cGMP regulatory and legal requirements as applied to quality assurance of pharmaceuticals manufacturing.
- Ability in handling and organizing multiple workflows
- Ability to understand the functionalities of systems and link with usage capabilities
- Understanding of regulatory compliance issue
- Good interpersonal and communication skills
- Good facilitation and presentation skills
- Good organizational skills
- Ability to apply optimal quality assurance standards to promote a business edge
- Ability to facilitate and influence business activities compatible to international regulatory environment
- Ability to communicate effectively within the site organization and across the network