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QA Remediation
- Permanent
- Good Clinical Practice (GCP)
- Germany
This vacancy has now expired. Please see similar roles below...
A company is currently looking for a (QA) Quality Assurance Remediator to help diagnose the situation and develop a remediation plan. This is an excellent opportunity for a talented QA Remediator to work for a global leader, but also change the effectiveness of medicine.
Job Responsibilities
- QA review and approval of executed test records.
- QA review and approval of records and reports related to area of responsibility.
- Provide QA expertise and approve environmental investigations.
- Provide QA expertise during investigations of deviations or OOS and approve these and their related CAPAs.
- Support and approve Change Control records related to area of responsibility.
- QA review and approval of Standard Operating Procedures (SOPs) related to area of responsibility.
- Participate in CAPAs resolution of inspection findings.
- Contribute to the preparation of inspections as per defined and agreed role.
- Train new members of the QA Operations (QC) team and other employees as needed.
- Participate in other quality related projects as needed.
Skills and Requirements
- Bachelor's Degree in physical /life science or pharmacy; Advanced degree preferable Compliance and thorough knowledge of applicable local and global regulatory requirements required for GDP, GXP compliance.
- Good knowledge of government regulations, laws and guidelines pertaining to GXP and Pharmacovigilance required
- GMP expert, 10-15 years of experience minimum
To Apply
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Caleb Mensah at +44 203 854 1080 or upload your CV on our website - www.proclinical.com/send-cv
A full job description is available on request.
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