Job Description
As a Quality Assurance Officer, you will work closely with the site management and collaborate with various internal teams to ensure the adherence to corporate governance requirements and regulations.
Responsibilities:
- Reviewing and approving batch-related records and deviations in a timely manner
- Coordinating with different departments to communicate the status of batch documentation
- Assisting in SBB, NSBB, FPU, and QC activities
- Maintaining the change control system and ensuring timely review, implementation, and closure of changes
- Acting as the quality representative for investigations, assigning actions, raising CAPAs, and managing change control processes
- Conducting internal and external inspections and audits
- Participating in regulatory inspections as required
- Performing VMD amendments
- Responsibilities for QA admin of GMP documentation
- Responsibilities for departmental admin
Qualifications/Skills:
- A graduate or equivalent with a solid understanding of cGMP principles and experience working within a quality management system
- Some experience in the pharmaceutical industry, preferably in Quality Assurance, Quality Control, or production
Closing date for applications: 30th September 2024
Current Contingent Workers apply
Project Temps (Fixed Term)
Not Applicable
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.