Were looking for a Quality Assurance Administrator experienced in ISO13485 to support product release and compliance within a fastpaced pharmaceutical environment.
What youll do:
- Facilitate product release in line with ISO13485 requirements.
- Compile review and maintain SOPs and quality documentation.
- Oversee batch records retention samples and stability data.
- Support quality systems audits and risk management procedures.
- Handle QA administration including permits courier services and tender applications.
What were looking for:
- Matric certificate (administrative experience advantageous).
- Post Matric Qualification preferably in compliance
- Experience with ISO13485 Administration and compliance
- Strong Microsoft Office skills (Excel Word PowerPoint Outlook).
- Attention to detail integrity and deadlinedriven mindset.
- Excellent communication organisation and problemsolving skills.
Why join
This role offers exposure to quality systems in a regulated industry collaboration across departments and the opportunity to grow your career in pharmaceutical quality assurance.
To apply click on the link or send your CV to response
Required Experience:
Unclear Seniority
IntroductionWere looking for a Quality Assurance Administrator experienced in ISO13485 to support product release and compliance within a fastpaced pharmaceutical environment.What youll do:Facilitate product release in line with ISO13485 requirements.Compile review and maintain SOPs and quality docu...
Were looking for a Quality Assurance Administrator experienced in ISO13485 to support product release and compliance within a fastpaced pharmaceutical environment.
What youll do:
- Facilitate product release in line with ISO13485 requirements.
- Compile review and maintain SOPs and quality documentation.
- Oversee batch records retention samples and stability data.
- Support quality systems audits and risk management procedures.
- Handle QA administration including permits courier services and tender applications.
What were looking for:
- Matric certificate (administrative experience advantageous).
- Post Matric Qualification preferably in compliance
- Experience with ISO13485 Administration and compliance
- Strong Microsoft Office skills (Excel Word PowerPoint Outlook).
- Attention to detail integrity and deadlinedriven mindset.
- Excellent communication organisation and problemsolving skills.
Why join
This role offers exposure to quality systems in a regulated industry collaboration across departments and the opportunity to grow your career in pharmaceutical quality assurance.
To apply click on the link or send your CV to response
Required Experience:
Unclear Seniority
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