Our client a major manufacturer in Clare has a vacancy for a QA Supervisor
The role is structured so that he/she will have :
Responsibility for the production of certificates to include:
- Authenticity and quality
- Ease of access / availability.
- Layout and embellishing
Ideally the candidiate should possess, 2-3 years experience within a GMP manufacturing facility.
The successful candidate will have the following:
- 3 Years experience in QA within a regulated environment ie. Pharma, Med Devices etc..
- Providing QA and oversight of cGMP activities across the site.
- Ensure operations and support departments are in compliance with cGMP.
- Internal auditing. Carry out preparation, scheduling, reporting & follow up of internal audits.
- In conjunction with the internal audit team.prepare, schedule, carry out, generate audit reports.
- Ensure Qualified Person support for site and global batch release.
- Documentation – working closely with the QA Officers responsible for control of documentation.
- Responsibility for production of documentation, communication & training to appropriate stakeholders
- Updating of the intranet and review on an ongoing basis. Intranet, update, review, training records
- Ensure preparation and support for internal & external audits.
- Work collaboratively with support departments while ensuring high cGMP standards.
- Ensure effective stakeholder management for corporate support departments.
- Strong leadership and personnel development skills.
An excellent salary package is on offer.
Diploma/Degree in Science required with IS0 9001:2000 & 17025 an advantage.
For more information please mail firstname.lastname@example.org
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