Beschreibung
Currently I am looking for a CAPA Consultant to support one of my clients, a global medical devices company in Germany Baden-Wuerttemberg.This Project will be for one year with an option of being permanently employed afterwards.
Major Responsibilities:
Manage CAPA System, which includes:
- Review CAPA submissions
- Assess risk of CAPA submissions and intiate CAPAs
- Follow up on CAPA status and commitments
- Assure CAPAs are applied across all relevant company facilities and functions
- Verify effectiveness of completed CAPAs
- Track CAPA metrics for reporting at Management Review
Required Experience:
- Experience with developing and improving CAPA systems
- Hands on experience in using Risk Analysis methodologies in decision making
- Hands on experience with CAPA as required by ISO 9001, ISO 13485 and/or 21 CFR part 820
- Participate in other QMS efforts such as complaints, supplier corrective action, non-conformances, document control, training, supplier quality, etc.
Minimum Requirements/Qualifications:
- 3 years of active involvement in CAPA.
- 3 years of experience in Quality Assurance or Quality Control role.
- Proficient knowledge of CAPA practices in accordance with standards such as ISO9001, ISO 13485, 21 CFR 820
If this position is of interest to you or someone you know, please reply with an update CV and we will be in contact with you shortly. Please feel free to share this email with your network.
Best Regards,
Sthree Germany is acting as an Employment Business in relation to this vacancy.