QA Specialist
| Branche | logistiek en vervoer |
| Dienstverband | Direct bij werkgever |
| Uren | Zie onder |
| Locatie |
Schiphol-Rijk, Haarlemmermeer |
| Salarisindicaties | 0-5.000 |
| Opleidingsniveau | Zie onder |
| Organisatie | Hoofdkantoor Standaard |
| Contactpersoon |
Mike Mulder +31 (0)6 27997795 |
Informatie
Quality is what we stand for at Bausch + Lomb, and it is exactly what drives you. A global scope with daily alignment inside and outside the organization. Plenty of decision-making power and real ownership of cases that truly matter. A key role in preparing the QMS for the future and the move to the new facility. You will deepen your expertise quickly by doing, supported by strong guidance and the freedom to steer your own work. This is what you get. Here you are allowed to learn, to make mistakes and to grow in your role and as a person. All of this in an environment where you are seen. Do not wait any longer and apply.
Through your work, releases run smoothly, you reduce the risk of backorders and you keep the supply chain alert to deviations, ensuring that products reach customers on time and safely and that incidents receive the right follow up straight away. You do this by taking ownership in an international setting, liaising quickly with stakeholders inside and outside the organization and getting the QMS ready for the move. You work independently, with the privilege to make decisions, and to grow fast. You are closely involved in challenging real life cases.
Your responsibilities include:
Managing CAPAs end to end: analyzing root cause, securing actions and keeping Catsweb fully under control.
Managing holds and recalls: ensuring traceability and coordinating on a global level.
Monitoring MDR verification and release: addressing questions and avoiding delays.
Sharpening the QMS in preparation for the new facility: with consistency and accountability of the full process.
Omschrijving
Quality is what we stand for at Bausch + Lomb, and it is exactly what drives you. A global scope with daily alignment inside and outside the organization. Plenty of decision-making power and real ownership of cases that truly matter. A key role in preparing the QMS for the future and the move to the new facility. You will deepen your expertise quickly by doing, supported by strong guidance and the freedom to steer your own work. This is what you get. Here you are allowed to learn, to make mistakes and to grow in your role and as a person. All of this in an environment where you are seen. Do not wait any longer and apply.
Through your work, releases run smoothly, you reduce the risk of backorders and you keep the supply chain alert to deviations, ensuring that products reach customers on time and safely and that incidents receive the right follow up straight away. You do this by taking ownership in an international setting, liaising quickly with stakeholders inside and outside the organization and getting the QMS ready for the move. You work independently, with the privilege to make decisions, and to grow fast. You are closely involved in challenging real life cases.
Your responsibilities include:
Managing CAPAs end to end: analyzing root cause, securing actions and keeping Catsweb fully under control.
Managing holds and recalls: ensuring traceability and coordinating on a global level.
Monitoring MDR verification and release: addressing questions and avoiding delays.
Sharpening the QMS in preparation for the new facility: with consistency and accountability of the full process.
Functie eisen
You feel at home in a role where you can take responsibility and where you have international contacts. You communicate clearly, liaise smoothly with different departments and keep a cool head when situations become urgent.
You also bring:
A completed bachelor level (HBO) degree.
More than 2 years of experience in QA within medical devices or logistics quality, working with ISO 13485 and MDR.
Strong skills in CAPA and root cause analysis and a good sense of when this is and is not necessary.
A good command of English; Dutch is not required.
