Associate Manager - Montmorency, France - BALT

BALT

Entreprise vérifiée

Montmorency, France

il y a 2 semaines

Posté par:

Sophie Dupont

beBee Recruiter

Description

About Balt
Our purpose is to improve the lives of 150,000 patients in 2026.

Our story
Balt is a rapidly growing pioneer in an exceptional field.

For 45 years, Balt has been leading the way - collaborating with physicians and institutions to develop elegant medical devices.

Our products are being used by physicians across the world, and we have 13 offices in 11 countries - and counting.

We introduced one of the first neurovascular intervention devices in 1977 and now offer the world's broadest portfolio of medical devices for stroke.

As the premier global neurovascular platform always seeking to expand beyond boundaries, we are now bringing our innovation to the peripheral vascular space.

We are proud of our mission, our people, and the incredible work we accomplish together as we empower physicians to save lives.

Why Join Balt? Join a passionate team, dedicated to making a difference.
Working at Balt means giving meaning to your work Pride is a strong part of our identity.

We are a close-knit team, with strong mission, vision and values that guide our day-to-day.

Recognition of work, respect, and our multicultural community are key aspects of the employee experience and contribute to our continued success.

No matter the country, we take care of you.

Would you like to be part of our story? Don't hesitate, come and join us

About the Opportunity
Provide support on the maintenance, development, and control of the Quality system.

This mission also includes the evaluation of the current QMS according to the applicable standards and the implementation of the new medical device regulation 2017/745.

You participate in continuous improvement projects and ensure the organization's compliance with regulatory requirements.

Job responsibilities:

Is responsible for the management of Quality System elements including monitoring of system performance (Nonconformance System; CAPA System; Change Control)
Act as a SME for the listed processes and coordinate site committees to ensure the best followup
Define the relevant KPIs and ensure an adequate reporting to the site leaderships
Lead projects to improve the Quality System through Change Control Processes
Development and execution of crossfunctional process and system improvements to improve Quality, Compliance, and Service Level to customers
Participate/support in QMS Project Planning
Maintenance and improving the mapping of the current QMS/ Evaluation of the consequences of QMS modifications in terms of quality (organization, documentation, validation, training, premises, investments, suppliers...)
Participate to worldwide QMS communities as part of project of harmonization and global monitoring
Participate and/or carry out internal and external audits (ensure that identified corrective actions are carried out, prepare and participate in national authorities' inspections)
Participate in NCA inspection and NB audits
Provide necessary training to stakeholders once required
Participate to the Management Reviews as SME

Qualification requirements:

Master's degree in a scientific discipline
Minimum of 710 years' experience in Medical Device Industry (Quality, Regulatory or related function)
Fluent in English
Excellent technical written and verbal communication skills
Experience with creating/integrating Quality Systems
Experience with Transitional MDR requirements implementation
Strong knowledge of IS013485:2016, European MDR o Lead auditor certification to IS013485:2016 is ideal

Type d'emploi :
Temps plein, CDI

Avantages: