Trabajos de director de control de calidad en industrias/directora de control de calidad en industrias en Luxemburgo

What you'll do

Contribute to the creation and implementation of the strategy and development in

terms of Quality Assurance activities.

Establish the company's Quality Management System (QMS) compliance to ISO

standards, applicable regulations, and all associated tasks around Quality

Management

Support and collaborate with different internal departments in relation to

Operational Quality (Production Quality, Quality Control, Supplier Quality), including

participation in Quality Circle, support and overview of the CAPA activities.

Act as companVs representative for all activities related to product certification and

the registration of products in and outside the European Union

Carry out and/or support all risk management activities and conduct risk

assessments of processes and tasks

Ensure the conformity in terms of Safety Officer for Medical Devices

Develop and maintain strong relationships with internal and external stakeholders to

ensure optimal performance

According to Article 15 of the European Regulation (EU) 2017/745 for medical

devices, T

The PRRC (Person responsible for regulatory compliance) responsibilities are

according to the article 15 of the European Regulation (EU) 2017/745 for medical

devices

What you'll bring

Successfully completed master's degree in engineering

Diploma, certificate or other evidence of formal qualification, awarded on

completion of a university degree or of a course of study recognized as equivalent by

the Member State concerned, in law, medicine, pharmacy, engineering or another

relevant scientific discipline

5 years of experience, ideally in regulatory affairs or in quality management systems

relating to medical devices

Work experience in an international and multicultural environment

Excellent leadership and management skills

Ability to manage cross-functional teams and to collaborate with business partners

across multiple functions

Planning and organization skills

Strong communication skills — written, verbal and presentation

Competent in problem solving, team building, planning and decision making

Attention to detail

Commercially aware

Mircosoft suite

Languages: English is mandatory any other language will be appreciated.

Our Offer

Become part of a company that makes a positive contribution to launching

groundbreaking scientific developments and therapies.

Contribute to innovative cell therapies and be a part of revolutionary cancer

therapies.

Take advantage of the operational opportunities in a growing, modern, and

innovative company within the health care/life science industry.

Experience an intensive exchange of experiences and close cooperation in a

worldwide network with our customers, friends and partners.

We offer participation in national and international company events.

After your initial training, you will receive regular training and further education

opportunities that are tailored to your needs.

A workplace that promotes your maximum.

You will participate in capital-forming benefits, numerous corporate benefits.

33 days of vacation.

Positive corporate culture and practiced teamwork across all locations.

Individual development opportunities of your international competencies and

language skills.