This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

THE ROLE

Coordinate, support activities related to Quality Systems (audit, NCR and CAPA, QMR preparation and presentation, Change Control, training, SOP implementation, SCAR’s, Scorecards, CAPA review Board preparation).Carry out the administrative operations necessary for the Documentation Management (Corporate and European’s documents implementation + local procedures).Coordinate documentation management and follow up of actions in regard to Audits (Internal Audits, Global Compliance, TÜV, MoH and CQA EMEA)Participate in the implementation of EMEA QS projects.Participate as auditor for internal and supplier audit program.

ESSENTIAL DUTIES & RESPONSIBILITIES

Coordinate, support activities related to Quality Systems (audit, NCR and CAPA, QMR preparation and presentation, Change Control, training, SOP implementation, SCAR’s, Scorecards, CAPA review Board preparation).Coordinate documentation management and follow up of actions in regard to Audits (Internal Audits, Global Compliance, TÜV, MoH and CQA EMEA)Carry out the administrative operations necessary for the Documentation Management (Corporate and European’s documents implementation + local procedures).Participate as auditor for internal and supplier audit program.Participate to the supplier relationship management as SCAR initiator, reviewer and approver.Participate to Global Compliance Audits and external quality audits (ISO9001/ISO13485 accreditation – TÜV and MoH)Perform statistics related to the efficiency of the QA Department.Manage administrative tasks as the QA Metrics and give QA related trainings.Manage periodic reviewHandle SOP implementation (Local, global and EMEA SOPs)Participate in the implementation of EMEA QS projects.

QUALIFICATIONS

Degree in pharmaceutical, engineering or life sciences, or equivalent by experience.You have an experience in a similar function of 1 to 5 years in the pharmaceutical industry (manufacturing or warehousing)You speak fluently French and have a very good level in EnglishProficiency in the Office Suite and software, TrackwiseTeam playerProactiiveRigorous, organizational with planning skillsGood communicator

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.