A Quality System Documentation Specialist
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 mission of Baxter is to save and sustain lives.
This mission is embedded into everything we do.
This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality.
Our patients come first, always.
A great opportunity has recently arisen for a Quality System Documentation Specialist to join our Quality System Team in Medolla (MO).
The Quality function values both working together as a team and independently.
We draw energy from working in a plant or an office where there are opportunities to collaborate.
As the company evolves, so does the way our team approaches work as it strives to create top-of-the-line products.
We build relationships with each other to get work done.
Building these relationships is easy because we all share common traits of being reliable, ethical, and caring.
We lean on our colleagues for their expertise and hold each other accountable.
We feel empowered to speak up when there's a new insight or opportunity to improve something.
This open dialogue builds trust within the team and helps create a better product for our customers.
**What you'll be doing
- Act as Document Author, Quality approver, Electronic System for Documentation Management Local administrator
- Act as Local Administrator of the Electronic System for the management of printed versions of paper document
- Coordinate the local implementation of global Quality Management System requirements and collaborate with Global Entity Review process for impact assessment of global QMS requirements for local implementation
- Performs periodic training to local Users on Documentation Electronic Systems
- Acts as local contact and site coach for Documentation Electronic Systems issues and supports local deployment of system enhancements
- Supports Sr Manager QA Medolla for QMS integration for the site
- Supports the local internal training process of QMS Documents
- Train colleagues on Quality System principles (e. g Quality Policy, Quality Objectives, GDP, Data Integrity)
**What you'll bring
- Scientific or Foreign Languages Bachelor's Degree
- Experience in QMS Documentation Management and knowledge in relevant quality documents and standards (eg.
ISO 13485 and 21 CFR Part 820) are welcome
- Very good knowledge of English language, both verbal and in writing.
- Attitude to work with focus on implementation, result driven and ability to accomplish agreed objectives
- Communication skills and ability to work with different stakeholders (located on the Site and other locations)
If you are looking for a place where you choose to work with dedicated and dynamic people whose primary focus is to save and sustain lives and whose work values focus on speed, simplicity, courage and collaboration.
Then we would love to hear from you.
**Reasonable Accommodations
**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.
083656
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