Quality Assurance 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 Systems Specialist to join a team a temporary contract supporting our site in Valtellina.

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**
- Drafting and review of documentation (e.g. specifications, DMR, procedures)
- Management and monitoring of internal changes related to labeling
- Product labeling management ensures that it is in compliance with product specifications and applicable regulations
- Lead and maintain the Documentation System. Manage site archive, storage, retrieval and destruction processes.
- Supporting all departmental administration systems as required
- Collating information and preparation of reports about Annual Product reviews for all products manufactured on-site.
- Conduct training
- Assist in the internal and external audit program. Participation in regulatory and corporate/internal audits. Conduct audits as per the internal audit schedule.

**What you'll bring**
- Degree in Science or a related field
- Previous experience in quality dept/activities is an advantage
- Excellent interpersonal, organizational and team-building skills
- Good knowledge of written and spoken English
- Run all compliance requirements and ensure an ethical, equal opportunity, and safe work environment.
- Good professional standards and demonstrates good attention to detail
- Prioritize and lead multiple tasks and work to meet project deadlines.
- Highly motivated self-starter and team worker
- Ability to work in a team-based environment and ability to lead a wide range of specific tasks
- Excellent organisational, coordination and communication skills
- Good influencing and interpersonal skills

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**

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