Senior Associate - EMEA Supplier Quality

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. Youll feel a sense of purpose throughout the organization as we know our work improves outcomes for millions of patients.

Baxters 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 liveswhere your purpose accelerates our mission.

Summary

Independently handles Supplier Quality System activities for assigned suppliers. Responsible for activities such as execution of quality assessments and audits negotiation and implementation of Quality Agreements monitoring and reporting of metrics. Lead Quality and Compliance related issues between suppliers and Baxter.

Essential Duties and Responsibilities:

• Set Quality system requirements to suppliers.

• Perform Qualification of suppliers of Raw Materials Medical Devices Pharmaceutical Services Finished Products and oversee their placement on the Approved Entity List (AEL) including ensuring the creation and maintenance of supporting evidence.

• Conduct and oversee supplier audits qualification and requalification; Collect trend and report supplier quality metrics also management of global audits performed by third party service.

• Oversee and negotiate Quality Agreements between suppliers and Baxter.

• Improve/develop quality systems at selected suppliers for QMS and compliance improvement.

• Evaluate and improve the effectiveness of purchasing controls and supplier quality processes and procedures.

• Assist in preparing for and defending Purchasing Controls in inspections by external agencies or internal Baxter audits of Purchasing Controls processes; Handle and oversee audits CAPA including root cause identification and effective and timely closure.

• Develop and/or deliver training to internal teams and suppliers.

• Reviewing and assessing suppliers and addressing any blocking issues that arise.

• Support Manufacturing Regulatory Quality and Purchasing organization or all other Location of Use (LOU) organization for third party suppliers related activities as applicable.

• Support other projects as appropriate.

• Willingness to travel up to 40% as necessary.

Qualifications:

• Prior auditing experience; Lead auditor qualification is beneficial; Knowledge of pharmaceutical and/or medical device regulationse.g. ISO 13485 ISO 9001 ISO 17025 FDA cGMP MDD Eudralex GMP GAMP 5.

• Experience in Product/process development and/or supplier quality improvement.

• Understanding of Business Insight; knowledgeable in current and possible future policies practices trends technology and information affecting their industry business and organization.

• Collaboration and Teamwork: Strong communication facilitation coordination and team skills excellent time-management abilities attention to details and a passion for quality outstanding written and oral communication skills.

• Proficient English is mandatory!

Education and/or Experience:

• Higher level of technical education (e.g. Science degree Diploma or Alternative technical bachelors degree or non-technical degree diploma or Certificate).

• Requires 5 years of experience in Quality Manufacturing Engineering or related field combination products medical devices and pharmaceuticals. Experience with other commodities relevant to medical devices or pharmaceuticals will also be considered.

• Experience in root cause analysis corrective and preventive action methods; Expertise / experience in problem solving with quality tools such as 6-sigma / 8-D / CAPA / FMEA / 5WHY etc.

What do we offer

• Fixed-term contract for 3 months and then for an indefinite period.

• Competitive salary annual bonuses recognition award program.

• Possibilities for development on a personal and professional level in one of the leading global MedTech companies.

• Package of benefits including Private medical care (Lux Med) Life Insurance Multisport card.

• Bax4U - cafeteria/lunch cards (300 PLN).

• PPE program with very attractive conditions available for each employee after 3 months.

• Educational support: fully covered language courses (English or other languages according to business needs) financial certifications (ACCA CIMA).

• Co-financing of holidays and an additional 2 days off from work annually.

• Day off for birthday.

• Employee Stock Purchase Plan.

• Bax Flex - hybrid model.

• Outstanding Warsaw office location - Powile!

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race color religion gender national origin age sexual orientation gender identity or expression protected veteran status disability/handicap status or any other legally protected characteristic.

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.

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