PV Auditor (EMEA)

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.

What You'll do:

• Developing and maintaining the PV high-level audit strategy (3-5 year audit plan).

• Writing the annual audit schedule for PV audits based on annual risk assessments and PV audit strategy plan.

• Leading, planning, conducting PV audits, and reporting out of both routine and for-cause/ad hoc PV audits inaccordancewith the approved schedule.

• Delivering PV audit reports and reviewing. Approving proposed preventive and corrective action (CAPA) plans inaccordancewith internal timelines.

• Maintaining responsibility for and oversight of audits conducted by PV contractors, when applicable. This includes identifying suitable PV audit consultants, working with Procurement to establish contracts and providing relevant training inaccordancewith company procedures.

• Participating in PV inspections in core and supporting roles, assisting with the preparation and delivery of appropriate training materials, advising and supporting interviewee coaching.

• Contribute to quality standards of internal cross-functional processes, e.g., involving GPS, Regulatory Affairs, Worldwide Medical and/or Quality activities that apply throughout the product lifecycle.

• Collaborating with the audited functions and providing advice and support where required in execution of remediation actions (CAPAs) to ensure compliance to regulatory andGlobalQuality expectations and requirements.

• Contributing to the Global Quality Assurance (GQA) team by conducting peer review of audit reports conducted by other team members.

• Building the continuous improvement and maintenance of the GQA andGlobalquality management system (QMS) by writing SOPs and guidance documents.

• Acting as the Expert/Point of Contact to provide expertise and knowledge to less experienced auditors, business partners and company entities on quality and compliance processes/procedures.

We are looking for someone who:

• In-depth knowledgeandexperienceof GxP guidance and global regulations fordrugs/biologics.

• Multitasking, project management, and execution skills.

• Oral and written proficiencyin English, second language capability is preferred.

• Strong interpersonalskills and ability to develop interdepartmental relationships, including in communication, presentation, persuasion, and influence.

• Strong organizational and prioritization skills, including efficiency, punctuality, and collaboration in a teamenvironment.

• computerskills, such as Microsoft Office/Office 365. Experience with Trackwise isanadvantage.

• Bachelor's degree in a scientific or health-related field, with a Master's degree preferred.

• 8to10yearsofexperiencein pharmaceutical industries, with 5yearsofexperiencein a Good Pharmacovigilance Practices (GVP) function/environment.

• Certification as a Quality auditor with at least 5yearsof PV auditing experience, primarily as lead auditor.

• 2 yearsofexperiencein Regulatory Inspections Management (e.g. MHRA, FDA, EU inspections).

• Experience in multi-national/ remote-group work environment.

• Computer Systems Validation (CSV) experience isanadvantage

• Competitivetotalcompensationpackage

• Professionaldevelopment opportunities

• High importance is placed on work-lifebalance

• Commitment to growing and developing an inclusive and diverse workforce

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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

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