Senior audit associate Work, Jobs in Swindon, Wil (with Salaries)

Clinical Post Market Surveillance Sr Specialist
Zimmer Biomet —Swindon
- Full-time
- Analysis skills
- Travel
- Health & wellbeing programme
Research Integrity Associate
Taylor and Francis —Abingdon
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Organisational skills
- Annual leave
- Work from home
Quick apply
8d
Anaesthetic Consultant
Great Western Hospitals NHS Foundation Trust —Swindon
- £113,565 - £150,569 a year
- Full-time
16h
Head of BBSRC Estates
UK Research and Innovation —Swindon
- £58,589 a year
- Full-time
- Engineering
- Microsoft Office
- Presentation skills
- Annual leave
- Employee assistance programme
8d
Senior Surveyor/Associate | Compulsory Purchase & Compensation
Knight Frank —Hendred
- Full-time
- Business development
- Analysis skills
- Travel
Locum Foot & Ankle Consultant
Great Western Hospitals NHS Foundation Trust —Swindon
- £113,565 - £150,569 a year
- Full-time
16h
Process Owner - Double Days
Rich Products Corporation —Andover
- Management
- Supervising experience
- Bakery
- Annual leave
Consultant in Stroke Medicine
Great Western Hospitals NHS Foundation Trust —Swindon
- £109,725 - £145,478 a year
- Full-time
Locum Consultant in T&O with special interest in Paediatrics
Great Western Hospitals NHS Foundation Trust —Swindon
- £113,565 - £150,569 a year
- Full-time
- Patient care
16h
Deputy Shift Manager
Rich Products Corporation —Andover
- Management
- Bakery
- Annual leave
Consultant in Respiratory Medicine
Great Western Hospitals NHS Foundation Trust —Swindon
- £113,565 - £150,569 a year
- Full-time
- Leadership
- Communication skills
- Teaching
13d

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senior audit associate jobs near swindon, wil

Clinical Post Market Surveillance Sr Specialist

Zimmer Biomet -
Swindon

Apply Now

Job details

Full-time

Benefits

Health & wellbeing programme

Qualifications

Analysis skills
FDA regulations

Full job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

As a Clinical Post Market Surveillance Sr Specialist, you will independently lead Post Market Surveillance (PMS) activities for assigned products. You will serve as a subject matter expert for PMS documentation, Post Market Clinical Follow-up (PMCF) commitments, trend analyses, and cross-functional coordination. You will provide guidance, mentorship, and technical oversight for less experienced PMS staff.

How You'll Create Impact

Leads authorship of PMPSs, Periodic Safety Update Reports (PSUR), PMS Reports, and PMCF-related documentation
for complex or high-risk product families.
Performs quality control checks for formatting, references, and traceability.
Performs in-depth trend analyses of PMS and complaint data, escalating potential safety signals as appropriate.
Interprets multi-source clinical and safety data to develop evidence-based conclusions.
Advises product teams on corrective actions, monitoring thresholds, and risk mitigation strategies.
Serves as document owner for PMS Plans, Periodic Safety Update Reports and PMS reporting.
Partners with Regulatory Affairs to ensure PMS documentation alignment and Notified Body readiness.
Provides expert peer review and mentorship to Specialists and Associate clinical PMS Specialists.
Troubleshoots Notified Body or internal QA questions related to PMS evidence, trends, or data integrity.
Supports audit readiness and participates in internal, external, and Notified Body audits/inspections by preparing,
reviewing, and defending PMS-related documentation, evidence, data, and responses.
Tracks execution of PMS plans, monitors risks or delays, and communicates status to senior stakeholders.
Contributes to improvements in templates, methodologies, and writing standards.

What Makes You Stand Out

Independent ownership of PMS processes and documentation
Strong working knowledge of global PMS regulations (EU MDR, FDA, ISO 14155)
Advanced analytical skills, critical thinking and ability to interpret multi-source data
Effective cross-functional communication and influence without authority
High attention to detail, audit-readiness, and inspection preparedness
Ability to efficiently prioritize multiple project tasks simultaneously, focusing on critical aspects while maintaining
strategic oversight to deliver high-quality results and meet deadlines
Ability to escalate and resolve compliance or risk concerns

Your Background

You hold a degree in Health, Life Sciences, or related field combined with at least 4 years of relevant experience in medical device across Clinical, Regulatory, or Quality department.

Travel Expectations

Up to 5%.

EOE/M/F/Vet/Disability

Apply Now

Refine Your Search

senior audit associate jobs in swindon, wil

Clinical Post Market Surveillance Sr Specialist

Research Integrity Associate

Anaesthetic Consultant

Head of BBSRC Estates

Senior Surveyor/Associate | Compulsory Purchase & Compensation

Locum Foot & Ankle Consultant

Process Owner - Double Days

Consultant in Stroke Medicine

Locum Consultant in T&O with special interest in Paediatrics

Deputy Shift Manager

Consultant in Respiratory Medicine

Other jobs to consider

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