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
- Work from home
- Employee assistance programme
Quick apply
2d
Quality Documentation Technician
Becton Dickinson —Swindon
- Microsoft Office
- SharePoint
- Communication skills
Quick apply
Administration Associate
Evlo —Trowbridge
- Microsoft Office
- Communication skills
- Time management
- Employee discount
- Life insurance
Quick apply
Consultant in Respiratory Medicine
Great Western Hospitals NHS Foundation Trust —Swindon
- £113,565 - £150,569 a year
- Full-time
- Leadership
- Communication skills
- Teaching
8d
Consultant in Stroke Medicine
Great Western Hospitals NHS Foundation Trust —Swindon
- £109,725 - £145,478 a year
- Full-time
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
2d
VodafoneThree - Associate Accountant - Retail Property
Three UK —Newbury
- Full-time
- Hybrid work
- Analysis skills
- No degree
- Accounting
- Employee discount
Quick apply
7d
HR Assistant Apprentice
Eurofins UK Forensic Services —Abingdon
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Free parking
- Annual leave
Quick apply
14d
Group HR Systems and Compliance Associate
Avon Protection —Melksham
- £35,000 - £80,000 a year
- BLS Certification
- Human resources
- Organisational skills
- Employee stock purchase plan
- Annual leave
Quick apply
Process Owner - Weekend Days
Rich Products Corporation —Andover
- Weekend availability
- Management
- Supervising experience
- Bakery
- Annual leave
Senior Surveyor/Associate | Compulsory Purchase & Compensation
Knight Frank —Hendred
- Full-time
- Business development
- Analysis skills
- Travel
Deputy Shift Manager
Rich Products Corporation —Andover
- Management
- Bakery
- Annual leave
Management Accountant
Littelfuse —Chippenham
- Full-time
- Microsoft Excel
- ERP systems
- Analysis skills
Quality Control Inspector
ZeroAvia —Kemble
- Full-time
- Oracle
- ERP systems
- English
- Employee assistance programme
Quick apply
Oral Surgeon
PracticePlusGroup —Devizes
- Monday to Friday
- Hospital
- Annual leave
Warehouse Team Leader - Weekends Nights
Rich Products Corporation —Andover
- Weekend availability
- Management
- ERP systems
- Bakery
- Annual leave

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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

audit associate jobs in swindon, wil

Clinical Post Market Surveillance Sr Specialist

Research Integrity Associate

Quality Documentation Technician

Administration Associate

Consultant in Respiratory Medicine

Consultant in Stroke Medicine

Head of BBSRC Estates

VodafoneThree - Associate Accountant - Retail Property

HR Assistant Apprentice

Group HR Systems and Compliance Associate

Process Owner - Weekend Days

Senior Surveyor/Associate | Compulsory Purchase & Compensation

Deputy Shift Manager

Management Accountant

Quality Control Inspector

Oral Surgeon

Warehouse Team Leader - Weekends Nights

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