Last updated: 2025-05-22

11 Quality Engineering jobs in Reading.

Hiring now: Sr Regulatory Affairs Spe @ Johnson Jo, Sr Analyst Trade Customs @ Baxter, Sr Mgr Clinical Data Stan @ Johnson Jo, Sr Pv Auditor @ Ergomed.Explore more at at kaamvaam.com

🔥 Skills

pharmacovigilance (4) audits (4) regulatory compliance (3) quality assurance (3) regulatory inspections (3) medical devices (2) product development (2) Healthcare (2) Operations (2) process improvements (2)

📍 Locations

Guildford (4) Reading (3) High Wycombe (2) Wokingham (1) Oxford (1)
🔍 Go to full job search

Johnson & Johnson Medtech

Senior Regulatory Affairs Specialist Wokingham
Skills & Focus: regulatory compliance, medical devices, EU regulations, UK regulations, ISO standards, IEC standards, product development, regulatory submissions, clinical standards, quality systems
About the Company: A division of Johnson & Johnson focused on innovative medical technologies, including cardiovascular and surgical devices.
Experience: at least 5 years in regulatory affairs in the medical device industry

Baxter

Senior Analyst, Trade & Customs Reading
Skills & Focus: Supply Chain, Trade, Customs, Analyst, Healthcare, Medical Devices, Logistics, Regulatory Compliance, Operations, Global Fulfillment
About the Company: Baxter is a global medical products company that develops therapies for people with chronic and acute medical conditions.
Type: Full-time
Benefits: Comprehensive benefits options reflecting the value placed on employees.
Commercial Compounding Lead Reading
Skills & Focus: compounding, regulatory, pharmaceutical, quality, regulatory compliance, automation, digital software, AI, stakeholder, partnership
About the Company: A global healthcare company committed to saving and sustaining lives through innovative medical products and solutions.
Benefits: Competitive total compensation package, professional development opportunities, work-life balance, inclusive and divers…
Commercial Compounding Lead Reading
Skills & Focus: sales, medical devices, healthcare, customer support, clinical education, supply chain, manufacturing, product development, quality assurance, regulatory compliance
About the Company: A healthcare company focused on medical products and therapies.
Type: Full-time

Johnson & Johnson

Senior Manager Clinical Data Standards High Wycombe
Skills & Focus: Clinical Data Standards, SDTM, Data Management, Regulatory Requirements, Data Transfer, Controlled Terminology, CRF, DTA, CDISC standards, GCP
About the Company: Johnson & Johnson is a multinational corporation focused on healthcare innovation, including pharmaceuticals, medical devices, and consumer health products.
Experience: At least 8 years in pharmaceutical/scientific fields, with minimum 5 years SDTM experience
Type: Full-time
Director Medical & Regulatory Excellence High Wycombe
Skills & Focus: Regulatory Affairs, Medical Excellence, Medical Operations, Cross-functional Teams, Quality System, Project Management, Leadership, Medical Compliance, Global Initiatives, Team Building
About the Company: A renowned healthcare company focused on innovative medicines and medical technologies.
Experience: Minimum of 5-7 yrs. of regulatory or medical affairs proven experience in relevant roles.
Type: Full-time

Ergomed

Senior PV Auditor Guildford
Skills & Focus: pharmacovigilance, audits, quality assurance, risk-based audit strategies, process improvements, audit reports, cross-functional teams, regulatory inspections, quality management systems, project management
Executive Director, PV Strategy Guildford
Skills & Focus: pharmacovigilance, regulations, EU/UK QPPV, PV processes, audits, gap analysis, consultancy services, training, drug safety, client-facing reports
Senior PV Auditor Guildford
Skills & Focus: pharmacovigilance, audits, compliance, risk-based, recommendations, cross-functional, regulatory inspections, mentorship, quality management, project management