14 Quality Engineering jobs in Reading.

Hiring now: Regulatory Affairs Spec @ Johnson Jo, External Tmf Mgr Sponsord @ Iqvia, Sr Raqa Mgr @ Intuitive , Manufacturing Jobs @ Baxter, Aggregate Report Sr Scien @ Biogen, Mgr Immunology Regulatory @ Johnson Jo, Exec Dir Pv Strategy @ Ergomed.Explore more at jobswithgpt.com.

🔥 Skills

Project Management (4) Compliance (3) Medical Devices (3) process improvement (3) Manufacturing (3) Healthcare (3) Quality (3) Regulatory (3) Pharmaceutical (3) Regulatory Affairs (2)

đź“Ť Locations

Oxford (4) High Wycombe (4) Reading (3) Wokingham (1) Maidenhead (1) Guildford (1)
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Johnson & Johnson Medtech

Regulatory Affairs Specialist Wokingham
Skills & Focus: Regulatory Affairs, Compliance, Medical Devices, Legislation, Impact Assessments, Documentation, Database Management, Project Management, Customer Focused, Communication Skills
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 10% Travel
Type: Hybrid

Iqvia

External TMF Manager, sponsor-dedicated Reading
Skills & Focus: TMF management, clinical trial, quality review, regulatory compliance, data analytics, established timelines, TAF health, documentation, cross-functional teams, GCP
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Minimum 5 years pharmaceutical / biotechnology industry experience, Minimum 3 years records management experience in a GCP-regulated environment.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
RBQM - Risk Surveillance Lead (Director/Assoc. Director) - Sponsor Dedicated Reading
Skills & Focus: Risk-Based Quality Management, clinical trials, risk assessment, quality tolerance limits, data analytics, root cause analysis, clinical quality, risk governance, stakeholder satisfaction, process improvement
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Minimum of 6 years of experience in the pharmaceutical or CRO industry. Minimum of 2 years of experience in Risk Based Quality Management.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Intuitive Surgical

Senior RAQA Manager Reading
Skills & Focus: regulatory compliance, quality system management, medical device regulations, post-market surveillance, QMS, audit/inspection, SRQA, UK Responsible Person, EU MDR, ISO 13485
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: At least 8+ years’ experience in medical device industry operating according to US or EU regulation including at least 3 years in medical devices quality system management.

Baxter

Manufacturing Jobs Oxford
Skills & Focus: Manufacturing, Production Technician, Medical Devices, Healthcare, Quality, Innovation, Pharmaceuticals, Patient Care, Laryngoscopes, Compliance
About the Company: Baxter is a global healthcare company that is dedicated to saving and sustaining lives through innovative healthcare solutions.
Type: Full time
Benefits: Comprehensive benefits options reflecting the value placed in employees.
GMP Production Technician Oxford
Skills & Focus: GMP, Production Technician, Medical Devices, Manufacturing, Quality, Healthcare, Innovation, Operations, Teamwork, Regulatory
About the Company: Baxter is a leading manufacturer of medical devices and solutions, committed to saving and sustaining lives around the globe through innovation and high-qualit…
Type: Full-time
Benefits: Comprehensive benefits options reflecting the value placed on employees.
EMEA Quality Systems Senior Manager Oxford
Skills & Focus: Quality Management System, pharmaceutical manufacturing, leadership, continuous improvement, quality systems, compliance, collaboration, communication, technical expertise, strategic initiatives
About the Company: 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. For over 85 yea…
Experience: Strong leadership and management skills with experience in pharmaceutical manufacturing.
Benefits: Paid Time Off, 2 Days a Year to Volunteer, Continuing Education/Professional Development, Employee Health & Well-Being.

Biogen

Aggregate Report Senior Scientist Maidenhead
Skills & Focus: aggregate reports, PSURs, DSURs, PADERs, pharmacovigilance, safety queries, medical safety, scientific safety, process improvement, global safety compliance

Johnson & Johnson

Manager, Immunology Regulatory Medical Writing High Wycombe
Skills & Focus: Immunology, Regulatory, Medical Writing, Clinical Documents, Project Management, Cross-Functional, Team Leadership, Process Improvement, Pharmaceutical, Communications
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience.
Type: Full-time
Analyst II, Regulatory Medical Writing High Wycombe
Skills & Focus: Regulatory, Medical Writing, Pharmaceutical, Clinical Documents, Protocols, Clinical Study Reports, Team Environment, Writing, Quality Control, Project Management
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 2 years of relevant pharmaceutical/scientific experience is required.
Type: Full-time
Benefits: We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority,…
Associate Director, Global Labeling Product Leader High Wycombe
Skills & Focus: Regulatory Affairs, Labeling, Pharmaceutical, Documentation, Compliance, Project Management, Scientific Communication, Continuous Improvement, Global Labeling Strategy, Team Leadership
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 8 years of professional work experience required, with 6 years of direct regulatory labeling content experience.
Type: Hybrid

Ergomed

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