Regulatory specialist Work, Jobs in Chingford, Gtl (with Salaries)

Quality and Regulatory Manager
Advanced Healthcare Technology Ltd —Waltham Cross
- £50,000 - £60,000 a year
- Full-time
- No degree
- Organisational skills
- In-person
- Free parking
Quick apply
LAB Cross Border Working Senior Specialist
Boston Consulting Group —London
- Full-time
- English
- Bachelor's degree
- Continuous improvement
Nutrition Specialist (Global Regulatory & Corporate Affairs)
Oatly AB —London
- Part-time
- Hybrid work
- English
- Master's degree
- Travel
Quick apply
Global Benefits Senior Specialist
Boston Consulting Group —London
- Full-time
- Microsoft Excel
- Data analysis skills
- Analysis skills
Senior Mobility Specialist - UK
Remote —London
- £54,900 - £61,750 a year
- Remote
- English
- Mentoring
- Relocation assistance
- Annual leave
Compliance Reporting Specialist
Hampshire Trust Bank —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Quick apply
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- University
- Time management
- Annual leave
3d
Medical Information Specialist - Afterhours
EVERSANA —London
- Weekend availability
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
6d
Analyst - Regulatory Market Access and Compliance
Access Partnership —London
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Regulatory Change Implementation Specialist - 2026
Suade —London
- £50,000 - £75,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- English
- Bachelor's degree
- Annual leave
- Work from home
Quick apply
FSQRN Data & Analytics Specialist
Starbucks —London
- Full-time
- Analysis skills
5h
Clinical Evaluation Specialist
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care
Regulatory Specialist - Commodity Chemicals
Synthomer (UK) Limited —Harlow
- Databases
- Continuous improvement
- Employee assistance programme
Quick apply
5d
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Responsible AI Specialist (Governance, Ethics & Compliance)
Talan —London
- Full-time
- Hybrid work
- Travel
- AI
- Communication skills
- Employee assistance programme
Quick apply
HM Inspector of Railway Human Factors Specialist
Office of Rail and Road —London
- £58,827 - £64,237 a year
- Part-time
- Hybrid work
- Presentation skills
Quality Assurance Specialist
MSD —London
- Full-time
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Quality control
5d
Cancer Referral Specialist
Lloyds Clinical —Harlow
- £48,000 a year
- Hybrid work
- IT
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
Regulatory Data Specialist - Contract Role 12 months
Synthomer (UK) Limited —Harlow
- Hybrid work
- Continuous improvement
- Employee assistance programme
Quick apply
4d
Student Support Specialist (SSO)
QA —London
- Travel
- Communication skills
- Annual leave
- Employee assistance programme

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regulatory specialist jobs near chingford, gtl

Quality and Regulatory Manager

Advanced Healthcare Technology Ltd
Waltham Cross

Quick apply

Job details

Full-time
£50,000 - £60,000 a year

Benefits

Free parking
Casual dress
Company pension
On-site parking

Qualifications

Quality assurance
HACCP
Organisational skills
Root cause analysis
Internal audits

Full job description

Role Purpose

The Quality and Regulatory Manager is responsible for leading the company’s quality management and regulatory compliance activities to ensure that products are developed, manufactured, released and marketed in compliance with applicable requirements. This is a hands-on role with broad responsibility across the quality management system, technical documentation, post-market activities, supplier quality, internal auditing, and regulatory support for global market access. The jobholder will work closely with senior leadership and cross-functional teams to maintain compliance with applicable international medical device regulations and standards, including ISO 13485, MDSAP and relevant market-specific requirements.

Key Responsibilities

· Maintain and continuously improve the company’s Quality Management System in line with ISO 13485, MDSAP and applicable regulatory requirements.

· Manage the relationship between the company and key regulatory bodies including the company’s Notified Body / Auditors

· Ensure products are correctly classified for regulatory clearance in proposed markets.

· Support and maintain technical documentation, declarations of conformity, labelling compliance, and product records in line with product classification.

· Act as the internal lead for quality assurance and regulatory compliance.

· Plan and conduct internal audits and support external audits by certification bodies, regulatory authorities, customers, and other third parties.

· Manage non-conformances, deviations, CAPA, complaints, and change control processes.

· Support clinical evaluation and human factors processes to ensure that these are met throughout the product life cycle.

· Support post-market surveillance, vigilance reporting, field safety corrective actions, and trend analysis where required.

· Ensure document control processes are effective and that quality records are complete, accurate, and audit-ready.

· Work with Senior Management to ensure culture of compliance is embedded in business processes.

· Support supplier qualification, monitoring, and re-evaluation activities, including supplier audits where appropriate.

· Provide regulatory input for product changes, new product introduction, and international market expansion.

· Monitor changes in applicable regulations, standards, and guidance and assess their impact on the business.

· Coordinate management review inputs, quality metrics, and compliance reporting for leadership.

· Deliver training and guidance to staff on quality and regulatory requirements and promote a strong quality and compliance culture.

· Support product registration and market access activities in territories where the company sells its products, using external specialists where required.

Management Responsibilities

· Direct Reports – Currently none

· Consultants and contractors – as appropriate

Qualifications and Experience

· Degree or equivalent experience in a relevant scientific, engineering, quality, or regulatory discipline.

· Lead Auditor qualified or extensive experience with internal auditing, CAPA, complaints handling, supplier quality, and change control.

· Proven experience in quality assurance and regulatory affairs within the medical device sector.

· Strong working knowledge of ISO 13485 and medical device regulatory requirements relevant to Class I and II devices especially in the USA.

· Experience maintaining technical documentation and quality system records in a regulated environment.

· Experience supporting international regulatory compliance and market access activities is essential.

· Supervise quality and document control activities.

Key Skills and Attributes

· Ability to work independently and pragmatically in an environment with limited resources.

· Strong organisational skills, attention to detail, and the ability to prioritise across multiple responsibilities.

· Confident communicator able to work effectively across departments and with external stakeholders.

· Ability to interpret regulations and translate them into workable internal processes.

· Strong problem-solving and root cause analysis skills.

· Ability to influence without unnecessary bureaucracy.

· Comfortable balancing compliance requirements with business needs and operational realities.

· High integrity, accountability, and commitment to patient safety and product quality.

Reporting and Working Relationships

This role reports to the Managing Director.

Key relationships with manufacturing, engineering, supply chain, customer service, and commercial teams.

Pay: £50,000.00-£60,000.00 per year

Benefits:

Casual dress
Company pension
Free parking
On-site parking

Work Location: In person

Quick apply

Refine Your Search

regulatory specialist jobs in chingford, gtl

Quality and Regulatory Manager

LAB Cross Border Working Senior Specialist

Nutrition Specialist (Global Regulatory & Corporate Affairs)

Global Benefits Senior Specialist

Senior Mobility Specialist - UK

Compliance Reporting Specialist

Research Regulatory Facilitator

Medical Information Specialist - Afterhours

Analyst - Regulatory Market Access and Compliance

Regulatory Change Implementation Specialist - 2026

FSQRN Data & Analytics Specialist

Clinical Evaluation Specialist

Regulatory Specialist - Commodity Chemicals

Medical Information Specialist - US Hours

Responsible AI Specialist (Governance, Ethics & Compliance)

HM Inspector of Railway Human Factors Specialist

Quality Assurance Specialist

Cancer Referral Specialist

Regulatory Data Specialist - Contract Role 12 months

Student Support Specialist (SSO)

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