Senior quality specialist Work, Jobs in Batley, Wyk (with Salaries)

Senior Regulatory Affairs Specialist
Medasil Surgical Ltd —Leeds
- £45,000 - £55,000 a year
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
Quick apply
1h
Audit Quality - Corporate Reporting Advisory Senior Manager
BDO —Leeds
- Full-time
- Accounting
- Communication skills
Senior Talent Acquistion Partner
StepChange —Leeds
- £50,000 - £55,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Project management
- Travel
Quick apply
14d
Programme Manager - Senior Quality Control Inspector
Baily Garner —Leeds
- £65,000 - £75,000 a year
- Full-time
- Hybrid work
- Business development
- Quality control
- Organisational skills
- Annual leave
- Flexible schedule
Quick apply
Deputy Head Teacher
High Peak School —High Peak
- £66,368 - £75,049 a year
- Full-time
- Data analysis skills
- Analysis skills
- Leadership
- Employee assistance programme
Senior Policy Adviser, MoJ/HMPPS Joint Strategic Policy Unit
Ministry of Justice —Leeds
- £40,001 - £60,000 a year
- Part-time
- Hybrid work
- Presentation skills
- Travel
- IT
- Annual leave
- Employee discount
10d
Large and Complex Loss Handler
Leeds City Council —Leeds
- £46,142 - £500,000 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Lead Clinician
Outcomes First Group —Wakefield
- £50,000 - £60,000 a year
- Monday to Friday
- Doctoral degree
- Psychology
- Leadership
3d
Senior HR Advisor
Locala Health and Wellbeing —Dewsbury
- £39,959 - £48,177 a year
- Travel
- Human resources
- Leadership
- Referral programme
7d
Senior Payroll Specialist
Schneider Electric —Leeds
- Full-time
- Hybrid work
- Customer service
- English
- Organisational skills
- Annual leave
Managing Director
Techbelt —Elland
- £110,000 - £125,000 a year
- Full-time
- Sales
- Engineering
- Master's degree
- Relocation assistance
Quick apply
Lead ER Specialist
Anchor —Bradford
- £42,000 a year
- Hybrid work
- Management
- Supervising experience
- Human resources
- Employee discount
18h
Associate Director - FM Operational Readiness
Turner & Townsend —Leeds
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
SHEQ Manager
Dawsongroup —Brighouse
- Full-time
Quick apply
Data Protection Consultant / Outsourced Data Protection Officer
Clinical DPO / Amicis Data Ltd —Harrogate
- £37,500 - £47,500 a year
- Full-time
- Bachelor's degree
- In-person
- Communication skills
- Work from home
Quick apply
7d
Register Your Interest Regional Facilities Services Manager Opportunities in Leeds!
Sodexo —Leeds
- Full-time
- Hospitality
- Travel
- Contracts
- Employee assistance programme
Quick apply
6d
Senior Acoustics Officer
Leeds City Council —Leeds
- £37,280 - £42,839 a year
- Full-time
- Project management
- No degree
- Mentoring
- Annual leave
Maintenance & Grounds Manager
Catgill Campsite Ltd —Skipton
- £35,000 - £40,000 a year
- Weekend availability
- Maintenance
- Hotel
- Supervising experience
- Employee discount
Quick apply
Implementation Senior Lead
Sopra Steria —Leeds
- Up to £45,000 a year
- Hybrid work
- Microsoft Excel
- Oracle
- Analysis skills
- Annual leave
Head of Health and Safety
Yorkshire Ambulance Service NHS Trust —Wakefield
- £66,582 - £77,368 a year
- Full-time
- Hybrid work
- Leadership
- Annual leave
- Employee assistance programme
4d

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Senior Regulatory Affairs Specialist

Medasil Surgical Ltd
Leeds

Quick apply

Job details

Full-time
£45,000 - £55,000 a year
1 hour ago

Qualifications

Engineering
Quality management
Diagnostic evaluation
Analysis skills
Bachelor's degree
Organisational skills
Communication skills

Full job description

About Us

Medasil Surgical Limited is a leading UK-based medical device company specialising in the design, manufacture, and supply of single-use surgical products. With a strong reputation for quality, and customer focus, we are committed to delivering safe and effective solutions to healthcare professionals worldwide.

The Opportunity

We are looking for a Senior Regulatory Affairs Specialist to join our team in Leeds. This role offers the opportunity to play a key part in maintaining and enhancing regulatory compliance across our product portfolio in a fast-paced and collaborative environment. This is a Full-time position, mainly onsite with occasional flexible working possible.

Key Responsibilities

Ensure compliance with all applicable medical device regulations, standards, and legislation
Create, update, and maintain Technical Documentation and Technical Files
Conduct regular reviews to ensure alignment with harmonised standards and regulatory requirements
Perform regulatory gap analyses against new or updated standards
Review and approve design changes, engineering updates, CAPA, and nonconformances for regulatory impact
Monitor regulatory changes and support updates to SOPs and internal systems
Manage and support product registrations with Competent Authorities (e.g., MHRA, EUDAMED)
Ensure post-market surveillance activities are effectively integrated into Technical Documentation
Review and approve labelling, promotional materials, and product claims
Participate in internal and external audits
Collaborate cross-functionally to support compliant product lifecycle management
Responsible for delivering high-quality, audit-ready technical documentation
Ensuring timely regulatory submissions and approvals
Proactively identifying regulatory risks and recommending solution

Skills & Experience

Minimum 5 years’ experience in a Medical Device Regulatory Affairs role
Bachelor’s degree in Science, Engineering, Regulatory Affairs, or related discipline
Strong understanding of:
MDD 93/42/EEC, MDR 2017/745, and UKCA requirements
ISO 13485 Quality Management Systems

Proven experience in:

Creating and maintaining Technical Documentation
Conducting regulatory gap analyses
Interpreting and applying harmonised standards and regulatory guidance
Reviewing design changes, CAPA, and nonconformances
Post-market surveillance and Technical File maintenance
Knowledge of risk management, clinical evaluation documentation, and labelling requirements
Familiarity with device registration systems such as MHRA and EUDAMED
Strong analytical, organisational, and communication skills

Why Join Medasil?

Be part of a respected and growing medical device company
Work within a collaborative and quality-driven environment
Opportunity to contribute to products that support patient care globally
Career development within Regulatory Affairs
Competitive salary dependent on experience.

Medasil Surgical Limited is an equal‑opportunity employer. We welcome applications from all qualified individuals regardless of background and identity

If you are passionate about regulatory compliance and want to grow your career with Medasil Surgical Limited, we would love to hear from you.

Job Type: Full-time

Pay: £45,000.00-£55,000.00 per year

Application question(s):

Do you have experience working with MDD 93/42/EEC and/or MDR 2017/745?
Are you familiar with UKCA regulatory requirements?
Do you have experience creating and maintaining Technical Documentation / Technical Files?
This is full time onsite role in Leeds are you able to work full-time onsite in Leeds?

Education:

Bachelor's (required)

Experience:

Medical Device Regulatory Affairs: 5 years (required)

Work authorisation:

United Kingdom (required)

Work Location: In person

Quick apply

Refine Your Search

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Senior Regulatory Affairs Specialist

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Deputy Head Teacher

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Managing Director

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Data Protection Consultant / Outsourced Data Protection Officer

Register Your Interest Regional Facilities Services Manager Opportunities in Leeds!

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I want to receive the latest job alerts for senior quality specialist in batley, wyk

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