Regulatory specialist Work, Jobs in Ashdon, Ess (with Salaries)

Regulatory Affairs Specialist
Cambridge Consultants —Cambridge
- Continuous improvement
- Leadership
IT GRC SOX Specialist - Regulatory Frameworks
Aveva —Cambridge
- Full-time
- Hybrid work
- In-person
- Annual leave
4d
Academic Quality and Enhancement Administrator
CATS Global Schools —Cambridge
- £35,000 - £45,000 a year
- Bachelor's degree
- Communication skills
- School
- Employee assistance programme
- Referral programme
Quality Compliance Officer
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £39,959 - £48,117 a year
- Full-time
- Microsoft Outlook
- Computer literacy
- Project management
1d
Procurement Specialist
GCB Cocoa UK Ltd —Sudbury
- £30,000 - £35,000 a year
- Full-time
- Analysis skills
- Continuous improvement
- In-person
- Free parking
- Annual leave
Quick apply
Technical Specialist
University of Cambridge —Cambridge
- £35,608 - £46,049 a year
- Call to connect
- Laboratory experience
- Research
- Communication skills
14d
Senior Quality Associate – Accredited Diagnostic Development Laboratory
AstraZeneca —Cambridge
- Analysis skills
- Bachelor's degree
- Continuous improvement
10d
SEND School Development and Quality Lead
Eastern Education Group —Bury St. Edmunds
- £57,612 - £66,726 a year
- Full-time
- Mentoring
- Training & development
- School
- Free parking
- Employee assistance programme
EHS Specialist
Abcam —Cambridge
- Full-time
- Laboratory experience
- Continuous improvement
- In-person
10d
Quality Assurance Administrator
Hologic —Cambridge
- £32,000 - £40,000 a year
- Microsoft Powerpoint
- Microsoft Word
- Engineering
Divisional Activities Lead - Central Division
Barchester Healthcare —Cambridge
- Up to £43,775 a year
- Travel
- Training & development
Quick apply
Laboratory Technician (Special Processes)
Marshall of Cambridge (Holdings) Limited —Cambridge
- Full-time
- Analysis skills
- Maths
- Continuous improvement
Supply Chain Specialist
AdventBio —Sawston
- Communication skills
- Time management
Quick apply
10d
Head of Development & Partnerships
Calm Futures Limited —West Mersea
- £65,000 - £75,000 a year
- Full-time
- Travel
- In-person
- Communication skills
Quick apply
4d
Contract Management Specialist
Aveva —Cambridge
- Full-time
- Hybrid work
- English
- Bachelor's degree
- No degree
- Annual leave
10d
Statistician & Data Manager
Resolian —Fordham
- Full-time
Deputy General Manager
Cambridgeshire and Peterborough NHS Foundation Trust —Cambridge
- £66,582 - £77,368 a year
- Full-time
- Business development
- Team management
- Travel
2d
Service Design Specialist
Arm —Cambridge
- £52,400 - £71,000 a year
- Hybrid work
- Analysis skills
Band 6 Senior Research Nurse/Senior Clinical Trials Co-ordinator
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £39,959 - £48,117 a year
- Full-time
- University
Lecturer in Digital and Creative Technologies
Eastern Education Group —Bury St. Edmunds
- £23,666 - £33,571 a year
- Part-time
- Software development
- In-person
- Teaching
- Free parking
- Employee assistance programme
Quick apply
10d

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regulatory specialist jobs near ashdon, ess

Regulatory Affairs Specialist

Cambridge Consultants -
Cambridge

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Job details

Qualifications

Stakeholder liaison
Quality assurance
Continuous improvement
Multidisciplinary collaboration
Project leadership
Quality management system (QMS) implementation
Leadership
ISO 13485

Full job description

Overview

We're looking for a Regulatory Affairs Specialist to join us, working across multidisciplinary teams to support and enable breakthrough innovation.

Cambridge Consultants is a global technology and product development consultancy that helps ambitious organisations turn complex ideas into commercially successful products and services.

We combine strategy, science, engineering and design to solve tough technical challenges, across a variety of industries, and this role is key to ensuring this can happen.

What we do

Breakthrough innovation challenges traditional approaches. At Cambridge Consultants our approach to quality applies technical expertise to provide a platform which encourages and facilitates creativity and innovation to meet global regulatory requirements.

The QA Group is responsible for maintaining the quality management system that supports our business processes, complies with regulatory requirements, and satisfies our clients' expectations.

What you will be doing

We are looking for a Regulatory Affairs Specialist to join our team.

Your role will focus on providing company-wide regulatory support to our project teams, spanning both medical and non-medical disciplines, as well as supporting the QA Director and Regulatory Affairs Manager with operational activities of the Quality Management System and related management systems. This is a great opportunity for you to gain experience in a variety of different market areas and expand and deepen your knowledge across multiple industries.

Responsibilities

Your responsibilities will be varied and there is plenty of opportunity for your role to evolve over time. We have listed below the types of things you can expect to be doing:

Use your experience in compliance to product regulations and quality standards (ISO 9001:2015, ISO 13485:2016, FDA QMSR 21 CFR 820), to provide a strategic advantage to client projects while expanding our knowledge and experience of European, US and Asian regulations (for both medical and non-medical applications).

Take initiative in identifying and monitoring key changes in relevant international regulations, guidance and standards, and interpret and communicate what they mean for both the QA team and the wider business.

Lead communications on quality and regulatory updates and run internal improvement initiatives, owning meaningful contributions to CC's global systems as a quality and regulatory technical lead.

Working alongside colleagues in QA and the wider business, support the fulfilment of external audit requirements.
Strongly demonstrate and develop your leadership and project management skills to facilitate the work done by client project teams.
Apply excellent attention to detail, quality assurance expertise and a collaborative approach to process improvements and the maintenance of QMS documentation.

Find pragmatic but robust solutions in problem-solving under tough commercial, technical, time and regulatory constraints. You must understand and demonstrate the need to balance freedom to innovate on the one hand, with rigour in the design process on the other by applying your knowledge and experience of quality management appropriately to the individual project situation.

Be resourceful in your approach to contribute to projects with a widely varying breadth of disciplines, scale, complexity and requirements.

What you can bring

To be successful in this role, we are looking for someone who:

Is a clear thinker, who can work independently, flexibly and inventively to facilitate others and show leadership in managing and undertaking activities
Is a proactive communicator and has the ability to develop relationships across a range of stakeholders, takes ownership of initiatives, delivers results, and strives for continual improvement.
Can demonstrate a track record of developing and executing regulatory strategies that align with business needs and deliverables
Has the skill and experience to interpret regulatory and standard requirements to clarify the downstream implications for our processes
Knowledge of medical device compliance requirements

By submitting an application to Cambridge Consultants, you confirm that the information provided in this application, together with any supporting documentation, is true, complete, and accurate to the best of your knowledge and belief. You understand that any false statement, misleading information, or material omission may render you liable to disqualification from the recruitment process, withdrawal of any offer of employment, or dismissal without notice if discovered following appointment. You acknowledge that the organisation reserves the right to verify the information supplied.

Apply Now

Refine Your Search

regulatory specialist jobs in ashdon, ess

Regulatory Affairs Specialist

IT GRC SOX Specialist - Regulatory Frameworks

Academic Quality and Enhancement Administrator

Quality Compliance Officer

Procurement Specialist

Technical Specialist

Senior Quality Associate – Accredited Diagnostic Development Laboratory

SEND School Development and Quality Lead

EHS Specialist

Quality Assurance Administrator

Divisional Activities Lead - Central Division

Laboratory Technician (Special Processes)

Supply Chain Specialist

Head of Development & Partnerships

Contract Management Specialist

Statistician & Data Manager

Deputy General Manager

Service Design Specialist

Band 6 Senior Research Nurse/Senior Clinical Trials Co-ordinator

Lecturer in Digital and Creative Technologies

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