Regulatory affairs lead Work, Jobs in Girton, Cam (with Salaries)

Regulatory Affairs Specialist
Cambridge Consultants —Cambridge
- Project management
- Leadership
Head of Quality Assurance and Regulatory Affairs
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Project management
- Bachelor's degree
- Machine learning
- Annual leave
- Life insurance
Quick apply
4d
Regulatory Affairs Manager
TOGL (Holdings) Limited —Cambridge
- Full-time
- English
- AI
- Business
- Annual leave
Quick apply
3d
Global Medical Advisor - Anti-Infectives
Mundipharma —Cambridge
- Full-time
- Doctoral degree
- ICU experience
- Communication skills
Senior QA Auditor - 60% - 80%
Healx —Cambridge
- Part-time
- Hybrid work
- Analysis skills
- Bachelor's degree
- Travel
- Annual leave
- Work from home
Quick apply
Global Medical Advisor - Rescue Treatments
Mundipharma —Cambridge
- Full-time
- Doctoral degree
- Communication skills
Medical Director, UK and Ireland
Mundipharma —Cambridge
- Full-time
- English
- Leadership
Senior Medical Writer - FSP
IQVIA —Cambridge
- Full-time
- Remote
- Microsoft Word
- Doctoral degree
- Master's degree
- Work from home
Regulatory Affairs Director
AstraZeneca —Cambridge
- Leadership
- Communication skills
10d
(Senior) Global Medical Director, Established Brands
Mundipharma —Cambridge
- Full-time
- Doctoral degree
- Leadership
Head of Programme Management
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Machine learning
- AI
- Communication skills
- Annual leave
- Life insurance
Quick apply
Regulatory Affairs Systems and Data Manager
Mundipharma —Cambridge
- Full-time
- Hybrid work
- Communication skills
Medical Director, Medical Safety
Jazz Pharmaceuticals —Cambridge
- £113,600 - £170,400 a year
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Quality Assurance Specialist
TOGL (Holdings) Limited —Cambridge
- Full-time
- Engineering
- Microsoft Office
- Analysis skills
- Annual leave
Quick apply
3d
Clinical Site Manager
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Machine learning
- Organisational skills
- Time management
- Annual leave
- Life insurance
Quick apply
Project Manager (AI models)
Qureight Ltd —Cambridge
- £56,000 - £61,000 a year
- Full-time
- Hybrid work
- Machine learning
- Communication skills
- Annual leave
- Life insurance
Quick apply
5d
Associate Director, Portfolio Project Management
Bicycle Therapeutics —Cambridge
- Full-time
- Hybrid work
- PMP
- Project management
- Organisational skills
- Annual leave
- Employee assistance programme
Quick apply
10d
Data Partnerships Project Manager
Qureight Ltd —Cambridge
- £56,000 - £61,000 a year
- Full-time
- Hybrid work
- Machine learning
- Negotiation
- Annual leave
- Life insurance
Quick apply
5d
Senior Director, Business Development
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- English
- Annual leave
- Life insurance
Quick apply
Marketing Communications Manager
Cycle Pharmaceuticals —Cambridge
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Gym membership
- Flexible schedule
6d

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Regulatory Affairs Specialist

Cambridge Consultants -
Cambridge

Apply Now

Job details

Qualifications

Quality management
Project management
Quality assurance
Leadership

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 affairs lead jobs in girton, cam

Regulatory Affairs Specialist

Head of Quality Assurance and Regulatory Affairs

Regulatory Affairs Manager

Global Medical Advisor - Anti-Infectives

Senior QA Auditor - 60% - 80%

Global Medical Advisor - Rescue Treatments

Medical Director, UK and Ireland

Senior Medical Writer - FSP

Regulatory Affairs Director

(Senior) Global Medical Director, Established Brands

Head of Programme Management

Regulatory Affairs Systems and Data Manager

Medical Director, Medical Safety

Quality Assurance Specialist

Clinical Site Manager

Project Manager (AI models)

Associate Director, Portfolio Project Management

Data Partnerships Project Manager

Senior Director, Business Development

Marketing Communications Manager

I want to receive the latest job alerts for regulatory affairs lead in girton, cam

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