Indo Search

100% fill rate on search with MedTech, and HealthTech Organisations. 
90% + vacancy fill rate on Contingent Assignments
92% have stayed in their roles over 24 months

* Regulatory Affairs / Quality / Clinical Research
* Commercial – including Sales/Marketing/Market Access
* Product Management
* Compliance & Risk
* Clinical & Medical Affairs – including Chief Medical Officer / Medical Director
* Leadership – including C-Suite & Director
* Change & Transformation
* Operations – including Finance/HR/Recruitment

Co-Founder

Practicus

Our mission is to help people navigate change.
Recruiting Change and Transformation consultants mainly in the Life Science and Healthcare space including the NHS

Principal Consultant

Gleeson Recruitment Group

Managed Finance Team for Thames Valley/South of England

Business Development Director

JWS Resources Ltd.

Management of Employee Benefits & HealthTech recruitment business with a broad range of clients including SMEs, Scale-Ups/Start-Ups and Large Enterprises

Associate Director

Business Manager

Regulatory Professionals

Regulatory Professionals focus on providing staffing solutions with Life Science organisations. As part of the Clinical Professionals Group we aim to offer candidates the most accurate and informed advice on careers within Regulatory Affairs. 

Took on the task to help turnaround the division's fortunes into a profitable business unit with influence over a new brand and identity in a competitive marketplace.

Project Resource Ltd

Joined a few months after Project Resource was established working closly with Directors to help grow market presence in the Commercial/QS recruitment market in the UK. My time at Project Resource was a fulfilling and enjoyable one that taught me the value of building internal and external relationships and how much I enjoy making a positive impact on someone's career.  Went on to be the top performing consultant over my time there while also coaching/growing teams to give clients and candidates the best of our market knowledge and recruitment experience.

Recruitment Consultant through to Manager

Huxley Associates

Recruitment Consultant

The Courier

Telesales Executive

How We Helped a High-Growth MedTech Company Fill Critical Positions and Launch Their Cutting-Edge Product…
This company aimed for rapid growth and substantial investment, requiring them to fill critical positions in technical and commercial roles.

They were seeking out seasoned professionals who could guide their product launch and maintain their competitive edge.

Despite their urgent need to fill positions, the company's recruitment team was having difficulty keeping pace with the volume of open roles.

This bottleneck risked delaying the release of their cutting-edge medical device, jeopardizing the company's ability to generate revenue from their investments.

By leveraging our expertise, the company successfully streamlined their hiring process and made more informed decisions, achieving a 100% acceptance rate for initial job offers.

Moreover, our team provided valuable input on clinical research and regulatory approval strategies, as well as sales and marketing efforts to support the global launch of their product.

We are proud to have filled all 17 vacancies for the company, including key roles such as…
> Multiple Regulatory Affairs professionals including Labelling, Pre and Post Market
 
> Multiple Sales and Marketing hires.

> Head of Clinical/Medical Director to work closely with their CMO Co-Founder

> Head of Quality to facilitate the company's US FDA approval process.

One of our unique strengths is our ability to create immersive digital job descriptions that effectively highlight the company's strengths and unique selling points, setting them apart from their competitors.

They’ve been highly effective in generating more interest resulting in a larger pool of applicants and real-time market analysis.

Ridda Michail

IMed Group 

Chief Executive Officer

IMed Consultancy Ltd

Managing Director and Quality & Regulatory Consultant

Lasersure Limited 

Director

Emergo Group

Senior Consultant (QA / RA)

Kimal

Regulatory Affairs Manager

High Edge Consulting Ltd

Medical Device Regulatory Specialist

Renishaw

Regulatory Affairs Officer

Summit Medical Ltd

Regulatory Affairs Executive

Ansell UK Ltd

Regulatory Affairs Assistant

QA/RA Medical Device & IVD Consultant assisting with UKRP, UKCA, CE Marking, MDR, ISO 13485, FDA, QMS, Global Registrations & Audits

Medical Device consultant with extensive experience of both regulatory and quality projects in accordance with both European and United States standards. 
My previous roles within Neurological, Orthopedic, Contraceptive Device and Procedure Pack companies have made me routinely work on product Technical Files and Design Dossiers including Essential Requirements, Risk Management and Clinical Literature Evaluations for CE marking and 510(k) projects as well as submissions for worldwide markets including Australia, New Zealand, Canada and Japan. 
EXPERIENCE
• MDR transition 
• MDSAP 
• Compilation of regulatory submission including Design Dossiers / Technical Files
• CE-Marking Class I, and II a and III MDD and Class III AIMD medical devices
• Biological Evaluation reviews  & Clinical Evaluations including clinical literature reviews in line with the requirements of the revised MDD Annex X
• Risk analysis & risk management activities
• Implementation of various standards, Directives and Regulations including ISO 13485, EU Directive 93/42/EEC, MDR 
• Implementation of ISO 13485, FDA 21 CFR Part 820, Canadian ISO 13485 and Japanese GMP requirements into quality management systems 
• On-site regulatory support to ongoing design projects bringing various medical devices to market including Class II b and III
• Control of Internal Quality System Audits 
• Internal Auditor and Supplier Auditor
• Representative during third party audits including BSI, LRQA and TUV
• Maintenance and reporting of Non-Conformity Reports and Observation Actions Plans
• Review of labeling materials and evaluation of marketing collaterals
• Designing, writing and conducting training courses
• Complaint handling

Specialties: ISO 13485:2016, MDR Transition, Clinical Evaluations, Regulatory Strategy, Auditing, World wide Medical Device Regulations and Quality Assurance

Contact me at leeanne@imedconsultancy.com

Leeanne Baker

taplio

The Battle

Ridda Michail

Leeanne Baker

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