Careers

Medovate is a dynamic and growing company. As we grow, we look for high calibre candidates for arising vacancies to support our revolutionary product portfolio and work with partners.

We currently have the following opportunities to join the Medovate team.

Business Development Manager

Quality Assurance (Q/A) Controller


Full details about each role, including how to apply, are below.

** No agencies please **


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Role: BUSINESS DEVELOPMENT MANAGER

Download a copy of the job description here or see details below.

Applications for this vacancy are currently being accepted.


Brief Description:

Medovate is a medical device company dedicated to the development and commercialisation of innovative medical technologies created within the NHS. By providing funding at a crucial point in development, Medovate will ensure that novel medical technologies with high growth potential are accelerated through development, clinical trials and regulatory approval into manufacture so that they can reach the market as quickly as possible to benefit patients and healthcare delivery.

To support these efforts and enable Medovate products to gain uptake and adoption upon market launch Medovate is looking to recruit a Business Development Manager. The successful candidate will be a key member of the commercial team and will be responsible for supporting distributors in the delivery of corporate revenue targets ensuring successful pull through of Medovate products.


Key responsibilities:

• Achievement of monthly, quarterly and annual sales and KPI targets
• Contribute to the development and management of product forecasting S&OP process
• Work closely with marketing team to implement marketing and promotional campaigns with distributor partners
• Work with distributors to educate and train on current and new products
• Develop and create key business opportunities as part of a wider matrix structured team.
• Build key relationships with and educate distributors & 3rd party customers to help drive success.
• Create bespoke business solutions on a customer by customer basis that meet and exceed requirements.
• Work to identify and develop new areas for distributor expansion, sometimes by working with external organisations.
• Provide regular sales and KPI reporting and updates to the Sales and Marketing Director.
• Actively develop internal and external stakeholder relationships in line with business principles and overall strategy.
• Develop sustainable business plans which are aligned to the changing customer environment.
• Work across the organisation to capitalise on the wealth of resources available to ensure service and solution delivery to the customer
• Represent the business at national and international trade and clinical shows and events


Person Specification:

• Enthusiastic and entrepreneurial approach to solution sales.
• Ideally you will be experienced either within Healthcare, Medical Devices or Medical services solutions
• Experience of managing distributors supporting both commercial and clinical requirements.
• Strong cross cultural communication skills, understand, appreciate, and adapt to international cultural variances and values.
• A history of working with and bringing together matrix teams in the delivery of a solution.
• Experience with clinically differentiated or similar products.
• Strong Commercial & analytical ability (Financial modelling, forecasting and assessment etc.)
• Excellent organisational and presentation skills.
• Freely able to travel internationally if required.


How to Apply:

If you believe you have what it takes to excel in this role, tell us why in a covering letter and send it along with your CV and any supporting information to: enquiries@medovate.co.uk

Closing date for applications: Friday, 20th August 2021

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Role: QUALITY ASSURANCE (Q/A) CONTROLLER

One year fixed term contract

Download a copy of the job description here or see details below.

Applications for this vacancy are currently being accepted.


Brief Description:

The QA Controller will be responsible for ensuring documents and records are created, approved and maintained in accordance with company procedures and available at point of use. The role will also play a key role in establishing an electronic document management system as well as maintaining and refining the quality system in line with business needs.


Knowledge & Experience:

- Minimum two years Document Control experience ideally in pharmaceutical, medical device or other related industries
- Working within an ISO 13485 Quality Management System under the Medical Devices Directive (MDD)/Medical - Devices Regulation (MDR) for product development and/or manufacturing in the UK/EU is desirable
- An HNC or degree in a related subject, or equivalent level of experience
- Competent in MS Office Suite and Windows applications e.g. Word, Outlook, SharePoint, Excel, PowerPoint, Visio etc
- Proficient in document formatting
- Experience of implementing an electronic documentation management system is desirable
- Excellent oral, written communication and interpersonal skills
- Attention to detail, commitment to Quality, accuracy, efficiency, and consistency
- Some exposure to regulatory agency inspections (e.g. FDA, notified bodies, etc.) is desirable
- Ability to work under limited supervision, manage multiple tasks and prioritise assignments within established time constraints
- A strong team player who is motivated by the success of the business
- A self-starter committed to making things happen


Responsibilities:

- Ensure documents are reviewed, approved and maintained in accordance with defined processes.
- Support in maintaining and continuously improving the quality management system in compliance with regulatory requirements
- Ensure documents remain legible and readily identifiable
- Prevent deterioration or loss of documents
- Prevent the unintended use of obsolete documents
- Support systems integration and deployment of electronic document management system
- Manage training records
- Support Audits, CAPA’s, Change Control, Deviations/Concessions, Root-Cause Analysis, and Complaint handling where required
- Maintain design change and equipment logs
- Monitor quality related KPI’s
- Monitor and control documents of external origin e.g. industry standards
- Make available, notify and distribute documents to relevant recipients
- Keep abreast of new developments in QA/RA e.g. standards and regulations
- Work closely with internal and external multi-disciplinary product development teams to ensure project success
- Deliver relevant training on the QMS to existing and new staff within remit of responsibilities


How to Apply:

If you believe you have what it takes to excel in this role, tell us why in a covering letter and send it along with your CV and any supporting information to: enquiries@medovate.co.uk

Closing date for applications: Friday, 30th July 2021