Regulatory Affairs Assistant – Leeds

Alex Tosney is recruiting for a Regulatory Affairs Assistant to join a leading medical device company in Leeds on a 12 month contract.

Your main responsibilities will include providing full support to all registration activities and product registration submissions throughout the world to ensure submissions are achieved in a timely manner in accordance with regulatory and company requirements.

To apply for this position you should have significant regulatory affairs experience in a medical device environment and have extensive knowledge of worldwide regulatory procedures.

Click here for more information or to apply 

 

 

 

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Senior Regulatory Affairs Officer – Edinburgh

Barney Smith is recruiting for a Senior Regulatory Affairs Officer to join a Contract Research Organisation based in Edinburgh on a permanent basis.

Responsibilities include managing the product licence registration process with the appropriate regulatory authorities on a worldwide basis.

To be considered for this role you must have a proven track record of working in regulatory affairs within a medical devices, diagnostics, biologics or virology environment. Our client is growing rapidly and will soon be a global leader in their field so this is a great opportunity to join.

For more information or to apply click here >

 

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Regulatory Affairs Manager – Edinburgh

Barney Smith is recruiting for a Regulatory Affairs Manager to join a Contract Manufacturing Organisation based in Edinburgh on a permanent basis.

Responsibilities include managing the product license registration with regulatory authorities on a worldwide basis and managing the regulatory affairs team. You will also be expected to manage, prepare and maintain regulatory documentation to ensure compliance with quality standards and FDA Regulations.

This could be a great opportunity for you if you have significant experience in managing a Regulatory Affairs department within a diagnostic, medical device, virology or immunology related environment. As this client is experience substantial growth due to the success of their core business so this is an opportunity to join a company at an exciting time.

Click here for more information or to apply >

 

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Global Raw Material Compliance Coordinator

Jason at CK Science is recruiting for a Global Raw Material Compliance Coordinator to join a global pharmaceutical company at their UK Site in London/Kent on a full time, permanent basis.

Our client designs and supports advanced coating systems, modified release technologies and functional excipients for pharmaceutical dosage form and are looking for someone to manage the Raw Material Risk Assessment programme.

If you have experience in a QC, A or regulatory affairs at an intermediate level, and are competent at the day to day management of base raw material data and specifications in the Oracle Quality Module and Master items, our client would like to speak to you.

For more information on this role and to apply click here

 

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