Exciting opportunity to join our Life Sciences Team who have had a extremely succesful year and won a numbe of large client projects.

Life Sciences recruitment consultant working with organisations that need help to find top talent that can help them succeed in their endeavour to save patients lives across the globe.

The role of a PageGroup recruitment consultant combines business development and commercial customer service, generating revenue by successfully engaging with clients, candidates and colleagues.

The role of a PageGroup recruitment consultant combines business development and commercial customer service, generating revenue by successfully engaging with clients, candidates and colleagues.

My client is a top 10 CRO who are at the forefront of scientific discoveries into new treatments. Offering a wide range of bio-pharmaceutical services to a diverse portfolio of clients. They are looking for a Senior Clinical Research Associate who is an innovative, tech-savvy problem solver that is confident and resourceful. The successful candidate will be joining a business that is dedicated to both the personal and professional growth of their team.

The creation, management and maintenance of Technical Files for product range in accordance with the requirements of the IVDD 98/79/EC and MDD Directive 93/42/EC, including CE-marking activities.

As a Quality Engineer you will be supporting design, development and manufacture of medical devices. You will be carrying out quality processes and generating, reviewing and approving associated records as required by associated regulations

As a Senior QC Analyst you will be responsible for supervising a team of analysts performing QC analysis for the business. You will be involved in escalation processes along with additional supporting QC related functions.

As a QC Analyst you will be responsible for RM, PM, In Process and Finished Product Sampling and both physical and chemical testing within QC lab. You will have high attention to detail and maintaining GMP/GLP compliance at all times.

Exciting and unique opportunity to join my client at a very important period of growth as Head Of Global Regulatory Affairs.

You will be supporting PURP and relevant Group Financial Reporting team in the month end close process which include:

Quality Assurance Associate for Biopharmaceutical company based in the Liverpool. Working in a QA team you will be responsible for QA front-line support, documentation review and project participation.

A fantastic opportunity to oversee a number of global EAP and NPP studies.

• Experience within LC-MS/MS platforms.
• Based in London.

• Experienced in a clinical research environment.
• Based in Hatfield.

As a principal programmer you will provide and support the statistics programming department with a range of projects, therapeutic areas and working with many clients.

The role of the Senior/Principal Statistician is to provide statistical support to the statistics and programming department across a range of projects, clients and therapeutic areas.

Quality Management, QMS management and implementation. Team leader of QA/QC department, based in North england, with a competitive salary and benefits package.

• Ensure laboratory services and equipment maintenance is run efficiently.
• Support lab scientists by producing stocks and general reagents.

The Biocide Registration Specialist will bring expert knowledge of Biocidal Products Regulation and relevant guidance. You will support the team by evaluating and validating data sources and ensuring regulatory compliance by: submission of registrations, resolving customer or regulatory body questions and working as a team.

Exciting opportunity to join a fast growing and innovative consultancy looking for a Associate Director to join the high performing team.

An exciting pre-clinical project management opportunity within a rapidly growing Biotech. You will be joining the business at a pivotal expansion point and will be immersed in cross-functional teams both internally and externally to deliver revolutionary new therapeutics and support critical company decisions.

• Laboratory and Facilities management experience.
• Based in Cambridge.

Exciting brand new opportunity to join a growing pharmaceutical services provider as a Commercial Lead at a pivotal point of there growth strategy. This research centre provide world leading sample management and high capacity bioprocessing.

There centre is based in the east of England but the the role can be relatively flexible for the right candidate.

I've partnered with a leading pharmaceutical business based in Devon who are actively recruiting a full-time QP to join their team.

Managing external suppliers to ensure that Pharmaceutical R&D projects run effectively and efficiently.

Managing KOL's.

Providing expertise and training to a range of HCP's.

To combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured and distributed to meet applicable regulatory requirements and applicable technical standards

The primary task for this Regulatory Affairs Executive role is to compile regulatory submissions. This position requires a professional with good organisational and communication skills, at every level in various departments.

Exciting opportunity to join a growing diagnostics company , due to growth they are looking for a Medical Science Liaison to join the team.