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

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

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.

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.

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

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

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.

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.

QA Administrator, based in Bedfordshire on a 6 month FTC. The Quality Assurance Administrator works closely with QA teams in support function to ensure compliance to relevant Standard Operating Procedures (SOPs) and cGDMP standards and internal policies.

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 ensure continued compliance with all relevant regulatory requirements of both internal corporate standards

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

This exciting role will effectively manage the Drug Regulatory Affairs (DRA) team responsible for global products and act as Deputy Head, in the absence of department head.

As a Senior Verification Engineer you will be responsible for developing product verification strategies as the business looks to drive innovative and new medical device products to market

Job overview

Being able to make use of developing computational tools and perform omics data analysis to support internal target identification and therapeutics development platforms.

Working closely with biology teams and team different range of diseases.

As Toxicology Engineer you will be critical to the companies success as you will be responsible for supporting new product development with critical care devices. You will be instrumental in supporting safety initiatives, ensuring that the toxicology and biocompatibility procedures are accurate, and conducting engineering activities of intermediate scope or degree of difficulty.

The Senior Regulatory Affairs Specialist will develop Regulatory strategies related to regulatory documents, submissions, investigations, product development planning and regulatory agency interaction

The Regulatory Affairs Specialist is responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval for products globally