Testing of routine release of raw materials, intermediates, finished product and stability as requested. Actively participate in analytical method transfers and…

The QA Specialist is responsible for supporting operation of core Quality Systems used in the Drug Substance Manufacture Facility and providing QA support to…

Nurture existing customer relationships, supporting their clinical requirements. Gain a deeper understanding of this clinical field and become a product expert.

Our client, a global pharmaceutical organisation are currently recruiting for a Fluent Romanian speaking Clinical Trials Start Up Associate to join their team…

The QA Snr Associate will serve primarily as a Quality point of contact for batch record review for complaints received related to products manufactured and…

As a Clinical Trial Coordinator the successful candidate will be responsible for leading the development, execution, completion, and reporting of clinical trial…

Working closely with cross functional team to define the regulatory and quality roadmaps for the business and then budget, plan, approve and execute these.

A third level qualification in science or engineering is desirable. Manage the complete recruitment process lifecycle for Life Science professionals.

Working with the Shift Supervisors to start and stop machines and troubleshoot processing problems to. Maximize and maintain machine up time.

We are seeking to appoint a Process Technician to carry out daily process monitoring to meet. Production targets and ensure tool set-up and change-over…

Develop market plan, taking account of product life cycle, market trends and maturity. The successful person shall support and grow our clients existing…

At least 3-5 years’ experience in Quality role, ideally in a heavily regulated industry, preferably in a life science sector (Pharma or medical device).

BS degree in engineering or technical sciences. Reporting to Quality Manager The Staff Quality Engineer will be accountable for supporting new product…

QA specialists will be required to understand and grasp a broad range of quality related competencies. Participation in self-inspection program in a lead…

Degree in a pharmaceutical development (science/engineering) discipline, or equivalent. Director will be responsible for all aspects of Regulatory Affairs for…

BA/BS, preferably in science. Requirements will revolve around QMS activities e.g. change controls and completion of change actions, Quality agreements, SOP…

Develop knowledge and skillset of clinical trials and the recruitment and retention space to support the overarching strategy.

Our client a high potential medical device start up is currently seeking a Manufacturing Technician to join their team for a 12 month contract.

The role of Staff Engineer involves, customer facing, technical leadership in a cross functional project core team guiding the design, development, verification…

Managing the activities of the Quality Inspectors to ensure optimal efficiency and compliance with all regulatory requirements; High level of computer literacy.