Jobs from ARx Recruitment Services

We're supporting a global Pharmaceutical company with sites all over the UK and Europe, with a search for freelance QPs primarily based in South West United Kingdom. The ideal QP will be experienced in Sterile and Non-sterile pharmaceuticals, have 3 years contract QP experience, likely 5 years total QP experience, and will have come from a high volume environment already. If you are a freelance QP

An Excellent Career Opportunity for an Experienced Quality Control Analyst, Supporting the QC Supervisor and QC Lead Analyst ROLE * Perform Routine Analytical Testing on Incoming Materials and Finished Products * Ensuring All Analytical Standards, Methods, Sampling Processes, and Training Requirements are Executed in Full Compliance with SOP’s * Coordinate with QC Lead Analyst and Other Team Membe

Our Client, a Pharmaceutical Manufacturer, Located Close to Watford has a Requirement for a Quality Risk Management Specialist on a 6 Month Fixed Term Basis. The Successful Candidate will Deliver Targeted Quality Risk Management, (QRM), Activities within Defined Projects or Timeframes. The Role Focuses on Rapid Identification, Assessment, Mitigation, and Communication of Quality Risks, Consistent

Every pharmaceutical innovation, whether biotechnology, or pharmaceutical, starts out life within the Clinical Research stage. Our client is a leading Clinical Research Organisation, at the forefront of the innovative life science industry, supporting hundreds of blue chip companies in getting their drugs to market and into the hands of patients that need these lifesaving drugs. Due to securing ne

We are seeking an experienced Qualified Person (QP) with IMP experience to join a leading pharmaceutical company in Greater London. This is a fantastic opportunity to play a key role in ensuring the highest standards of compliance and product quality within a dynamic and growing organisation. Key Responsibilities: * Act as a QP for the certification and release of IMPs in compliance with EU GMP re

CMDO is Seeking to Appoint a Qualified Person. The Organisation is Engaged in Developing and Manufacturing New Medicines and Novel Formulations, Including a Wide Range of Oral Solid and Liquid Dosage Forms, Sterilised and Aseptically Filled Products, as well as Manufacturing and QP Certification of a Range of Phase I/II Clinical Trials for the UK and EU Markets, ROLE * Perform the Legal Duties of