Clearline Recruitment Ltd

Role: Laboratory Applications Specialist Location: Field-Based - Devon (Remote with ad hoc visits to Burgess Hill) Hours: Full-time Pay: £180 - £230 per day (PAYE) or £245.27 - £305.06 per day (UMB) Contract: 12-month contract, inside IR35An excellent opportunity has arisen for a Laboratory Applications Specialist to join one of our longstanding global healthcare clients, supporting NHS laboratories across the Devon region.This field-based role will provide applications support, customer training and technical troubleshooting across diagnostic laboratory platforms. Benefits: 12-month contract opportunity Field-based role with autonomy and variety Opportunity to work with leading diagnostic platforms Exposure to NHS pathology laboratories Travel for meetings and training The Requirements: Degree in Biomedical Science or equivalent experience Experience within diagnostics, pathology or a hospital laboratory environment Biomedical Scientist or Applications Specialist background preferred Strong troubleshooting and problem-solving skills Excellent communication and customer relationship skills Full UK driving licence Must be based in Devon, nearby or willing to relocate Experience with cobas 8000, cobas 6000, cobas Pure, cobas Pro, Infinity or pre-analytic systems desirable The Role: Provide frontline applications support across NHS laboratory sites Deliver customer training on diagnostic systems Troubleshoot and investigate technical and application issues Minimise laboratory downtime through effective customer support Support software, applications and IT-related queries Work closely with laboratory teams to ensure successful system use Travel throughout Devon and occasionally to Burgess Hill for meetings/training Please note: candidates must live within the Devon region or be willing to relocate to meet customer response times. The recruitment process will include a pre-screen interview, presentation and potentially a second-stage interview.If you're keen to join an exceptional team who can offer exposure to leading diagnostic technologies and autonomy in a field-based role, then please apply to this Laboratory Applications Specialist role below or call Chloe McCausland on between 8:30am - 5:00pm .

Role: Senior Regulatory Medical Writer Location: Hybrid - Welwyn Hours: Full-time Pay: £45.50 - £56.40 per hour PAYE basic excluding holiday pay or £60 - £75 per hour LTD/UMB Contract: 12-Month Contract (Outside IR35) An excellent opportunity has arisen for a Senior Regulatory Medical Writer to join one of our longstanding global pharmaceutical clients. This senior-level role will focus on developing regulatory content strategies and delivering high-quality clinical, safety and medical device documentation for global submissions. The successful candidate will work independently, lead cross-functional contributors and help shape submission content throughout the product lifecycle. Benefits: 25 days holiday + bank holidays 12-month contract outside IR35 Hybrid working based in Welwyn Free, on-site parking Opportunity to support global regulatory submissions Exposure to pharmaceutical and medical device programmes Senior-level strategic and cross-functional responsibility The Requirements: Degree in Life Sciences or an equivalent scientific discipline At least 5 years of relevant experience within the pharmaceutical or biotechnology industry Strong medical and regulatory writing experience Experience independently managing complex regulatory writing projects Experience producing clinical protocols and pharmacovigilance documents, including DSURs and PBRERs Strong understanding of clinical, safety and medical device regulatory documentation Familiarity with drug and device development regulations, including GCP, GVP, ICH, ISO and MDR/IVDR Experience supporting global filings and regulatory submissions strongly preferred Proven ability to lead cross-functional teams and manage stakeholder input Excellent scientific writing, editing and project-planning skills Experience with Veeva Vault, Adobe Acrobat, Microsoft Office and Google Workspace desirable The Role: Lead the development and delivery of regulatory content strategies Prepare and oversee clinical, safety and medical device documentation Produce protocols, DSURs, PBRERs and other regulatory submission documents Plan document timelines and manage content from initiation through approval Review documentation for scientific quality, clarity, consistency and compliance Lead cross-functional contributors and resolve content-related issues Support global regulatory filings and submission planning Contribute to content standards, strategic reuse and process improvement initiatives Maintain awareness of relevant regulatory, scientific and medical developments Mentor less experienced writers or Content Strategists where required If you're keen to join an exceptional team who can offer strategic regulatory exposure, global submission work and senior-level ownership across clinical, safety and device content, then please apply to this Senior Regulatory Medical Writer role below or call Chloe McCausland on between 8:30am - 5:00pm .

Role: Production Operative (Early Shift) Location: Hailsham, East Sussex Hours: 48 hours per week (Monday-Thursday: 6:00 am - 4:45 pm / Friday: 6:00 am - 2:45 pm) Pay: £12.21 - £13.68 per hour Temporary Ongoing An excellent opportunity has arisen for Production Operatives to join one of our clients, a forward-thinking manufacturing business based in Hailsham, East Sussex. This role is offered on a full-time temporary contract, working as part of the production team on the early shift. Please note: You must be able to drive and have access to your own vehicle due to the remote location. Benefits: Weekly pay On-site parking The Requirements: Safety footwear required Physically fit with knowledge of manual handling Due to the site's location, own transport is required Good understanding of Health & Safety in a production environment Willingness to learn and follow written and verbal instructions Excellent attention to detail and strong quality standards Basic maths and measurement skills Reliable, with good timekeeping and strong work ethic Basic computer skills Flexibility to work alternative shifts if required The Role: Set up machinery at the beginning of each shift Carry out safety and quality checks before and during runs Monitor and optimise machine performance during production Accurately log run-time and downtime data Perform basic maintenance and cleaning at the end of shift Operate pallet jacks and other relevant equipment Maintain a clean and safe working environment Report progress, issues, or hazards to the Production Manager If you're keen to join a supportive and growing company with excellent opportunities for development, then please apply to this Production Operative role below or call Martin Davis on between 8:00am - 4:30pm.

Role: Medical Device Training Specialists Location: Field-Based - South East (London / Sussex) Hours: Full-time Pay: £185 - £240 per day PAYE basic excluding holiday pay or £230 - £300 per day UMB Contract: 12-Month Contract (Inside IR35) An excellent opportunity has arisen for two Medical Device Training Specialists to join one of our longstanding global healthcare clients. This field-based role will focus on delivering high-quality diagnostic product training and supporting customers across healthcare environments. Benefits: 12-month contract opportunity Field-based role with regional autonomy Opportunity to work within diagnostics and healthcare training Exposure to NHS and healthcare customers The Requirements: Strong training experience, ideally within diagnostics, medical devices or healthcare Excellent communication and presentation skills Ability to deliver engaging face-to-face training Strong organisational and time management skills Full UK driving licence and access to a vehicle Must be able to start within a maximum one-month notice period The Role: Deliver product training to healthcare customers Support customer implementations and onboarding Provide training support and basic troubleshooting Maintain accurate training records and documentation Travel across customer sites within the South East region Work closely with internal teams to ensure effective training delivery If you're keen to join an exceptional team who can offer autonomy, customer engagement and the opportunity to support innovative diagnostic solutions, then please apply to this Medical Device Training Specialists role below or call Chloe McCausland on between 8:30am - 5:00pm .