14 Contract Biotechnology & pharmaceutical found

Role: Laboratory TechnicianLocation: DartfordContract Length: 3 MonthsSalary: £27500 Randstad has partnered with a leading scientific manufacturing organisation. The role The successful candidate will be working within a manufacturing lab, preparing reagents, intermediates and carrying out testing using standard operating procedures and production documentation ensuring they meet performance specifications and good manufacturing practice standards. Attenti

Please note that this role requires your own car and a valid UK driving licence.Capital Equipment Service CoordinatorJob Location - SolihullJob Type - Onsite - Monday - Friday (08:30-16:30 or 09:00 - 17:00)Contract Duration - 12 MonthsPay Rate - £13.39 per hourDepartment - Capital ServiceReporting Relationship - Capital Service Team LeadJob SummaryThe Capital Equipment Service Coordinator is responsible for providing operational, administrative, and logist

Clinical Development Lead - Cardiovascular & Metabolic Diseases (CVMD) Location: Burgess Hill, UK (Hybrid: Up to 2 days per week on-site) Contract Duration: 6 MonthsAre you a senior clinical development expert with a strong background in Cardiovascular and Metabolic Diseases? We are seeking a high-calibre Clinical Development Lead to join a global diagnostic leader driving innovation in early diagnosis and personalised medicine.The RoleIn this senior strat

Service Demand Planning AssociateLocation: Burgess HillRole Type: 6-Month ContractAbout the RoleWe are currently recruiting for a Service Demand Planning Associate to join a leading healthcare technology organisation based in Burgess Hill.In this role, you will be a core member of the Technical Support organisation, coordinating the supply-demand balancing process to ensure exceptional service delivery to clients across the UK and ROI. You will play a vita

Global Studies Asset ManagerLocation: Welwyn Garden City (Hybrid - 2 to 3 days on site per week)Position Type: 6-Month ContractAre you an experienced Clinical Operations professional with a strong track record in Phase 3 global trial delivery? A leading global pharmaceutical organisation is seeking a Global Studies Asset Manager (GSAM) to lead and drive operational study management across key therapeutic areas, including Oncology, Neurology, Immunology, an

Job Title: Diagnostics Specialist / Healthcare Support SpecialistLocation: Burgess Hill (Hybrid: 2-3 Days On-Site per Week)Contract Duration: 12 Months (Inside IR35)Work Pattern: Full-Time | 37.5 Hours per WeekPay Rates:Umbrella: £305.93 - £331.10 / dayPAYE Basic: £231.00 - £250.00 / day (+ Holiday Pay)Notice Period: 1 MonthAbout the RoleWe are seeking a motivated Healthcare / Diagnostics Specialist to join a global leader in medical diagnostics based in B

Job Title: Senior Clinical Study Startup SpecialistLocation: Welwyn Garden City (Hybrid - Minimum 2-3 Days On-Site)Contract Duration: 6 Months (Inside IR35)Work Pattern: Full-Time | 37.5 Hours per WeekPay Rates:Umbrella: £450.00 - £500.00 / dayPAYE Basic: £339.27 - £376.97 / day (+ Holiday Pay)About the RoleWe are seeking an experienced, country-facing Study Startup Specialist to lead and accelerate clinical trial site activation across the UK. Based out o

Manufacturing Technician ILocation: CramlingtonPosition Type: Full-time (12-Month Contract)Shift Pattern: Day shift ( 4 days on and 4 days off) rotation, 6:00 AM - 6:00 PM)Pay Rate: £13.46 per hour + 20% shift allowanceRole OverviewSafely and efficiently produce single-use medical products within a cGMP-compliant cleanroom environment, working to a defined schedule to meet customer orders.Key ResponsibilitiesFollow detailed Standard Operating Procedures (S

Location in West side of Singaporepaying up to $65001 year contract About the RoleJoin a Clinical Research Unit (CRU) in Singapore to play a central role in driving high-quality clinical trial operations across global markets.We are seeking a detail-oriented Clinical Trial Assistant (CTA) with direct sponsor-side experience and a strong foundation in Trial Master File (TMF/eTMF) management. In this role, you will work closely with Clinical Project Managers

Laboratory TechnicianLocation: Dartford, UK (Onsite)Contract Type: Full-time, 6-Month ContractWorking Hours: Monday - Friday, 08:00 - 16:00 (37.5 hours per week)Pay Rate: £14.14 per hourRole OverviewWe are seeking a detail-oriented Laboratory Technician to join a growing microbiology manufacturing team. Working within a regulated manufacturing laboratory, you will prepare reagents and intermediates, carry out in-process testing, and ensure all work adheres

Visual Inspector ILocation: SwindonPosition Type: Full-time (37.5 hours per week)Contract Duration: 12-month contractWorkplace: OnsiteShift Pattern: Monday - Friday (Rotating shifts: 07:00 - 15:00 or 15:00 - 23:00)Pay Rate: £13.86/hr + 22% shift allowanceOpenings: 7 Positions availableAbout the RoleWe are looking for detail-oriented Visual Inspectors to join our production team in Swindon. In this role, you will perform manual visual inspections of filled

Located in Tuas 1 year contract Great Pharma Brand about the companyA multinational processing and manufacturing organization known for maintaining high standards in global facility operations.about the jobThis 1-year contract role offers a monthly remuneration of up to S$8750 to drive site-wide environmental, health, and safety operational execution.Direct site EHS operations and ensure compliance with regulatory and corporate guidelines during facility s

about the companyOur client is a global leader in the B2B food ingredients industry, trusted by world-class food manufacturers, confectioners, and food service brands worldwide. Operating across the world, they are renowned for their cutting-edge R&D, commitment to sustainability, and consumer-centric innovation. Their centre in Singapore serves as a primary hub for regional and worldwide product development. about the jobIn this role, you will hold techni

We are seeking a Sr QA Technician (Batch Release) to join our team in Birmingham. In this role, you will be responsible for performing batch release activities, ensuring regulatory compliance, verifying Device History Records (DHRs), and maintaining high quality standards. You will serve as a key point of contact for GXP documentation and support ongoing quality management initiatives.Key ResponsibilitiesBatch Release & DHR Review: Review Device History Re