Register Your Interest Here - Technical Operators – (Swindon | Double Days Shifts)
Thermo Fisher Scientific
Register Your Interest Here - Technical Operators – (Swindon | Double Days Shifts)
Job Description
Work ScheduleRotational shift daysEnvironmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job DescriptionTechnical Operator Opportunities – Register Your Interest Here For Double Days Shift Pattern OnlyWorking shift pattern: Double Days shift - Monday Friday (1 week on early shift, followed by 1 week on late shifts)When you’re part of Thermo Fisher Scientific, you’ll do challenging work and be part of a team that values performance, quality, and innovation. As a successful, growing global organisation, we empower our people to perform at their best.We have upcoming Technical Operator positions in Swindon and are inviting candidates to apply now. In addition to these roles, we welcome applications from individuals interested in future Technical Operator opportunities as they arise.Apply today to be considered for upcoming roles only on Double Days shifts and to register your interest for further opportunities.DESCRIPTIONResponsibilities:Setting up and operating bulking and/or aseptic filling lines in line with SOPsManufacturing pharmaceutical products following Batch Manufacturing Records (BMRs)Performing manufacturing, filling, and packaging activities in compliance with cGMPSupporting equipment set-up, start-ups, changeovers, and cleaning to minimise downtime and wasteMonitoring equipment performance and reporting faults or issuesMaintaining cleanroom environments and equipment to regulatory standardsPerforming Clean In Place (CIP) and Steam In Place (SIP) activitiesOperating airlocks, autoclaves, and automated cleaning systemsSupporting investigations into non-conformance and quality eventsContributing to validation projects and new product introductionUsing SAP and quality systems for GMP documentation and reportingCarrying out basic equipment maintenanceRequirements:Experience in a pharmaceutical or regulated environment (MHRA/FDA)Cleanroom experience, with aseptic manufacturing knowledge desirableExperience in spray drying, GMP powder manufacturing, or powder filling is advantageousStrong English and Maths skills, with a scientific background (e.g., A-Levels) preferredEquivalent experience in a science-based discipline will also be consideredStrong teamwork, communication, and organisational skillsExperience with Lean / Continuous Improvement methodologiesFamiliarity with HMI-driven pharmaceutical systemsAseptic block license (desirable but not essential)Why Join Thermo Fisher Scientific?With over 120,000+ colleagues globally and significant investment in R&D, we offer the opportunity to work on meaningful projects that make a real-world impact.Apply now to be considered for Double Days shifts
Locations
- United Kingdom, Swindon, Covingham
Skills Required
- pharmaceuticalintermediate
- spray dryingintermediate
- science-based discipline will also be consideredintermediate
- Lean / Continuous Improvement methodologiesintermediate
- HMI-driven pharmaceutical systemsintermediate
Required Qualifications
- Experience in a pharmaceutical or regulated environment (MHRA/FDA) (experience)
- Cleanroom experience, with aseptic manufacturing knowledge desirable (experience)
- Experience in spray drying, GMP powder manufacturing, or powder filling is advantageous (experience)
- Strong English and Maths skills, with a scientific background (e.g., A-Levels) preferred (experience)
- Equivalent experience in a science-based discipline will also be considered (experience)
- Strong teamwork, communication, and organisational skills (experience)
- Experience with Lean / Continuous Improvement methodologies (experience)
- Familiarity with HMI-driven pharmaceutical systems (experience)
- Aseptic block license (desirable but not essential) (experience)
- Experience in a pharmaceutical or regulated environment (MHRA/FDA) (experience)
- Cleanroom experience, with aseptic manufacturing knowledge desirable (experience)
- Experience in spray drying, GMP powder manufacturing, or powder filling is advantageous (experience)
- Strong English and Maths skills, with a scientific background (e.g., A-Levels) preferred (experience)
- Equivalent experience in a science-based discipline will also be considered (experience)
- Strong teamwork, communication, and organisational skills (experience)
- Experience with Lean / Continuous Improvement methodologies (experience)
- Familiarity with HMI-driven pharmaceutical systems (experience)
Responsibilities
- Setting up and operating bulking and/or aseptic filling lines in line with SOPs
- Manufacturing pharmaceutical products following Batch Manufacturing Records (BMRs)
- Performing manufacturing, filling, and packaging activities in compliance with cGMP
- Supporting equipment set-up, start-ups, changeovers, and cleaning to minimise downtime and waste
- Monitoring equipment performance and reporting faults or issues
- Maintaining cleanroom environments and equipment to regulatory standards
- Performing Clean In Place (CIP) and Steam In Place (SIP) activities
- Operating airlocks, autoclaves, and automated cleaning systems
- Supporting investigations into non-conformance and quality events
- Contributing to validation projects and new product introduction
- Using SAP and quality systems for GMP documentation and reporting
- Carrying out basic equipment maintenance
- Setting up and operating bulking and/or aseptic filling lines in line with SOPs
- Manufacturing pharmaceutical products following Batch Manufacturing Records (BMRs)
- Performing manufacturing, filling, and packaging activities in compliance with cGMP
- Supporting equipment set-up, start-ups, changeovers, and cleaning to minimise downtime and waste
- Monitoring equipment performance and reporting faults or issues
- Maintaining cleanroom environments and equipment to regulatory standards
- Performing Clean In Place (CIP) and Steam In Place (SIP) activities
- Operating airlocks, autoclaves, and automated cleaning systems
- Supporting investigations into non-conformance and quality events
- Contributing to validation projects and new product introduction
- Using SAP and quality systems for GMP documentation and reporting
- Carrying out basic equipment maintenance
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