Register Interest - Technical Operators | Double Days Shifts
Listed on 2026-08-28
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Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Quality Engineering, Validation Engineer
Work Schedule
Rotational shift days
Environmental 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 Only
Working 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 we are welcoming applications from individuals interested in future Technical Operator opportunities as they arise.
DESCRIPTIONResponsibilities:
- 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
- Experience in a pharmaceutical or regulated environment (MHRA/FDA)
- Cleanroom experience, with aseptic manufacturing knowledge desirable
- Experience in spray drying, GMP powder manufacturing, or powder filling is advantageous
- Strong English and Maths skills, with a scientific background (e.g., A-Levels) preferred
- Equivalent experience in a science-based discipline will also be considered
- Strong teamwork, communication, and organisational skills
- Experience with Lean / Continuous Improvement methodologies
- Familiarity with HMI-driven pharmaceutical systems
- Aseptic block license (desirable but not essential)
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.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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