Technical Operator (24/7 shift pattern)

ThermoFisher Scientific; Swindon; On-site; GBP 25,000 - 35,000; Full time

Job summary

Thermo Fisher Scientific in Swindon is hiring 3 Technical Operators for 24/7 shifts to support bulking and aseptic filling lines in a regulated environment. You will work across rotating day and night schedules, adhere to SOPs and cGMP standards, and contribute to production throughput.

The role requires experience in pharmaceutical or regulated settings, familiarity with cleanrooms, and the ability to operate SAP and quality systems.

Qualifications

• Experience in a pharmaceutical or regulated environment (MHRA/FDA).
• Experience in cleanroom working and aseptic manufacturing desirable.
• Experience with spray drying systems and bulk GMP powder manufacturing.
• Strong English and math skills; scientific background essential.
• Equivalent science-based experience acceptable.

Responsibilities

• Set up and operate bulking and aseptic filling lines per SOPs.
• Maintain access to production areas and requalification every 2 years.
• Manufacture pharmaceuticals following SOPs and BMRs.
• Perform manufacturing, filling and packaging duties to cGMP.
• Set equipment to minimize downtime and assist start-ups/changeovers/cleaning.
• Monitor equipment status and report faults to supervision.
• Clean and maintain clean rooms and equipment to regulatory standards.
• Perform CIP and SIP activities; operate autoclaves and automated cleaning systems.
• Communicate non-conformances for investigation and rectification.
• Support project validation work and new product introductions.
• Perform SAP transactions and use quality systems for GMP changes and reports.
• Conduct basic equipment maintenance as needed.

Skills

Excellent communication

Teamwork

English proficiency

Math proficiency

Lean systems

Continuous Improvement

GMP knowledge

Aseptic manufacturing awareness

Education

A-Levels in science or equivalent

Tools

SAP

Quality systems

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Fluctuating Temps hot/cold, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials, Working at heights

Job Description

Working shift pattern: 24/7 – 2 shifts on, 2 days off, 3 shifts on, 2 days off, 2 shifts on, 3 shifts off, etc.. Shifts will rotate between Day shift, 6.45am to 7pm, and Night shifts 6.45pm to 7am.

We are currently hiring 3 Technical Operators to join our expanding team on 24/7 shifts —this is a fantastic opportunity to join a global leader with multiple openings available.

With revenues of $20 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

Responsibilities:

• Set up and operate bulking and/or aseptic filling lines in accordance with Standard Operating Procedures (SOPs)

• Complete all activities to acquire and maintain, as a minimum, a Bronze License Badge – Production areas (Grade C/D) access, including requalification every 2 years

• Manufacture pharmaceuticals following SOPs and Batch Manufacturing Records (BMRs)

• Perform Manufacturing, Filling, and Packaging operational duties, ensuring compliance with cGMP

• Set equipment to minimize downtime and product damage/waste, supporting start-ups, changeovers, and cleaning activities

• Monitor equipment status and report any faults or issues to supervision

• Clean and maintain clean rooms and equipment to regulatory standards

• Perform Clean In Place (CIP) and Steam In Place (SIP) activities

• Operate airlocks, autoclaves, and automated equipment cleaning systems

• Communicate instances of non-conformance for investigation and rectification

• Support project validation work and new product introduction

• Perform SAP transactions and use Quality systems for GMP changes and report writing

• Conduct basic equipment maintenance as needed

Requirements:

• Experience in a pharmaceutical or regulated environment (MHRA and FDA regulations)

• Experience in cleanroom working, with knowledge of aseptic manufacturing and filling desirable

• Experience in spray drying systems, bulk GMP powder manufacturing, and powder filling

• Strong competency in English and Math, with a scientific background (e.g., A-Levels) essential

• Equivalent experience in a science-based subject is also acceptable

• Excellent communication and teamwork skills, with the ability to manage workload

• Experience in Lean systems and Continuous Improvement

• Understanding of HMI-driven pharmaceutical systems

• Aseptic block license will be considered a plus

At Thermo Fisher Scientific, every single one of our 120,000 remarkable individuals has an unusual narrative to reveal. Join one of our new hires and become part of our outstanding mission—helping our customers make the world healthier, cleaner, and safer.

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.