Work Schedule
Other
Environmental Conditions
Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed
Job Description
When you join Thermo Fisher Scientific at our Swindon site youll work in a leading UK sterile manufacturing hub. This facility is committed to quality innovation and global impact. As part of a growing global organization you will be empowered to deliver your best work with support and resources.
Responsibilities
- Set up and operate bulking and/or aseptic filling lines under strict SOPs and GMP conditions including liquid and lyophilized product fill-finish operations.
- Complete all activities required to acquire and maintain a Bronze license badge for production-area access (Grade C/D) including successful requalification every 2 years.
- Manufacture pharmaceutical products according to cGMP following Batch Manufacturing Records (BMRs).
- Operate and maintain equipment to minimize downtime and product waste; support start-up change-over cleaning CIP/SIP activities.
- Clean and maintain cleanrooms and equipment to regulatory standards; perform airlocks autoclaving automated cleaning systems and maintain aseptic environment integrity.
- Monitor equipment status report faults immediately and support corrective actions to ensure continuous compliance.
- Support validation processes new product introductions and continuous improvement initiatives.
- Perform required SAP transactions and documentation in line with GMP/site quality systems.
- Support packaging operations and secondary packaging where required.
- Enforce rigorously to hygiene and cleanroom requirements (PPE no permitted contamination: hair products jewelry cosmetics etc.).
- Work collaboratively across teams (engineering material handling QA) to ensure smooth production and high quality standards.
Requirements
- Previous experience in a regulated pharmaceutical or sterile manufacturing environment preferred experience in aseptic fill/cleanroom manufacturing is a strong advantage.
- Knowledge of GMP regulations (MHRA/FDA) cGMP processes and cleanroom SOPs desirable.
- Strong scientific or technical background (science-based qualification or equivalent experience).
- Proven communication skills and ability to work both independently and within a team.
- Experience or willingness to embrace Lean/Continuous Improvement practices.
- Skilled at functioning within a cleanroom environment and maintaining strict hygiene and safety protocols.
- Comfortable with manual handling prolonged standing and shift work if required.
Apply now
Work ScheduleOtherEnvironmental ConditionsCleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowedJob DescriptionWhen you join Thermo Fisher Scientific at our Swindon site youll work in a leading UK sterile manufacturing hub. This facility is commit...
Work Schedule
Other
Environmental Conditions
Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed
Job Description
When you join Thermo Fisher Scientific at our Swindon site youll work in a leading UK sterile manufacturing hub. This facility is committed to quality innovation and global impact. As part of a growing global organization you will be empowered to deliver your best work with support and resources.
Responsibilities
- Set up and operate bulking and/or aseptic filling lines under strict SOPs and GMP conditions including liquid and lyophilized product fill-finish operations.
- Complete all activities required to acquire and maintain a Bronze license badge for production-area access (Grade C/D) including successful requalification every 2 years.
- Manufacture pharmaceutical products according to cGMP following Batch Manufacturing Records (BMRs).
- Operate and maintain equipment to minimize downtime and product waste; support start-up change-over cleaning CIP/SIP activities.
- Clean and maintain cleanrooms and equipment to regulatory standards; perform airlocks autoclaving automated cleaning systems and maintain aseptic environment integrity.
- Monitor equipment status report faults immediately and support corrective actions to ensure continuous compliance.
- Support validation processes new product introductions and continuous improvement initiatives.
- Perform required SAP transactions and documentation in line with GMP/site quality systems.
- Support packaging operations and secondary packaging where required.
- Enforce rigorously to hygiene and cleanroom requirements (PPE no permitted contamination: hair products jewelry cosmetics etc.).
- Work collaboratively across teams (engineering material handling QA) to ensure smooth production and high quality standards.
Requirements
- Previous experience in a regulated pharmaceutical or sterile manufacturing environment preferred experience in aseptic fill/cleanroom manufacturing is a strong advantage.
- Knowledge of GMP regulations (MHRA/FDA) cGMP processes and cleanroom SOPs desirable.
- Strong scientific or technical background (science-based qualification or equivalent experience).
- Proven communication skills and ability to work both independently and within a team.
- Experience or willingness to embrace Lean/Continuous Improvement practices.
- Skilled at functioning within a cleanroom environment and maintaining strict hygiene and safety protocols.
- Comfortable with manual handling prolonged standing and shift work if required.
Apply now
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