Location: Ballasalla, Isle of Man
Salary: £27,00.00 - £32,000.00 per annum Dependent on Experience
SOC Code: 3115
Closing Date: 31st October 2026
About the Role
We are looking for a motivated and detail-oriented Quality Control Analyst to join our Quality Control team in the Isle of Man. This is an exciting opportunity to contribute to the testing and release of specialist products while supporting quality standards, laboratory operations and continuous improvement initiatives. This role offers exposure to a variety of analytical techniques and opportunities to develop within a regulated laboratory environment.
Key Responsibilities
Conduct testing of raw materials, intermediates and finished products, maintain laboratory records, perform environmental monitoring activities, support equipment maintenance and calibration, assist with investigations, train colleagues and contribute to continuous improvement activities.
About You
A degree in a scientific discipline is desirable, together with strong organisational skills, attention to detail and the ability to work independently. Previous laboratory experience within a pharmaceutical, biotechnology or chemical manufacturing environment would be advantageous.
Working Environment
Laboratory-based role involving analytical testing, the use of laboratory equipment and adherence to quality and safety procedures. The role may require occasional flexibility to support operational requirements.
Why Join Us?
Opportunity to work within a quality-focused environment, gain experience across a range of analytical techniques and products, and develop your skills through ongoing training and professional development.
If you are looking for a challenging and rewarding opportunity within a quality control environment, we would love to hear from you.
Closing Date: 31st October 2026.
Skills Required
- At least 1 year of laboratory experience in the pharmaceutical, biotechnology, or fine chemical industry
- Understanding of GMP principles, Quality Management Systems, and laboratory compliance requirements
- Knowledge of pharmacopoeias, ICH guidelines, and industry standards
- Experience with HPLC, GC, AKTA systems, TLC, UV-Visible spectroscopy, titrations, FlowCam, bioburden testing, endotoxin testing, and environmental monitoring
- Strong technical troubleshooting and problem-solving skills
- Excellent attention to detail and an organized, methodical approach
- Strong computer literacy, analytical skills, and numerical skills
- Ability to work independently and collaboratively in a fast-paced environment
- Strong verbal and written communication skills
- Ability to write clear, concise scientific and technical reports
- Willingness to train, coach, and support colleagues
- Flexibility to support overtime or weekend work when required
What We Do
Biotage is a global partner in drug discovery, development, and analytical testing, providing expertise in separation and purification technologies and intelligent workflow solutions to advance human health and optimize scientific processes.
