QC Analyst (Biotechnology)

Location: Isle of Man; approximately 80% laboratory-based and 20% office-based

Company

hirify.global develops products and technologies for pharmaceutical, biotechnology, and fine chemical applications.

What you will do

• Perform QC testing of raw materials, intermediates, in-process samples, and finished products according to approved procedures.
• Conduct stability studies and environmental monitoring for cleanrooms and purified water systems.
• Support manufacturing and customer shipping schedules through timely laboratory testing.
• Maintain GMP-compliant laboratory records and support equipment maintenance, calibration, reagent preparation, inventory, and document archiving.
• Participate in investigations of deviations, out-of-specification results, change controls, and corrective actions.
• Provide analytical support to Technology Transfer, R&D, manufacturing, external laboratory partners, and other cross-functional teams.

Requirements

• At least 1 year of laboratory experience in the pharmaceutical, biotechnology, or fine chemical industry.
• Good understanding of GMP principles, Quality Management Systems, laboratory compliance requirements, 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, problem-solving, analytical, numerical, and computer skills.
• Excellent attention to detail, clear scientific and technical writing, and an organised, methodical approach.
• Ability to work independently and collaboratively, including occasional overtime or weekend work when required.

Culture & Benefits

• Collaborative and supportive quality-focused team environment.
• Exposure to multiple areas of quality control, manufacturing support, and product development.
• Ongoing training and professional development opportunities.
• Opportunity to work with a wide range of analytical techniques and technologies.
• Focus on quality, innovation, continuous improvement, and patient safety.