QC Analyst: GMP Lab & R&D Support

Biotage; Ballasalla; On-site; GBP 32,000 - 42,000; Full time

Job summary

Biotage is seeking a QC Analyst to join our Quality Control team. You will perform laboratory testing of raw materials, intermediates and finished products in a GMP-regulated environment, supporting TT/R&D and ensuring compliance with quality systems.

You will contribute to investigations, documentations, and drive continuous improvement within the QC department while mentoring colleagues as needed.

Qualifications

• At least 1 year of laboratory experience in pharma, biotech or fine chemicals.
• Knowledge of GMP principles, Quality Management Systems and laboratory compliance.
• Understanding of pharmacopoeias, ICH guidelines and industry standards.

Responsibilities

• Perform QC testing of raw materials, intermediates, in-process samples and finished products per approved procedures.
• Conduct stability studies and environmental monitoring testing.
• Support manufacturing and shipping schedules with timely testing results.
• Maintain GMP-compliant laboratory records and documentation.

Skills

GMP principles

Quality Management Systems

pharmacopoeias & ICH guidelines

Analytical techniques

Troubleshooting

Attention to detail

Team collaboration

Communication

Tools

HPLC

GC

AKTA systems

TLC

UV-Visible Spectroscopy

Titrations

FlowCam

Bioburden Testing

Endotoxin Testing

Environmental Monitoring

Job description

Biotage is seeking a QC Analyst to join our Quality Control team. You will perform laboratory testing of raw materials, intermediates and finished products in a GMP-regulated environment, supporting TT/R&D and ensuring compliance with quality systems.

You will contribute to investigations, documentations, and drive continuous improvement within the QC department while mentoring colleagues as needed.