QC Analyst: cGMP Testing, HPLC & Tech Transfer

Catalent, Inc; Dartford; On-site; GBP 27,000 - 36,000; Full time

Benefits offered by this job

Site performance bonus

Pension scheme (10% matching)

Life assurance

BUPA private medical insurance

Job summary

Catalent Micron Technologies Dartford seeks a QC Analyst to perform analytical testing using HPLC, FTIR/Raman, and DSC, support method development and validation, and contribute to technology transfer projects and batch release processes.

The role requires accurate documentation, strong IT skills, and knowledge of cGMP environments. On-site role with opportunities to contribute to critical pharmaceutical analysis and reporting.

Qualifications

• Degree in a Scientific, Biotechnology, or related discipline or equivalent laboratory experience.
• Experience using HPLC and Empower software would be advantageous.
• Strong IT skills including Word, Excel, PowerPoint.
• Knowledge of analytical laboratory techniques and cGMP environments.

Responsibilities

• Perform analytical testing including HPLC, FTIR/Raman, DSC, particle size analysis and pharmacopoeial testing.
• Support method development, validation, optimisation and troubleshooting.
• Participate in technology transfer projects and method implementation.
• Complete testing accurately and efficiently in line with cGMP requirements.
• Maintain clear, accurate, and compliant laboratory documentation.
• Prepare and maintain analytical test methods and procedures.
• Conduct environmental monitoring and microbiological testing as required.
• Review QC data and prepare analytical reports to support batch release activities.

Skills

Attention to detail

Communication & teamwork

Prioritisation

MS Office proficiency

cGMP awareness

Education

Degree in sciences or related lab discipline

Tools

HPLC

Empower software

Job description

Catalent Micron Technologies Dartford seeks a QC Analyst to perform analytical testing using HPLC, FTIR/Raman, and DSC, support method development and validation, and contribute to technology transfer projects and batch release processes.

The role requires accurate documentation, strong IT skills, and knowledge of cGMP environments. On-site role with opportunities to contribute to critical pharmaceutical analysis and reporting.