Quality Control Lab Analyst: Right-First-Time in GMP Pharma

Clear Destination Inc.; Loughborough; Hybrid; GBP 30,000 - 40,000; Full time

Benefits offered by this job

Company pension

Private Medical Insurance

25 days holiday per year

Job summary

Kindeva, located at Derby Road, Loughborough, seeks a Quality Control Laboratory Analyst to test pharmaceutical materials, support batch release and stability studies, and investigate customer complaints. You will uphold GMP/GLP standards and data integrity while delivering right-first-time results.

You will train colleagues, author documentation, calibrate equipment and participate in audits. The role offers a competitive package and 37.5 hours/week on-site.

Qualifications

• 2+ years' experience in testing within a pharmaceutical, QC or regulated laboratory environment.
• A BTEC HND or above in a science-based discipline, or a similar relevant qualification.
• Practical experience working within GMP and/or GLP environments.
• Good knowledge of laboratory specifications and test methods.
• Experience with HPLC, GC or related analytical techniques.
• Good computer skills, including familiarity with Microsoft Office.

Responsibilities

• Providing technical expertise and support to help resolve laboratory and testing issues.
• Ensuring testing is completed accurately and within required timelines, with a strong focus on right-first-time performance.
• Working in accordance with GMP, GLP, ALCOA principles, specifications, test methods and laboratory procedures.
• Performing physical and analytical testing, including HPLC, to support batch release, stability studies and customer complaint investigations.
• Completing laboratory investigations with minimal support and contributing to quality investigations and GMP deviations within your area of expertise.
• Maintaining accurate, complete and compliant laboratory documentation.
• Authoring laboratory documentation within your areas of technical knowledge.
• Supporting continuous improvement initiatives and participating in wider team improvement projects.
• Taking responsibility for the maintenance and calibration of basic laboratory equipment.
• Supporting and training colleagues, sharing technical knowledge and good laboratory practices.
• Representing the QC laboratory during customer and regulatory audits.
• Maintaining excellent laboratory housekeeping and consistently following site safety procedures.
• Championing safety, quality, data integrity and continuous improvement in everything you do.

Skills

Laboratory knowledge

Team collaboration

Education

BTEC HND or above (science)

Tools

HPLC

GC

Job description

Kindeva, located at Derby Road, Loughborough, seeks a Quality Control Laboratory Analyst to test pharmaceutical materials, support batch release and stability studies, and investigate customer complaints. You will uphold GMP/GLP standards and data integrity while delivering right-first-time results.

You will train colleagues, author documentation, calibrate equipment and participate in audits. The role offers a competitive package and 37.5 hours/week on-site.