Senior Pharmaceutical QC Lab Technician (GMP/GLP)

Kindeva-Drug-Delivery-Careers; Loughborough; On-site; GBP 28,000 - 38,000; Full time

Benefits offered by this job

Private Medical Insurance

Company pension scheme (up to 10%)

25 days holiday plus service days

Free on-site parking

Cycle to work scheme

Job summary

Kindeva is seeking a QA/Testing role on site at Charnwood Campus, Loughborough. The successful candidate will test pharmaceutical finished products, perform stability assessments, and handle customer complaints in line with GMP/GLP practices.

You will input data into LIMS, support audits, and participate in investigations while maintaining rigorous documentation and equipment calibration.

Qualifications

• 3+ years’ experience of testing within a Pharmaceutical or laboratory environment.
• BTEC HND in Science or similar field.
• Experience with GLP, GMP, specifications and test methods.
• Hands on experience of HPLC, UV techniques and GLC.
• Knowledge of pharmaceutical testing requirements, equipment and methods.
• Proficient with Microsoft Office.

Responsibilities

• Test finished products, stability and customer complaints in line with site procedures.
• Input results onto the LIMS system and maintain documentation.
• Represent the department during regulatory and customer audits.
• Maintain lab equipment calibration and housekeeping.
• Support investigations and continuous improvement within the group.
• Ensure compliance with safety, GMP/GLP standards and regulatory requirements.
• Assist in developing understanding of tests carried out and their product impact.

Skills

Pharmaceutical testing

GLP/GMP knowledge

HPLC

UV techniques

GLC experience

MS Office

Education

BTEC HND in Science

Tools

LIMS system

Job description

Kindeva is seeking a QA/Testing role on site at Charnwood Campus, Loughborough. The successful candidate will test pharmaceutical finished products, perform stability assessments, and handle customer complaints in line with GMP/GLP practices.

You will input data into LIMS, support audits, and participate in investigations while maintaining rigorous documentation and equipment calibration.