GMP Equipment Compliance Analyst (Calibration & QA)

Eurofins; Liverpool; On-site; GBP 36,000 - 48,000; Full time

Benefits offered by this job

Pension

Private Medical Insurance

Annual discretionary bonus

Birthday Holiday entitlement

Free parking onsite

Job summary

Eurofins is seeking an Equipment Compliance Analyst to maintain GMP-compliant equipment and assist with introducing new systems at a client site. The role involves calibration checks, documentation, and supporting audits and inspections.

The successful candidate will have a scientific degree, knowledge of analytical chemistry, and experience validating analytical equipment in GMP settings. The position offers full-time hours and a competitive benefits package.

Qualifications

• Degree in pharmaceutical sciences, chemical engineering or chemistry is required or significant relevant experience may be considered in lieu of educational qualifications.
• Sound knowledge of analytical chemistry techniques.
• Experience of pharmaceutical product analysis/manufacturing and validation of analytical equipment in a GMP setting.

Responsibilities

• Check instrument calibration and service data for multiple analytical instruments (e.g., HPLC, Dissolution, KF, stability chambers).
• Support introduction of new equipment/technology via documentation processes.
• Write or update reports, SOPs and calibration protocols.
• Support internal audits and regulatory inspections and document data per client policies.
• Ensure compliance and integrity of quality systems to maintain GMP and handle client queries.

Skills

Analytical chemistry

Quality documents

GMP experience

Education

Pharmaceutical sciences

Chemical engineering

Chemistry

Job description

Eurofins is seeking an Equipment Compliance Analyst to maintain GMP-compliant equipment and assist with introducing new systems at a client site. The role involves calibration checks, documentation, and supporting audits and inspections.

The successful candidate will have a scientific degree, knowledge of analytical chemistry, and experience validating analytical equipment in GMP settings. The position offers full-time hours and a competitive benefits package.