Quality Compliance Officer- Analytical Services

HIRANI; United Kingdom; On-site; GBP 30,000 - 50,000; Full time

Job summary

HIRANI is seeking a Quality Compliance Officer to join their Analytical Services team. The role includes ensuring quality assurance across analytical projects, promoting GMP improvement initiatives, and supporting the Quality Management System.

The successful candidate will need to have a Life Sciences degree and experience in a quality or laboratory environment. Responsibilities include reviewing and approving analytical data and documentation to maintain compliance.

Qualifications

• Life Sciences degree level qualification is required.
• Experience in a quality or laboratory environment adhering to GMP principles.
• Proficient in preparing and reviewing analytical documents such as validation reports.

Responsibilities

• Provide quality assurance support for analytical projects.
• Promote Quality Compliance activities and improvements.
• Review and approve GMP analytical data and documentation.

Skills

Experience in quality assurance

GMP principles

Analytical document review

Investigating unplanned deviations

Analytical data review

Conducting internal audits

Education

Life Sciences degree level qualification

Job description

Quality Compliance Officer - Analytical Services

The Quality Compliance Officer within the Analytical Services team will provide quality assurance support across analytical projects and routine analytical operations, including the review and approval of quality‑related documentation.

The role involves actively promoting Quality Compliance activities and driving GMP improvement initiatives across Almac Sciences. The post holder will support the effective implementation of the Quality Management System, contribute to quality investigations, and ensure robust CAPA actions are implemented.

They will review and approve GMP analytical data and documentation, represent QA on relevant analytical project activities, and take ownership of quality assurance aspects, escalating issues where appropriate to maintain regulatory and GMP compliance at all times.

Key Requirements

• Life Sciences degree level qualification
• Experience working in a quality or laboratory environment operating to GMP principles or a recognised quality system (e.g., ISO)
• Experience preparing and/or reviewing analytical documents such as analytical method validation reports and Certificates of Analysis
• Experience performing investigations into quality issues such as Unplanned Deviations and OOS’s
• Experience reviewing analytical data (e.g., stability data)
• Experience performing internal audits to identify GMP compliance gaps