Quality Compliance Officer

4 weeks ago


Craigavon, United Kingdom Almac Group Full time

**Quality Compliance Officer - Analytical Services**

**Location**: Craigavon, Northern Ireland, UK

**Hours**: 37.5 Hours Per Week. Flexible working pattern.

**Business Unit**: Almac Sciences

**Open To**:Internal & External applicants

**Ref No.**: HRJOB9689

**The Team**

The Quality Compliance team at Craigavon are part of a global quality team, working to ensure patient safety, regulatory compliance, and product quality in an efficient and effective manner.

The team consists of Quality Compliance and Quality Validation teams. Team members are involved in all aspects of GMP operations across the site, performing quality inspections to verify GMP activities and act as a supportive/advisory role, both in the manufacturing and analytical laboratories.

As a contract organization, Quality is at the heart of our relationship with customers, therefore involvement in customer communications, visits and site audits may also form part of the role.

**The Role**

Quality Compliance Officers participate in Quality Compliance activities and GMP improvement initiatives throughout Almac Sciences.

Analytical Services provides support to analytical projects and operations, including review of quality related documents. The post holder will also be responsible for performing reviews of Quality issues (unplanned deviations and OOS) and assist in the management the Quality Management System, supporting operations to ensure it is effective, efficient and compliant.

As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group.
- Degree level (or equivalent) qualification in a Life Science related discipline. Relevant experience may be considered in lieu of academic qualification.
- Experience working in a quality or laboratory environment operating to GMP principles or recognised quality system (e.g. ISO)
- Experience working in a Quality Assurance role, supporting the analysis of APIs or Drug products
- Experience of preparation and or reviewing analytical documents such as analytical method validations reports
- Experience performing investigation into quality issues such as Unplanned Deviations and OOS’s
- Experience of review of analytical data for example Stability data
- Experience of perform internal audits to identify GMP compliance gaps

**Reward**

**Closing Date**: Sunday 2nd June 2024 at 17:00



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