Quality Control

4 days ago


Craigavon, United Kingdom Almac Group Full time

**Quality Control & Analytical Group Leaders - Pharma Services**

**Location**:Craigavon

**Hours**:37.5 Hours Flexi

**Salary**:Competitive

**Business Unit**: Pharma Services

**Open To**: Internal & External Applicants

**The Roles**:
Operating from state-of-the-art facilities in Craigavon, Almac Pharma Services is an FDA and MHRA approved company which partners with global pharmaceutical and biotechnology companies to develop and manufacture life-changing pharmaceutical products. We have over 50 years’ experience in providing a comprehensive range of tailored solutions.

We are currently on the lookout for Group Leaders (Job Descriptions Attached);
- **Quality Control Group Leader**:

- **Analytical Group Leader**

The role of each post holder is to provide technical and managerial leadership to several analytical teams. They will manage the progress of Analytical work and ensure that project schedules are met and that the work is carried out efficiently, compliantly, and accurately, providing regular updates to their Line Manager. They will actively support the Department Manager in delivering the Company’s operational and business objectives.

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.

For a full list of job specific responsibilities, please see attached Job Descriptions.

**Essential Criteria**
- Have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time, permanent employment in the UK
- Extensive experience of managing and leading analytical teams within a cGMP/GLP laboratory
- A proven ability for solving and coaching others to solve analytical challenges
- Experience of leading analytical drug product development/commercial analytical activities for many solid oral dose development projects.
- Significant experience in the interpretation of data from a wide range of analytical techniques
- Extensive experience of conducting and leading HPLC method development/method transfer and validation activities in support of drug product development/commercial release
- Experience of Stability study design and testing in support of drug product development/commercial release

**Desirable Criteria**
- (The following criteria may be applied if a large pool of applicants exist)_
- M.Sc./PhD (or equivalent) in a Analytical Chemistry or Chemistry
- Experience of statistical data analysis techniques
- Experience of preparing or supporting the preparation of CMC regulatory submission documentation.
- Experience of leading analytical development activities preferably within a contract research environment.

**Closing Date**

LI-AMC



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