Senior Validation Officer

3 days ago

Craigavon, United Kingdom Almac Group Full time

**Senior Validation Officer**

**Location**:Craigavon

**Hours**:37.5 Hours Per Week. Mon Friday with core hours 10:00-16:00

**Salary**:Competitive

**Business Unit**: Almac Sciences

**Open To**: Internal & External Applicants

**Ref No.**:HRJOB9349/1

**Please note this is a re-advertisement, if you have applied for this position recently there is no need to re-apply**

**The Business Unit**

Almac Sciences provides a wide range of custom synthesis services, technology, and products to the pharmaceutical industry, supporting our clients from drug discovery to commercialisation of new chemical entities. We can offer a complete set of solutions aimed at accelerating entry into early-stage clinical development.

**The Role**

The primary purpose of this role is to assist in the maintenance of activities within the validation lifecycle of all GMP systems requiring validation.

Furthermore, the role requires practical execution of qualifications which may include equipment, utilities and facilities used in manufacture, storage, analytical testing or controlling and/or monitoring of cGMP systems.

The Senior Validation Officer will ensure the validation status of equipment, facilities and associated software is maintained in accordance with cGMP and other regulatory standards at all times.

They will be a positive role model, demonstrating excellence in technical and practical knowledge, customer care, planning, HSE, QA and results delivery.

This role assumes an excellent understanding, and demonstrated knowledge, of validation, operation of equipment as well as regulatory guidelines.

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.

**Essential Criteria**:

- GCSE (or equivalent) Grades A-C, in Mathematics and English Language
- Degree (or equivalent) in Analytical Chemistry, Chemistry, Biochemistry, Engineering or a related field
- Previous experience of validation/qualification within a GMP environment.
- Previous plant engineering or facility qualification within industry (i.e. pharmaceuticals/fine chemistry/chemical engineering) in a GMP environment.

**Desirable Criteria**:

- Previous validation/qualification experience of production equipment or utilities.

**Reward**

**Closing Date

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