Product Quality Auditor

Almac Group

Craigavon

On-site

GBP 26,000 - 38,000

Full time

2 days ago
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Benefits offered by this job

Paid Time-Off for Vacation and Sick</n
Equal Opportunity Employer

Job summary

Almac Group in Craigavon is seeking a Product Quality Auditor to join the Pharma Services unit. The role focuses on reviewing batch records before QP certification and release, ensuring adherence to customer requirements and KPI targets within OTIF timelines, and logging constraints as needed.

The position is full time and on-site at headquarters. You will work in a busy Product Quality Team, with opportunities for professional development across a rapidly growing organisation.

Qualifications

  • 5 GCSEs (or equivalent) at Grade C or above including English Language and Maths.
  • Previous significant experience working within an established Quality System (e.g. GMP, ISO)
  • Level 5 qualification or above

Responsibilities

  • Review batch records prior to QP certification and release.
  • Support Product Quality objectives in relation to delivery of batches on OTIF timelines.
  • Generate KPI data from electronic transactions.
  • Ensure customer requirements for batch release are met in relation to Promise Date and log constraints as required.

Skills

Quality systems
Production
GCSE Maths
GCSE English

Education

GCSEs including English Language and Maths
Level 5 qualification or above

Job description

Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.

Skills and attributes
  • GCSE Maths & English - Grade C or above
  • quality systems
  • Production
Description

Hours: 37.5 Hours (Full time on-site)

Business Unit: Pharma Services

Open To: Internal & External Applicants

Ref No.: HRJOB12018

The Role

Working as part of the Pharma Services Business Unit, based in our Headquarters in Craigavon, the Product Quality Auditor will work as part of the Product Quality Team responsible for review of batch records prior to QP certification and release.

They will support the Product Quality department objectives in relation to the delivery of batches in line with OTIF timelines, including performing the associated electronic transactions required to generate KPI data.

They will also ensure customer requirements for batch release are met in relation to Promise Date, escape any anticipated issues in meeting these timelines to the Product Quality Team Leader and log constraints as required.

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 Description.

*Please note that if you have applied for this role within the past 6 months your interview score will remain valid and you do not need to reapply*

  • 5 GCSEs (or equivalent) at Grade C or above including English Language and Maths
  • Previous significant experience working within an established Quality System (e.g. GMP, ISO)

(The following criteria may be applied if a large pool of applicants exist)

  • Level 5 qualification or above
  • Previous experience in review/auditing of GMP records
  • Previous experience working within a production environment
  • Previous experience working within a pharmaceutical manufacturing environment

Paid Time-Off for Vacation and Sick Days

Almac Group is an Equal Opportunity Employer

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