QA Batch release specialist (Orals) - new job in Worthing, UK

QA Batch release specialist (Orals)
  • Competitive
  • Temporary
  • Worthing, West Sussex, England, UK Worthing West Sussex UK BN14 8QH
Job Ref: J2166583
Sector: Science
Sub-sector: Pharmaceuticals
Date Added: 21 September 2022
QA Batch release specialist (Orals) - Worthing

Job Title: QA Batch release specialist (Orals) - Global Pharmaceutical Company

Location: Worthing, UK

Contract: 12-month contract

SRG are working with a global pharmaceutical company to help them find a QA batch release specialist to join their busy team.

As the QA specialist, you will be responsible for reviewing and releasing fully compliant material while helping to maintain quality and safety standards on site. You will also be performing the quality assurance activities and quality oversight of the GMP (Good Manufacturing Practice) functions performed at the site. Throughout your day-to-day work you will promote quality and compliance, including monitoring of improvement activities where applicable.

The role includes a strong focus on raising collective performance and continuous quality improvement. As part of the quality assurance team, you will actively promote team working and effective communication across the site.


  • Review and verdict documents from production areas for bulk and intermediate product release while maintaining an efficient service in line with customer demands for the release of manufactured batches.
  • Give advice and assistance across site on a range of GMP topics.
  • Deviations, vendor complaints and associated CAPAs.
  • To participate in root cause analysis of deviations as a QA person to ensure GMP impact is considered and recorded. Ensure that they are fully investigated such that appropriate steps/measures are assigned and the risk to product quality and compliance is fully assessed.
  • Represent QA at value stream accountability and compliance meetings.
  • Review and approval of SOPs and other technical documents.
  • Use GPS process tools such as GEMBA/Process Confirmation/5S techniques to review and identify weaknesses and recommend improvements within Quality and Orals Manufacturing processes.


  • You will be an experienced Quality Assurance professional with relevant experience
  • Working knowledge of cGMP, across aligned manufacturing and/or packaging areas.
  • Ideally a minimum of 2 years GMP experienced in a quality assurance setting.
  • Knowledge of deviation management and FDA/MHRA regulatory requirements.
  • Understanding of laboratory testing including out of specification investigations.
  • The ability to work in and lead cross functional teams
  • Good organisation and attention to detail, great interpersonal and teamwork skills.
  • Relevant degree in Biology/ chemistry related degree would be an advantage.

To apply click the link or send your CV to

21/10/2022 13:25:26
GBP 0.00 0.00 Annum
Contact Consultant:
Thomas Ramsey

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