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Synexa Life Sciences

Senior Quality Assurance Auditor
MacclesfieldPermanentOn-SiteFull-TimeSenior

Posted 5 days ago

Description

Role Overview
The Senior QA Auditor is responsible for ensuring that all organisational processes and services comply with established quality standards and regulatory requirements. The role focuses on conducting audits, identifying gaps, and driving continuous improvement across quality systems.

Key Responsibilities
  • Follow and where applicable implement appropriate laws, regulatory guidelines, SOPs, Study Plans.
  • Support QA Manager in implementing the quality assurance program and assist in continuous improvement of the site's quality systems.
  • Participating in the maintenance of the quality system.
  • Forecast, monitor and control the work volume within Quality Assurance Unit.
  • Plan and organise all activities within the Quality Assurance Unit.
  • Schedule and perform study, facility and process audits in compliance with SOPs.
  • Communicate the audit outcome to relevant personnel and site management and ensure that audit responses are appropriate.
  • To maintain the CAPA system and follow up CAPA actions.
  • Prepare and sign QA statements for inclusion in reports in accordance with SOPs.
  • Submit audit reports for archiving in accordance with the applicable SOP.
  • To approve GMP documentation where applicable.
  • To participate in computerized system validation team where applicable.
  • Review Standard Operating Procedures for consistency and compliance and maintaining QA SOPs.
  • Manage and conduct assessment of key company suppliers as requested by management to ensure compliance with regulatory guidelines.
  • Provide guidance, training and consultation in quality-related issues.
  • Support QA Manager in management and hosting of sponsor and monitoring authority inspections
  • Observe appropriate regulatory guidelines, SOPs, policies and study documentation

Qualifications & Experience
Required:
  • Minimum 2 years’ auditing experience in GLP, GCP, GMP, or ISO environments.
  • Degree in a relevant natural science.
  • Strong understanding of national laws and relevant regulations and guidelines and SOPs and site related functions.
  • Proficient in written and spoken English.
  • Strong attention to detail, communication, problem-solving, and organisational skills.
  • Able to work independently and collaborate effectively in a team.
  • Proactive and decisive with a scientific background (desirable).
  • Willing to travel as needed.

PLEASE ENSURE THAT YOUR CV/RESUME IS SUBMITTED IN ENGLISH.
Synexa Life Sciences cover
Synexa Life Sciences logo

Synexa Life Sciences

Leading biomarker and bioanalytical CRO advancing therapeutic pipelines through precision science

MacclesfieldContract Research51 - 250
Synexa Life Sciences logo

Synexa Life Sciences

Contract Research

Shape drug development alongside 120+ specialist scientists. Work on pioneering biomarker assays across oncology, autoimmune and vaccine development, tackling complex scientific challenges that directly accelerate therapeutics to patients.