Quality Assurance Analyst

2 weeks ago


Halstead Kent, United Kingdom SRG Full time
Quality Assurance Specialist

Company: SRG

Type: Permanent Position

Salary: Competitive Package

SRG is pleased to assist a clinical trial manufacturer in their search for a Quality Assurance Specialist. As the company continues to grow, they are seeking two professionals with expertise in sterile environments.

Key Responsibilities:
  • Engage with stakeholders to ensure the effective progression and timely execution of quality assurance initiatives.
  • Manage deviations, conduct investigations, and implement corrective actions.
  • Oversee the documentation system, including the review and approval of standard operating procedures, batch manufacturing records, and other controlled documents.
  • Ensure the efficient management of the document lifecycle, maintaining compliance with regulatory standards and industry best practices.
  • Assess site compliance and drive improvements through internal audits.

Requirements:
  • Proven experience in quality assurance within a pharmaceutical setting.
  • Familiarity with process validation and cleaning validation and verification.
  • Experience in a sterile site is preferred.
  • Ability to manage validation lifecycles from inception to retirement.
  • Expertise in equipment, facility, and process change management.
  • Strong communication skills, both written and verbal, along with computer proficiency.
  • Capacity to manage individual workload, meet deadlines, and prioritize effectively.
  • Attention to detail and a commitment to high standards in all work outputs.

This position offers a dynamic and motivated professional the opportunity to work within an ambitious organization while enhancing their professional profile with valuable skills that will advance their career.



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