Quality Assurance Analyst
2 weeks ago
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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