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Job Summary
About SRG
SRG is a leading recruitment agency specializing in the pharmaceutical and life sciences industry. We are delighted to be supporting a clinical trial manufacturer with their search for a quality assurance specialist.
Key Responsibilities
- Collaborate with Stakeholders
- Work closely with cross-functional teams to ensure the timely execution of quality assurance activities.
- Manage Deviations and Investigations
- Oversee the investigation and resolution of deviations, ensuring compliance with regulatory requirements.
- Document Control
- Review and approve standard operating procedures, batch manufacturing records, and other controlled documentation.
- Compliance and Audits
- Evaluate site compliance and implement improvements through internal audits.
Requirements
- Experience
- Minimum 2 years of experience in quality assurance within a pharmaceutical facility.
- Skills
- Excellent communication and interpersonal skills.
- Strong attention to detail and organizational skills.
- Ability to manage multiple priorities and deadlines.
What We Offer
As a quality assurance specialist at SRG, you will have the opportunity to work with a dynamic and driven team, contributing to the success of a clinical trial manufacturer. This role offers a chance to develop your skills and expertise in quality assurance, while working in a fast-paced and challenging environment.
