Data Quality Assurance Specialist
13 hours ago
About the Role:
This is an exciting opportunity to join our Global Systems Audit team within the Quality Assurance department at C Psystems. As a Quality Specialist - Computer Systems Validation, you will play a crucial role in ensuring the quality and integrity of our computer systems.
Key Responsibilities:
- Develop and implement validation strategies for computer systems, ensuring compliance with FDA and EU regulations.
- Collaborate with cross-functional teams to identify and implement improvements in our systems and processes.
- Provide technical guidance and support to peers and management on computer systems validation and related technical issues.
- Contribute to the development of technical or strategic direction and operational decision making in your specialization.
- Travel occasionally to support global initiatives and projects.
Requirements:
- Degree level or equivalent in a science or technical area.
- 4+ years of experience in validation, QA validation, validation testing, or related technical field within a pharmaceutical, life sciences, or biotechnology GXP environment.
- Thorough knowledge of FDA and EU computer systems validation, including IT system development life cycle and software quality assurance in a regulated environment and associated regulations.
- Strong problem-solving, organizational, and communication skills.
What We Offer:
C Psystems is committed to accessibility in its workplaces, including during the job application process. We strive to create an inclusive environment where everyone can thrive. If you require accommodation during the application process, please reach out to our HR Services team.
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