Automated Validation and Qualification Specialist
3 days ago
Key Responsibilities:
- Develop and implement comprehensive validation plans
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements
- Create and maintain high-quality documentation, including protocols, reports, and deviations
- Provide technical oversight and lead the overall validation and qualification of equipment and processes
Requirements:
- Must have process/equipment validation experience with CSV knowledge
- Strong understanding of automation process validation and CSV methodologies
- Familiarity with GxP guidelines, FDA 21 CFR Part 11, and ISO standards
- Excellent communication and project management skills
What We Offer:
- Competitive salary and benefits package
- Opportunity to work on exciting projects in the medical device industry
- Collaborative and dynamic work environment
- Professional growth and development opportunities
How to Apply:
If you are a motivated and experienced professional looking for a new challenge, please submit your application, including your resume and cover letter.
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