Quality Validation Specialist
Quality Validation Specialist
Posted on :
06-06-2025
Employer Active
1 Vacancy
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Job Description
Inteldot has over 14 years of experience in the life sciences industry with allocations across Puerto Rico the United States Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Time required- 1000 hrs. @ 6 months
Start date - Mid June 2025
Requirements
- Ensure all validation activities are documented accurately and comply with regulatory requirements and industry standards.
- Review and approve validation protocols and reports to ensure they meet quality standards.
- Identify opportunities for improving validation processes and implement changes to enhance efficiency and effectiveness.
- Work closely with cross-functional teams including Quality Assurance Manufacturing and Engineering to coordinate validation activities.
Qualifications
- Experience in validation within a regulated industry such as pharmaceuticals biotechnology or medical devices.
- Strong understanding of validation principles regulatory requirements and industry standards.
- Excellent analytical problem-solving and communication skills.
- Ability to work independently and as part of a team.
- Flexibility to work weekends and extended hours as needed to meet project deadlines and support team efforts.
- Strong organizational skills and attention to detail.
- Pragmatic approach to validation processes ensuring efficient and effective validation outcomes.
Education
- Bachelors degree in Engineering Life Sciences or a related field.
Required Experience:
Unclear Seniority
Employment Type
Full-Time
Key Skills
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