Supplier Component Validation Specialist
Humacao, Puerto Rico, United States
Job Description
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
Description:
Qualifications:
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
- Supplier Component Validation Specialist
Description:
- Responsible for component testing, sampling, and acceptance criteria
- Write, edit, and complete writing protocols, supplier quality agreements, and acceptance reports
- Analyze batch/component data and reconcile discrepancies including common component materials and basic failure modes.
- Support procurement, receiving, QA, and engineering teams
Qualifications:
- Bachelor's degree in Biology, Chemistry, Materials Science, Engineering, or related
- 25 years in supplier qualification, incoming component testing supplier assessments
- Knowledge of GxP/GMP and supplier qualification expectations
- Bilingual (English/Spanish)
- Full-time on-site; able to support occasional weekends/extra hours
- Preferable: Prior experience with supplier quality programs in medical device industry
- Preferable: Familiarity with ISO 13485 and supplier quality metrics
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
Apply
Career Focus: Validation
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