Quality Engineer
Quality Engineer Empleos Puerto Rico
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Qualifications & Requirements – Quality Engineer We are seeking a driven, detail-oriented Quality Engineer to join our team. The ideal candidate is passionate about quality systems and thrives in a highly regulated environment. If you are eager to drive change, improve processes, and ensure world-class product quality, we want to hear from you!

Requisitos:
Requirements:
Key Requirements: Bachelor’s degree in Chemical, Biomedical, Mechanical, or Industrial Engineering required. 5 to 7+ years’ experience in an FDA-regulated environment. Prior experience working in ISO-classified cleanrooms. Experience with Quality System Regulation (QSR), ISO standards, Design Controls, and Process Validation. ASQ Certified Quality Engineer (CQE) and/or Quality Auditor (CQA) preferred. Medical device industry experience preferred but not required. Knowledge of lyophilization and qualifying facility expansions (HVAC, water filtration systems). Proven ability to develop technical documentation such as Validation Protocols, SOPs, Validation Plans, Technical/Investigation Reports, and Change Controls. Deep understanding of developing, documenting, and implementing quality systems to meet domestic and international standards. Basic understanding of audit processes including planning, executing, and reporting audits. Fully bilingual (English/Spanish) required.



Requiere Mucha Experiencia Requires Expert

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Empleos en Puerto RicoJobs in Puerto Rico
Kelly Science, Engineering, Technology & Telecom

Empleos en Puerto RicoJobs in Puerto Rico Ingenieros
Anasco PR 00600 Anasco
DescripciónDescription Qualifications & Requirements – Quality Engineer We are seeking a driven, detail-oriented Quality Engineer to join our team. The ideal candidate is passionate about quality systems and thrives in a highly regulated environment. If you are eager to drive change, improve processes, and ensure world-class product quality, we want to hear from you! Requisitos Requirements Key Requirements: Bachelor’s degree in Chemical, Biomedical, Mechanical, or Industrial Engineering required. 5 to 7+ years’ experience in an FDA-regulated environment. Prior experience working in ISO-classified cleanrooms. Experience with Quality System Regulation (QSR), ISO standards, Design Controls, and Process Validation. ASQ Certified Quality Engineer (CQE) and/or Quality Auditor (CQA) preferred. Medical device industry experience preferred but not required. Knowledge of lyophilization and qualifying facility expansions (HVAC, water filtration systems). Proven ability to develop technical documentation such as Validation Protocols, SOPs, Validation Plans, Technical/Investigation Reports, and Change Controls. Deep understanding of developing, documenting, and implementing quality systems to meet domestic and international standards. Basic understanding of audit processes including planning, executing, and reporting audits. Fully bilingual (English/Spanish) required.

Requiere Mucha Experiencia Requires Expert
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AVISO de ClasificadosOnline
Los patronos NO le piden dinero ni un depósito para trabajar, si lo piden es un negocio, inversión o Fraude.
NO envíe dinero para trabajar, tampoco ofrezca información personal, por teléfono o email.
 Evite el Fraude
ClasificadosOnline Warning
Employers DON'T ask for money or deposits for work, if they do is a bussiness, invertion or Fraud.
DON'T send money for work, neither offer personal information, by phone or email.
 Avoid the Fraud

Empleos en Puerto RicoJobs in Puerto Rico
Kelly Science, Engineering, Technology & Telecom

Empleos en Puerto RicoJobs in Puerto Rico Ingenieros
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