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Specialist Quality Control
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We are seeking a Specialist in Quality Control to join a highly regulated pharmaceutical environment. This role is ideal for professionals with a strong background in engineering or science and hands-on experience in equipment validation. You will support validation activities, maintain compliance with GMP, and collaborate with cross-functional teams to ensure quality standards.

Requisitos:
 Requirements:
 Doctorate in Engineering OR Master’s degree + 2 years of directly related experience OR Bachelor’s degree in Engineering (Chemical, Environmental, Mechanical, Electrical) or Science (Chemistry/Biology) + 4 years of directly related experience OR Associate degree + 8 years of directly related experience OR High school diploma / GED + 10 years of directly related experience Experience in equipment validation (IQ/OQ/PQ). Knowledge of GMP compliance and quality control standards. Ability to document and resolve deviations or non-conformance issues. Strong analytical, problem-solving, and communication skills. Lean or Six Sigma experience for process improvement. Familiarity with quality management systems and GMP documentation.

Requiere Mucha Experiencia Requires Expert

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Empleos en Puerto RicoJobs in Puerto Rico
PRPDG, Corp.

Empleos en Puerto RicoJobs in Puerto Rico Profesionales
Area Este PR 00600 Area Este
# Clasificado 2214784 Classified # 2214784
PRPDG, Corp.
DescripciónDescription We are seeking a Specialist in Quality Control to join a highly regulated pharmaceutical environment. This role is ideal for professionals with a strong background in engineering or science and hands-on experience in equipment validation. You will support validation activities, maintain compliance with GMP, and collaborate with cross-functional teams to ensure quality standards. Requisitos Requirements Doctorate in Engineering OR Master’s degree + 2 years of directly related experience OR Bachelor’s degree in Engineering (Chemical, Environmental, Mechanical, Electrical) or Science (Chemistry/Biology) + 4 years of directly related experience OR Associate degree + 8 years of directly related experience OR High school diploma / GED + 10 years of directly related experience Experience in equipment validation (IQ/OQ/PQ). Knowledge of GMP compliance and quality control standards. Ability to document and resolve deviations or non-conformance issues. Strong analytical, problem-solving, and communication skills. Lean or Six Sigma experience for process improvement. Familiarity with quality management systems and GMP documentation.
Requiere Mucha Experiencia Requires Expert
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PRPDG, Corp.

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