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Principal Process Scientist
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We are seeking a temporary technical resource to provide specialized support to our Sterile Manufacturing Operations. The role requires expertise in process science and parenteral inspection technologies, supporting ongoing operations, technology transfers, and continuous improvement initiatives. Key Responsibilities Serve as a Subject Matter Expert (SME) for sterile manufacturing processes, including liquid and lyophilized parenteral products Perform troubleshooting and investigations (e.g., deviations and CAPAs) Support process validation activities Contribute to technology transfer efforts Drive process optimization initiatives Ensure compliance with cGMP regulations and site procedures Collaboration Work cross-functionally with manufacturing, engineering, quality, and validation teams Ensure alignment with site priorities and regulatory requirements

Requisitos:
 Requirements:
 Strong technical expertise Problem-solving capabilities Experience in pharmaceutical sterile manufacturing environments Education & Experience • Bachelor’s degree in Science (Engineering, Chemistry, Microbiology, Biotechnology, or related field) • Approximately 8–12+ years of experience in sterile pharmaceutical manufacturing, including parenteral processes • Experience supporting investigations, validations, and technology transfers in a SME capacity



Requiere Mucha Experiencia Requires Expert

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Empleos en Puerto RicoJobs in Puerto Rico
QRC GROUP LLC

Empleos en Puerto RicoJobs in Puerto Rico Ingenieros
Manati PR 00600 Manati
DescripciónDescription We are seeking a temporary technical resource to provide specialized support to our Sterile Manufacturing Operations. The role requires expertise in process science and parenteral inspection technologies, supporting ongoing operations, technology transfers, and continuous improvement initiatives. Key Responsibilities Serve as a Subject Matter Expert (SME) for sterile manufacturing processes, including liquid and lyophilized parenteral products Perform troubleshooting and investigations (e.g., deviations and CAPAs) Support process validation activities Contribute to technology transfer efforts Drive process optimization initiatives Ensure compliance with cGMP regulations and site procedures Collaboration Work cross-functionally with manufacturing, engineering, quality, and validation teams Ensure alignment with site priorities and regulatory requirements Requisitos Requirements Strong technical expertise Problem-solving capabilities Experience in pharmaceutical sterile manufacturing environments Education & Experience • Bachelor’s degree in Science (Engineering, Chemistry, Microbiology, Biotechnology, or related field) • Approximately 8–12+ years of experience in sterile pharmaceutical manufacturing, including parenteral processes • Experience supporting investigations, validations, and technology transfers in a SME capacity

Requiere Mucha Experiencia Requires Expert
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INGENIEROS
Ingenieros (Ingenieros - Otros) Engineering (Engineers - Others)
Sra Maldonado Galeria


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
QRC GROUP LLC

Empleos en Puerto RicoJobs in Puerto Rico Ingenieros
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