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Última actualización: hace 5 horas
LL02-032525 Validation Specialist (Drug Substance)

LL02-032525 Validation Specialist (Drug Substance)

Validation & Engineering Group00777, PR, US
Validation & Engineering Group, Inc.V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the ...Mostrar másÚltima actualización: hace más de 30 días
JT098 - ENGINEER

JT098 - ENGINEER

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Quick Apply
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  • Nueva oferta
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T Mobile Authorized Retailer Sales Associate

T Mobile Authorized Retailer Sales Associate

GP Mobile, An Authorized T-Mobile Retailer (Southeast)00777, PR, US
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LL02-032525 Validation Specialist (Drug Substance)

LL02-032525 Validation Specialist (Drug Substance)

Validation & Engineering Group00777, PR, US
Hace más de 30 días
Descripción del trabajo

Job Description

Job Description

Validation & Engineering Group, Inc. (V&EG) 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 :

  • Validation Specialist for Drug Substance Equipment

Qualifications :

  • Bachelor's Degree in Science or Engineering.
  • Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.
  • Experience in drug substance process / manufacturing areas.
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
  • SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT) & Site Acceptance Test (SAT).
  • Strong knowledge in drug substance equipment C&Q (Bioreactors, Mixing, Filtration, Centrifuges, Incubators, Chromatography Systems, Lyophilizers)
  • Technical Writing skills and investigations processes.
  • Available to work extended hours, possibility of weekends and holidays.