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Sr Validation Scientist
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Sr Validation Scient....
QRC Group, LLC
drjobs Sr Validation Scientist العربية

Sr Validation Scientist

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1 Vacancy
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Jobs by Experience

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5 years

Job Location

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Juncos - Puerto Rico

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 1142280
Sr Validation Scientist with experience in utilities validation, facilities and critical systems qualification, Controlled Temperature Chambers (CTC), Controlled Room Temperature (CRT), Validation, validation lifecycle documents Validation protocol generation and execution, commissioning and qualification process, IQ,/OQ/PQ process.

  • Applies advanced and diverse validation engineering principles to the design and implementation of major system or process modifications and/or capital projects.
  • Develop validation engineering policies and procedures that affect multiple organizational units.
  • Work with manufacturing, process development, utilities, facilities, labs, and/or quality assurance in developing requirements and recommendations for large and/or highly complex process, system/facility modifications.

Requirements

  • Doctorate or Master s degree and 3 years of directly related experience or Bachelor s degree and 5 years of directly related experience orAssociate s degree and 10 years of directly related experience.
  • Bilingual (Spanish/English)
  • Technical writing
  • Advanced validation knowledge (equipment qualification, cleaning, sterilization).
  • Applies extensive technical validation expertise, and has full knowledge of other related disciplines.

Regular first shift but will support of hours activities as required by specific project schedules.

Doctorate or Master s degree and 3 years of directly related experience or Bachelor s degree and 5 years of directly related experience or Associate s degree and 10 years of directly related experience. Bilingual (Spanish/English) Technical writing Advanced validation knowledge (equipment qualification, cleaning, sterilization). Applies extensive technical validation expertise, and has full knowledge of other related disciplines. Regular first shift (8 hrs) but will support off hours activities as required by specific project schedules.

Employment Type

Full Time

Company Industry

Pharma / Biotech / Clinical Research

About Company

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