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Validation Engineer
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Validation Engineer
Fladger Associates
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Validation Engineer

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1 Vacancy
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Job Location

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others - USA

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 1703239
Gaithersburg, MD
Contract Duration: 12-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Validation Engineer in the Gaithersburg, MD area.
  • Will be responsible for developing and implementing equipment (facilities, formulation/fill, packaging, and Quality Control), cleaning, sterilization, computer/automation, shipping, and method validation strategies by incorporating good engineering practices, risk-based validation principles and the regulatory requirements.
  • Collaborate with internal and external customers by providing oversight and technical guidance throughout the system lifecycle.
  • Will continually ensure systems and facilities comply with regulatory and Quality process requirements.
  • Participates in system design and commissioning project phases.
  • Provides oversight and technical guidance for Facilities, Formulation/Fill, and Packaging Engineers during Installation and Operational Qualification.
  • Generates Validation Project Plan for complex projects and systems
  • Supports Risk Assessments documentation including but not limited to, System Impact Assessments, Components Criticality Assessments, Data Integrity Assessments and Automation Risk Assessments
  • Authors Validation Protocols and Reports for cleaning, sterilization computer /automation, shipping and method processes.
  • Authors Validation Protocols and Reports for Controlled Temperature Units.
  • Supports Periodic Assessments on required frequency intervals
  • Performs Revalidations on required frequency interval
  • Resolves technical issues encountered during study execution
  • Schedules resources to approve and execute validation documents
  • Participating in SOP development as needed
  • Supports equipment start-up, shakedown, and cycle development
  • Interacts with regulatory agencies during inspections to speak to validation program and questions related to process validation life cycle
  • Implements/maintains governing cGMP procedures
  • Ensures training of employees and contractors to assure up-to-date knowledge of practices and procedures
  • Author and review change control documents

Experience:

  • Bachelor's Degree and 1-2 years of related experience.

Employment Type

Full Time

Company Industry

About Company

100 employees
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