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Project Engineer

$ 6,000 - $ 9,000 / month

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Job Description

Roles & Responsibilities

Key Responsibilities:

  • Lead and support commissioning, qualification, and validation (CQV) activities for assigned projects.
  • Manage project timelines, ensuring deliverables are met within scope, budget, and regulatory compliance.
  • Develop and execute validation protocols (FAT/SAT, IQ, OQ, PQ) for equipment and systems.
  • Coordinate with cross-functional teams, including manufacturing, quality, and engineering, to ensure seamless project execution.
  • Identify and resolve technical issues during commissioning and qualification phases.
  • Support continuous improvement initiatives to optimize processes and enhance project outcomes.

Qualifications and Experience:

  • Bachelor's degree in Engineering or a related field.
  • 5-7 years of experiencein CQV, validation, and commissioning, preferably within the pharmaceutical or biotech industry.
  • Strong understanding of GMP standards and regulatory compliance.
  • Proven ability to manage multiple projects and priorities effectively.
  • Excellent problem-solving and communication skills.

Job Description

Roles & Responsibilities

Key Responsibilities:

  • Lead and support commissioning, qualification, and validation (CQV) activities for assigned projects.
  • Manage project timelines, ensuring deliverables are met within scope, budget, and regulatory compliance.
  • Develop and execute validation protocols (FAT/SAT, IQ, OQ, PQ) for equipment and systems.
  • Coordinate with cross-functional teams, including manufacturing, quality, and engineering, to ensure seamless project execution.
  • Identify and resolve technical issues during commissioning and qualification phases.
  • Support continuous improvement initiatives to optimize processes and enhance project outcomes.

Qualifications and Experience:

  • Bachelor's degree in Engineering or a related field.
  • 5-7 years of experiencein CQV, validation, and commissioning, preferably within the pharmaceutical or biotech industry.
  • Strong understanding of GMP standards and regulatory compliance.
  • Proven ability to manage multiple projects and priorities effectively.
  • Excellent problem-solving and communication skills.