Process Equipment Engineer II – GMP Pharma

BeOne Medicines

Hopewell (NJ)

On-site

USD 96,000 - 131,000

Full time

13 days ago

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Job summary

BeOne Medicines, based in Hopewell, NJ, is seeking an experienced engineer to support a new small molecule manufacturing facility. The role ensures compliant operation of a 24x7 GMP facility and provides technical direction across equipment, commissioning, and validation with cross-functional collaboration.

The position requires a BS in Engineering or Life Sciences, 4+ years in GMP environments, and strong communication skills.

Qualifications

  • BS or higher in engineering and/or related discipline.
  • 4+ years of experience in GMP facilities/maintenance support or operations.
  • Strong understanding of Quality in GMP environment including Good Documentation Practices, Deviation and CAPA management.
  • Excellent communication and interpersonal skills, with the ability to collaborate across functional teams.
  • Bachelor’s degree in Engineering, Life Sciences, or related field with 4+ years of GMP pharmaceutical experience required, or Masters degree with 2+ years required.

Responsibilities

  • Provide SME input into Equipment and Facility for Small Molecule projects.
  • Provide SME input for commissioning, qualification and validation of responsible systems.
  • Develop and maintain technical, operational procedures, preventative maintenance plans for responsible systems.
  • Work in cross functional team to hit project milestones and KPI’s.
  • Manage the assets of buildings & facility, focusing on downstream equipment such as tablet press and coating machines.
  • Directly support operations with troubleshooting and issue resolution.

Skills

Analytical problem-solving
Communication
Project management

Education

BS in Engineering
Life Sciences degree

Tools

Maximo CMMS
Microsoft Project
AutoCAD
Smartsheet
Power BI
Veeva Vault/eQMS

Job description

BeOne Medicines, based in Hopewell, NJ, is seeking an experienced engineer to support a new small molecule manufacturing facility. The role ensures compliant operation of a 24x7 GMP facility and provides technical direction across equipment, commissioning, and validation with cross-functional collaboration.

The position requires a BS in Engineering or Life Sciences, 4+ years in GMP environments, and strong communication skills.

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