[MNC] Equipment Qualification Specialist / Engineer (Biopharmaceutical) -West #HAC

Recruit Express Pte Ltd

Singapore

On-site

SGD 28,000 - 39,000

Full time

6 days ago
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Job summary

Recruit Express Pte Ltd in Singapore seeks a focused entry-level professional to support qualification activities for equipment in a GMP-regulated biopharmaceutical environment. You will assist in IQ/OQ/PQ processes, verification, and documentation while coordinating with Engineering, Manufacturing and QA teams.

No prior experience is required as training will be provided; a Diploma/Degree in Biomedical, Chemical Engineering or Biotechnology is preferred, and a 1-year commitment is expected to

Qualifications

  • Min Diploma or Degree in Biomedical / Chemical Engineering / Biotechnology or relevant courses
  • No Experience required, training will be provided
  • Able to commit for 1 year contract

Responsibilities

  • Support the execution of equipment qualification and decommissioning activities within a GMP-regulated biopharmaceutical manufacturing environment.
  • Assist in the preparation, review and execution of qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ), where applicable.
  • Perform equipment verification, testing and documentation to ensure compliance with approved procedures and regulatory requirements.
  • Support equipment decommissioning activities, including documentation, equipment status verification and closure of relevant records.
  • Maintain and update equipment qualification documentation, reports, checklists and validation records.
  • Coordinate with cross-functional teams, including Engineering, Manufacturing, Quality Assurance (QA) and Validation, to ensure timely completion of qualification activities.
  • Assist in identifying, documenting and following up on deviations or discrepancies identified during qualification activities.
  • Ensure all activities are performed in accordance with Good Manufacturing Practices (GMP), site procedures and safety requirements.
  • Provide general technical and administrative support for equipment qualification projects

Skills

GMP compliance
Documentation
Cross-functional coordination

Education

Diploma/degree in Biomedical/ Chemical Engineering/ Biotechnology

Tools

IQ
OQ
PQ

Job description

  • Support the execution of equipment qualification and decommissioning activities within a GMP-regulated biopharmaceutical manufacturing environment.
  • Assist in the preparation, review and execution of qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ), where applicable.
  • Perform equipment verification, testing and documentation to ensure compliance with approved procedures and regulatory requirements.
  • Support equipment decommissioning activities, including documentation, equipment status verification and closure of relevant records.
  • Maintain and update equipment qualification documentation, reports, checklists and validation records.
  • Coordinate with cross-functional teams, including Engineering, Manufacturing, Quality Assurance (QA) and Validation, to ensure timely completion of qualification activities.
  • Assist in identifying, documenting and following up on deviations or discrepancies identified during qualification activities.
  • Ensure all activities are performed in accordance with Good Manufacturing Practices (GMP), site procedures and safety requirements.
  • Provide general technical and administrative support for equipment qualification projects
Requirements:
  • Min Diploma or Degree in Biomedical / Chemical Engineering / Biotechnology or relevant courses
  • No Experience required, training will be provided
  • Able to commit for 1 year contract
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