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CSV Engineer (Pharma) (SG)

Date Posted: September 27, 2024

Job Description

We are urgently seeking a highly experienced CSV Engineer to join our pharmaceutical team in Singapore. The ideal candidate will have a minimum of 5-7 years’ experience in the pharmaceutical manufacturing environment, with a strong proficiency in computer system validation (CSV) protocols and reports execution and review

Key Responsibilities

  • Prepare, execute, and review CSV protocols and reports for various systems including laboratory instruments, manufacturing equipment, utility systems, IT, and enterprise systems.
  • Manage CSV deliverables, ensuring alignment with the Validation Master Plan and timely completion of validation-related activities.
  • Assess vendor documents for CSV deliverables and conduct risk assessments for computerized systems, focusing on data integrity and security.
  • Participate in cross-functional team (CFT) meetings related to IT systems, providing expertise on CSV matters.
  • Familiarity with electronic validation systems and proficiency in quality management systems (QMS), enterprise resource planning (ERP) systems, and supervisory control and data acquisition (SCADA) systems.

Required Qualifications and Skills

  • Bachelor’s degree in IT or related field.
  • Minimum of 5-7 years’ experience in CSV within the pharmaceutical manufacturing environment.
  • Strong analytical skills and attention to detail.
  • Excellent communication and interpersonal skills.
  • Ability to work effectively in a cross-functional team environment.

If you are keen to grow your career with this job, apply with us and send us your resume now. All shortlisted candidates will be contacted shortly.

Reference no.: 122-4948-2918-NW

Registration no.: 968446516E

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