loader image

Lab CQV Engineer

Date Posted: March 28, 2024

Job Description

We are seeking a highly skilled and detail-oriented Lab CQV (Commissioning, Qualification, and Validation) Engineer to join our team in Singapore’s pharmaceutical industry. The Lab CQV Engineer will be responsible for executing commissioning, qualification, and validation activities specific to laboratory equipment and facilities to ensure compliance with regulatory requirements and industry standards.

Key Responsibilities

  • Plan and execute commissioning, qualification, and validation activities for laboratory equipment, instruments, and facilities in accordance with regulatory guidelines and company procedures.
  • Develop and execute validation protocols (IQ/OQ/PQ) for laboratory equipment and systems, ensuring thorough testing and documentation.
  • Collaborate with cross-functional teams, including laboratory personnel, engineering, and quality assurance, to coordinate validation activities and ensure alignment with project timelines.
  • Conduct risk assessments and impact assessments for laboratory validation activities, identifying potential issues and developing mitigation strategies.
  • Review and approve validation documentation, including protocols, reports, and deviations, to ensure completeness and accuracy.
  • Perform troubleshooting and investigation of validation issues and deviations, implementing corrective and preventive actions as necessary.
  • Support regulatory inspections and audits by providing validation documentation and participating in inspections as required.
  • Stay updated on regulatory requirements and industry best practices related to laboratory validation and quality assurance.

Required Qualifications and Skills

  • Bachelor’s degree in Science, Engineering, or related field.
  • Minimum of 2-3 years of experience in commissioning, qualification, and validation activities within a laboratory setting, preferably in the pharmaceutical industry.
  • Strong knowledge of regulatory requirements (GMP, GAMP, FDA) and industry guidelines related to laboratory validation.
  • Experience in developing and executing validation protocols (IQ/OQ/PQ) for laboratory equipment and instruments.
  • Familiarity with laboratory equipment and instrumentation commonly used in pharmaceutical laboratories.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with laboratory personnel and cross-functional teams.
  • Detail-oriented with strong analytical and problem-solving abilities.
  • Ability to work independently and manage multiple projects simultaneously.

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

Apply for this position

Allowed Type(s): .pdf, .doc, .docx