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    Validation Engineer - Singapore - COALESCE MANAGEMENT CONSULTING PTE. LIMITED

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    Description
    Roles & Responsibilities

    Position: Validation Engineer in Singapore

    Job Description

    We are currently expanding our team and are looking for a CQV Engineer for our project on site with our client.

    You will be responsible for planning, writing, implementing and reviewing Validation protocols in place within highly regulated environments. Your expertise will lend a hand in tactical problem-solving, effective communication, and creating a progressive growth culture.

    Key Responsibilities:

    • Create, review and approve qualification protocols such as FAT, SAT, IQ, OQ, PQ of existing manufacturing process equipment, package units (e.g. Ultrafiltration Unit, Chromatography Columns, autoclave, FIT testers), commercial off the shelves (COTS) analytical instruments, freezers
    • Experience in writing and executing validation documents and SOPs for IQ, OQ, PQ for automated systems, and cleanrooms
    • Excellent communication skills

    Requirements:

    • Degree in Science or Engineering with 3 years of working experience in GMP environment
    • Understanding of manufacturing engineering experience in a Pharmaceutical/ Biotechnological company

    What's in it for you?

    • Exposure to the most renowned Pharmaceutical companies in the industry
    • Annual leave benefits
    • Full Medical coverage
    • Training and Development allowance

    If you are interested in applying for this position, please send an email to

    Coalesce Management Consulting operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.

    Tell employers what skills you have

    Excellent Communication Skills
    Validation
    Management Consulting
    Manufacturing Engineering
    Risk Assessment
    Test Validation
    Computer Validation
    Ultrafiltration
    Chromatography
    GMP
    Validation testing
    Python
    Writing
    Regulatory Requirements
    Terminology
    Manufacturing
    Commissioning
    Analytical Instruments
    Autoclave
    Data Validation

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