CQV Engineer

3 weeks ago


Singapore No Deviation Pte. Ltd. Full time

No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.

We strongly uphold our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive work environment that fosters personal growth and development.

By joining our team, you will have the opportunity to make a meaningful impact in the pharmaceutical industry while advancing your career.

Scope and Responsibilities

  • Perform Commissioning and Qualification/Validation for Project in compliance with GMP regulations, specification requirements.
  • Protocol generation or review for the assigned areas and summary reports for initial and subsequent re qualification programs related to E/F/U systems.
  • Review vendor or construction turnover document
  • Participate/lead system walkdowns to assure compliance with design.
  • Support or direct execution of full Commissioning and Qualifying project lifecycle, including URS, Design Verification, FAT, SAT, DQ, IQ, OQ and PQ etc.
  • Trouble shooting equipment with cross functional teams.
  • Support or lead summary report writing
  • Support the review and revision of design document
  • Support the handover of assigned system
  • Support the management of project schedule.
  • Compliant to quality and safety requirements.

Qualifications:

  • Bachelor of Science, Engineering or related scientific degree
  • Experience in Pharma Industry is preferred
  • Min. 3 years of experience in Commissioning and Qualifying project is required
  • Knowledge of cGMP regulations and industry standards such as ISPE GAMP, and FDA guidance documents
  • Ability to work in a fast-paced environment.
  • Time management skill and attention to detail
  • Strong interpersonal and communication skills

At No deviation, we strive to deliver our best every day. We apply our core values of empathy, integrity, and transparency to every activity, including engagement with our candidates. We are an equal opportunity employer, value diversity, and promote inclusivity at our company. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

EA Licence: 19C9587


  • CQV Engineer

    3 weeks ago


    Singapore Anter Consulting Pte. Ltd Full time

    Job Summary: The Commissioning, Qualification, and Validation (CQV) Engineer will play a crucial role in ensuring the successful commissioning, qualification, and validation of pharmaceutical manufacturing processes and facilities. The ideal candidate will be responsible for planning, executing, and documenting the validation activities in compliance with...


  • Singapore Pharmeng Technology Pte. Ltd. Full time

    Commissioning / Qualification and Verification (CQV) Engineer (Singapore)PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure...

  • CQV Engineer

    3 weeks ago


    Singapore Pharmeng Technology Pte. Ltd. Full time

    PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective...

  • CQV Engineer

    7 days ago


    Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Roles & ResponsibilitiesPharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world...


  • Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Roles & ResponsibilitiesCommissioning / Qualification and Verification (CQV) Engineer (Singapore)PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering,...

  • Validation Engineer

    1 week ago


    Singapore Coalesce Management Consulting Pte. Limited Full time

    Position: Validation Engineer in SingaporeJob DescriptionWe 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...

  • Validation Engineer

    2 weeks ago


    Singapore COALESCE MANAGEMENT CONSULTING PTE. LIMITED Full time

    Roles & ResponsibilitiesPosition: Validation Engineer in SingaporeJob DescriptionWe 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...


  • Singapore Pharmeng Technology Pte. Ltd. Full time

    Responsibilities:Provide direct services to site Technical Services management, contributing to increased throughput of commissioning and qualification activities across the site.Collaborate with Technical Services management while independently performing required validation activities.Support C&Q activities across the site as directed by site Technical...


  • Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Roles & ResponsibilitiesResponsibilities: Provide direct services to site Technical Services management, contributing to increased throughput of commissioning and qualification activities across the site. Collaborate with Technical Services management while independently performing required validation activities. Support C&Q activities across the site as...