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CQV/CSV Specialist

  • Location

    Boston, Massachusetts

  • Sector:

    Life Sciences, Technology

  • Job type:


  • Salary:

    Competitive salary

  • Contact:

    Kimia Kazerouni

  • Contact email:

  • Salary high:


  • Salary low:


  • Published:

    16 days ago

  • Expiry date:


Hamlyn Williams are currently working with a global manufacturing consultancy who work with high-end Pharmaceutical and Biotechnology clients - providing intelligent technology systems and solutions to enhance manufacturing products.


Due to an increased amount of project work you will be working on a very well-known Pharmaceutical manufacturing facility in Massachusetts carrying out start-up, commissioning and validation activities within FDA regulated environments.


Key responsibilities:

  • Act as the primary point of contact for providing CQV technical support.
  • Coordinate and execute activities across documentation review, approval on change controls, user requirements, system acceptance testing protocols etc.
  • Participate on cross-functional project teams in development and deployment teams.
  • Commissioning, qualification and validation of process equipment and associated software to support utility and process equipment.
  • Document preparation of commissioning, qualification and verification protocols (CQV) for process equipment CSV.

What they can offer:

  • Enhanced level of career growth from working with highly skilled teams, enabling further exposure to market leading training and access to the newest systems and technologies 
  • Very competetive salary and overall package 
  • Flexible working 

Please not that Visa sponsorships are NOT provided 

If this role is of interest please get in contact with me on +1 646-847- 2703 or