Job

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 k.kazerouni@hamlynwilliams.com