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  • 2 weeks ago

jobs description

Cambridge, Massachusetts (onsite)

12 month...

About The Job

One of the world-leading biotech companies is looking for a Senior CQV Engineer to join them at their site in Cambridge, MA on a contract basis. This contract will give you the opportunity to perform meaningful missions and there are countless opportunities for growth and furthering your career track. A great company with quality products.

Responsibilities

Assist CQV team members with validation activities during the tech transfer of new products in the manufacturing facility

Generate documentation (e.g., SOPs, commissioning and qualification protocols) to support CQV project initiatives

Maintain validation test equipment and systems used during protocol execution

Ensure all test equipment is fully functioning, calibrated and ready for use

Assist with CQV revalidation program for the site

Requirements

A minimum of 5 years in the Biotechnology, Pharmaceutical or related industry

Experience working in GxP pharmaceutical and/or biotechnology regulated environment.

Strong interpersonal and communication skills

Strong technical writing skills

This is an opportunity to work for a company that has a flexible schedule, that allows employees to balance their work/life well-being. The company has brilliant reviews from current and previous employees and it is an excellent organization to have on your resume.

Pankaj

IT Technical Recruiter

Phone: (201) 584-1186

Email: pankaj.sharma@stellentit.com

Gtalk: pankaj.sharma@stellentit.com

LinkedIn: https://www.linkedin.com/in/pankaj-sharma-63510b241
Cambridge MA United States

salary-criteria

Apply - CQV Engineer Cambridge