Senior CQV Engineer

Senior CQV Engineer - Competitive Salary, Bonus, Benefits, Work/Life BalanceThis Jobot Job is hosted by: Tony BarhoumAre you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume.Salary: $80,000 - $125,000 per year

A bit about us:We are an Award-Winning Consulting, Architecture, Engineering, Construction Management, and CQV firm helping Life Sciences Companies usher in the next generation of life-saving therapies, treatments, and technologies. Whether it's providing AE support for existing sites; commissioning, validation, and qualification for specific processes or equipment; or turnkey design-build solutions, our team blends sound science and technical expertise with quality and safety to deliver unparalleled results. Headquartered in Pennsylvania, since 1996, we've expanded with multiple office on the East and West Coast. Our award-winning team is looking for top talent who want to make a difference in the world. Ranked within the Top 5 Pharmaceutical Design Firms by ENR magazine, we're advancing worldwide health through the design and construction of facilities where life-saving drugs are manufactured. We believe that putting our employees first is not only the right thing to do, but it also gives us the competitive edge to ensure our clients have an excellent experience! Over the years our reputation for providing our people with the very best has caught the eye of some reputable clients who have chosen to use us as their primary firm! Some of these clients include Public & Private institutions, Google, Meta, Amazon, and many more!If you are an experienced Commissioning, Qualification, Validation (CQV) Engineer with Pharmaceutical or Biotech experience, then please apply!

Why join us?Do you want to work with some of the nation's best Clients AND enjoy time at home w/ family? We do too!

• Meaningful Work!
• Best in Class Firm!
• Competitive Compensation Package!
• Complete Benefits Package!
• Flexible Work Schedules!
• Accelerated Career Growth!
• Fun Company Activities!
• Many More!

Job DetailsIs your background a fit? Apply if you meet this criterion:

• BS/MS or Associates Degree in Engineering or related field
• 7-10+ years of experience as a CQV Specialist
• Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.
• Experience in writing and execution of PFC, FC, IQ, OQ, and PQ forms/protocols for GMP Utilities, Equipment, Systems, and Software a plus.
• General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA helpful.
• Primary duties include C/Q/V of equipment & systems, including CSV & automation, supporting pharmaceutical, biotech, and medical device industries.
• Read, understand, and utilize the Firms Best Practices and SOPs for delivery of compliance services;
• Perform work to meet budget requirements and quality standards.
• Provide consistent, complete, and timely feedback & reports to project leaders, project managers, or management, of project status and issues, as requested.

We can offer you the opportunity to work with State-of-the-Art Clients making a meaningful impact on today's society and the next generation! Help us revolutionize the way firms treat their employees! Join us and enjoy accelerated career growth with exciting life balance at a premium best in class firm!Interested in hearing more? Easy Apply now by clicking the "Apply Now" button.