MEP- Responsible System Engineer

Location: Boston, MA
Department: Azzur Worcester, LLC

Job Description

About Azzur:

Our employees are fueled by an entrepreneurial spirit and the desire to make a difference in the lives of our customers, coworkers and our partners. If you’re ready to put in the work, take personal responsibility and test the limits of what’s possible, we’re ready to provide the reward.

Do What You Love

At Azzur, we look for talented individuals who take pride in the work they do. We foster employee growth by encouraging our employees to focus on doing what they love and what they do best.­­

Azzur is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers.

Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever-changing healthcare field while simultaneously and organically exuding Azzur’s core values:

Put Others First, Courage to Take Action, Take Personal Responsibility and Have Fun!


Essential Duties and Responsibilities:

  • Technical responsibility for all Base Building utility systems and GMP process Utilities
  • Support construction activities (RFI’s, submittal approvals etc)
  • Coordinate all Start-up activities and schedules
  • Support all commissioning activities
  • Develop all maintenance SOP’s and ensure data is properly entered in CMMS
  • Define spare parts inventory and work with procurement team to purchase
  • Review and approve all vendor ETOP packages

Skills & Qualifications

  • BS in Engineering, Science or equivalent technical degree.
  • 5+ years’ experience in a regulated, manufacturing environment within the biotechnology or pharmaceutical industry.
  • Excellent written and verbal communication skills; excellent technical writing skills.
  • Strong interpersonal skills and the ability to work in a team environment.
  • Ability to work effectively in a fast paced multitasking environment.
  • Strong working knowledge of FDA and cGMP regulations and documentation practices.
  • Proficient in Microsoft Word, Excel, PowerPoint.
  • Is able and open to working for multiple clients throughout the New England region.

 



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