Project Manager - CSV

Location: Summit, NJ
Department: Azzur Consulting LLC

Job Description

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

Azzur personnel are expected to live up to our core values at all times and exhibit a high level of integrity and personal responsibility, especially when interacting with our valued clients. The following is a short list of the typical responsibilities and deliverables of any given project. The level of knowledge expected will be commensurate with level of incoming experience.

  • Lead, direct and develop company personnel through all technical aspects of the project lifecycle
  • Develop project plans, define roles and responsibilities and the scope of work for each project with input from key stakeholders
  • Understand and manage deliverables of all project requirements originating from the proposal, specifications, meetings, verbal direction, or other means
  • Write engineering and design specifications (URS/FS/DS) and protocols (IQ/OQ/PQ/CSV)
  • Perform (hands on) field execution of commissioning and/or validation documentation
  • Responsible for working with all team members to ensure timely delivery of project requirements (schedule, budgets, and costs). Ensure project team members work within the project schedule and budgets. Provide updates to client and management indicating status of project as required
  • Perform business development work as necessary to procure additional work at their site as well as additional clients
  • Actively participate in the mentoring, training of junior engineers and development of internal company policies and procedures

Qualifications

  • BS Engineering or related discipline
  • 5-7 years’ project management experience in the pharmaceutical and/or biotechnology industry is required
  • Cell Gene Therapy and CAR-T experience required
  • Has worked in PMO setting
  • Experience with FDA compliance and cGMP
  • Demonstrated experience managing others as well as fostering a team focused approach. The ideal candidate shall excel in the areas of communication, leadership, client loyalty, initiative and business integrity
  • Excellent verbal, oral, and technical writing communication skills
  • Proficient in Microsoft Word, Excel, Power Point and able to quickly learn new computer applications
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