Location: Summit, NJ
Department: DNU - Azzur Princeton, LLC
Apply Now
Department: DNU - Azzur Princeton, LLC
Job Description
About Azzur
Azzur is a GxP compliance and consulting organization dedicated to providing high quality,
expertly backed, assistance that drives life science companies to success.
At Azzur Group we work in tandem to provide the innovations of tomorrow, today! We’re proud
to be one of the fastest growing companies in the United States. With a national network of
engineers and consultants, we offer comprehensive quality assurance, regulatory compliance,
and validation services specifically geared for the complexities of life science.
We are seeking highly motivated individuals that have the desire to learn, can adapt to the ever-
changing life sciences field and are flexible to work on various projects throughout the Mid-
Atlantic region all while exuding Azzur’s core values: Put Others First, Courage to Take Action,
Take Personal Responsibility and Have Fun!
Responsibilities
Liaise with global project manager, giving site (CMC team for development transfers)
and site functions
Ensure knowledge transfer from giving site to receiving site including to operators.
Ensure transfer timelines align with overall site project plans
Contribute to inspection (Pre-Approval Inspection PAI) readiness.
Ensure site readiness for campaign start-up.
Preferred Requirements
● Relevant work experience in validation and/or quality in a regulated, manufacturing
environment within the biotechnology, pharmaceutical or medical device industry
● Excellent communication and interpersonal skills and ability to interact with all levels of
management, clients, and vendors
● Bachelor or Master’s degree in Bioengineering, Biomedical Engineering, Mechanical
Engineering, Chemical Engineering, or Science related technical degree preferred
● Proficient Computer Skills (Google Professional Services, Project Software)
● Willing and able to travel as necessary for project requirements to include but not be
limited to project work activities, client meetings, company sponsored meetings,
trainings, industry related forums, or conventions, etc.
Perks of Working at Azzur
Medical, Dental and Vision
Competitive 401K plan
Flexible Paid Vacation Time
Employee Recognition Program
Diversity and Inclusion Initiatives
Training and Mentorship Opportunities
Travel Expense Reimbursement
Learn more about who we are and what makes us great at Azzur
https://youtu.be/9VmKkBLkoFQ
Azzur Group is an equal opportunity employer and promotes a diverse culture in our workplace. We
believe that promoting diversity plays an important role in developing top-quality talent, fostering greater
innovation and creativity, and enhancing our relationships with customers and the communities in which
we operate. All qualified applicants will receive consideration for employment without regard to race,
color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age,
marital status, pregnancy, genetic information, or other legally protected status. #LI-GN1
Azzur is a GxP compliance and consulting organization dedicated to providing high quality,
expertly backed, assistance that drives life science companies to success.
At Azzur Group we work in tandem to provide the innovations of tomorrow, today! We’re proud
to be one of the fastest growing companies in the United States. With a national network of
engineers and consultants, we offer comprehensive quality assurance, regulatory compliance,
and validation services specifically geared for the complexities of life science.
We are seeking highly motivated individuals that have the desire to learn, can adapt to the ever-
changing life sciences field and are flexible to work on various projects throughout the Mid-
Atlantic region all while exuding Azzur’s core values: Put Others First, Courage to Take Action,
Take Personal Responsibility and Have Fun!
Responsibilities
Liaise with global project manager, giving site (CMC team for development transfers)
and site functions
Ensure knowledge transfer from giving site to receiving site including to operators.
Ensure transfer timelines align with overall site project plans
Contribute to inspection (Pre-Approval Inspection PAI) readiness.
Ensure site readiness for campaign start-up.
Preferred Requirements
● Relevant work experience in validation and/or quality in a regulated, manufacturing
environment within the biotechnology, pharmaceutical or medical device industry
● Excellent communication and interpersonal skills and ability to interact with all levels of
management, clients, and vendors
● Bachelor or Master’s degree in Bioengineering, Biomedical Engineering, Mechanical
Engineering, Chemical Engineering, or Science related technical degree preferred
● Proficient Computer Skills (Google Professional Services, Project Software)
● Willing and able to travel as necessary for project requirements to include but not be
limited to project work activities, client meetings, company sponsored meetings,
trainings, industry related forums, or conventions, etc.
Perks of Working at Azzur
Medical, Dental and Vision
Competitive 401K plan
Flexible Paid Vacation Time
Employee Recognition Program
Diversity and Inclusion Initiatives
Training and Mentorship Opportunities
Travel Expense Reimbursement
Learn more about who we are and what makes us great at Azzur
https://youtu.be/9VmKkBLkoFQ
Azzur Group is an equal opportunity employer and promotes a diverse culture in our workplace. We
believe that promoting diversity plays an important role in developing top-quality talent, fostering greater
innovation and creativity, and enhancing our relationships with customers and the communities in which
we operate. All qualified applicants will receive consideration for employment without regard to race,
color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age,
marital status, pregnancy, genetic information, or other legally protected status. #LI-GN1
Apply Now