Sr. Principal Engineer

Location: Raleigh Consulting

Job Description

Displays standard engineering principles to resolve difficult problems, from conception to final design with team input. Plans, schedules and leads project assignments in the evaluation, selection and adaptation of various engineering techniques, procedures and criteria with minimal guidance. This project will be focused on the implementation of new technology for visual inspection on, IV/ medication delivery bag fabrication machines. This project will be upgrading the plant's 32 plant machines requiring drafting, validation testing, protocol writing, execution, troubleshooting, and continuous improvement

Primary Responsibilities
1) With minimal guidance, schedules and leads a team through the planning and execution of a smaller project or defined piece of a larger project. This includes constructing detailed, accurate project schedules, interfacing with development groups and technical support groups.
2) Demonstrates new approaches to complex problems through adaptations and modifications of standard technical principles.
3) Ability to prioritize multiple tasks.
4) Supervises/coordinates an engineer and/or technician on assigned work.
1) Display a solid understanding of theories/practices utilized by other disciplines outside primary area of expertise.
2) Ability to communicate with all levels of management on courses of action using both written and verbal methods.
3) Effectively work on cross-functional teams and facilitate with guidance.
4) Must be able to provide solutions that reflect understanding business objectives and cost implications.
5) Technical skill (Software or other):
• Must have at least 5-8+ years of recent Rockwell PLC experience
• Ability to read and write electrical schematics
• Proven hands on mechanical skill set
• Solid works drafting skills is a plus
Education / Experience
• B.S. Engineer (Discipline: Mechanical or Electrical, possibly Biomedical with the right experience)
• 8-10 years related experience in upgrading manufacturing machines within a regulated environment.
• Track record for successfully driving deliverables on time.
• Previous experience as a project lead, strongly preferred.
• Recent and relevant experience with Allen Bradley Control Systems and Automation
Previous experience with Validation, Allen Bradley Control Systems, Automation, 8-10 years related experience in upgrading machines within a regulated environment,  prefer medical device / pharma background

Physical Requirements (Manufacturing site)
• Requires continuous grasping, pushing/pulling up to 15 pounds and reaching with hands and arms.
• Lifting and carrying on average up to 15 pounds frequently throughout the shift.
• Must have the ability to complete quick and precise repetitive processes using both arms and both hands
• Must be able to squat, climb, reach above shoulder level, reach at or below shoulder level, kneel, twist and bend at the neck, twist and bend at the waist and balance
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!

Apply Now