Reliability Engineer

job
  • Arcadis
Job Summary
Location
Greenville ,NC 27834
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
23 Jan 2025
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Job Description

About The Job

Arcadis is the world's leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets.


We are more than 36,000 people, in over 70 countries, dedicated to improving quality of life. Everyone has an important role to play. With the power of many curious minds, together we can solve the world’s most complex challenges and deliver more impact together.


Role description:


Arcadis is seeking a Reliability Engineer to support our client on a calibration, instrumentation, and reliability drug substance manufacturing project in Greenville, NC. The Reliability Engineer will set up new project equipment and standalone instruments for calibrations, as well as prioritize and coordinate activities according to validation schedules, according to GMP guidelines. The ideal candidate has strong knowledge of drug substance manufacturing equipment and instruments, GMP regulations, excellent communication skills, and proven experience to problem solve.

Role accountabilities:

  • Participate in project design reviews and communicate discrepancies and corrections required to design review team.
  • Complete Project Readiness activities necessary for validation, PQs, and Media Fill activities in a timely manner as to eliminate or minimize impacts to those activities.
  • Prioritize and coordinate activities according to validation schedule and equipment/instrument installations completion activities. Note that all instruments to be calibrated must be fully installed and fully connected to and set up on their automation systems/instrument loops before any calibrations can be performed.
  • Review P&ID’s and other relevant drawings and develop comprehensive equipment and instrument lists.
  • Set up new project equipment and standalone instruments with Functional Location Numbers and tags.
  • Coordinate instrument classification process to classify all instruments as either Critical, Non-Critical, or Reference.
  • Facilitate Instrumentation/Calibration scheduling meetings and discussions as required to meet project goals.
  • Complete spare parts assessments and set up spare parts for equipment as necessary.
  • Set up equipment maintenance strategies (PM’s) for equipment and instruments. Note that some equipment maintenance strategies may be Run-To-Failure.
  • Collect instrument data necessary to complete FORM-400’s for instrument calibrations.
  • Complete QR’s related to Reliability/Project Readiness as assigned prior to due dates.
  • Track all work in an equipment and instrument tracker to be shared on the project TEAMs site.
  • Track instruments and PMs through SAP entry.
  • Expedite HOT items through the approval and SAP entry process.
  • Complete project decommissioning tasks (if necessary) to take equipment and calibrations out of SAP and the accounting system.
  • Other duties as assigned


Qualifications & Experience:

  • Bachelor’s degree in Industrial, Process, Chemical, or Mechanical Engineering
  • Candidate must possess an aptitude for mechanical and electrical systems. How they operate, how they fail, ways to extend equipment reliability and life.
  • Strong experience working in a GMP-regulated environment and knowledge of GMP guidelines
  • Knowledge of typical biotech/pharmaceutical manufacturing systems and equipment
  • Excellent communication skills, both written and verbal
  • Excellent teamwork and interpersonal skills
  • Excellent analytic, problem-solving and decision-making skills
  • Advanced time management and organizational skills
  • Leadership skills, with a view to managing people
  • Results and customer-oriented
  • Demonstrated ability to learn and quickly apply new concepts and technical information
  • Ability to work onsite in Greenville, NC
  • Ability to provide legal US work authorization documents required. Will consider US domestic travelers and relocation.


Why Arcadis?


We can only achieve our goals when everyone is empowered to be their best. We believe everyone's contribution matters. It’s why we are pioneering a skills-based approach, where you can harness your unique experience and expertise to carve your career path and maximize the impact we can make together.


You’ll do meaningful work, and no matter what role, you’ll be helping to deliver sustainable solutions for a more prosperous planet. Make your mark, on your career, your colleagues, your clients, your life and the world around you.


Together, we can create a lasting legacy.


Join Arcadis. Create a Legacy.


Our Commitment to Equality, Diversity, Inclusion & Belonging


We want you to be able to bring your best self to work every day which is why we take equality and inclusion seriously and hold ourselves to account for our actions. Our ambition is to be an employer of choice and provide a great place to work for all our people. We are an equal opportunity and affirmative action employer. Women, minorities, people with disabilities and veterans are strongly encouraged to apply. We are dedicated to a policy of non-discrimination in employment on any basis including race, creed, color, religion, national origin, sex, age, disability, marital status, sexual orientation, gender identity, citizenship status, disability, veteran status, or any other basis prohibited by law.


Arcadis offers benefits for full time and part time positions. These benefits include medical, dental, and vision, EAP, 401K, STD, LTD, AD&D, life insurance, paid parental leave, reward & recognition program and optional benefits including wellbeing benefits, adoption assistance and tuition reimbursement. We offer nine paid holidays and 15 days PTO that accrue per year. Salaries will vary and are based on several factors, such as experience, education, budget, internal equity, project and location.

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