Reliability Engineer

2 weeks ago


Chicago, Illinois, United States Sterling Engineering Full time

Position: Equipment Reliability Engineer - Pharmaceutical Manufacturing

About Sterling Engineering: Sterling Engineering is dedicated to fostering successful career trajectories for professionals. With a team of expert recruiters, we connect talented individuals with leading employers across the nation.

Role Overview:

The Equipment Reliability Engineer plays a pivotal role in managing and overseeing engineering functions within a pharmaceutical manufacturing setting.

Key Responsibilities:

  • Supervise various engineering divisions to ensure operational efficiency.
  • Develop and implement engineering strategies focused on reliability standards and mechanical systems.
  • Guarantee compliance with health and safety regulations throughout all processes.
  • Maintain and enhance the Engineering Change System.
  • Oversee the current and future facility layouts.
  • Create and uphold preventative maintenance schedules and criteria.
  • Revise equipment specifications and technical drawings.
  • Propose cost-effective improvements to equipment and facilities.
  • Apply Lean Manufacturing principles to enhance productivity.
  • Recommend and execute modifications to equipment.
  • Participate in Health, Safety, and Environmental initiatives.
  • Stay informed on the latest advancements in control technology and safety measures.
  • Manage equipment across various laboratory environments.
  • Conduct feasibility studies to optimize design efficiency.
  • Select, mentor, and evaluate engineering personnel.
  • Provide guidance within organizational frameworks and suggest policy enhancements.
  • Collaborate with cross-functional teams to address challenges.
  • Lead and coordinate team projects effectively.
  • Oversee Engineering department operations, including budgeting and methodologies.
  • Ensure compliance with regulatory standards.
  • Monitor and complete routine and non-routine tasks.
  • Conduct GAP analyses and offer recommendations.
  • Tackle technical issues while managing multiple priorities.
  • Oversee engineering projects from initial concept through to validation.

Qualifications:

  • Bachelor's or Master's Degree in Engineering is required.
  • 3 to 5 years of managerial and supervisory experience in biotech, pharmaceutical, or medical device manufacturing.
  • Project Management experience is preferred.

All applicants will be considered based on qualifications and competencies, irrespective of race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or genetic information.


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