Reliability Engineer in Pharmaceutical Sector

2 weeks ago


Chicago, Illinois, United States Sterling Engineering Full time

Position: Equipment Reliability Engineer - Pharmaceutical Manufacturing

Location: Chicago, IL

Hire Type: Direct Hire, Onsite

Salary Range: $110,000 - $120,000/year

About Sterling Engineering: Sterling Engineering is a leading staffing company dedicated to creating successful career paths for professionals. Our expert recruiters connect candidates with top employers across the nation.

Role Overview:

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

Key Responsibilities:

  • Oversee multiple engineering teams to ensure operational efficiency.
  • Develop and execute engineering strategies focused on reliability, mechanical systems, and electronic components.
  • Guarantee compliance with health and safety regulations throughout all engineering processes.
  • Establish and manage the Engineering Change System effectively.
  • Design and maintain optimal layouts for the facility.
  • Create and uphold preventative maintenance schedules and criteria.
  • Revise equipment specifications and technical drawings as necessary.
  • Implement cost-effective improvements to equipment and facilities.
  • Utilize Lean Manufacturing principles to enhance operations.
  • Propose and execute modifications to equipment.
  • Participate in Health, Safety, and Environmental initiatives actively.
  • Stay informed about the latest advancements in control technology and safety standards.
  • Manage equipment across various laboratory environments.
  • Conduct feasibility studies to assess design efficiency.
  • Recruit, develop, and evaluate engineering personnel.
  • Provide guidance in line with organizational policies and recommend policy changes.
  • Collaborate with cross-functional teams to resolve engineering challenges.
  • Lead and coordinate team projects effectively.
  • Oversee the Engineering department's operations, including budgeting and workforce management.
  • Ensure compliance with FDA and EU regulations.
  • Monitor and complete routine and special tasks as required.
  • Perform GAP analyses and offer recommendations for improvement.
  • Tackle technical issues while managing multiple priorities.
  • Supervise 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, without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or genetic information.


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