Reliability Engineer
2 weeks ago
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 leader in connecting talented professionals with top-tier employers across the nation. Our dedicated team of expert recruiters is committed to guiding candidates through their career journeys.
Job Overview:
The Equipment Reliability Engineer plays a pivotal role in overseeing and directing all engineering functions within a pharmaceutical manufacturing setting.
Key Responsibilities:
- Oversee multiple engineering teams and their operations.
- Develop and execute engineering strategies focused on reliability standards, mechanical systems, and electronic components.
- Ensure compliance with health and safety regulations throughout all engineering processes.
- Establish and manage the Engineering Change System effectively.
- Supervise the current and future layouts of manufacturing facilities.
- Create and maintain preventative maintenance schedules and criteria.
- Revise equipment specifications and technical drawings as necessary.
- Implement cost-effective improvements to equipment and facility operations.
- Utilize Lean Manufacturing principles to enhance efficiency.
- Recommend and implement modifications to existing 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 assess design efficiency.
- Select, mentor, and evaluate engineering personnel.
- Provide guidance in line with organizational policies and suggest necessary adjustments.
- Collaborate with cross-functional teams to resolve engineering challenges.
- Lead and coordinate team projects and initiatives.
- Oversee the Engineering department's operations, including budgeting and methodologies.
- Ensure compliance with FDA and EU regulations.
- Monitor and finalize both routine and special projects.
- Conduct GAP analyses and offer recommendations for improvement.
- Address 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 experience in a managerial and supervisory role within the biotech, pharmaceutical, or medical device manufacturing industry.
- Project Management experience is preferred.
All applicants will be evaluated based on their 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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