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Reliability Engineer for Pharmaceutical Equipment
2 months 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. With a focus on building successful career paths, our expert recruiters provide guidance throughout the hiring process.
Role Overview:
The Equipment Reliability Engineer plays a pivotal role in overseeing engineering functions within a pharmaceutical manufacturing context.
Key Responsibilities:
- Oversee multiple engineering divisions to ensure operational efficiency.
- Develop and execute strategies for engineering processes, focusing on reliability standards and mechanical and electronic systems.
- Ensure compliance with health and safety regulations throughout all operations.
- Establish and maintain the Engineering Change System for continuous improvement.
- Manage current and future facility layouts to optimize workflow.
- Create and implement preventative maintenance schedules and criteria.
- Update and maintain equipment specifications and technical drawings.
- Propose and implement cost-effective improvements to equipment and facilities.
- Utilize Lean Manufacturing principles to enhance operational efficiency.
- Recommend and execute modifications to equipment as necessary.
- Participate in Health, Safety, and Environmental initiatives to promote workplace safety.
- Stay informed on the latest advancements in control technology and safety protocols.
- Manage equipment across various laboratory settings.
- Conduct feasibility studies to assess design efficiency.
- Select, mentor, and evaluate engineering personnel.
- Provide leadership within organizational guidelines and recommend policy enhancements.
- Collaborate with cross-functional teams to address engineering challenges.
- Lead and coordinate team projects effectively.
- Supervise engineering operations, including budgeting and resource management.
- Ensure compliance with FDA and EU regulations.
- Monitor and complete routine and non-routine tasks efficiently.
- Conduct GAP analyses and provide actionable recommendations.
- Resolve 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 a biotech, pharmaceutical, or medical device manufacturing environment.
- 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.
