Key Responsibilities:
- Define and continuously improve site maintenance strategy for all equipment.
- Execute asset lifecycle management to meet global standards.
- Lead the site reliability program using data-driven approaches.
- Mentor and manage engineers supporting 24/7 operations.
- Own and optimize master data for process, utility, Quality Control, and Technical Research and Development equipment.
- Develop, monitor, and enhance Key Performance Indicators (KPIs) for system reliability.
- Drive change management and Corrective and Preventive Actions (CAPA) to ensure equipment reliability.
Essential Requirements:
- Bachelorโs degree in Engineering.
- Minimum 5 years of engineering experience in a Good Manufacturing Practice (GMP)โregulated environment.
- Proven experience with regulatory audits and inspections.
- Demonstrated use of Root Cause Analysis tools (5 Whys, Fishbone, Failure Modes and Effects Analysis).
- Strong background in leading or supporting investigations.
- Excellent communication and leadership skills.
Desirable Requirements:
- Professional experience in Reliability Engineering.
- Experience in the pharmaceutical industry.
Benefits (if applicable):
- Performance-based cash incentive; eligibility to be considered for annual equity awards.
- US-based comprehensive benefits (health, life and disability), 401(k) with company contribution and match, time off (vacation, personal days, holidays, and other leaves).
Application instructions:
- For reasonable accommodations, email [email protected] or call +1(877)395-2339; include the job requisition number.