Sr. Maintenance Specialist

Scorpion Therapeutics; Morrisville (NC); On-site; USD 90,000 - 130,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Maintenance Specialist to lead maintenance planning, CMMS administration, and asset reliability for manufacturing, facility, utilities, and laboratory equipment in a biopharma GMP environment.

Responsibilities include optimizing preventive and corrective maintenance programs, ensuring GMP compliance, and supporting site startup and continuous improvement efforts through cross-functional collaboration.

Qualifications

• Bachelor's degree in engineering or related field with 12+ years of regulated manufacturing experience, or equivalent technical experience with fewer years.
• Strong CMMS knowledge, especially Blue Mountain RAM.
• Proficiency in GMP, data integrity and maintenance best practices.

Responsibilities

• Perform maintenance planning for manufacturing, facility, utilities, and laboratory equipment in a biopharma GMP environment.
• Administer CMMS systems and ensure data accuracy and traceability.
• Develop and optimize preventive and corrective maintenance schedules.
• Analyze equipment data to drive reliability improvements and reduce downtime.
• Collaborate with Manufacturing, Engineering and Quality to ensure site reliability.

Skills

CMMS

Data integrity

Education

Bachelors in engineering or related field

Tools

Blue Mountain RAM

Job description

Role: Senior Maintenance Specialist responsible for maintenance planning, CMMS administration, and asset reliability for manufacturing, facility, utilities, and laboratory equipment in a biopharma GMP environment. Objectives include optimizing preventive and corrective maintenance programs, ensuring GMP compliance, and supporting site startup and continuous improvement efforts. Responsibilities involve managing Blue Mountain RAM system, developing maintenance schedules, analyzing equipment data for reliability improvements, and collaborating cross-functionally with Manufacturing, Engineering, and Quality.

Requirements: Bachelor's degree in engineering or related field with 12+ years of regulated manufacturing experience, or equivalent technical experience with fewer years; strong CMMS knowledge, especially Blue Mountain RAM; proficiency in GMP, data integrity, and maintenance best practices.

Preferred qualifications include experience supporting GMP startup, commissioning, and qualification activities, and expertise in risk-based maintenance strategies. High-value details: emphasis on regulated manufacturing, GMP compliance, maintenance of manufacturing and laboratory assets, and integration within biopharma production systems. Work setup details are not specified, but the role involves collaboration across operational teams and supports site reliability initiatives.