Pharma Maintenance Planner: Specialist Engineering

Scorpion Therapeutics; Pennsylvania; On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Medical/dental/vision

401(k) retirement plan

paid holidays

vacation

compassionate and sick days

Job summary

Scorpion Therapeutics seeks a maintenance planning professional to join our operations team. You will assign codes to work orders, inspect sites, and develop maintenance plans to optimize scheduling and execution.

You will maintain plant history files, use data to anticipate delays, coordinate with stakeholders, and support GMP, safety, and regulatory requirements across vaccine manufacturing areas. This role requires a BS in science/engineering or equivalent experience, 3+ years in

Qualifications

• Bachelor’s degree in Science/Engineering or a technical field, or equivalent maintenance-industry experience.
• 3+ years manufacturing or technical support experience.
• Knowledge of large industrial equipment and components; strong computer skills (CMMS, Excel).

Responsibilities

• Assign codes to work orders and perform field inspections.
• Develop maintenance work plans for scheduling and execution.
• Create and maintain plant history/technical files and use data to prevent delays.
• Perform purchasing duties and stage materials.
• Support safety, GMP, and environmental regulations.
• Coordinate with stakeholders to execute planned preventive, predictive, and corrective work orders.
• Provide planning support for vaccine manufacturing areas.

Skills

CMMS

data management

detail-oriented

equipment maintenance

hazard recognition

teamwork

preventive maintenance

system upgrades

manufacturing support

technical auditing

Education

Bachelor's in Science/Engineering/technical field

Job description

Scorpion Therapeutics seeks a maintenance planning professional to join our operations team. You will assign codes to work orders, inspect sites, and develop maintenance plans to optimize scheduling and execution.

You will maintain plant history files, use data to anticipate delays, coordinate with stakeholders, and support GMP, safety, and regulatory requirements across vaccine manufacturing areas. This role requires a BS in science/engineering or equivalent experience, 3+ years in