Engineering Specialist

Engineering Specialist – Novartis – Advanced Accelerator Applications

Engineering Specialist at Novartis
, located on site. Responsible for engineering activities (design, implementation, maintenance) to ensure technical quality and support site objectives, including maintenance, calibration, and commissioning for projects.

• Adhere to Novartis Quality Policies and procedures to ensure product safety, purity, effectiveness, and quality.
• Perform a wide range of maintenance repair activities on production equipment, laboratory equipment, and building management systems.
• Provide guidance and leadership to team members.
• Assist in troubleshooting and repair of process equipment (containment isolator systems, filling line equipment, utility connections), including mechanical, electrical, pneumatic, motors, pumps, vacuum, HVAC, control systems, and compressed gases.
• Interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications to perform maintenance and repairs.
• Support 24x7 site-based operations after startup.
• Write and revise accurate operational procedures, training documents, and maintenance procedures for production and utility systems.
• Provide radiation safety program support, including calibration of all radiation detection equipment.
• Complete equipment work orders thoroughly and accurately, documenting them in the system.
• Supply information and technical data for securing spare parts.
• Provide responsive customer support with emphasis on customer satisfaction.
• Perform startup and commissioning activities as required.
• Support investigations and deviations from an engineering/maintenance perspective and help close CAPAs.
• Perform preventative and corrective maintenance on manufacturing process equipment within a cleanroom environment.
• Complete accurate documentation in cGMP operations.
• Oversee work and provide training of less experienced maintenance technicians and new technicians.
• Execute other related duties as assigned.
• Use CMMS system for documentation of relevant work.

• High School diploma or equivalent required;
  Bachelor’s degree preferred.
• 3+ years of hands‑on plant maintenance experience in a regulated GMP environment required.
• Prior supervisory or team/project lead experience preferred.
• Experience in aseptic fill/finish or radio pharmacy preferred.
• Experience in pharmaceuticals or medical devices preferred.
• Completed training in radioactive or hazardous materials environment preferred.
• Ability to adhere to all applicable procedures, policies, and quality or regulatory requirements (OSHA, DEA, FDA, etc.).
• Strong communication and organizational skills in a team environment.
• Proficient computer skills using MS Office, Building Management Systems, and Computerized Maintenance Management Systems (CMMS) or similar.
• Ability to climb ladders and lift up to 50 lbs.
• Work in protective clothing, including respiratory protection, confined space entry, and cleanroom environments.
• Flexibility to work nights, weekends, and holidays as required.

The salary range for this position is expected to be between $85,400 and $158,600 per year, with performance‑based cash incentives and potential annual equity awards.

Comprehensive benefits package including health, life, disability, 401(k) with company match, and generous time‑off (vacation, personal days, holidays).

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

We are committed to working with individuals with disabilities. For reasonable accommodation requests during the application process or for essential functions, contact [email protected] or +1(877)395‑2339. Include the job requisition number in your message.