Computerized maintenance management systems (cmms)
The Engineering Specialist leads CQV development and execution for new and modified processing equipment, systems, and critical utilities in pharmaceutical operations
Job Summary
The Engineering Specialist leads CQV development and execution for new and modified processing equipment, systems, and critical utilities in pharmaceutical operations.
Joining this team offers meaningful opportunities for talent growth and to make a sustained impact on product reliability and patient safety to continue advancing our mission.
The role is based in Rahway, NJ, includes a hybrid work model, and offers a comprehensive benefits package including medical, dental, vision, retirement, and paid time off.
Matching Summary
The Engineering Specialist leads CQV development and execution for new and modified processing equipment, systems, and critical utilities in pharmaceutical operations.
Salary
Base: $87,300.00 - $137,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation, and sick days
Skills & Requirements
Must-have
Commissioning and qualification/validation
Good Manufacturing Practices (GMP)
Computerized Maintenance Management Systems (CMMS)
Good Documentation Practices
Equipment commissioning and validation
Process engineering and optimization
Nice-to-have
Paperless electronic validation systems
Lean and Six Sigma methodologies
Strong organizational and communication skills
Ability to lead or facilitate tasks
Experience with oral solid dosage equipment
Knowledge of regulatory requirements for CQV
Key Requirements
Bachelor's Degree in Engineering or Science
Minimum 2 years qualification/validation experience
Experience with cGMP and GDocP
Familiarity with CMMS and CCMS systems
Ability to work independently and lead small projects
Experience in pharmaceutical manufacturing plant operations