Manufacturing Maintenance Supervisor - GMP Focus

jj; Añasco (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

Johnson & Johnson in Anasco, Puerto Rico seeks a Production Equipment Supervisor to oversee maintenance and repair of production equipment ensuring reliable, safe operations. You will direct Technicians, apply asset-management methods, and ensure regulatory compliance with GMP and environmental standards.

Ideal candidates show strong leadership, 2+ years in manufacturing maintenance, and fluency in Spanish and English. Join a team focused on excellence in a regulated medical device environment.

Qualifications

• Bachelor’s Degree in Engineering is required.
• Minimum 2 years of experience in a maintenance manufacturing environment is required.
• Experience working in the medical device industry preferred.
• Able to read, speak, and write Spanish and English.
• Strong leadership and supervisory skills.
• Knowledge of FDA regulations is preferred.
• Must be computer literate in email, word processing, and spreadsheets.

Responsibilities

• Directs and coordinates maintenance and repair of production equipment.
• Maintains GMP compliance and environmental standards.
• Leads technicians and ensures schedule adherence.
• Carries out preventive, corrective, and predictive maintenance.
• Collaborates with QA, Operations, and EHS.

Skills

Leadership

Bilingual Spanish/English

Regulatory compliance knowledge

GMP experience

Facility maintenance

Team supervision

Education

Bachelor's Degree in Engineering

Tools

MS Office

Asset management systems

Job description

Johnson & Johnson in Anasco, Puerto Rico seeks a Production Equipment Supervisor to oversee maintenance and repair of production equipment ensuring reliable, safe operations. You will direct Technicians, apply asset-management methods, and ensure regulatory compliance with GMP and environmental standards.

Ideal candidates show strong leadership, 2+ years in manufacturing maintenance, and fluency in Spanish and English. Join a team focused on excellence in a regulated medical device environment.