Maintenance Supervisor

Astrix; New Jersey; On-site; USD 80,000 - 100,000; Full time

Job summary

A leading company in the pharmaceutical manufacturing sector is seeking a Manufacturing Supervisor to oversee maintenance operations. The role involves managing maintenance activities, ensuring compliance with cGMP and FDA standards, and supporting operational efficiency. Candidates should have a relevant Bachelor's degree and significant industry experience.

Benefits

Medical insurance

Vision insurance

Qualifications

• Minimum of 8 years of experience in the pharmaceutical industry.
• At least 5 years of experience working in a cGMP-regulated environment.
• Willingness to work flexible shifts based on business needs.

Responsibilities

• Lead and manage projects related to equipment acquisition and maintenance.
• Coordinate scheduled and emergency maintenance, repairs, and equipment upgrades.
• Support the development and execution of a robust Preventive Maintenance Program.

Skills

Strong computer skills

Proficiency with maintenance management systems

Education

Bachelor’s degree in Mechanical Engineering, Chemical Engineering, or a related field

Job description

2 days ago Be among the first 25 applicants

This range is provided by Astrix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$80,000.00/yr - $100,000.00/yr

Direct message the job poster from Astrix

Scientific and technical staffing recruiter connecting top talent with leading companies

We are seeking a skilled Manufacturing Supervisor to oversee maintenance operations and support equipment-related projects within a pharmaceutical manufacturing environment. This role will be responsible for managing maintenance activities, ensuring compliance with cGMP and FDA standards, and supporting overall operational efficiency.

Middlesex County, NJ

Full Time/Perm Role

Key Responsibilities:

• Lead and manage projects related to equipment acquisition and maintenance to support the company’s operational goals.
• Coordinate both scheduled and emergency maintenance, repairs, and equipment upgrades.
• Oversee the ERP work order system, assigning tasks and preventive maintenance (PM) schedules to the maintenance team.
• Identify future equipment and maintenance needs to align with business objectives.
• Procure parts and materials necessary for preventive maintenance, routine repairs, and emergency fixes.
• Support the development and execution of a robust Preventive Maintenance Program, ensuring equipment operates efficiently and remains in compliance with FDA regulations.
• Contribute to the Quality Improvement Program by conducting investigations, preparing reports, and implementing corrective and preventive actions (CAPAs) related to production maintenance.

Qualifications:

• Bachelor’s degree in Mechanical Engineering, Chemical Engineering, or a related field.
• Minimum of 8 years of experience in the pharmaceutical industry.
• At least 5 years of experience working in a cGMP-regulated environment.
• Willingness to work flexible shifts based on business needs.
• Strong computer skills and proficiency with maintenance management systems.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Manufacturing

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

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