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Supervisor, Facilities Engineering

Amneal

Piscataway, NJOnsitePosted 1 day ago$95,000 - $110,000/year
Full TimeMid LevelManufacturing & CMCPharmaceutical
Original posting ↗

Summary

The Supervisor, Facilities Engineering is responsible for overseeing facilities and engineering operations within a pharmaceutical manufacturing environment to ensure regulatory compliance, operational reliability, and cost-effective execution of projects and maintenance activities. This role provides leadership and technical guidance to engineering staff while ensuring the proper functioning, qualification, and maintenance of facility systems, utilities, and equipment in accordance with GMP, safety, and regulatory requirements.

Job description

Essential Functions

  • Oversee engineering and facilities programs to ensure the compliant, safe, and reliable operation of machinery, equipment, and utilities. Responsibilities include validation activities, preventive maintenance (PM), building management systems (BMS), environmental controls, fire system maintenance, building permit management, and the development, implementation, and training of engineering SOPs.
  • Plan and supervise workloads for direct reports while overseeing facilities management services, including building systems operations, maintenance, repairs, and capital improvement projects. Review and evaluate operational procedures and personnel practices, and establish and implement enhanced processes to support efficient, compliant, and cost-effective operations.
  • Provide direct supervision and leadership to the Project Engineers, Validation Engineers, and Junior Mechanics, including performance management, coaching, and development. Promote a culture of safety, quality, and continuous improvement.
  • Coordinate preparation and management of the engineering and facilities budget; monitor expenditures; analyze staffing requirements; and oversee maintenance contracts, service agreements, and construction activities related to facility modifications and repairs.
  • Review, evaluate, and continuously improve operating procedures and practices to enhance compliance, efficiency, and reliability of facilities and engineering operations.

Qualifications

Education: Bachelors Degree (BA/BS) Engineering (Mechanical, electrical, facilities, or related field) - Required

Experience: 4 years or more in Engineering in a pharmaceutical manufacturing environment; 2 years or more in Supervisory level or lead experience

Requirements

  • Bachelor's degree in Engineering (Mechanical, electrical, facilities, or related field)
  • 4+ years of engineering experience in a pharmaceutical manufacturing environment
  • 2+ years of supervisory or lead experience

Benefits

  • Health Insurance
  • Insurance Benefits
  • 401(k) Matching
  • Short-term Incentive
  • Performance-based Award

Company overview

Amneal Pharmaceuticals, Inc. (NYSE: AMRX) is a leading American publicly traded pharmaceutical company headquartered in Bridgewater, New Jersey. Founded in 2002 by brothers Chirag and Chintu Patel, the company has grown to become one of the largest and fastest-growing generic pharmaceutical manufacturers in the United States. Amneal operates as an integrated pharmaceutical company focused on developing, manufacturing, and distributing generic, brand, and biosimilar products. With approximately 8,100 employees globally, the company maintains operations across North America, Asia, and Europe. Amneal's business is organized into three main segments: a robust U.S. generics business with over 250 product families, a growing specialty pharmaceuticals division focused on central nervous system disorders and endocrine conditions, and an expanding biosimilars portfolio. The company has established itself as a leader in complex dosage forms and difficult-to-manufacture products, with manufacturing capabilities spanning oral solids, injectables, ophthalmics, liquids, topicals, transdermals, and respiratory devices. Amneal's mission 'We make healthy possible' reflects its commitment to providing affordable access to essential medicines while maintaining high-quality standards across its global operations.

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