Pharma Maintenance Engineering Lead

Pine Pharmaceuticals

City of Tonawanda (NY)

On-site

USD 90,000 - 125,000

Full time

14 days+
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Job summary

Pine Pharmaceuticals seeks an Engineering Supervisor to lead a small maintenance and engineering team, providing hands-on support for automated manufacturing equipment and facility systems. The role emphasizes safety, regulatory compliance, and uptime in a cGMP environment.

You will supervise technicians and engineers, develop PM programs, and collaborate with Production, Quality, Engineering, and EHS to align maintenance with production goals.

Qualifications

  • Bachelor's degree in Engineering (Mechanical, Industrial, Electrical) or related field required.
  • Minimum 7 years in automated manufacturing; 3+ years in pharma/cGMP environment preferred.
  • Experience with automated manufacturing equipment (PLCs, HMIs, robotics) required.
  • Capital projects, facility layout or commissioning experience strongly preferred.

Responsibilities

  • Lead a small engineering/maintenance team; supervise scheduling, tasks, and development.
  • Hands-on maintenance and engineering tasks alongside team members.
  • Maintain preventive and predictive maintenance programs; use vibration analysis or thermal imaging as applicable.
  • Collaborate on facility design, layout, utility routing, and new equipment installation from concept through qualification.
  • Maintain documentation to meet FDA, OSHA, ISO, and local regulatory requirements.
  • Ensure safety, EHS compliance, and incident investigations; support root cause analyses.

Skills

Hands-on troubleshooting
Automation & controls
Team leadership
CMMS proficiency
Documentation & compliance

Education

Bachelor's degree in Engineering

Tools

PLC/SCADA systems
HMI systems
Pneumatics & Hydraulics

Job description

Pine Pharmaceuticals seeks an Engineering Supervisor to lead a small maintenance and engineering team, providing hands-on support for automated manufacturing equipment and facility systems. The role emphasizes safety, regulatory compliance, and uptime in a cGMP environment.

You will supervise technicians and engineers, develop PM programs, and collaborate with Production, Quality, Engineering, and EHS to align maintenance with production goals.

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