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Process & Instrumentation Supervisor

Job in Silver Spring, Montgomery County, Maryland, 20901, USA
Listing for: United Consulting Hub, Inc.
Full Time position
Listed on 2026-11-01
Job specializations:
  • Manufacturing / Production
    Instrumentation Tech, Validation Engineer, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 110000 - 150000 USD Yearly USD 110000.00 150000.00 YEAR
Job Description & How to Apply Below

Role:

-Process & Instrumentation Supervisor

Location:

- Maryland, USA

Duration:

-12+ Months W2 contract

Industry: Biologics / Biotechnology / Pharmaceutical Manufacturing

Position Overview

We are seeking an experienced Process & Instrumentation Supervisor to oversee process equipment, instrumentation, calibration, and maintenance activities within a GMP-regulated manufacturing facility. The ideal candidate will have hands-on experience with pharmaceutical or biologics manufacturing equipment, process automation, clean utilities, and technician supervision.

Key Responsibilities
  • Supervise daily process instrumentation, equipment maintenance, and troubleshooting activities.
  • Oversee maintenance of bioreactors, fermenters, centrifuges, chromatography skids, filtration systems, and CIP/SIP equipment.
  • Monitor critical process parameters, including temperature, pressure, pH, dissolved oxygen, flow, and conductivity.
  • Lead instrument installation, calibration, loop checks, and functional testing of sensors, transmitters, meters, and control valves.
  • Troubleshoot PLC, SCADA, DCS, and HMI systems, including alarms, interlocks, and control loops.
  • Manage preventive and corrective maintenance schedules, calibration activities, and critical spare parts.
  • Oversee instrumentation for purified water, WFI, clean steam, HVAC, and other critical utilities.
  • Support FAT/SAT, commissioning, IQ/OQ/PQ, and equipment performance testing.
  • Participate in deviation investigations, root cause analysis, CAPA, change controls, and risk assessments.
  • Maintain accurate maintenance, calibration, and qualification documentation in compliance with GMP and data integrity requirements.
  • Assign daily tasks, guide technicians, and ensure compliance with safety procedures.
  • Coordinate with OEMs, service providers, Engineering, Manufacturing, Quality, and Utilities teams.
  • Support regulatory audits, inspections, and GMP readiness activities.
Required Qualifications
  • Hands-on experience in process instrumentation, calibration, and equipment maintenance within pharmaceutical, biologics, or biotechnology manufacturing.
  • Knowledge of GMP requirements, instrumentation systems, process automation, and clean utilities.
  • Experience troubleshooting manufacturing equipment and instrumentation control systems.
  • Familiarity with PLC, SCADA, DCS, and HMI platforms.
  • Experience supervising technicians and coordinating maintenance activities.
  • Knowledge of equipment qualification, commissioning, and validation documentation.
  • Strong troubleshooting, communication, leadership, and problem-solving skills.
Preferred Experience
  • Biopharmaceutical manufacturing and process equipment maintenance.
  • Bioreactors, chromatography, filtration, and CIP/SIP systems.
  • Critical utility instrumentation, including WFI and clean steam.
  • GMP documentation, deviation management, CAPA, and change control.

Ideal Candidate Profile: A hands-on technical supervisor with strong instrumentation and maintenance expertise in a GMP-regulated pharmaceutical or biologics manufacturing environment.

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