Overview
On Site
Contract - Independent
Skills
Process Engineering
Repair
Electrical Engineering
Programmable Logic Controller
INSPECT
Collaboration
Quality Assurance
Continuous Improvement
Preventive Maintenance
Project Management
Performance Management
CMMS
Regulatory Compliance
GMP
Documentation
Pharmaceutics
Manufacturing
Critical Thinking
Good Manufacturing Practice
Technical Writing
Communication
Analytical Skill
Power Tools
DVM
First Aid
ISO 9000
Auditing
IQ
OQ
PQ
HVAC
Mechanical Engineering
HMIS
Privacy
Marketing
Job Details
Location: Indianapolis, IN
Description: Our client is currently seeking a Process Development Engineer
Position: Process Development Engineer
Location: Indianapolis, IN (100% onsite)
Duration: 12+ months contract
Job Description:
Summary:
The Process Maintenance Technician plays a critical role in ensuring the reliability and performance of production and support equipment in a regulated pharmaceutical manufacturing environment. This role involves executing reactive, preventive, and predictive maintenance, troubleshooting mechanical, hydraulic, pneumatic, and control systems, and supporting GMP-compliant operations. The technician may work one of various shift patterns, including 8, 10, or 12 hours, occurring on days or nights, weekdays or weekends, and be 100% on-site at the client facility.
Key Responsibilities
Perform maintenance activities in compliance with cGMPs and SOPs.
Assemble, disassemble, install, repair, and replace components for pharmaceutical-grade machinery and cleanroom equipment.
Troubleshoot and resolve issues in mechanical, electrical, pneumatic, and PLC-controlled systems.
Maintain accurate documentation including Maintenance and Calibration Records per cGMP standards.
Inspect equipment for wear, irregularities, and potential failures.
Collaborate with cross-functional teams (Quality, Engineering, Production) to ensure equipment reliability and compliance.
Execute scheduled PMs and CMMS updates in a timely and accurate manner.
Maintain tools and workspaces in accordance with cGMP housekeeping standards.
Adhere to OSHA, and site-specific safety protocols.
Participate in continuous improvement initiatives and equipment reliability programs.
Support audits and inspections by regulatory bodies and internal quality teams.
Other duties as assigned. Metrics for Success
PM completion rate and CMMS accuracy
Equipment uptime and reliability
Compliance with GMP documentation standards
Audit readiness and deviation reduction
Responsiveness to unplanned maintenance events
Experience Required
Minimum 3-5+ years of experience in mechanical maintenance within pharmaceutical, biotech, or regulated manufacturing environments.
Strong mechanical aptitude with troubleshooting and critical thinking skills.
Familiarity with the demands of performing maintenance activities in a cGMP environment.
Ability to interpret technical documentation and engineering drawings.
Strong communication, organizational, and analytical skills.
Comfortable working in confined spaces, heights, and around chemicals.
Ability to use basic hand tools, power tools and meters (DVM, Amp and Ohm).
Desired Skills:
Certification in First Aid or CPR
Familiarity with ISO standards and FDA audit processes.
Experience supporting equipment qualification (IQ/OQ/PQ).
Experience with aseptic processing, HVAC systems, and utility maintenance is a plus.
Technical diploma or degree in Mechanical Engineering or equivalent.
Proficiency in troubleshooting PLCs, HMIs, and automated systems.
Skilled in using lathes, mills, grinders, and precision instruments
By providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes. Message & data rates apply and message frequency may vary. Consistent with Judge's Privacy Policy, information obtained from your consent will not be shared with third parties for marketing/promotional purposes. Reply STOP to opt out of receiving telephone calls and text messages from Judge and HELP for help.
Contact:
This job and many more are available through The Judge Group. Please apply with us today!
Description: Our client is currently seeking a Process Development Engineer
Position: Process Development Engineer
Location: Indianapolis, IN (100% onsite)
Duration: 12+ months contract
Job Description:
Summary:
The Process Maintenance Technician plays a critical role in ensuring the reliability and performance of production and support equipment in a regulated pharmaceutical manufacturing environment. This role involves executing reactive, preventive, and predictive maintenance, troubleshooting mechanical, hydraulic, pneumatic, and control systems, and supporting GMP-compliant operations. The technician may work one of various shift patterns, including 8, 10, or 12 hours, occurring on days or nights, weekdays or weekends, and be 100% on-site at the client facility.
Key Responsibilities
Perform maintenance activities in compliance with cGMPs and SOPs.
Assemble, disassemble, install, repair, and replace components for pharmaceutical-grade machinery and cleanroom equipment.
Troubleshoot and resolve issues in mechanical, electrical, pneumatic, and PLC-controlled systems.
Maintain accurate documentation including Maintenance and Calibration Records per cGMP standards.
Inspect equipment for wear, irregularities, and potential failures.
Collaborate with cross-functional teams (Quality, Engineering, Production) to ensure equipment reliability and compliance.
Execute scheduled PMs and CMMS updates in a timely and accurate manner.
Maintain tools and workspaces in accordance with cGMP housekeeping standards.
Adhere to OSHA, and site-specific safety protocols.
Participate in continuous improvement initiatives and equipment reliability programs.
Support audits and inspections by regulatory bodies and internal quality teams.
Other duties as assigned. Metrics for Success
PM completion rate and CMMS accuracy
Equipment uptime and reliability
Compliance with GMP documentation standards
Audit readiness and deviation reduction
Responsiveness to unplanned maintenance events
Experience Required
Minimum 3-5+ years of experience in mechanical maintenance within pharmaceutical, biotech, or regulated manufacturing environments.
Strong mechanical aptitude with troubleshooting and critical thinking skills.
Familiarity with the demands of performing maintenance activities in a cGMP environment.
Ability to interpret technical documentation and engineering drawings.
Strong communication, organizational, and analytical skills.
Comfortable working in confined spaces, heights, and around chemicals.
Ability to use basic hand tools, power tools and meters (DVM, Amp and Ohm).
Desired Skills:
Certification in First Aid or CPR
Familiarity with ISO standards and FDA audit processes.
Experience supporting equipment qualification (IQ/OQ/PQ).
Experience with aseptic processing, HVAC systems, and utility maintenance is a plus.
Technical diploma or degree in Mechanical Engineering or equivalent.
Proficiency in troubleshooting PLCs, HMIs, and automated systems.
Skilled in using lathes, mills, grinders, and precision instruments
By providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes. Message & data rates apply and message frequency may vary. Consistent with Judge's Privacy Policy, information obtained from your consent will not be shared with third parties for marketing/promotional purposes. Reply STOP to opt out of receiving telephone calls and text messages from Judge and HELP for help.
Contact:
This job and many more are available through The Judge Group. Please apply with us today!
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.