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Process Engineer III, MSAT

Job in Owensboro, Daviess County, Kentucky, 42302, USA
Listing for: Resilience
Full Time position
Listed on 2026-07-31
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 121250 USD Yearly USD 80000.00 121250.00 YEAR
Job Description & How to Apply Below
## Process Engineer III, MSATApplylocations:
USA - OH - West Chester time type:
Full time posted on:
Posted 3 Days Agojob requisition :
R-107015A career at Resilience is more than just a job – it’s an opportunity to change the future.

Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

For more information, please visit (Use the "Apply for this Job" box below). Process Engineer III, MSAT independently owns all technical aspects of assigned technology transfers from feasibility through PPQ completion and commercial introduction, serving as the primary technical escalation point for complex process issues. This role coaches Process Engineer I/II staff and partners cross-functionally with Validation, PMO, Supply Chain, Operations, and Quality. #
** Job Responsibilities
**** Technology Transfer & Process Engineering**:
* Independently owns all technical aspects of assigned technology transfers from feasibility through PPQ completion, ensuring process capability at each phase gate.
* Leads continuous improvement work streams across multiple assigned processes — including changeover reduction, yield improvement, OEE improvement, maintenance reliability, and waste reduction —, applying structured problem-solving (e.g., DMAIC, RCA) to drive improvements.
* Authors and independently approves URS, FAT, SAT, commissioning, and IQ/OQ/PQ protocols and reports for assigned process areas.
* Independently manages engineering projects from initiation to completion, including project justification, resourcing, timelines, and capital planning input.
* Coordinates and supports Manufacturing/Facility improvement initiatives that define equipment data, capabilities, utilization, and efficiencies; manages the equipment life cycle, including obsolescence planning.
** Continuous Improvement &

Risk Management:

*** Independently leads change control development and implementation, evaluating cross-functional impact and applying risk-based judgment.
* Performs and maintains risk management activities for assigned processes and equipment using structured risk assessment tools.
* Initiates deviations and leads complex technical investigations across multiple processes, defining CAPAs and assessing impact.
* Leads complex technical troubleshooting across multiple assigned processes, developing systematic approaches to recurring issues.
** Documentation & Compliance:
*** Authors, reviews, and independently approves controlled documents (SOPs, Batch Records, Rework procedures) for assigned process areas.
* Authors, reviews, and independently approves validation and change control documents, including master plans, protocols, and summary reports.
* Leads validation activities and periodic reviews — including validation required as a result of changes to validated processes, evaluating compliance status and driving corrective actions.
** Training & Development:
*** Coaches and mentors Process Engineer I and II staff on technology transfer, GMP practices, and problem-solving methodology.
* Independently manages external technical relationships with equipment and material suppliers, evaluating solutions and resolving issues.
* Designs and delivers technical training programs for Operations, Engineering, and Maintenance.
* Serves as key technical contact for regulatory inspections; participates in annual product review and biennial critical systems review.# Education & Experience
*
* Minimum Qualifications:

*** Demonstrated GMP experience in a regulated pharmaceutical manufacturing environment, with ability to independently apply controlled procedures and quality standards.
* Training or experience in one or more of the following applicable MSAT-relevant technology areas: programmable logic controllers, computerized systems, vision systems, aseptic/controlled environment, formulation, aseptic filling, assembly, packaging, process validation, technology transfer, change control.
* Demonstrated proficiency in more than one of the following disciplines:…
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