Top 19 Manufacturing process engineer Jobs in Lexington, Ky

Manufacturing Process Engineer
Piramal Pharma Solutions —Lexington, KY
- Up to $100,000 a year
- Full-time
- Background check
- Maintenance
- Research
- Health savings account
- Health insurance
Quick Apply
Manufacturing Process Engineer
Piramal Enterprises —Lexington, KY
- Full-time
- Research
- Mid-level
- Windows
Assembly Engineer – Automotive Manufacturing
CrossSafety Solutions Inc. —Lexington, KY
- Overtime
- Engineering
- Mid-level
- Travel
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Automation Engineer - Life Sciences (KY)
Excel Engineering, Inc. —Lexington, KY
- $86,700 - $160,000 a year
- Full-time
- Management
- Engineering
- Mid-level
- Health insurance
- Dental insurance
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Senior Application Engineer, CNC Machining
Xometry —Lexington, KY
- Hybrid work
- 7 years
- US work authorization
- Welding
Conveyor Engineer – Automotive Manufacturing
CrossSafety Solutions Inc. —Lexington, KY
- Overtime
- Spanish
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Paint Engineer – Automotive Manufacturing
CrossSafety Solutions Inc. —Lexington, KY
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Engineering
Quick Apply
Mechanical Engineer – Automotive Manufacturing
CrossSafety Solutions Inc. —Lexington, KY
- Overtime
- Microsoft Outlook
- Up to 50% travel
- Construction site
Quick Apply
Electrical Engineer – Automotive Manufacturing
CrossSafety Solutions Inc. —Lexington, KY
- Overtime
- Microsoft Outlook
- Up to 50% travel
- 5 years
Quick Apply
Operational Excellence Engineer
Piramal Pharma Solutions Inc. —Lexington, KY
- Full-time
- Engineering
- 3 years
- Master's degree
10h

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manufacturing process engineer jobs near lexington, ky

Manufacturing Process Engineer

Piramal Pharma Solutions -
Lexington, KY

Quick Apply

Job Details

Full-time
Up to $100,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Life insurance
Referral program
Retirement plan

Qualifications

Incident investigation techniques for hazard identification
Manufacturing plant facilities maintenance experience
Computer operation
Industrial automation
Defect resolution root cause analysis
Chemical Engineering
Pharmaceutical regulatory compliance
Maintenance
Software administration
Industrial equipment troubleshooting
Manufacturing facility
Bachelor’s degree in engineering
Production validation processes
Bachelor's degree
Pharmaceutical company experience
Productivity software
Commissioning phase involvement
Electrical Engineering
Process engineering
Failure analysis
Pharmaceutical manufacturing facility experience

Full Job Description

Company Overview
Piramal Pharma Solutions (PPS) is a leading Contract Development and Manufacturing Organization (CDMO) dedicated to delivering comprehensive solutions across the entire drug development and manufacturing spectrum. With a global network of state-of-the-art facilities, we specialize in innovative pharmaceutical services, including biologics, potent APIs, sterile fill/finish, and advanced manufacturing technologies. Our commitment is to partner with clients worldwide to bring life-changing therapies to market efficiently and reliably.

Job Overview

Reporting to the Engineering Manager, the Manufacturing Process Engineer serves as subject-matter-expert and provides real-time, process engineering support to the manufacturing process. This position is responsible for design, project management, and implementation of new and existing systems, utilities and equipment, and ensures Quality, Compliance, and improved OTIF for all products produced at the manufacturing facility in Lexington, Kentucky.

Reporting Structure

This position reports to the Engineering Manager.

Key Responsibilities:

Designs and project manages changes, improvements, new systems and or equipment.
Prepares Change Control Records (CCRs), Design Specifications, User Requirements Specifications, System Specifications, Design documents, Drawings, and Validation Documents for improvement, planned and corrective maintenance and system or process improvements
Leads/assists in Continuous Improvement Projects, including identification of opportunities, researches literature and vendors, prepares and presents proposals, develops and executes projects, and closes projects, all following appropriate change control methodologies
Represents Technical Subject Matter Expert (SME) in teams assembled to specify, install, troubleshoot and maintain systems, equipment and processes
Supports day-to-day production and maintenance activities
Provides training support as required.
Develops and or modifies SOPs for the Processes and Equipment.
Participates in deviation investigations to identify root causes and define corrective and preventive actions (CA/PA).
Creates and maintains drawings and sketches.
Manages Technical Publications Library to ensure the relevant manuals, specifications, design information for all of our facilities, utilities, equipment and products are on hand
Primary/First Line responsibility for operation and maintenance of the Validated Systems to maintain production capability required.
Primary/First Line responsibility for enhancements and upgrades of manufacturing related systems to maintain production capability.

Qualifications:

Bachelor’s degree in Mechanical, Electrical, or Chemical Engineering
Minimum 3-5 years of pharmaceutical manufacturing/maintenance experience required (parenteral/sterile filling experience preferred)
Expertise in troubleshooting production equipment/systems
Ability to work flexible schedule to support 24-hour operation (requires assignment on shift for 4 shift rotating days off schedule)
PC literate with standard office application (Word, Excel, PowerPoint) competency
Experience with maintenance and administration of both Windows-based and industrial (e.g., PLC) computer networks.
Experience with Allen-Bradley ControlLogix and Siemens PLCs; experience with HMI software applications; experience with automating processes and equipment
Knowledge and understanding of cGMPs including FDA, PMDA, and EU regulations; knowledge of cGMP validation requirements and techniques; experience with commissioning and validation protocol development and execution.
Knowledge and experience in cGMP CA/PA, root-cause analysis, risk assessment and investigation tools and techniques.

Pay: Up to $100,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Parental leave
Referral program
Retirement plan
Tuition reimbursement
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

manufacturing process engineer jobs in lexington, ky

Manufacturing Process Engineer

Manufacturing Process Engineer

Assembly Engineer – Automotive Manufacturing

Automation Engineer - Life Sciences (KY)

Senior Application Engineer, CNC Machining

Conveyor Engineer – Automotive Manufacturing

Paint Engineer – Automotive Manufacturing

Mechanical Engineer – Automotive Manufacturing

Electrical Engineer – Automotive Manufacturing

Operational Excellence Engineer

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