Senior Manufacturing Engineer I
Onsite Requirement
100% onsite
Location
Lexington, KY 91324
Position Id
2570
Recruiter Contact
SARAH
Job Description
Responsibilities:
Equipment Performance and Troubleshooting
- Lead efforts to monitor and optimize the performance of manufacturing equipment, ensuring compliance with CGMP standards.
- Troubleshoot and resolve complex issues to minimize production downtime and ensure optimal operational efficiency.
- Identify and implement opportunities for continuous improvement through upgrades, process modification, or alternative solutions. Lead in the development and implementation of procedural or automation improvement changes.
- Lead lean manufacturing initiatives, six sigma projects, and other process optimization efforts to improve productivity, quality, and cost efficiency.
- Assist with new product/equipment design reviews, process development, and commercialization activities, including training and development of manufacturing staff on operation and process.
- Serve as a technical point of contact for client and contract services.
Data Analytics and Performance Analysis
- Develop and maintain measurement systems to visualize key performance indicators (KPIs) in manufacturing.
- Use data analytics tools and techniques to analyze equipment performance, identify trends, and recommend corrective action and process improvement.
Quality System / Equipment Qualification Support
- Assist with manufacturing equipment-related deviations and root cause analysis as the equipment SME.
- Support the development and execution of Corrective and Preventive Actions (CAPA) and Change Controls to address root causes of equipment failures and performance issues.
- Support equipment Installation, Operation, and Performance Qualification (IOPQ) activities.
- Experience supporting client and regulatory audits as well as responding to action items.
- Provide SME input on equipment qualification processes, ensuring fit for commercial manufacturing use, compliance with FDA and other regulatory requirements.
Qualifications:
Basic Qualifications:
- Bachelor’s degree in Engineering or related field and/or equivalent experience
- 5+ years of manufacturing of relevant experience in the pharmaceutical industry with a Bachelor’s degree; and 3+ years’ experience in the pharmaceutical industry and a Master’s degree.
- Proven track record of successfully implementing improvement initiatives in a pharmaceutical manufacturing environment.
- Strong analytical and problem-solving skills with the ability to use data to drive decision-making.
- Excellent communication and interpersonal skills, with the ability to influence and collaborate effectively across multiple departments.
- Ability to manage multiple projects and priorities in a fast-paced environment.
- Technical writing experience, such as SOPs, Maintenance PMs, user requirement specs, vendor requests for proposal
- Experience with automation, nasal, or related drug delivery device manufacture and packaging.
Preferred Qualifications
- Lean manufacturing or Six Sigma certifications
- Proficiency in using Lean tools and software applications such as Smartsheet, Power BI, Power Apps, etc.
- Experience with site-level automation systems, ex.
- Serialization - Antares, Tracelink
- Data historian – Aveva OSI PI
- Reporting Systems – OSI PI, MS Report Builder, SQL Development
- Kepware, Matrikon, AB Factory Talk
- Automated Visual Inspection
- Other duties as assigned