RCI-TEVA-9979 Process Automation Engineer (Oral Solid Dosage) - Davie, FL

Job Description

We are looking for a candidate with deeper manufacturing automation and continuous improvement execution experience who can independently identify, drive, and implement larger-scale opportunities.

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RCI-TEVA-9979 Process Automation and Continuous Improvement Engineer (Oral Solid Dosage/ BioPharma) - Davie, FL

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Full JD & Apply:

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Interested? Send me your resume + availability for a quick call: View email address on ziprecruiter.com

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Job Title: Lean and Automation Engineer

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Location: US-FL-Davie

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Shift Schedule: Standard working hours of 8:00 AM to 5:00 PM

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Employment type: Full-time.

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Education :

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• Master's degree in industrial, manufacturing, mechanical engineering, or a related technical discipline is required.
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Experience :

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• 2-3 years of pharmaceutical industry experience is required, including at least 2 years supporting Oral Solid Dosage (OSD) or tableting/compression operations.
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• Demonstrated completion of waste-reduction or automation projects with the candidate as the primary executor, not a coordinator.
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Required Core Essential Skill Set:

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• Lean Manufacturing, DMAIC, Value Stream Mapping, SMED, OEE improvement, statistical analysis, Root Cause Analysis, and hands-on process analysis.
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• Ability to identify opportunities, develop business cases, quantify benefits, and build practical workflows, dashboards, or data tools.
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• Strong project ownership and effective cross-functional execution within GMP, data-integrity, safety, and quality requirements.
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Preferred Skills:

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• Lean Six Sigma Black Belt; strong Green Belts with proven hands-on delivery considered. A practical project example will be discussed on site.
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• Power BI, Power Automate, advanced Excel, SQL, SAP, MES/EBR, and historian or manufacturing analytics platforms.
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• Experience applying modern analytics and AI-enabled tools to improve operational reliability and performance.
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• Self-starter with strong analytical, troubleshooting, systems-thinking, communication, documentation, and compliance skills.
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• Ability to challenge historical practices and carry an approved idea through build, training, implementation, handoff, and sustainment.
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Job Summary

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• We're looking for a hands-on Continuous Improvement & Automation Engineer who identifies, assesses, builds, and implements solutions that reduce waste and improve manufacturing performance - not a facilitator or meeting coordinator.
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• You will personally bring approved projects to life through analysis, solution development, automation build, training, implementation, and sustainment.
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• Success is measured by high-quality opportunities identified, approved projects implemented, Finance-validated benefits delivered, and compliant results sustained.
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• This role offers meaningful ownership and impact in a regulated Oral Solid Dosage environment.
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Key Responsibilities

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• Personally perform process studies, time studies, waste assessments, and bottleneck analysis to identify improvement and automation opportunities.
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• Develop evidence-based opportunity assessments covering the baseline, expected operational and financial benefit, implementation needs, cost, risk, timing, and sustainment approach.
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• Present opportunities to the Site Leadership Team (SLT) for prioritization, approval, and sponsorship; project priority and resource commitment remain with the SLT.
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• Own approved projects from analysis through solution build, training, implementation, benefit realization, and sustainment, working with Operations, Finance, Quality, Engineering, and IT/OT as required.
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• Develop and deploy practical digital and analytics tools, including Power BI dashboards, Power Automate workflows, and electronic data collection, to eliminate non-value-added work.
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• Improve OEE, cleaning and changeover/setup time, labor productivity, throughput, and capacity across manufacturing, laboratories, offices, and warehouse operations.
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• Partner with Finance to classify and validate benefits consistently, maintain one agreed view of project value, and prevent duplicate reporting or double counting.
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• Establish process ownership, standard work, training, controls, documentation, and performance tracking before project closure.
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• Ensure all improvements comply with GMP, data integrity, safety, quality, change-control, and validation requirements in an FDA-regulated environment.
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