Program Manager, Technical Operations
Job in
Edison, Middlesex County, New Jersey, 08817, USA
Listed on 2026-11-01
Listing for:
DSJ Global
Full Time
position Listed on 2026-11-01
Job specializations:
-
Manufacturing / Production
Lean Manufacturing / Six Sigma, Operations Management, Quality Engineering
Job Description & How to Apply Below
A leading pharmaceutical manufacturer is seeking a Technical Operations Program Manager to join its Manufacturing Science & Technology team. This is a high-impact role responsible for leading strategic operational excellence initiatives, driving continuous improvement programs, and partnering with cross-functional teams to enhance manufacturing performance across a complex pharmaceutical production environment. This opportunity offers direct exposure to site leadership, global initiatives, and the ability to influence manufacturing operations through data-driven decision making and Lean Six Sigma methodologies.
Key Responsibilities
- Lead site-wide continuous improvement initiatives focused on operational excellence, efficiency, quality, and performance improvement.
- Implement and support global technical operations programs and process improvement strategies.
- Collect, analyze, and interpret manufacturing data to identify opportunities for process optimization and operational improvements.
- Facilitate root cause investigations and problem-solving activities using Lean principles and structured methodologies.
- Collaborate with Manufacturing, Quality, Engineering, Supply Chain, Materials Management, and R&D teams to establish goals and key performance indicators.
- Drive Lean Six Sigma initiatives that improve process robustness, productivity, and overall manufacturing performance.
- Conduct value stream mapping, risk assessments, and FMEA activities to identify and mitigate operational risks.
- Lead cross-functional teams to execute strategic projects from planning through completion.
- Manage project timelines, milestones, budgets, and resource requirements using project management best practices.
- Serve as a liaison across manufacturing sites to promote the sharing of best practices and continuous improvement tools.
Qualifications
- Bachelor's degree in Pharmaceutical Sciences, Engineering, Life Sciences, or a related technical discipline.
- 5+ years of experience in pharmaceutical manufacturing, technical operations, process engineering, or operational excellence.
- Strong understanding of pharmaceutical manufacturing processes, packaging operations, and testing equipment.
- Experience leading cross-functional process improvement, operational excellence, or strategic initiatives.
- Knowledge of statistical analysis, root cause analysis, risk management, and process optimization techniques.
- Experience with project management tools and methodologies; PMP certification is a plus.
- Strong communication, leadership, and stakeholder management skills.
- Experience working within a GMP-regulated pharmaceutical manufacturing environment.
Why Consider This Opportunity?
- Opportunity to lead high-visibility strategic initiatives that directly impact manufacturing performance.
- Significant exposure to senior leadership and cross-functional decision makers.
- Influence operational excellence efforts across a complex pharmaceutical manufacturing site.
- Drive meaningful process improvements using Lean Six Sigma and data-driven methodologies.
- Join a growing organization committed to continuous improvement and operational excellence.
- Competitive compensation package, benefits, and long-term career advancement opportunities.
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