Operational Excellence Engineer
2 weeks ago
We are seeking a **Process Improvement Specialist** to enhance operational efficiency and drive excellence within our organization.
Catalent Inc. is a prominent, rapidly expanding public company, recognized as a key partner in the pharmaceutical sector, dedicated to the development and production of innovative treatments for patients globally. Your skills, insights, and enthusiasm are vital to our mission: to improve the quality of life for individuals.
The **Process Improvement Specialist** will work closely with multiple departments to pinpoint, eradicate, and maintain the reduction of inefficiencies within the facility. This role serves as a crucial change agent, consistently collaborating with frontline staff and dedicating significant time to areas requiring enhancement. **This is a full-time, salaried role based entirely on-site, with a Monday to Friday schedule during first shift hours.**
Catalent Biologics operates a cutting-edge, GMP-certified manufacturing site, offering over one million square feet dedicated to drug substance and product manufacturing, alongside related pharmaceutical services. This award-winning facility is instrumental in accelerating biologic drug development initiatives, delivering improved treatments that contribute to healthier lives.
**Key Responsibilities**
+ Employ lean methodologies, Six Sigma, and other continuous improvement strategies to solve problems.
+ Develop and implement solutions addressing challenges in manufacturing and business operations.
+ Balance role responsibilities with 70% focus on shop-floor execution and 30% on project management.
+ Coordinate improvement initiatives across various departments.
+ Provide updates and visibility to organizational leaders.
+ Prepare and manage project timelines.
+ Facilitate Kaizen events aimed at achieving rapid and ongoing process enhancements.
+ Perform additional duties as assigned.
**Candidate Qualifications**
+ Bachelor’s degree or higher in Industrial, Mechanical, or Process Engineering.
+ At least 2 years of relevant experience.
+ Experience in cGMP environments is preferred.
+ Background in the pharmaceutical industry is advantageous.
+ Six Sigma Green Belt certification is preferred.
**Why Join Catalent?**
+ Comprehensive medical, dental, vision, and wellness benefits starting on your first day.
+ Opportunities for career advancement within a growing team and organization.
+ Generous paid time off policy, including 152 hours annually plus 8 paid holidays.
+ Commitment to community engagement and sustainability initiatives.
+ Active Diversity & Inclusion Employee Resource Groups.
+ Tuition reimbursement program available.
+ Competitive 401K matching program.
**Catalent offers fulfilling career opportunities** Join the global leader in drug development and delivery, contributing to the advancement of over 7,000 life-saving and life-enhancing products for patients worldwide. Catalent is a dynamic and expanding international organization where employees collaborate directly with pharmaceutical, biopharmaceutical, and consumer health companies of all sizes to propel new medicines from early development through clinical trials to market. Catalent produces over 70 billion doses annually, each one vital to someone in need. Join us in making a significant impact.
Catalent is dedicated to ensuring the health and safety of its employees, visitors, and the customers and patients we serve. In response to the global pandemic, we have adapted many of our recruitment and onboarding processes to prioritize safety. The Human Resources team will communicate all necessary safety protocols throughout each stage of the process.
**Catalent is an Equal Opportunity Employer, including disability and veterans.**
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