Logo of Huzzle

Home

Matches

Explore

Manage

Continuous Improvement Specialist I/II/III

image

Genezen

4d ago

  • Job
    Full-time
    Junior, Mid & Senior Level
  • Research & Development
    Engineering
  • Indianapolis
  • Quick Apply

AI generated summary

  • You need a relevant Bachelor’s degree, 2-5 years in biopharma, lean manufacturing experience, proficiency in MS Office and data visualization, strong communication skills, and project management abilities.
  • You will analyze workflows, lead workshops, train staff on improvement practices, manage project frameworks, and support daily visual management for continuous improvement initiatives.

Requirements

  • Bachelor's Degree in a relevant science or engineering discipline (Industrial Engineering, Mechanical Engineering, Chemical Engineering, Biomedical engineering)
  • 2-5 years of biopharma manufacturing experience
  • Experience with lean manufacturing methodologies (A3, process map, kaizen practices)
  • Proficiency in MS Office including Word, Excel, and PowerPoint
  • Skills in data visualization (Power BI, Power Query, PowerApps)
  • Experience with quality system compliance
  • Interest in human factors & system safety (aka human & organizational performance)
  • Ability to travel domestically (5-10%)
  • Excellent Communication And Presentation Skills
  • Skilled in humble inquiry and creating a psychologically safe work environment
  • Strong leadership, collaboration, and cross-functional team building skills
  • Ability to teach and train others
  • Skilled in managing a project schedule, progress, risks, and communications to stakeholders
  • Openness to change and flexible for shifting project priorities
  • Skilled in meeting facilitation and effectiveness
  • Understanding of manufacturing and supply chain systems, including production planning, scheduling, and material management
  • Curiosity and creative problem solving
  • Adaptability required as work schedule may change based on business needs
  • Criminal background check required
  • Other duties as assigned

Responsibilities

  • Defines complex internal/external problems by collecting data and information to understand how normal work-is-done
  • Interacts with cross-functional stakeholders to understand work-flow impediments and other wastes throughout the business. Selects appropriate lean tools to improve them. Ensure effective sustainment of results to close gaps to targets.
  • Lead cross-functional workshops, kaizen events
  • Maintains continuous improvement tools, templates, dashboards and internal communications
  • Develops and deploys formal, informal, and on-the-floor training on continuous improvement principles and improvement practices
  • Provide on-the-floor training of manufacturing and lab staff on human factors & system safety (aka human & organizational performance)
  • Supports visual daily management (Tier meeting), including development of leading indicators
  • Manage site project funnels and frameworks, including designing dashboards, templates, tools
  • Leads proactive-learning activities such as After Action Reviews

FAQs

What is the job title for this position?

The job title is Continuous Improvement Specialist I/II/III.

Where is the location of this job?

The job is located in Lexington, MA.

What does the Continuous Improvement Specialist do?

The Continuous Improvement Specialist is responsible for supporting continuous improvement initiatives in daily operations, implementing ideas, and deploying continuous improvement principles across the organization.

What qualifications are required for this role?

A Bachelor's Degree in a relevant science or engineering discipline and 2-5 years of biopharma manufacturing experience are required.

What experience is essential for applicants?

Applicants must have experience with lean manufacturing methodologies, proficiency in MS Office, skills in data visualization, and experience with quality system compliance.

Is training provided for continuous improvement principles?

Yes, the role involves developing and deploying training on continuous improvement principles and practices.

Are there physical demands associated with this job?

Yes, the role involves frequent standing, lifting, and working in a GMP clean room environment with personal protective equipment.

Is travel required for this position?

Yes, the position requires the ability to travel domestically about 5-10% of the time.

Are there opportunities for professional development?

Yes, employees are encouraged to engage in continuous improvement activities and training, which contributes to their professional growth.

Does Genezen offer benefits to employees?

Yes, Genezen offers a range of benefits including paid vacation days, healthcare plans, 401(k) plans with company match, and more.

Is Genezen an equal opportunity employer?

Yes, Genezen is an Equal Opportunity Employer and participates in EVerify.

Can the job responsibilities change?

Yes, the job description does not restrict management’s right to assign or reassign duties and responsibilities at any time.

Can Genezen sponsor work visas for this position?

No, Genezen is interested in candidates eligible to work in the United States but is not able to sponsor visas.

image

Genezen

Accelerating the Pace of Cell Therapy CMC and Clinical Development

Science & Healthcare
Industry
51-200
Employees
2014
Founded Year

Mission & Purpose

Genezen is a biotechnology company specialising in cell and gene therapy manufacturing. They focus on providing comprehensive services for the production of advanced therapies, including vector production and cell processing. Genezen’s approach combines expertise in cutting-edge technology with rigorous quality standards to support the development and delivery of innovative treatments. Their goal is to advance therapeutic solutions and facilitate the progress of gene and cell-based therapies through their state-of-the-art facilities and customised support.