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Kimberly-Clark

Global maker of personal care products

Lead Process Engineer

Process EngineeringConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's or advanced degree in an Engineering or Scientific discipline.
  • At least 4 years of experience, or a combination of an advanced degree and a lesser amount of relevant experience.
  • Strong working knowledge and background in the safe operation of high-speed converting equipment.
  • Experience working with external technical service providers and sourcing and supply vendor partners.
  • Analytical skills to design experiments and collect and assess data to support technical recommendations.
  • Practical experience and knowledge in installation qualification, operational qualification, and performance qualification, and understanding of process validation.
  • Ability to effectively influence alignment to technical recommendations.
  • Ability to work in a matrix organization and collaborate across functions and departments.
  • Ability to effectively communicate to individuals and groups.
  • Ability to work under normal office conditions.
  • Ability to travel by air and ground as necessary up to 25% of the time.

Responsibilities

  • Lead and support process development and implementation of Adult and Feminine Care product formats and assets from conception through commercialization.
  • Work closely with product, materials, engineering leads, quality, regulatory, and product safety to provide functional guidance in the design, development, or optimization of converting equipment and processes to meet unit objectives and comply with design control requirements for Class 2 medical device manufacturing.
  • Provide functional guidance in the design, development, or optimization of converting equipment and processes to meet unit objectives.
  • Acquire and transfer technical knowledge in Adult and Feminine Care manufacturing.
  • Work closely with the process validation leader to identify and lead process characterization, support process validation, and deliver documentation for proper process design control.
  • Apply engineering solutions to address root causes of complex issues.
  • Document and support required process-related documentation for design review steps of the design control process for Class 2 medical devices, supporting FDA procedures and requirements.
  • Manage project responsibilities typically ranging from $0.5 million to $5.0 million, with project teams of 3 to 15 people and single or multiple projects, as assignments vary.

Desired Qualifications

  • Experience in both Kimberly-Clark plant and staff roles, or equivalent experience in an outside industry.

About the Company

Kimberly-Clark

Global maker of personal care products

Kimberly-Clark makes and sells everyday hygiene and personal care products worldwide, including Kleenex tissues, Huggies diapers, Scott paper products, Kotex feminine care, and Depend incontinence products, plus workplace solutions through K-C Professional. Products are produced at large-scale manufacturing facilities and sold through retailers to consumers, as well as to businesses and healthcare facilities. It differentiates itself with a global brand portfolio, wide distribution, and a commitment to sustainability and social impact. Its goal is to provide essential hygiene products at scale while advancing ESG initiatives, such as renewable energy use and sanitation programs.

Company size
10,001+
Company stage
IPO
Headquarters
Irving, TX
Founded
1871

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