Senior Quality Engineer

Job Description

You’re not the person who will settle for just any role. Neither are we. Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference. Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands. In this role, you’ll help us deliver better care for billions of people around the world. It starts with YOU. 

The Senior Quality Engineer participates in the validation of new and existing equipment and processes, application development and maintenance of quality standards of both in-process materials and finished products, ensures the application of approved test methods and develops instructions for use and calibration of equipment, testing, management, control and monitoring of the system of corrective actions and handling of non-conforming material for
process improvement, application and monitoring of environmental control requirements, performs adequate training in them to all personnel involved.

In this role, you will:

Review and approve validation protocols for new and existing equipment through the use of approved procedures to ensure their quality. Continue with the best practices and safety guidelines in the area, in order to achieve KC's objectives.Participate in the planned inspections and investigations of accident incidents for the EHS system; Follow the requirements of the environmental policyAssisting the Manager of Quality Assurance in the planning, organization of the activities and work carried out in the quality department, such as the systems put into practice and maintaining the standards according to the FDA and the GMP, for the quality and conformation of the product.Contribute by ensuring the maintenance of the required certifications, ensuring the availability of the product in the global market. This includes ISO 13485 and EN46002Coordinate, review and apply the methods of material and process inspection through the use of approved procedures to ensure their quality in all stages of manufacturing.Review, verify, develop and validate the test methods for products and / or processes by using applicable procedures to ensure that they meet the established requirements.Handle, execute and control the calibration and test equipment based on the requirements to ensure that the tests are performed with reliable measurements based on the standards.Contribute to the investigation of the client's claims through the use of the claims system established for the generation of the RCA and AP, as well as contributing to maintain the responses to customers in a timely manner.Comply with all security requirements that have been established as well as active participation in all development and monitoring activities of the EHS system.Analyze the necessary statistics to be able to monitor the non-conforming product, the DPM of receipt, process and packaging with trends that allow us to determine its capacity.Ensure compliance with the requirements of quality standards and regulations (ISO-13485, FDA / GMP, and others applicable), in accordance with established policies and procedures.Lead the improvement projects to processes with the greatest impact on the plant, relying on the quality engineering group to comply with all the corresponding plans.

About Us

Huggies®. Kleenex®. Cottonelle®. Scott®. Kotex®. Poise®. Depend®. Kimberly-Clark Professional®. You already know our legendary brands—and so does the rest of the world. In fact, millions of people use Kimberly-Clark products every day. We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.

At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact. We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity. It’s all here for you at Kimberly-Clark.

Led by Purpose. Driven by You.

About You

You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring.  You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.

You love what you do, especially when the work you do makes a difference. At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results. When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and the business.

In one of our technical roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center. To succeed in this role, you will need the following qualifications:

Professional degreeEnglish - Advanced level.4+ years in the area of quality and experience in regulations for medical devices.Statistics (Tools of quality control, Graphical analysis, Capability Analysis, DOE, ANOVA, R&R).ISO 13485 standard, GMP.Knowledge of the EHS; Sampling systems by AQL or similar.

And finally, the fine print….

For Kimberly-Clark to grow and prosper, we must be an inclusive organization that applies the diverse experiences and passions of its team members to brands that make life better for people all around the world.  We actively seek to build a workforce that reflects the experiences of our consumers.  When you bring your original thinking to Kimberly-Clark, you fuel the continued success of our enterprise. We are a committed equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity, age, pregnancy, genetic information, citizenship status, or any other characteristic protected by law.

The statements above are intended to describe the general nature and level of work performed by employees assigned to this classification. Statements are not intended to be construed as an exhaustive list of all duties, responsibilities and skills required for this position.

Employment is subject to verification of pre-screening tests, which may include drug screening, background check, and DMV check.

Veterans and members of the Reserve and Guard are highly encouraged to apply.

This role is available for local candidates already authorized to work in the role’s country only. Kimberly-Clark will not provide relocation support for this role

Grade 10/ P3

Primary LocationNogales AFC - Plant 2476

Additional Locations

Worker TypeEmployee

Worker Sub-TypeRegular

Time TypeFull time