*job function*:
quality
*job sub function*:
quality assurance
*job category*:
professional
*all job posting locations*:
ciudad juarez, chihuahua, mexico
this position is related to support i-prevent improvement projects and active participation during mes implementation.
Impact: unable to achieve the goals and objectives committed during 2025
share point request id: 240
*about medtech*
fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
*about cardiovascular*
fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of cardiovascular? Ready to join a team that’s reimagining how we heal? Our cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (afib) patients.
*we are searching for the best talent for quality engineer ii to be in ciudad juarez, mexico.*
*responsabilities*:
in accordance with all applicable federal, state and local laws/regulations and corporate
johnson & johnson, procedures and guidelines, this position:
- primary responsibilities include assisting in a supporting role on new product development,
sustaining and supply chain quality projects. Assist in the development of effective quality
control and associated risk management plans.
- write process and product validation protocols and reports, equipment qualifications,
engineering change orders.
- use statistical tools to analyze data, make acceptance decisions, and improve process
capability (six sigma, spc, doe).
- help to ensure that development activities follow design control requirements, product is tested
per applicable standards, european essential requirements are met per the mdr, and product
is properly transferred to manufacturing.
- provide support in quality improvement opportunities as appropriate to legacy products,
continuous improvement, and customer satisfaction
- assist in planning necessary to ensure effective product acceptance. This includes, but is not
limited to, inspection instructions, equipment and gage requirements, and sampling plans.
- support vendor audits as technical lead as needed and support supplier quality as franchise
quality representative as appropriate.
- support nc, capa, internal audit, training and qs activities as needed and ensures
compliance to all applicable due dates.
- initiate and investigate corrective and preventative actions (capa) as appropriate.
- assist in complaint analysis as appropriate.
- assist regulatory affairs in developing submissions for process changes, inspection changes,
and new processes/devices as necessary.
- moderate exercise of judgment is required on details of work and in making selections and
adaptations of engineering alternatives.
- supervisor or sr./staff/pmgr screens assignments for unusual or difficult problems and reviews
techniques and procedures to be applied on non-routine work.
- receives general direction on new aspects of assignments.
- performs work which involves conventional types of plans, investigations, surveys, structures, or
equipment with relatively few complex features for which there are precedents.
- responsible for communicating business related issues or opportunities to next management
level.
- responsible for ensuring subordinates, if applicable, follow all company guidelines related to
health, safety and environmental practices and that all resources needed to do so are available
and in good condition.
- responsible for ensuring personal and company compliance with all federal, state, local and
company regulations, policies, and procedures.
- performs other duties assigned as needed.
- responsible for communicating business related issues or opportunities to next management
level
- responsible for following all company guidelines related to health, safety and environmental
practices as applicable.
- for those who supervise or manage a staff, responsible for ensuring that subordinates follow all
company guidelines related to health, safety and environmental practices and that all
resources needed to do so are available and in good condition, if applicable
- responsible for ensuring personal and company compliance with all federal, state, local and
company regulations, policies, and procedures
- performs other duties assigned as needed
*experience/ education/ qualifications*:
- bachelor’s degree in a related field, along with minimum 2 - 4 years of quality, manufacturing, or
- research and development experience in a medical device or other regulated industry is required.
- master’s degree is preferred.
- bilingual: english / spanish, preferab