Sr Quality Engineer
hace 6 meses
Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.
**We are searching for the best talent for SR QUALITY ENGINEER to be in Juarez, Chih., in Plant Independencia.**
**Purpose**:
To perform various technical duties of quality control and quality assurance such as: establish inspection procedures and methods
**You will be responsible for**:
Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
- Monitor all FGQA quality assurance functions.
- Establish and maintain appropriate documentation as required for Quality Assurance activities and the Quality Documentation Systems.
- Develop statistical sampling plans and perform process capability studies.
- Implement process control systems and provide technical support for process validations.
- Provide QS support in Product transfers and new products development.
- Assist in training new engineers, train technicians and supervisors in process changes.
- Perform Complaint analysis investigation as needed.
- Participate in process/ quality improvement projects.
- Support COGs initiatives.
- Responsible for following and administering safety.
- Compliance with safety policies and procedures.
- Follow J&J and EES Records Management Policies for Convenience Information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and third party vendor if applicable.
- Follow J&J and EES Records Management Policies for Convenience Information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and third party vendor if applicable.
- Assist, review & approve non-conformances investigations & non-conforming product dispositions.
- Other responsibilities may be assigned and not all responsibilities listed may be assigned.
- Responsible for communicating business related issues or opportunities to next management level.
- 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
**Qualifications**:
**Qualifications and requirements**:
- Bachelor’s degree in engineering-mechanical, electrical, industrial, preferred, or Applicable science or business degree.
- CQE, CRE, CQA 2-Ratings, GB preferred
- Generally requires (4-6) years related experience.
- Bilingual: English/ Spanish required.
- GMP/ ISO knowledge preferred.
- PC experience.
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