Job Information
J&J Family of Companies QUALITY OPERATIONS MANAGER (SEGUNDO TURNO) in Juarez, Mexico
QUALITY OPERATIONS MANAGER (SEGUNDO TURNO) - 2406212493W
Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
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 QUALITY OPERATIONS MANAGER (2NDO TURNO) to be in Juarez Chih., MX Salvarcar Plant
Purpose:
Plans, coordinates, and directs the quality assurance programs designed to ensure continuous production consistent with the established standards through the following responsibilities, either personally or through his/her subordinates.
You will be responsible for:
Leads or support quality improvement initiatives, such as the characterization of processes and products that leads to continuous improvements / cost.
Revision / analysis of the effectiveness of PDCA, Six Sigma, Kaizen, Lean Techniques and other tools and improvement programs.
Performs benchmarking in order to develop more effective methods to improve quality.
Establishes and formulates the quality metrics to maintain the quality assurance objectives and alignment with the objectives of the plant.
Supports the development of quality engineering and the compliance with the quality with the adequate abilities for the introduction of new products and product life cycle management.
Promotes and supports the implementation of quality, product and process improvement projects.
Revises and approves Engineering Change Orders (ECOs).
Evaluation, monitoring and analysis of the quality costs in order to maintain a quality system according to the medical industry standards.
Revises / analyzes if the current products and processes (including performed actions or decisions) comply with the regulations, such as the QSRs, ISO 13485, etc.
Leads the preparations activities for regulatory agencies audits, including the active participation as SME or Escort (for example: FDA, JJRC, BSI, etc.).
Revises and approves the answers to internal and external audit observations ton ensure the compliance with the internal procedures and applicable regulations
Establishes and properly maintains the required documentation of quality assurance activitiesand/or quality systems.
Ensures the performance of periodical audits of the line to evaluate GMPs, production controls, lot segregation and process audit according to JJPS.
Checks the results of the audits of the area to ensure that the corrective and preventive actions are adequate.
Defines, monitors and administers the central budget of the department/cost
Collaborates with NPI and with the operations and engineering departments to develop, conduct and approve validation strategies of products and processes.
Directs and attends to Revision meetings of NCs as a member of MRB.
Revises and approves the investigations, bounding, documentation, revision and approval of the non-conformities (NCs), preventive and corrective actions (CAPAs), customer complaints and escalation of quality problems when applies.
Responsible and owner of the identification of material, material segregation, classification of the types of defects, including the successful application of these techniques in the day-to-dayin manufacturing.
Provides direction and assigns resources for the resolution of complex problems (technically) associated to the manufacturing process at a local or franchise level.
Revises and approves process validation strategies.
Ensures the realization of periodical maintenance and revision of the CTQs in the manufacturing process to guarantee the continuous satisfaction of the customer.
Approves the revision and maintenance of PFMEAs, Quality control Plans, Process Instructions and additional manufacturing documents.
Provides support to the development and proper implementation of process monitoring and control methods consistent with the process/product risk level.
Promotes the use of innovative tools for the timely detection and mitigation of risks. Determines the effectiveness of these techniques in the improvements previously implemented.
Responsible and owner of the risk assessment evaluation including the realization, documentation, revision, maintenance of current risk and documentation of the risk assessment such as FMEA of the process given to changes in the product/process
Collaborates with the quality leaders to identify the required quality engineering skills andcompetences that allow the execution of the strategic vision.
Performs the strategic planning with the site leaders and with the product engineering team. Works in team with other functions to establish the priorities of the business and assignment of resources.
Provides supervision, mentoring, coaching, performance revision, development plans andplanning of the succession for others (when applies).o Responsible for communicating business related issues or opportunities to next managementlevel
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
As minimum, Bachelor, preferably in engineering: Mechanical, Electrical, industrial or applicable science.
Master or Doctorate in applicable sciences, preferable.
Advanced English level
8 to 10 years of work experience, or demonstrated performance.
Use of computer packages.
Ability to effectively deal and negotiate with representatives of various governmental agencies and auditing agencies.
Excellent communication skills in English, spoken and written.
Ability to perform active involvement in the solution of problems and resolution of problems, preferably.
Capacity to solve problems providing good judgment is highly desired.
Certifications such as CQA, CQE, CQM (preferably), CBA, MBB or BB are a plus.
Primary Location Latin America-Mexico-Chihuahua-Juarez
Organization Cordis de Mexico S.A. de C.V. (8286)
Job Function Quality Assurance
Req ID: 2406212493W