COMPLAINTS ANALYST I - FIXED TERM 24 MONTHS - 1 OF 2

At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity.
That starts by creating the world’s healthiest workforce.
Through cutting-edge programs and policies, we empower the physical, mental, emotional, and financial health of our employees and the ones they love.
As such, depending on location and subject to local legislation, candidates offered employment may be required to show proof of COVID-19 vaccination or, in certain countries, secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work.
If you are invited to interview for the position, your recruiter will advise on the vaccine requirement status in your geographic location.  At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose.
to transform the history of health in humanity.
Diversity & 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.
At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives.
In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions.
We are in this for life.
We are changing the trajectory of human health, YOU CAN TOO.
Please visit https://www.
njmedicaldevices.
om/es-419 for more information.  Biosense Webster, Inc.
 is recognized worldwide as a leader in the science behind the diagnosis and treatment of cardiac arrhythmias.
Guided by the needs of electrophysiologists and cardiologists, Biosense Webster has pioneered innovative technological advancements for more than 30 years.
Some might call this quite a heritage.
At Biosense Webster, we say it's just the beginning.
For more information, visit www.
iosensewebster.
om  We are searching for the best talent for Complaints Analyst I to be in Juarez.   Purpose:   Under general supervision, the Complaints Analyst I will be responsible for maintaining the quality processes associated with product complaint handling, procedures, and controls to ensure that all complaints are processed in accordance with established company procedures and worldwide regulations and standards.
This individual will review documentation from incoming calls, faxes, and emails from all areas of the world.
This individual will also obtain adequate information to ensure proper documentation, investigation (including product testing), and closure of each complaint, in order to make and document sound regulatory reporting decisions/justifications for worldwide reporting.
The individual applies standard practices and techniques in specific situations, adjusts and correlates data, recognizes discrepancies in results, and follows operations through a series of related detailed steps and processes.  You will be responsible for.
·       Under general supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position.
Activities related Complaint Handling:   ·       Responsible for complaint management (Entry, Follow ups, Product Analysis, Closure, etc.).  ·       Possess a thorough understanding of the complaint database.  ·       Understands basic principles, theories, concepts, and techniques related to customer complaints.  ·       Establish reports for the prompt review of new complaints, regulatory reporting decisions, and follow-up.   ·       Develop, establish, prepare, and distribute dashboards and reports to assure complaints are processed in a timely manner.   ·       Responsible for coding the event and ensuring that all the required information for a complaint file is obtained and properly documented to make a final regulatory reporting decision.    ·       Evaluates all information from a clinical and technical perspective to ensure appropriate Analysis, Investigation, Root Cause, and Quality Engineering review is documented prior to.  ·       Responsible for tracking, receiving, and shipping products as needed.   ·       Execute the complaints analysis and failure investigations daily and document the analysis results and relevant information to the Med Watch reports in the assigned product families.   ·       Approve the complaints in the assigned product families.  ·       Set up complaint meetings and effectively communicate with worldwide complaint groups, as well as other internal departments such as Marketing, R&D, Customer Service, and Technical Services.  ·       Write customer response letters, as required.  ·       Provide support in the training of the complaints process for new analysts or technicians if the analyst has been identified as a subject-matter expert.   ·       Investigate and develop solutions related to procedures and process issues.
·       May receive technical guidance on complex problems, but independently determines and develops approaches and solutions.   ·       Participate in Quality improvement processes and projects.   ·       Provide support in product transfer and new product development as needed.   ·       Ensure compliance with the company's Quality System policies and procedures and applicable external requirements and standards, including FDA, ISO , CMDCAS, PMDA and other worldwide regulatory agencies, Johnson & Johnson Environmental, Health & Safety Practices, and other applicable standards as pertains to medical devices.  ·       Responsible for communicating business related issues or opportunities to next management level.   ·       Responsible for ensuring personal and Company compliance with all Federal, State, Local and Company regulations, policies, and procedures.  Qualifications Requirements.
·       Completed BS, preferably in computer science, engineering, physical, biological, or natural sciences.   ·       Preferably with 0 to 2 to years of quality, manufacturing, or regulatory experience in medical devices or other regulated industry.   ·       Preferably American Society for Quality (ASQ) certification, Six Sigma experience, and/or knowledge of Process Excellence tools.  ·       Critical thinking and investigation skills are required.  ·       Ability to multitask, including ability to understand customer requirements, retrieve relevant information, and provide responses satisfactorily and with immediacy is required.   ·       Employee must be able to effectively prioritize and manage multiple activities and responsibilities.   ·       Ability to understand and follow complex written procedures is required.
Candidates should be familiar with general quality management system concepts, including good documentation practice (GDP), corrective and preventive action (CAPA), and document change control practices.   ·       Ability to function in a team environment and deliver on team objectives is required.
Ability to influence and drive change.
Preferably, project management and/or process mapping experience.   ·       Communication Skills.
Strong written and verbal communication skills.
Must be highly proficient in reading, writing, and speaking the English language.
Preferably, presentation skills.   ·       Professional demeanor on the phone and in email is required.
Technical writing is a routine part of this position.
Strong attention to detail is required.   ·       Required Computer Skills.
Familiarity with computers and Windows-based PC applications.
Ability to learn and manipulate complex computer system applications is required.
Experience with word processor software (e.
.
Microsoft Word) and internet browsers (e.
.
Internet Explorer) is required.
Prefer experience with Enterprise Complaint Management System (ECM).   ·       Preferably, prior medical device complaint handling experience, or knowledge of medical.