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Inspector Complaint Vigilance Ii
2 semanas atrás
**INSPECTOR COMPLAINT VIGILANCE II**-2307008216W
Description
Kenvue is currently recruiting for a [INSPECTOR COMPLAINT VIGILANCE]. This position reports into LATAM Complaint Vigilance Manager] and is based at [São José dos Campos - SP]
**Who We Are**
At Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue), we believe there is extraordinary power in everyday care. Built on over a century of heritage and propelled forward by science, our iconic brands—including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® —are category leaders trusted by millions of consumers who use our products to improve their daily lives. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
Join us in shaping our future-and yours.
**What will you do**
Collaborates with Call Centers, Medical Safety, Marketing, Internal affiliates, External sites, and other business partners to ensure the integrity, consistency, compliance, and alignment of the end-to-end complaint vigilance process. Can assists with developing training presentations for complaint vigilance. This position will support the Triage function in LATAM & NA for consumer products and might support other Geographical regions as needed. This role reports directly to the LATAM Complaint Vigilance Manager and dotted line for the NA Complaint Vigilance Manager.
Participates directly or indirectly on regional and global complaint vigilance initiatives, and project teams to develop, consolidate, and/or improve complaint vigilance and related/interfacing processes.
**Responsibilities**:
- Contribute to Complaint Vigilance reports and presentations per established procedures. Prepares and issues meeting minutes, ensures action items are completed
- Assists with/participate in various projects and activities related to Central Complaint Vigilance process and system implementations and improvements, supports the identification of continuous improvement activities. Supports training and onboarding of peers, when necessary.
- Monitors Complaint Records in PQMS to ensure standard process is being followed and complaints are closed as required. Compile product and lot-specific complaint trending data and complaint closure metrics as requested. Supports internal and external audits and inspections as a Subject Matter Expert and backroom roles as needed. Support with Field sample room activities. Support with Field sample room activities.
**Qualifications**:
**What we are looking for**
**Required Qualifications***
- A minimum of a bachelor’s degree is required. A focus in Science, Engineering, or related discipline is preferred.
- A minimum of 2 years of related experience including Quality Assurance and/or Quality Control is required.
- Experience working in pharmaceutical, medical devices or other related or highly regulated industry is required.
- Demonstrated knowledge and expertise in quality processes and regulatory requirements is required.
- Able to write, read and communicate in English.
***
**Other Preferred Experiences**:
- Ability to write, read and communicate in Spanish is an asset.
- A customer-oriented profile and ability to balance processes execution excellence maintaining an innovative mindset is an asset.
- Experience working in highly regulated environment with agencies such as FDA, ANVISA, INVIMA, COFEPRIS, etc is an asset.
- Experience supporting manufacturing, packaging, and development operations is preferred.
- Experience supporting many/all aspects of the complaint vigilance life cycle for pharmaceutical, device, and /or cosmetic products is preferred.
- Experience with one or more technologies supporting complaint handling preferred.
- Experience in the creation, update, and management of complaint files from complaint identification through closure is desired.
- Expertise with root cause analysis techniques including but not limited to: Brainstorming, data analysis and collection tools, 5 Whys, Fishbone (Cause and Effect), FMEA, and DMAIC preferred
- Experience with tools and techniques supporting qualitative risk analysis including but not limited to: Probability and impact assessment (likelihood of recurrence and potential effect), probability and impact matrix (risk ratings, rating rules), and risk categorization (by root causes, other qualifiers) is prefered
- Experience with systems and tools supporting analysis and reporting preferred.
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Primary Location Latin America-Brazil-São Paulo-São José dos Campos
Organization J&J Brazil
Jo
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