**Franchise Quality Manager - R&D Ops | São José dos Campos**-2307004958W
Description
Johnson & Johnson New Planned Consumer Health Company is currently recruiting for a Franchise Quality Manager - R&D Ops to be based in São José dos Campos/Brazil and being responsible to provide direction and oversight for RD&E quality systems and R&D Q&C personnel, to ensure an integrated and comprehensive risk-based quality monitoring system for GMP is developed, implemented, and maintained within RD&E teams.
**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?
**
- Lead compliance projects to promote continuous improvement within R&D community and processes, and ensure innovative compliance solutions are identified, when possible, to address project and process challenges.
- Lead and/or support management reviews and Q&C dashboard processes.
- Ensure timely and accurate actions are implemented and documented for Escalation, NC, CAPA, Change Control and Audit processes.
- Participate on R&D Compliance committees (i.e.
Management Review, Project Meetings) in the region, and escalate issues appropriately.
- Interact and provide guidance to R&D leadership and professionals on GMP regulatory requirements.
- Develop and implement programs designed to increase employee awareness and knowledge of compliance requirements/policies.
- Review and approve standard operating procedures and GMP documentation within R&D Compliance processes and R&D processes.
- Interpret regulations and J&J standards to provide risk analysis guidance and make decisions about R&D GxP activities properly.
- Lead and/or support internal and external Q&C audit program, JJRC assessments, regulatory inspections, and Inspection Readiness Program.
- Lead R&D Q&C personnel, assuring they have appropriated qualification to perform their tasks & responsibilities and development plans to promote their growth.
- Represents department in cross-functional R&D groups and external partnership activities
- Ensure proper approach for product risk management, providing directions to R&D personnel.
**Other responsibilities include?
**
- Accountable for delivering the department objective as assigned by leadership.
- Possesses a high degree of independent judgment which directly impacts the operational results of the department.
- Support investigations, CAPAs, data analysis, change controls, trends and risk monitoring for Quality and Compliance topics.
- Provides guidance and coaching to direct reports based on the organizational and political objectives of the company.
Promotes and supports the development of Q&C people through the conversations, including definitions of G&Os, follow up actions, training, feedbacks, participating in local, regional, and global projects, cross training opportunities, Leadership courses among others.
- Supports and Ensures execution of actions and mitigation plans derived from self-assessments, internal audits, Regulatory Inspections and Corporate Audits.
Guarantee the proactive risk management of the quality processes (identification, evaluation, communication, prevention, mitigation).
- Ensures RD&E LATAM is in audit readiness status.
Ensures facilities (including labs, Pilot Plants, Human Use Tests) comply with applicable JNTL and regulatory GxP requirements.
- Ensures strong connection and partnership with other QC pillars, including Quality Make, Source Quality, Quality Systems & Performance and other Segments.
**Qualifications**:
**What do you need to know?
**
- 8+ years of experience in a regulated industry (GMP environment) with BS or equivalent degree in Pharmacy, Chemistry, Biology, Engineering, or related science.
- English is required and Spanish would be a differential
- 6+ years of experience in a regulated industry (GMP environment) with
- Lead auditor certificate is a differential
- 2+ years of experience as a people leader.
- Ability to manage a complex environment, complexes technical discussions and negotiations.
Out of the box thinking to provide solutions for complexes issues, with compliance mindset.
**Location: São José dos Campos**
**Our benefits**
- Health and Dental Plan
- Transportation or parking voucher
- Hybrid work and flexible hours
- Private pension fund
- Gympass
- Discount on the purchase of products, pharmacy aid
- Professional development programs in differe