Job Opportunities in Colombia
September 2, 2024
Kenvue
Cali
OTHER
QUALITY SUPERVISOR (Fixed Term 12 months)
Description
Kenvue is currently recruiting for:
Specialist, Quality Systems & Compliance
This position reports into Quality structure based at Kenvue SJC, BRAZIL site, but is based in Cali, Colombia.
Who we are
At Kenvue, part of the Johnson & Johnson Family of Companies, 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.
What will you do
The Project Quality Specialist will be responsible for Project management in the Quality Strategic Office organization, reporting to Regional Quality Project Manager . This role will be responsible for delivering quality plans across the region in order to achieve project separation milestones in several workstreams such as regulatory licensing , inspection readiness, quality management system adequacy, product label & codes change management, documentation updates including change control coordination and others.
Kenvue is currently recruiting for:
Specialist, Quality Systems & Compliance
This position reports into Quality structure based at Kenvue SJC, BRAZIL site, but is based in Cali, Colombia.
Who we are
At Kenvue, part of the Johnson & Johnson Family of Companies, 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.
What will you do
The Project Quality Specialist will be responsible for Project management in the Quality Strategic Office organization, reporting to Regional Quality Project Manager . This role will be responsible for delivering quality plans across the region in order to achieve project separation milestones in several workstreams such as regulatory licensing , inspection readiness, quality management system adequacy, product label & codes change management, documentation updates including change control coordination and others.
Key Responsibilities
- Take lead on quality projects related to separation program (spin off)
- Build collaboration across different functional areas with business partners
- Build alignment with Sponsor, aligns Core and Extended team to deliver the Final Project Objectives
- Develop, manage, and maintain up-to-date Project plans through collaboration with cross functional team members
- Ensure seamless coordination across all workstreams, fostering cross-functional collaboration to maintain synchronization and meet project deliverables following quality requirements.
- Provide project governance activities across all workstreams such as: resource management, risk management and scope management
- Change control opening and management to track all Gx P related activities on-time and in compliance with Kenvue procedures and country-specific quality/regulatory requirements
- Manage risks effectively, identify potential problems early, and assist in resolving or raising issues as appropriate.
- Effectively prepare and communicate project status updates regarding project milestones, deliverables, and risks within the workstreams and for the broader project
Qualifications
What We Are Looking For
What’s In It For You
What We Are Looking For
Required Qualifications
- Bachelor's degree in pharmacy, chemical engineering or equivalent technical field required
- A minimum of 7 (seven) years of relevant professional work experience in the field regulated health industry : Cosmetic/Device/Drug regulations environment
- Experience in Quality systems, audits/inspections and regulatory affairs
- Proven experience in leading virtual within dynamic settings in a regional /cross-functional environment. Ideally 3-5 years.
- Project management certification is preferred
- Solid technical (quality/regulatory) knowledge
- Understanding of LATAM Gx P regulations applicable for cosmetics, devices, pharmaceutical industries.
- Advanced English
Desired Qualifications /Technical competences
- Ability to lead and motivate teams
- Excellent problem-solving and conflict resolution skills
- Consistent track record to work cross-functionally
- Flexibility and adaptability to thrive in a multifaceted environment
- Attention to detail and a drive for ensuring data accuracy and integrity
- Strong demonstrated collaboration, sense of urgency, analytical, influencing skills
- Understanding of project controls and scheduling
- Must be able to develop and maintain relationships/partnerships and to work collaboratively
What’s In It For You
- Competitive Benefit Package
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
- Learning & Development Opportunities
- Employee Resource Groups
- This list could vary based on location/region
Primary Location Latin America-Colombia-Valle del Cauca-Cali
Job Function Quality (Generalist)
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