Em Quality Category Lead - Zug, Schweiz - Kenvue

Kenvue

Geprüftes Unternehmen

Zug, Schweiz

vor 4 Wochen

Geschrieben von:

Lena Schneider

beBee Recruiter

Beschreibung

External Manufacturer Quality Category
Leader

Physical Location of Role:
Zug CH

The External Manufacturing (EM) Quality Category Leader is responsible for the quality oversight and coordination of activities related to the EM category. This individual is accountable for developing and leading the execution of a quality strategy which is orchestrated as a part of the overall category for the lifecycle management of EM (new product development, commercialization, monitoring of
This individual will work with the EM teams in Procurement, Make and Quality to develop a comprehensive set of performance measures, implementing across the network of EM suppliers. He/she will also ensure strong, standardized processes are in place to scout and assess potential. EMs for compliance and reliability.
This individual collaborates closely with the regional teams who have responsibility for managing External Manufacturers from a Quality standpoint, ensuring standardization of approach across Kenvue. He/she is also responsible for ensuring appropriate and standardized controls are in place to detect and address the most frequently occurring failure modes for quality at EMs. This role is also

- accountable to ensure the correct framework of legal agreements (in the form of Quality Agreements or similar) are in place to ensure accountability with EMs.

Close collaboration with the regional Quality Systems teams is required to ensure alignment, and that necessary revisions or change management is standardized and cascaded globally. This individual is responsible for presenting data and information to the QHS leadership team to demonstrate the QSMS is in a state of control.

Approximate Percentage of Time Tasks/Duties/Responsibilities
60% - Strategy development for global management of external manufacturers. Ensure that standardized processes are in place to manage EM lifecycle, and executed consistently in the regions.

These processes include the assessment and selection of EM, Quality Agreement templates and frameworks, performance monitoring, reliability interventions, compliance assessment, risk assessment where required, and disengagement when necessary.

20% -Key global partner for Procurement EM category.

Collaborates closely with the global Procurement organization on the standardization of EM assessment, selection, and monitoring in order to develop a network of external partners to deliver Kenvue objectives.

20% -Influence and change management.

This role works closely with regional Quality EM teams to drive consistency across the regions, and ensure that learnings from one region are applied globally.

The organization must be able to balance a rapid pace of implementing transformational change, with the requirement to ensure compliance across all countries where Kenvue operates.

Qualifications:

Required Minimum Education:

Minimum of a bachelor's degree in chemistry, life sciences, engineering, or related field.

Required Years of Related Experience:
Minimum 8 years in pharmaceutical, medical device, cosmetics or similarly

Required Knowledge, Skills and Abilities:

Strong communication and interpersonal skills to collaborate with regional partners
Compliance mindset, to ensure systems are correctly executed at a global level
Fluent English is required
Knowledge of regulatory requirements for drugs, cosmetics, medical devices, and dietary supplements
Experience in Health Authority inspections
Experience in External Manufacturer management

Travel on the Job:
Yes 20%

People Management Experience:
required of at least 2 years

Direct Reports: 7

Primary Location Europe/Middle East/Africa-Switzerland-Zug-Zug

Job Function Quality Assurance