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Senior Manager, Product Quality Integrator
Senior Manager, Product Quality Integrator-March 2024
Cork
Mar 29, 2026
About Senior Manager, Product Quality Integrator

  Senior Manager, Product Quality Integrator - 2406161137W

  Description

  For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

  We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.

  That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

  Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”!

  Key Responsibilities

  The Senior Manager, Product Quality Integrator has end-to-end accountability for the quality strategy and quality aspects for new products from Early Development through commercialization in Launch and Grow for an assigned portfolio of products.

  Represents Global Quality on the CMC and Value Chain Team (VCT). Serves as liaison between VCT and Analytical group. Serves as the single point of Global Quality contact. Drives communication with all Q&C partners.

  Ensures Quality achievements and Quality stage gate deliverables are achieved. Quality reviewer/approver of health authority submissions (i.e.,BLA, NDA, MAA) and associated HA questions on the filings. Support PAI and agency audits for the product assigned.

  Defines and coordinates the vital QA resource for global and local QA of their assigned products.

  Leads a comprehensive Quality Sub team that assures Quality throughout clinical, DS, DP, FF & device.

  Supports QA communication/issue resolution with External Manufacturers and Business Partners, as applicable.

  Ensures standard Global Quality processes (new product introduction processes and norms) are used across sites and facilitates communication throughout Global Quality.

  Demonstrate knowledge of product launch (new filing, launches, regulatory impact, basic of clinical trials management) and supply network planning and supplier management.

  Gives input to the development of new strategies. Implements and deploys strategies. Aids in the creation of product portfolio guidelines on the control strategy for development products which will influence the development strategy and the total quality cost during commercial production. These include decisions for Design for manufacturability, quality by design versus the cost of development, time to market.

  Qualifications

  Education and Experience :

  Minimum of Master / Bachelor´s degree in a scientific field, and crucial you have excellent scientific & technical capabilities based on combination of qualification and minimum 7 years of experience in a regulated industry.

  Experience in at least one quality related subject area is a requirement including, but not limited to, manufacturing and packaging operations, analytical and micro testing and commercial distribution, basic knowledge of new product development.

  Experience within ADC (Antibody Drug Conjugates) is a nice to have.

  Demonstrate medium knowledge of financial management, budgeting, and cost benefit calculation.

  Fluent in English.

  Leadership & Behavioral Competencies

  Consistent track record in successful leadership role in building, inspiring and leading a global virtual team and influencing partners across a cross-functional organization structure.

  Well-developed leadership skills and shown efficiency to influence others in a cross-functional environment.

  Excellent communication and organization skills required. Excellent presentation, written and oral communication skills as well as the ability to meet targets. Strong attention to detail and analytical / problem-solving skills

  Business oriented, independent and driven.

  We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

  Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

  Primary Location Europe/Middle East/Africa-Belgium-Antwerp-Beerse

  Other Locations Europe/Middle East/Africa-Switzerland, Europe/Middle East/Africa-Italy-Lazio-Latina, Europe/Middle East/Africa-Netherlands-South Holland-Leiden, Europe/Middle East/Africa-Ireland-Cork-Cork, Europe/Middle East/Africa-Belgium-Antwerp-Geel

  Organization Janssen Pharmaceutica N.V. (7555)

  Job Function Quality Systems

  Req ID: 2406161137W

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