Sr Mgr Product Quality Integrator

• Job title Sr Mgr Product Quality Integrator
• Function Quality
• Sub function Quality Assurance
• Category Senior Manager, Quality Assurance (P8)
• Location Horsham / Malvern / Spring House / United States of America
• Date posted Jul 09 2026
• Requisition number R-085873
• Work pattern Hybrid Work

This job posting is anticipated to close on Jul 23 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

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Job Description:

The Senior Manager, Product Quality Integrator, Launch and Grow Biotherapeutics has end-to-end accountability for the quality strategy and quality aspects from Early Development through commercialization in Launch and Grow for an assigned group of large molecules (biological) products.

Main responsibilities include but are not limited to:

• Represents Global Quality on the Chemistry, Manufacturing, and Controls (CMC) and Value Chain (VCT) Teams. Serves as liaison between VCT and Analytical group. Serves as the single point of Global Quality contact.
• Ensures Quality stage gate deliverables are achieved.
• Quality reviewer/approver of health authority submissions (i.e., IND, IMPD, BLA, NDA, MAA) and associated HA questions on the filings. Approves filings and questions for secondary filings. Support PAI and agency audits for the product(s) assigned.
• Defines and oversees the necessary QA resource for global and local QA of his or her assigned products.
• Leads a comprehensive Quality new product integration team that assures Quality throughout clinical, DS, DP, FF & device: development through launch.
• Leads a comprehensive Quality Sub team that assures Quality throughout clinical, DS, DP, FF & device:
  • Ensures product quality development through Launch and Grow stage.
  • Supports the sites, represents the sites on CMC and VC teams.
  • Supports QA communication/issue resolution with External Manufacturers and Business Partners, as applicable.
  • Ensures patients get the right quality products
• Ensures standard Global Quality processes (new product introduction processes and norms) are used across sites and facilitates communication throughout Global Quality.
  • Manages preparation of the PPQS in advance of Review Board and Executive Management Review.
  • Supports preparation of the criticality analysis per schedule.
  • Ensures complaints are well managed, issues are understood, and addressed as necessary. Participate in product safety management teams to present Product Quality Complaints trends and topics. Coordinates and/or owner of complaints trend signal investigations.
  • Partners with Product Quality Owner (PQO) Value Optimize & Late Stage to complete Transfer of Ownership activities.
• Represents Global Quality on the Value Chain Teams (VCT).
  • Maintains the flow of communications between Global Quality and VCT teams.
  • Brings Quality issues to the VCT and assists with prioritization of projects and with key product decisions.
  • Supports the business continuity process including VCT strategy and BCP projects.
  • Reviews Proactive Product Quality Scans with the VCT and assures appropriate mitigating actions are defined there.
  • Prepare quality sections of Product Strategy and End-to-end Value Chain Mapping.
  • Participate in the F2F VCT meetings on PSR and VCM finalization and project prioritization.
  • Align and interface the JSC Product Strategy with other existing strategies: J&J corporate strategies, commercial strategies, R&D strategies, regulatory strategies, etc.
• Presents project updates to QM for Global Quality alignment.
  • Escalate issues when appropriate. Works with the cross functional/site teams to coordinate and hold Escalation meetings, minutes archival, follow up on actions.
  • Participates and actively engages on IMTs. Supports field/recalls as needed.
• Drives Decision making and Problem Solving:
  • Drives/coordinates decisions and makes decisions on behalf of Global Quality including sites.
  • Gives input to the development of new strategies and implements and deploys strategies. Aids in the creation of product portfolio guidelines on the control strategy for new 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.
  • Aware that quality decisions made at any time during the development of new products can be revisited years later during regulatory inspections and reviews.
  • Provides Quality structure, direction and decision making to the teams (Quality, CMC and VC Team) in situations of medium risk, uncertainty and ambiguity.
  • Expected to bring creative solutions to define a compliant quality strategy with flexibility for business needs and more complex L&A deals, thus providing the best total value to the company.

Qualifications Required

• A minimum of a bachelor’s degree (or University equivalent) with a major or concentration in one of the following: Pharmacy, Biology, Biochemistry, Biotechnology, Engineering, or a similar technical/scientific degree concentration
• A minimum of 8 years’ experience in the pharmaceutical, or biotechnology industry
• Knowledge in cGMP standards, policies and procedures
• Demonstrated ability to work across organizational boundaries through presenting, influencing, negotiation and partnering
• Ability to quickly assimilate new technologies, perform risk assessment and develop action plans

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The anticipated base pay range for this position is :

Additional Description for Pay Transparency: