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Senior Analyst, Business Process Quality
Job in
04100, Latina, Lazio, Italy
Listed on 2026-01-25
Listing for:
Johnson & Johnson Innovative Medicine
Full Time
position Listed on 2026-01-25
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst -
Healthcare
Data Scientist
Job Description & How to Apply Below
Learn more at
Job Function
Quality
Job Sub Function
Business Process Quality
Job Category
Professional
All Job Posting Locations
Beerse, Antwerp, Belgium;
Cork, Cork, Ireland;
Latina, Italy;
Leiden, Netherlands;
Schaffhausen, Switzerland
Job Description
At Johnson & Johnson Innovative Medicine (IM), we are committed to delivering transformative treatments that improve patient lives worldwide. We strive to set new standards in quality and excellence through innovation and collaboration.
Product Quality Management (PQM) plays a critical role in ensuring the highest standards of quality across our products. We are seeking a Senior Analyst, Business Process Quality to join our team, contribute to this mission, and make a significant impact on product quality and operational excellence.
This is a global position, preferably located at one of our major JJIM manufacturing sites. This role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s).
North America
- Requisition #R-052951. EMEA-Requisition (details omitted). Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
The Senior Analyst, Business Process Quality will be part of the Product Risk Management and PQM Support team, within Strategy Deployment & Excellence in PQM. The role involves ownership of selected Quality Management System (QMS) processes and provides essential support to PQM and other organizations across IM Supply Chain, IM Quality, and Therapeutics Development & Supply (TDS). Key responsibilities include managing processes related to budgeting, resource planning, and reporting, while ensuring compliance and driving continuous improvement.
Key Responsibilities
Quality Systems
Serve as PQM process owner for selected QMS processes, including Internal Audits.
Provide back-up support for other systems such as NC/CAPA, Change Control, Document Management, and Training.
Assume additional ownership of tactical support systems over time (e.g., COMET STAR user), ensuring compliance, system access, and oversight.
Actively participate in councils and forums related to QMS processes.
Continuously improve processes and systems to enhance efficiency and effectiveness.
Support Quality Review Meetings, metrics, and dashboards for PQM and TDS.
Business Support
Provide budget support for PQM, including headcount oversight, LRFP, and BP planning (currently for PQM-base and ECSQ), in alignment with other team members.
Support onboarding and training of new team members as well as document management and training activities to maintain PQM’s operational continuity.
Qualifications
Education
Bachelor’s degree required, preferably in Pharmaceuticals, Chemistry, Engineering, Sciences, or a related field.
Required
Proven experience in a regulated industry (pharmaceuticals, medical devices, biotechnology), preferably in Quality Assurance or Quality Engineering.
Experience in supporting or leading audits, NC/CAPA and/or change control activities.
Familiarity with budget and business support activities, including relevant systems and tools.
Strong written and verbal communication skills, with the ability to clearly present quality risks, decisions, and recommendations to cross-functional partners.
Demonstrated ability to manage multiple priorities, work independently, and adapt in a dynamic environment.
Global mindset with collaboration and relationship-building capabilities.
Ability to identify,…
Position Requirements
10+ Years
work experience
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