Senior Manager – Security, Data and Digital Core

Johnson & Johnson

Sr. Manager overseeing quality and compliance in technology systems at Johnson & Johnson.

Posted 7/18/2026full-timeRaritan • New Jersey, Pennsylvania • 🇺🇸 United StatesSenior💰 $122,000 - $212,750 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Quality Management Systems and Computerized System Validation within the pharmaceutical and biotech industries, ensuring compliance with regulations and effective risk control frameworks. Proven ability to manage end-to-end quality processes and provide strategic direction for technology-related projects.

Highest-signal resume keywords

Computerized System ValidationQuality Management SystemsValidation Protocols AuthoringPharmaceutical Industry ExperienceRegulatory Compliance Expertise

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Quality AssuranceValidation PlansSOP DevelopmentChange ControlNon-Conformities ManagementLIMSCAPAMESPLMSAP

Certifications & Qualifications

Bachelor’s Degree in Computer ScienceBachelor’s Degree in Information SystemsBachelor’s Degree in Business Administration

Industry Keywords

PharmaceuticalMedical DeviceBiotechRisk Control FrameworksStrategic Programs

About the role

Key responsibilities & impact

Building and Execution of Quality into Applications and Supporting Digital Core
Ensures/promotes early involvement of TQ in the design and development of applications and infrastructure to ensure automated and preventive controls are built in
Manages the end-to-end quality process and strategies for building and execution of applications and supporting infrastructure
Ensure that all Tech Quality related projects go through the Intake process
Provides strategic direction and operational support to the individual project teams
Supports the building and execution of quality into Strategic Programs across the enterprise where the use of technology supported by TQ is involved
Contributes to the creation of strategies for the qualification and validation of new and emerging technologies
Applies expert knowledge of regulations, technology, and risk control frameworks to develop and evolve tailored Quality Management System processes and approaches for security requirements

Requirements

What you’ll need

A Bachelor’s degree in Computer Science, Information Systems, Business Administration or another related field required; solid, relevant experience may be substituted when appropriate, additional certifications a plus
8-10 years of progressive experience in the pharmaceutical/medical device/biotech industry, with direct experience in Computerized System Validation activities is required
Experience in running large scale end-to-end Validation programs like LIMS, CAPA, MES, PLM, SAP, LMS, Complaints Handling, and Change Control is preferred
Experience authoring or approving validation protocols, non-conformities, Change Requests, SOPs, Validation Plans and Reports is required

Benefits

Comp & perks

Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year