Specialist Quality Assurance Auditor – Innovative Medicine
Johnson & Johnson is hiring a Specialist Quality Assurance Auditor – Innovative Medicine. Level rates it ; you can apply on Level.
Level's read on this job
- Little AI ●○○○ is how Level rates this role: aI is not part of the work.
- Tools and skills the posting cites include quality assurance, auditing and gxp.
- Level files it as a mid-level role.
- Level lists 1,800+ other open roles at Johnson & Johnson.
- The role was posted in the last few days.
AI in this role
Lead R&D Quality QA audits and support regulatory compliance and inspection readiness across international locations for Johnson & Johnson.
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.
Job Function:
QualityJob Sub Function:
Quality AssuranceJob Category:
ProfessionalAll Job Posting Locations:
Beijing, China, Chiyoda, Tokyo, Japan, Mumbai, Maharashtra, India, Petaling Jaya, Selangor, Malaysia, Shanghai, China, Singapore, Singapore, Taguig, National Capital Region (Manila), PhilippinesJob Description:
Main responsibilities will include but are not limited to:
Auditing:
Leads the planning, conduct and reporting of R&D Quality QA routine audits and supports non-routine audits of activities, data, internal facilities and processes in GxP/non-regulated areas to assure adherence to corporate policies, internal standards/requirements and compliance with applicable regulatory requirements. Non-routine audits include Due Diligence, for cause audits, cross-functional, complex/sensitive system/service provider audits as defined by the scope.
Ensures the relevant standard procedures, diagnostic tools, and audit plans are fully understood and applied in audit activities.
Inspection Support :
Supports regulatory inspections in various supporting roles.
Training & Development :
Completes assigned training requirements in a timely manner to ensure inspection readiness at all times.
May assist in the preparation of training material if requested.
People Management :
N/A
Project Management :
Participates in projects or serves on teams, as assigned by supervisor.
Meets priorities, checkpoints and timelines for all aspects of work and projects to achieve adequate progress.
Subject Matter Expert / Point of Contact :
Provides consultation to business partners on routine tasks with occasional supervision. Cooperates with business partners when contacted for compliance inquiries and seeks advice on non-routine and more complex issues to ensure a departmental unified position.
Job Requirements (Pharmacovigilance Auditor Focus)
Education & Experience:
Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related discipline.
Minimum 2 years of experience in Pharmacovigilance (PV) within the pharmaceutical or biotech industry.
Proven hands-on experience in PV operations (e.g., case processing, signal detection, risk management, safety surveillance) or other PV-related roles.
2+ years of QA auditing experience, specifically in Pharmacovigilance / GVP audits (internal, external, or vendor audits) is preferred.
Pharmacovigilance Expertise (Critical Requirement):
Knowledge of Pharmacovigilance regulations and guidelines, including: EU Good Pharmacovigilance Practices and Health Authority requirements in Asian countries
Understanding of end-to-end PV processes, including:
Individual Case Safety Report management
Aggregate reporting (i.e. PSUR/PBRER, DSUR)
Product risk management and implementation of risk minimization activities
Vendor oversight and PV compliance models
Experience auditing PV systems, processes, databases, and service providers is preferred.
Skills & Competencies:
Strong analytical thinking and attention to detail, particularly in safety data and compliance reviews.
Excellent communication skills, with the ability to influence and challenge stakeholders constructively.
Ability to manage multiple audits and priorities in a fast-paced, global environment.
High level of integrity, professionalism, and objective judgment in sensitive or high-impact audit situations.
Proven ability to work cross-functionally and across geographies.
Required Skills:
Preferred Skills:
Business Alignment, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Human-Centered Design, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality StandardsHow we rate this
Specialist Quality Assurance Auditor – Innovative Medicine at Johnson & Johnson rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.
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Skills and AI tools this role asks for
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- Tell me about a project where quality assurance was part of your work. What did you do?
- Tell me about a project where auditing was part of your work. What did you do?
- Tell me about a project where gxp was part of your work. What did you do?
- Tell me about a project where regulatory compliance was part of your work. What did you do?
- Tell me about a project where risk management was part of your work. What did you do?
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- List these exact terms on your resume: Quality Assurance, Auditing, Gxp, Regulatory Compliance, and Risk Management. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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