Surgery Commercial Quality Analyst

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:

Quality

Job Sub Function:

Customer/Commercial Quality

Job Category:

Professional

All Job Posting Locations:

Buenos Aires, Argentina

Job Description:

We are searching for the best talent for Surgery Commercial Quality Analyst – Argentina MedTech

Purpose:

At Johnson & Johnson MedTech, we are working to transform the future of healthcare by bringing innovative medical technologies to patients and healthcare professionals around the world. Joining our Commercial Quality team means helping ensure that our products, processes, and distribution channels meet high standards of quality, compliance, and patient safety.

As a Commercial Quality Analyst for Argentina MedTech, you will play a key role in supporting the execution and governance of Commercial Quality processes across the Local Operating Company, with a strong focus on quality oversight, compliance, and continuous improvement across warehouse and distribution operations.

You will partner with cross-functional teams and external partners to strengthen quality and compliance, maintain audit readiness, and support business continuity in a dynamic and highly regulated environment. In this role, you will support compliance with applicable J&J Quality Management System requirements, as well as global, regional, and local quality and regulatory requirements.

This is an exciting opportunity for a quality professional who enjoys working closely with the business, translating quality requirements into practical solutions, and contributing to meaningful outcomes for patients, customers, and stakeholders.

You will be responsible for:

Maintain and support the effectiveness of the Quality Management System (QMS) in compliance with applicable company standards, procedures, and local regulatory requirements, ensuring appropriate quality controls and product traceability throughout the supply chain.

Lead and support the timely and compliant investigation of deviations, nonconformances, and compliance gaps, including identification, documentation, root and/or assignable cause analysis, and follow-up through closure. Define and monitor appropriate corrective and preventive actions in collaboration with relevant cross-functional partners, in accordance with applicable requirements and company procedures.

Perform product release activities for commercialization in Argentina and provide support to the corresponding release process for Uruguay, ensuring compliance with applicable quality and regulatory requirements.

Ensure compliance with applicable quality requirements for marketing companies, external manufacturers, packaging, and labeling activities, including the local implementation of applicable Repack & Relabel standards.

Manage document control activities and Quality Management System documentation in accordance with company requirements, ensuring quality procedures remain current and aligned with corporate standards and applicable local regulations.

Provide Quality training to warehouse operations personnel on applicable procedures, standards, and requirements, ensuring appropriate understanding and consistent implementation of established processes.

Monitor and report Quality Management System performance, including monthly quality metrics and applicable Third-Party Logistics (3PL) performance indicators.

Support Product Complaint Management activities, including the appropriate handling, documentation, and coordination of complaint samples.

Coordinate Stop Shipment notifications and related quality activities in collaboration with Commercial, Regulatory Affairs, Deliver, and other relevant functions.

Support and participate in the Internal Audit Program, external regulatory inspections, and Corporate Audits, including preparation, execution support, follow-up, and management of resulting actions, as applicable.

Partner with Deliver Operations and 3PL partners to drive continuous improvement across warehouse and distribution processes, ensuring alignment with applicable Quality System requirements, company standards, and local regulations.

Ensure compliance with quality requirements associated with Master Data processes, including appropriate management and oversight of relevant quality activities.

Conduct GEMBA Walks at the 3PL warehouse to monitor adherence to applicable Quality procedures and identify opportunities for continuous improvement.

Mandatory Qualifications

Bachelor’s degree in Pharmacy, Biochemistry, Engineering, Life Sciences, or a related field.

Previous experience in Quality, Quality Assurance, Quality Systems, Operations Quality, or a related function within a regulated industry.

Intermediate English proficiency.

Intermediate to advanced proficiency in Microsoft Office applications.

Preferred Qualifications

The following qualifications will be considered a plus:

Previous experience in the Medical Device, Pharmaceutical, or Healthcare industry.

Experience working with warehouse, distribution, logistics, or Third-Party Logistics (3PL) operations.

Knowledge of product release, complaint management, audits, inspections, and distribution quality processes.

Familiarity with GxP requirements and risk-based Quality Management principles.

Experience collaborating with Regulatory Affairs, Supply Chain/Deliver, Commercial, or other cross-functional teams.

Knowledge of applicable Argentinian medical device regulatory requirements.

Experience with SAP or similar ERP systems.

Key Competencies

Strong knowledge of Quality Management Systems and quality principles in a regulated environment.

Strong analytical, problem-solving, and root cause investigation skills, with a risk-based mindset.

High level of attention to detail, organization, and accountability.

Ability to effectively manage multiple priorities and meet established timelines.

Strong communication and training skills, with the ability to translate Quality requirements into clear guidance for operational teams.

Strong collaboration and stakeholder management skills, with the ability to work effectively across cross-functional teams and external partners.

Continuous improvement mindset, with a proactive approach to identifying opportunities to strengthen Quality and operational processes.

Demonstrates an understanding of AI concepts and frameworks, including awareness of responsible and ethical AI practices, experience generating effective prompts to boost efficiency and productivity, and awareness of AI’s impact on the workforce.

Location

Buenos Aires, Argentina

J&J MedTech

Required Skills:

Preferred Skills:

Business Behavior, Compliance Management, Continuous Improvement, Data Analysis, Data Compilation, Detail-Oriented, Execution Focus, Goal Attainment, Internal Controls, Issue Escalation, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Report Writing