PM Eligibility, Rationalization & Compliance

Johnson Johnson; São Paulo; Presencial; BRL 180 000 - 320 000; Tempo integral

Resumo da oferta

Johnson & Johnson, a leader in healthcare solutions, is seeking a PM Eligibility, Rationalization, and Compliance specialist within the QARA International group in São Paulo, Brazil. The role focuses on ensuring regulatory readiness, managing product eligibility across markets, and driving portfolio rationalization processes to support patient access and business continuity.

Ideal candidates bring at least 5 years in regulatory affairs, quality, or related areas within medical devices or life

Qualificações

• Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, Quality, or related discipline.
• Advanced degree or certification in Regulatory Affairs, Quality Systems, or Business Administration may be preferred.

Responsabilidades

• Lead and support product eligibility assessments to determine regulatory readiness across international markets.
• Execute portfolio rationalization activities
• Ensure ongoing regulatory compliance across product lifecycle in alignment with international and local requirements.
• Partner with Regulatory Affairs, Quality, Supply Chain and Commercial teams to align product strategies.
• Maintain and update product compliance documentation and trackers for audit readiness.
• Support health authority interactions related to product changes, renewals, and remediation activities.
• Identify and drive process improvements to enhance efficiency in eligibility and rationalization workflows.

Conhecimentos

Regulatory affairs

Data analysis

Cross-functional collaboration

Lifecycle management

Quality systems

Formação académica

Bachelor's degree in Life Sciences

Regulatory Affairs certification

Ferramentas

Regulatory management systems

Descrição da oferta de emprego

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:

Regulatory Affairs Group

Job Sub Function:

Regulatory Affairs

Job Category:

People Leader

All Job Posting Locations:

Las Condes, Santiago,, Region Metropolitana de Santiago, Chile, São Paulo, Brazil

Job Description:

DePuy Synthes is recruiting for position, located in Sao Paulo, Brazil.

Alternate Hybrid locations may be considered at Las Condes, Chile.

Please note that 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):

SaoPaulo, Brazil - RequisitionNumber: R-097924

LasCondes, Chile - RequisitionNumber: R-099896

Remember, whetheryou apply to one or all of these requisition numbers,your applications will be considered as a single submission.

Job Overview

The PM Eligibility, Rationalization, Compliance role within QARA International plays a critical role in ensuring that DePuy Synthes products remain eligible, compliant, and optimally positioned across international markets. This position supports global and regional strategies by managing product eligibility assessments, driving portfolio rationalization activities, and ensuring ongoing regulatory compliance throughout the product lifecycle. The role offers strong cross‑functional exposure and the opportunity to influence portfolio decisions that directly impact patient access and business continuity.

Key Responsibilities

• Lead and support product eligibility assessments to determine regulatory readiness and market viability across international markets.
• Execute portfolio rationalization activities, including analysis of regulatory, quality, and business risks to support informed decision‑making.
• Ensure ongoing regulatory compliance of products throughout their lifecycle in alignment with international and localrequirements.
• Partner closely with Regulatory Affairs, Quality, Supply Chain, and Commercial teams to align product strategies and timelines.
• Maintain and update product compliance documentation, trackers, and databases to ensure audit and inspection readiness.
• Support health authority interactions related to product changes, renewals, discontinuations, and remediation activities.
• Identify and drive process improvements to enhance efficiency, transparency, and consistency within eligibility and rationalization workflows.

Qualifications

Education

• Required: Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, Quality, or a related discipline.
• Preferred: Advanced degree or certification in Regulatory Affairs, Quality Systems, or Business Administration.

Experience and Skills

• Required: Minimum 5 years of experience supporting product management, regulatory affairs, quality, compliance, or related activities within a medical device, healthcare, or life sciences environment.
• Working knowledge of international regulatory frameworks and product lifecycle management.
• Ability to analyze complex data sets to support eligibility and rationalization decisions.
• Preferred: Experience working in QARA International or global matrixed organizations.
• Familiarity with medical device regulations across Latin America and other international regions.
• Prior involvement in portfolio optimization, product discontinuation, or remediation initiatives.
• Experience using regulatory or product lifecycle management systems.
• Effective written and verbal communication skills for cross‑functional collaboration.
• Strong organizational skills with the ability to manage multiple priorities and stakeholders.

Other

• Languages: Fluency in English required; Spanish strongly preferred.
• Travel: Limited domestic and international travel may be required (up to ~10%).
• Certifications: Regulatory Affairs Certification (RAC) or Quality certification preferred but not required.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com .

Johnson & Johnson announced plans to separate our Orthopaedics business