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Senior Medical Affairs Analyst
1 semana atrás
At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for humanity.
Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Next Move Could Mean Our Next Breakthrough.The Sr.
Medical Affairs Analyst will be responsible for supporting the procedural documents activities, scientific affairs investigations, change project management and processes improvements initiatives.
Key Role Activities:
This function supports the procedural documents activities, operations investigations, change project management and processes improvements initiatives related to Scientific Affairs-Latin America.
The main activities are:
- Be responsible for supporting the procedural documents and change project management covering all scientific affairs areas. It requires a close interaction with local, regional, and global stakeholders, within and outside Medical Affairs, such as Scientific Affairs, Product Quality Vigilance, BRQC, Commercial Quality and others;
- Be responsible for performing data science analyses related to scientific operations and other MAF activities;
- Support SA process improvements managing the endtoend activities related to it (Define, Measure, Analyze, Improve and Control);
- Interface with MAF local team to identify impact and needs for regional process improvements;
- Responsible for monitoring SA process performance indicators;
- Proactively seeks out opportunities to collaborate and solve problems as a team and maximize performance focusing on all Scientific affairs areas;
- Lead and perform the applicable alignments with impacted areas involving investigation of issues related SA;
- Work in partnership with SA areas to support the change management of projects involving the regional and local areas;
- Preaudit preparation, audit support and management of corrective actions, preventive actions and effectiveness check as postaudit activity related to Medical Affairs Area.
Qualifications:
- Bachelor's or higher degree in preferentially in a healthcare area (pharmaceutical, biochemical or chemical/production engineering);
- Proficient in Portuguese (oral and written); advanced English and intermediate Spanish;
- 35 years of experience in managing and implementing Processes, mapping, improving and optimizing processes;
- Desirable previous experience in a quality management system or process excellence in the medical device and/or pharmaceutical industries;
- Experience with nonconformance investigations techniques;
- Process excellence knowledge;
- Knowledge of data science tools;
- Analytical skills to diagnose and manage demands;
- Quality & Compliance or correlated areas developing activities related to controlled procedural documents and quality issues/CAPAs;
- Knowledge in Office package tools;
- Good Communication skills;
- Home Based Position.
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