Regulatory Affairs Expert

2 semanas atrás


São Paulo, São Paulo, Brasil Bristol Myers Squibb Tempo inteiro
{"Key Responsibilities": "Working with Us
Discover a challenging and meaningful career at Bristol Myers Squibb, where you'll have the opportunity to work on life-changing projects that transform the lives of patients and your own career.

In this role, you will be responsible for ensuring the company's compliance with regulatory requirements, preparing major filings, and providing regulatory intelligence and support to various teams. You will work in a fast-paced environment, where you'll be expected to prioritize tasks, communicate effectively, and demonstrate commitment to delivering high-quality results.

As a key member of our Regulatory Affairs team, you will have the opportunity to work on a wide range of projects, including product registration, post-approval variations, and regulatory intelligence. You will also have the opportunity to collaborate with cross-functional teams, including Global Labeling Operations, CMC Managers, and Global Document Managers.

If you are a motivated and detail-oriented individual who is passionate about regulatory affairs, we encourage you to apply for this exciting opportunity.

Key Outputs and Measurements
The success of this role will be measured by the timely completion of assigned functions, the quality of deliverables, and the level of regulatory intelligence and support provided to various teams.

Key Contacts/Stakeholders
You will work closely with various stakeholders, including GRSB team, Local Regulatory team, International Strategic Liaisons, Global Labeling Operations, CMC Managers, and Global Document Managers.

Skills, Competencies, and Knowledge
To be successful in this role, you will need to have a strong understanding of regulatory requirements, excellent communication and interpersonal skills, and the ability to prioritize tasks and manage multiple projects simultaneously. You will also need to have a bachelor's degree in Pharmacy and experience in the regulatory area, with a focus on biological drugs.

If you are a motivated and detail-oriented individual who is passionate about regulatory affairs, we encourage you to apply for this exciting opportunity.

Uniquely Interesting Work, Life-changing Careers
At Bristol Myers Squibb, we value diversity, inclusion, and innovation. We offer a comprehensive benefits package, including health insurance, retirement plans, and paid time off. We also offer opportunities for professional development and career advancement, as well as a dynamic and inclusive work environment.

About Us
Bristol Myers Squibb is a global biopharmaceutical company that is dedicated to transforming patients' lives through science. We have a diverse portfolio of innovative medicines and vaccines, and we are committed to making a positive impact on the world through our work.

Equal Employment Opportunity
Bristol Myers Squibb is an equal opportunity employer and welcomes applications from diverse candidates. We are committed to creating a workplace that is inclusive and respectful of all employees, and we offer a comprehensive benefits package that includes health insurance, retirement plans, and paid time off. We also offer opportunities for professional development and career advancement, as well as a dynamic and inclusive work environment.

Contact Us
If you are interested in this opportunity, please submit your application, including your resume and cover letter, to the contact information provided below.

Thank you for considering this opportunity to join our team. We look forward to hearing from you soon.

Best regards,
[Your Name]"}

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