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Roche Product Development Intern Recruitment, Apply Online

Diluxi Arya
By Diluxi Arya
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Roche Product Development Intern

Roche Product Development Intern Recruitment, Apply Online

Roche Product Development Intern Recruitment, Apply Online. We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world.

Intern Product Development – Regulatory Program Management – I2ONE

Job ID: 202201-102019

Job Level: Entry Level

Location: California

Start Date: May 2, 2022 (Summer 2022)

Length of Assignment: 1 Year

Preferred Majors/Disciplines: Any major in, or related to, the biological sciences

Education Level: Bachelor’s, or Master’s, or PhD, or PharmD, or MBA

Product Development Regulatory (PDR) is responsible for maintaining product license applications and for the timely submission of such applications to Health Authorities for approval of new products and product line extensions. PDR is committed to regulatory strategies that are the most innovative, ethical, and influential in the industry.

This intern position is in the PDR Program Management department – I2ONE franchise (Immunology, Infectious Diseases, Ophthalmology, Neuroscience & Established Products). The department’s work involves global product development and post-marketing programs, working with key partners across product development.

Job Description/Responsibilities

Activities involve maintenance of US and global applications including, but not limited to INDs, CTAs, NDAs, or BLAs. The intern will, as necessary, be working with key partners in development, production, quality, marketing, and legal. The successful candidate will participate directly with one or more of our current molecule project teams. This is an opportunity to explore using your science background in a business environment. Under supervision, will develop and implement innovative regulatory strategies from pre-clinical through to Phase 4 drug development, including direct interactions with the FDA.

Requirements/Qualifications:

  • Understand the needs of the project and proactively drive them
  • Adapt and respond to changes in a positive and thoughtful manner
  • Be comfortable with uncertainty and support a team through challenges
  • Able to balance multiple priorities and organize their time effectively
  • Identify and solve problems and, if needed, escalate issues appropriately
  • Use of interpersonal skills and influence to accomplish work without formal authority
  • Knowledge of drug development is a plus

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Diluxi Arya
Diluxi Aryahttp://www.biotecnika.org
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