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Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of over $ 4.5 billion US Dollars. Supported by more than 40 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe including the United States. Sunology is a combination of Sun Values and Ideology and is the way of life at Sun Pharma. Sunology is Humility.Integrity.Passion.Innovation. It represents our promise to all stakeholders including patients, physicians, and employees.
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Our Global Code of Conduct governs every aspect of our operations. Sun Pharma is a family of thousands of people, working across many countries, speaking multiple languages, and all united, with one common purpose: to make good health accessible and affordable to local communities and society at large. Through active fieldwork, dedicated research teams, and in recognition of the efforts who work behind the scenes to combat illness and disease, the Sun Pharmaceutical Group helps as many people as possible, to secure their right to good health. The way we work every day is important to us.
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Sun Pharma Advanced Research Company (SPARC) is a pharmaceutical research and drug discovery organization that was formed in 2007 when SUN Pharmaceutical Industries Ltd separated out its active projects in drug discovery and innovation into a new company to provide the focus and the opportunity for growth of these projects which are now at different stages of preclinical and clinical development.
SPARC is seeking a Senior Director, Global Regulatory Affairs Strategist to join their team at the North American corporate headquarters in Princeton, NJ.
The position is to provide regulatory affairs strategic leadership for SPARC and supported Sun novel drug development programs. Of each program this position supports, the individual will be responsible for developing and executing the overall regulatory strategy, which includes developing the registration pathway, interacting with regulatory agencies, and being responsible for all associated regulatory filings.
The applicant should join SPARC to take the leadership position for clinical regulatory affairs strategy in a dynamic and rapidly growing novel drug discovery company.
Key responsibilities are to:
Technical Skills/Competencies (Software packages, experience with specific machines etc.)
Education Requirements:
IND123
Full Time
$151k-200k (estimate)
07/06/2023
06/03/2024
The job skills required for Senior Director, Regulatory Affairs include Regulatory Affairs, Leadership, Project Management, Drug Development, Innovation, Chemistry, etc. Having related job skills and expertise will give you an advantage when applying to be a Senior Director, Regulatory Affairs. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Senior Director, Regulatory Affairs. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Senior Director, Regulatory Affairs positions, which can be used as a reference in future career path planning. As a Senior Director, Regulatory Affairs, it can be promoted into senior positions as a Regulatory Affairs Director that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Senior Director, Regulatory Affairs. You can explore the career advancement for a Senior Director, Regulatory Affairs below and select your interested title to get hiring information.