Director of Regulatory Affairs
EnergyHubSalary not specified
Not SpecifiedCompensation
Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, BiotechnologyIndustries
Requirements
- Ability to serve as a group leader for developing and implementing regulatory strategies
- Capability to achieve regulatory submission and approval for new products/projects in Hematology LCM within agreed deliverables
- Ability to integrate future regulatory changes into global development discussions with the global full development team
Responsibilities
- Take full responsibility as a group leader for developing/implementing regulatory strategies
- Achieve regulatory submission and approval for new products/projects in Hematology LCM within agreed deliverables
- Integrate future regulatory changes into the global development discussion with the global full development team
Skills
Regulatory Strategy
Regulatory Submissions
Regulatory Approval
Hematology
Life Cycle Management
Global Development
Clinical Trials
Bristol-Myers Squibb
Develops and delivers biopharmaceutical medicines
About Bristol-Myers Squibb
Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.
New York City, New YorkHeadquarters
1887Year Founded
$33,706.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees
