The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in...
Job Summary: This position is vital to ensuring the timely and high-quality delivery of the carve-out project, making a significant impact on the overall success of the regulatory affairs team. Key...
DIRECTOR, GLOBAL REG AFFAIRS STRATEGY LEAD - ONCOLOGY Growing $1.5Bn+ revenue, $7Bn market cap, 550-person biotech1 approved cancer blockbuster with 1 anticipated blockbuster in late...
Aptar is a leader in the development and manufacture of dosing, delivery, closure, and protection systems for the pharmaceutical and consumer industries. With 3 Business Segments, Pharma, Beauty and Closures, Aptar has a turnover of $3.5 billion...
About the job Senior Manager Regulatory Affairs Senior Manager Regulatory Affairs A well-known large consumer products corporation is hiring for Regulatory Affairs Manager. Responsibilities include: ...
**_What Regulatory Affairs and Clinical Submissions contributes to Cardinal Health_** The _Manager, Regulatory Affairs (Clinical Submissions)_ is responsible for ensuring compliance with regulatory requirements for clinical trials and...
Location: Midtown Manhattan Compensation: $225K-$300K total compensation Job Description The Legal and Compliance Department consists of the General Counsel, the Chief...
Senior Director of Regulatory Affairs Job Ref: 112166 Category: Professional Department: OFFICE CORPORATE COMPLIANCE Location: 50 Water Street, 7th Floor, New York, NY 10004 Job Type: Regular Employment Type:...
CooperVision, a division of CooperCompanies (NASDAQ: COO), is one of the worlds leading manufacturers of soft contact lenses. The Company produces a full array of daily disposable, two-week and monthly contact lenses, all featuring advanced...
The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area.