- ThermoFisher Scientific (Greenville, NC)
- …years in the biotech/pharmaceutical industry with at least 2 years in regulatory labeling . **5+** years of management responsibility. Strong leadership skills. ... Lifecycle Document Specialist (GL&LDS) Team is responsible for managing global labeling activities and ensuring compliance with international regulatory … more
- Boehringer Ingelheim (Ridgefield, CT)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , DRA Product Labeling will lead and manage ... labeling initiatives in compliance with Corporate and local regulatory requirements. The AD, DRA Product Labeling ... labeling section of NDA Annual Reports. **Requirements** Associate Director : + Bachelor's degree with a… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... of labeling documentation and assures that Takeda labeling content and processes conform to regulatory ...Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions… more
- Ascendis Pharma (Princeton, NJ)
- …and committed to working together as one team to achieve extraordinary results. The Associate Director Regulatory Affairs, Advertising and Promotion will be ... the promotion of prescription drug and biologic products. The Associate Director Regulatory Affairs, Advertising... impact of new campaign concepts, target, or product labeling , and providing strategic regulatory guidance on… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director Commercial Regulatory Affairs** **Description** : The ... role of Associate Director of US Commercial Regulatory Affairs requires...and subpart E and H submissions + Ensure full regulatory compliance of all promotions with approved labeling… more
- Boehringer Ingelheim (St. Joseph, MO)
- …such as governance review, project team meetings, planning activities and FDA communications. Associate Director Act as Regulatory Affairs (RA) core or ... **Description** Manager The Manager, Regulatory Affairs (RA) Pharma Safety & Efficacy will...as defined. + Supports specific infrastructural projects as assigned. Associate Director + Responsibility for the safety… more
- Glenmark Pharmaceuticals Inc., USA (Elmwood Park, NJ)
- Associate Director , Regulatory Affairs Department: Regulatory Affairs Location: Elmwood Park, NJ START YOUR APPLICATION ... + Update the internal tracker that records all incoming and outgoing regulatory activities/communications for ANDAs/OTCs which may include submissions to FDA and… more
- Post Holdings Inc. (Lakeville, MN)
- …passionate about pet nutrition and regulatory excellence? Join our team as the ** Associate Director of Pet Food Regulatory Affairs** , where you'll lead ... You'll Do** + **Lead and inspire** a team of regulatory professionals, driving excellence in pet food labeling... regulatory professionals, driving excellence in pet food labeling , advertising, and product registration. + Serve as the… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …their aspirations. Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs, you will act as ... regulatory authorities. You will oversee preparation and maintenance of regulatory submissions, regulatory labeling and packaging for assigned products or… more
- Merck (Rahway, NJ)
- **Job Description** ** Associate Director , Regulatory Submissions Archive Operations** Location: Rahway, NJ (Hybrid role - onsite 3 days per week required) ... Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of Regulatory Submissions... Regulatory Affairs Management, Regulatory Compliance, Regulatory Documents, Regulatory Labeling , … more