- AbbVie (Mettawa, IL)
- …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Compliance will possess working knowledge ... Outcome Science Liaisons who provide clinical resources to Market Access stakeholders. The Associate Director , Compliance may perform the following with… more
- Catalent Pharma Solutions (Harmans, MD)
- ** Associate Director , Validation & Engineering** Catalent Pharma Solutions is looking to hire a ** Associate Director , Validation & Engineering** to lead ... and will house 8 CGMP manufacturing suites and cold storage warehousing. The ** Associate Director , Validation & Engineering** is responsible for the strategic… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the ... meet quality requirements, auditing and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards,… more
- Boehringer Ingelheim (St. Joseph, MO)
- …through activities such as governance review, project team meetings, planning activities and FDA communications. Associate Director Act as Regulatory Affairs ... of regulatory tools as defined. + Supports specific infrastructural projects as assigned. Associate Director + Responsibility for the safety and efficacy part of… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is responsible for ... Global Regulatory Affairs and Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly complex or multiple… more
- Takeda Pharmaceuticals (Boston, MA)
- …monitor the health of the QMS including the identification of systematic quality compliance risks and implementation of robust mitigation plans + Engage with CPMQ ... continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and support to the CPMQ team… more
- BeOne Medicines (Pennington, NJ)
- **_General Description:_** Responsible for the design, implementation, and management of Compliance programs for the Hopewell, NJ site. Programs which require ... the job_** **_:_** + Within the Quality Assurance organization, develop and implement Compliance programs for the Hopewell, NJ Site. Ensuring the strategy meets the… more
- Abbott (Alameda, CA)
- …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Associate Director , Medical Events Group** **Working at Abbott** At Abbott, ... glucose levels with our new sensing technology. As the Associate Director , Medical Events Group, you will...is responsible for filing Medical Device Reports to the FDA (US), Medical Problem Reports to Health Canada, Medical… more
- Takeda Pharmaceuticals (Boston, MA)
- …regulatory strategies in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly ... to achieve timely and efficient development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. + Is a leader both in the… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA A&P) ... to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you… more
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