- Merck & Co. (Millsboro, DE)
- …operations, formulation and fill/finish activities.Ensure compliance with corporate and regulatory requirements (cGMP/USDA) and lead IPT support for audits, ... Quality Notifications and technical documentation; collaborate cross-functionally with QA, Regulatory Affairs, EHS, Engineering, BTS, ATS and HR.Direct technical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director , Global Oncology Medical Affairs, Medical Analytics ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Merck & Co. (North Wales, PA)
- …Source Management Business Operations Lead is expected to understand the end-to-end regulatory submission process. The main focus will be on document production ... include:Function as Business System Owner (BSO) of the current Documentum-based global submission content management solutionCo-lead the implementation of the next… more
- Eisai, Inc (Nutley, NJ)
- …make a difference. If this is your profile, we want to hear from you. The Associate Director , Compliance Operations will be a key member of Eisai's US Ethics & ... US monitoring activities, managing in-house efforts and third-party vendor engagements. The Associate Director will also play a critical role in advancing… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director , Engineering, Packaging Commercialization will lead packaging development for new products including parenteral products ... erience developing and commercializing new products on cross-functional teams. - - The Associate Director will be accountable for the d efinition and execution… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …a global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the ... compliance activities and fosters a culture that seeks to constantly enhance global regulatory compliance to meet signal evaluation timelines.Develop quality… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …including the timely deployment of CDx assays that are compliant with applicable global regulatory guidelines. Collaborates wtih Regulatory Affairs to ... diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...trials or for approval of CDx. Keeps abreast of regulatory and policy updates in the external environment and… more
- Insmed Incorporated (San Diego, CA)
- …for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , EDC Programming will lead and oversee EDC ... Company DescriptionInsmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most… more
- Merck & Co. (Rahway, NJ)
- …execution, along with leadership skills to shape the technical capabilities lead a global , cross-modality technical team.The Associate Director will lead a ... into the Director , Logistics and Distribution Technology the Associate Director , Logistics and Distribution Technology will be responsible… more
- Merck & Co. (Upper Gwynedd, PA)
- …science that radically changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology ... Job DescriptionOur company is a global health care leader with a diversified portfolio...Group. Under the guidance of a supervisor, the Senior Director has primary responsibility for the planning and directing… more
- Genmab (NJ)
- …and feel like a fit? Then we would love to have you join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of ... as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …to execute daily production schedules.Will have 3-6 direct reports ranging from Associate Director , Senior Manager, and Manager.Oversee the hiring, development, ... Knowledge: Deep understanding of FDA, EMA, and other global regulatory requirements for pharmaceutical manufacturing.Operational Excellence: Expertise… more
- Merck & Co. (Rahway, NJ)
- …Procurement Project Execution within the Global Capital Procurement organization, the Associate Director will serve as the primary point of contact for ... Job Description Role Summary The Associate Director of Procurement for Capital...functions in their assigned area. They will collaborate with Global Capital category teams and cross-functional teams across the… more
- Merck & Co. (Rahway, NJ)
- …DescriptionReporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) Platform ... of commercialized products for the benefit of patients. The Associate Director of MDCP Platform Packaging and...generate gap analysis and mitigation strategies In-depth knowledge of global regulatory requirements for medical devices and… more
- Merck & Co. (Millsboro, DE)
- … Global Safety & Environment organization, and reports to the Associate Director of Safety & Environment at Millsboro, DE.Responsibilities:Ensure compliance ... records of incidents and ensure proper reporting to relevant regulatory authorities as required.Conduct regular inspections of laboratories and facilities… more
- Sandoz Group AG (Princeton, NJ)
- …and personally. Join us as a Founder of our 'new' Sandoz! As the Associate Director , Market Product Quality you will be responsible for the execution ... GMP policies, directives, procedures and processes that support the Global Supply Chain Security program, including Serialization, Anti-Counterfeiting, and Product… more
- Protagonist Therapeutics (Newark, CA)
- Associate Director , API Development Protagonist Therapeutics is seeking an experienced API process research and development chemist to support route scouting, ... regulatory starting materials, and drug substances that meet global regulatory expectations. Work with multiple CDMOs in sourcing amino acids, peptide… more
- BC Platforms (Somerville, MA)
- …a mission-driven team, we'd love to hear from you. Job key features: Title: Associate Director / Director , Sales Life Science Individual contributor role from ... Platforms is looking for a driven and results-oriented Sales Director , Life Sciences to join our growing global...have the unique ability to provide unmatched access to global , research-ready, regulatory -grade patient data. This is… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Global Regulatory Lead (GRL), reporting to the Executive Director , Senior Director ... projects in their assigned therapeutic area portfolio. **Responsibilities** The Associate Director will be responsible to: + Develop regulatory strategy for… more
- Takeda Pharmaceuticals (Boston, MA)
- …what is possible in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is ... responsible for developing innovative global regulatory strategies and providing strategic regulatory guidance...and Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly… more
