- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **OBJECTIVE / PURPOSE** + Providesprogram leadership and develops CMC regulatory strategy in support of global vaccine programs in various ... world-wide + Demonstrates leadership and comprehensive understanding of global vaccines CMC regulations and guidelines by applying interpersonal skills and expert… more
- UTMB Health (Dickinson, TX)
- …patients. Works under the supervision of a Psychologist, Mental Health Manager and/or Program Director . **_ESSENTIAL JOB FUNCTIONS_** **:** + Contributes to the ... Mental Health Clinician - CMC - Carole Young **Dickinson, Texas, United States**...or eligibility for licensure as a Professional Counselor, Psychological Associate , or Social Worker. Salary is commensurate with years… more
- Otsuka America Pharmaceutical Inc. (Rockville, MD)
- **Job Summary** Associate Director , Quality Control, Biologics is responsible for late development stage through commercial biologic products including product ... ability to understand and communicate impact of technical risks on CMC program timelines. + Review and interpret complex data, communicating clearly to… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Program Management in our Cambridge, MA office. At ... have responsibility for line management of Sr. Manager and/or Associate Director level GPMs as well as...related functions (eg Clinical Science, Clinical Operations, Research, Regulatory, CMC , Marketing) + Minimum of 5 years program… more
- Merck (West Point, PA)
- …clinical development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager ( Program CSPM) serves as the ... spokesperson at clinical and development related meetings. Working independently, the Program CSPM designs strategic and operational plans for all clinical supply… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Product Development Princeton, NJ, USA...a new and exciting role as part of growing CMC group at Taiho. You will be responsible not only ... the oncology space this is the role for you. Position Summary: + The Associate Director , Product Development will be responsible for product development, scale… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are seeking an ** Associate Director ** within the Formulation Development Group of Regeneron Pharmaceutical Inc. at Tarrytown, NY. This role will lead clinical ... Regeneron functions and stakeholders including Therapeutic Focus Areas, Pre-clinical Development, CMC and Manufacturing (DS and DP), Program Management,… more
- Lilly (Indianapolis, IN)
- …solutions to support communities through philanthropy and volunteerism. **Responsibilities** + The Associate Director - Sourcing Manager is a hands-on leadership ... subject matter experts (SMEs), and timely communication with the suppliers. + The Associate Director - Sourcing Manager will ensure compliance with all internal… more
- Merck (Rahway, NJ)
- …Reporting to the Director of Packaging Commercialization, the Associate Director , Engineering, Packaging Commercialization will lead packaging development ... prior experience developing and commercializing new products on cross-functional teams. The Associate Director will be accountable for the definition and… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The Associate Director / Director will operationalize content strategy central to portfolio ... demands and external expectations. This role will report to the Sr. Director , Global Scientific Communications (GSC) - Portfolio & Capability (Regulatory Strategy,… more
- Lilly (Indianapolis, IN)
- …and drug products. **Responsibilities** Through scientific training and relevant experience, the ( Associate ) Director - Quality and Compliance serves as a key ... resource for all Quality and Compliance related initiatives within SMDD. The ( Associate ) Director : + Manages key compliance activities which include: + SMDD… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …110 countries and regions. **Summary:** Grifols is looking to hire Global Program Leaders (GPLs) to support drug development programs across its therapeutic areas ... strategic project leadership and oversight within a cross-functional, highly matrixed, global program teams (GPT) to spearhead the development and execution of a… more
- Merck (West Point, PA)
- …development and manufacturing and ensure safety and quality of our products. The Director of Vaccines Potency in Analytical Research & Development is responsible for ... a portion of the Vaccines development portfolio from discovery to launch. The Director will oversee the design and development of robust and reliable vaccine potency… more
- Merck (Rahway, NJ)
- …of regulatory submissions. Under the general scientific and administrative direction of Director in the CCFS group and working in conjunction with internal and ... partners, this individual will support late stage and commercial large molecule program activities within CCFS. The individual will be responsible for leading a… more
- Shuvel Digital (Reston, VA)
- …a division. Has supervisory and developmental responsibilities within a functional area. The program director manages one or more projects or programs, may ... Desired Relevant Certifications: + Project Management Professional (PMP) + Certified Associate in Project Management (CAPM) + Program Management Professional… more
- LA Care Health Plan (Los Angeles, CA)
- …maintain a high level of based knowledge on benefits for all product lines (Medi-Cal, CMC , PASC, Healthy Kids and Covered California) as well as serve and act as the ... and Member Relations Unit). Provides unit managers and departmental director with analysis on the error trends and provide...subject matter expert for all Lines of Business (Medi-Cal, CMC , PASC/SEIU, Healthy Kids, LA Care Covered ); in… more
- University of Maryland, Baltimore (Baltimore, MD)
- …of the Department of Pharmaceutical Sciences with teaching responsibility to the Graduate Program Director and Associate Dean for Graduate Programs. ... activities such as student/alumni events and regulatory agency site visits. This program covers all major areas of drug product and biologics regulatory science,… more
- State of Georgia (GA)
- …for continuous student improvement and success and submits results to the program director . Requires strong computer skills, communication skills, and ability ... Coder (CPC), Certified Coding Specialist (CCS), Certified Medical Coder ( CMC ), Registered Health Information Administrator (RHIA), or Registered Health Information… more
- ThermoFisher Scientific (Boston, MA)
- …pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. Reporting to the Associate Director , CMC QC Stability, will be ... as required. + Support continuous improvement activities for VCGT stability program + Provide support to applicable stability sections of regulatory submissions… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …CRO/Partnered studies. Collaborates and interacts with clinical trial managers, development program managers, medical monitors, as well as staff from quality, ... clinical compliance, regulatory, formulations, and IOPS ( CMC , external manufacturing, stability). _We have a 3-day onsite minimum requirement in either Armonk, NY or… more