Manager, Global Regulatory Affairs CMC Submissions Management

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job...

Job Title: Manager, Global Regulatory Affairs CMC Submissions ManagementTakeda Development Center Americas, Inc. is seeking a highly skilled professional to join our team as a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA.Job Summary:We are looking for a seasoned regulatory affairs professional with expertise in CMC...

Job Title: Manager, Global Regulatory Affairs CMC Submissions ManagementJob Summary:Takeda Development Center Americas, Inc. is seeking a highly skilled Manager, Global Regulatory Affairs CMC Submissions Management to join our team in Lexington, MA. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with global...

Job SummaryTakeda Development Center Americas, Inc. is seeking a highly skilled Manager, Global Regulatory Affairs CMC Submissions Management to join our team in Lexington, MA. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with global CMC regulations for advanced therapies and biological compounds.Key...

Takeda Pharmaceutical Job OpportunityWe are seeking a highly skilled Manager, Global Regulatory Affairs CMC Submissions Management to join our team at Takeda Development Center Americas, Inc. in Lexington, MA.Job SummaryThe successful candidate will be responsible for managing global regulatory affairs and CMC submissions, ensuring compliance with worldwide...

Job Title: Director of Regulatory Affairs CMCWe are seeking a highly skilled and experienced Director of Regulatory Affairs CMC to join our team at GSK. As a key member of our Global Regulatory Affairs organization, you will play a critical role in ensuring the timely and successful submission of CMC regulatory documents to support the development,...

Job Title: Manager, Global Regulatory Affairs CMC Submissions ManagementTakeda Development Center Americas, Inc. is seeking a highly skilled professional to establish global submission activities and timelines in partnership with global and cross-functional stakeholders in Pharmaceutical Science, GMS, and Biologics.Key Responsibilities:Develop and implement...

Job DescriptionTakeda Pharmaceutical is seeking a highly skilled Manager, Global Regulatory Affairs CMC Submissions Management to join our team in Lexington, MA.Key Responsibilities:Develop and maintain strong working relationships with the regulatory CMC team and cross-functional teams.Participate on and/or lead multifunctional teams to deliver high-quality...

Job DescriptionTakeda Development Center Americas, Inc.is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA with the following requirements:Key Responsibilities:Develop and maintain strong working relationships with the regulatory CMC team and cross-functional teams, participate on and/or lead multifunctional teams,...

Job SummaryWe are seeking a highly skilled and experienced CMC Regulatory Specialist to join our team at AbbVie. As a key member of our regulatory affairs team, you will be responsible for leading global regulatory dossier preparation activities, coordinating cross-functional teams, and ensuring consistent preparation of high-quality regulatory submission...

As a key member of the Takeda Development Center Americas, Inc. team, you will play a critical role in ensuring the successful submission of CMC dossiers for advanced therapies and biological compounds. Your expertise in global CMC regulations will be essential in developing and maintaining strong working relationships with the regulatory CMC team and...

Senior Director, Global Regulatory Affairs Strategy The position will provide regulatory affairs strategic leadership for the company and novel drug development programs. Of each program this position supports, the individual will be responsible for developing and executing the overall regulatory strategy, which includes developing the registration pathway,...

Job Title: Regulatory Affairs DirectoruniQure is seeking a highly skilled Regulatory Affairs Director to join our team. As a key member of our Regulatory Affairs department, you will be responsible for ensuring our products meet the appropriate legislation in order to control their safety and efficacy from early development phases up to the coordination of...

Senior Director, Global Regulatory Affairs Strategy The position will provide regulatory affairs strategic leadership for the company and novel drug development programs.  Of each program this position supports, the individual will be responsible for developing and executing the overall regulatory strategy, which includes developing the registration...

Senior Director, Global Regulatory Affairs Strategy The position will provide regulatory affairs strategic leadership for the company and novel drug development programs.  Of each program this position supports, the individual will be responsible for developing and executing the overall regulatory strategy, which includes developing the registration...

Senior Director, Global Regulatory Affairs Strategy The position will provide regulatory affairs strategic leadership for the company and novel drug development programs. Of each program this position supports, the individual will be responsible for developing and executing the overall regulatory strategy, which includes developing the registration...

Director, Global Regulatory Affairs, Development StrategyProclinical Staffing is seeking a seasoned professional to fill the role of Director, Global Regulatory Affairs, Development Strategy for a leading global biotechnology company.Key Responsibilities:Develop and implement a comprehensive US regulatory development strategy to ensure successful...

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job...

COME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE!Hybrid work arrangementMedical, Dental, Vision BenefitsHealth Savings Account (HSA), Flexible Spending Account (FSA)  Prescription Drug CoverageTelehealth and Behavior Health ServicesIncome Protection – Short Term and Long Term Disability BenefitsRetirement Benefits - 401k Company Match on Day...

COME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE!Hybrid work arrangementMedical, Dental, Vision BenefitsHealth Savings Account (HSA), Flexible Spending Account (FSA)  Prescription Drug CoverageTelehealth and Behavior Health ServicesIncome Protection – Short Term and Long Term Disability BenefitsRetirement Benefits - 401k Company Match on Day...