Global Lead for Late Stage Synthetic Molecules Development

Job DescriptionThis role offers the opportunity to lead a global team of managers and scientists in the field of analytical development for late stage synthetic molecules. The successful candidate will oversee and manage analytical development efforts across three main areas: characterization and in vitro comparability, method development and validation for...

About the RoleTakeda Pharmaceutical is transforming patient care through the development of novel specialty pharmaceuticals and best-in-class patient support programs. Our team is dedicated to driving scientific and technical innovation in process modeling and simulation.We are seeking a highly skilled Senior Staff Engineer - Process Modeling to join our...

About the OpportunityWe are seeking a seasoned Regulatory Affairs Professional to join our Global Regulatory Affairs CMC team as a Director, GRA CMC Small Molecules. This role offers an exceptional opportunity to contribute to the development and execution of regulatory strategies for our small molecule products.Job Summary:Oversee the development and...

About the PositionWe are seeking a seasoned Global Regulatory Project Manager to join our team in Massachusetts, USA. As a key member of our Global Regulatory Affairs organization, you will be responsible for managing global regulatory projects from late stage filings.Key ResponsibilitiesPartner with the Global Regulatory Lead to ensure seamless execution of...

At Takeda Pharmaceutical, we are a world-class research and development organization that drives innovation and delivers life-changing therapies to patients worldwide.About the RoleWe are seeking a highly experienced Regulatory Affairs CMC Director to oversee the development and execution of regulatory strategies for our small molecules products. As a key...

Pharmaceutical Development Opportunity:We are seeking a highly skilled Lead Process Modeling Engineer to join our Synthetic Molecule Process Development (SMPD) team at Takeda Pharmaceutical. In this role, you will focus on developing robust and cost-effective processes for the manufacture of new small molecule pharmaceuticals.The successful candidate will...

Transform Patient Care with Takeda PharmaceuticalAbout the RoleWe are seeking a Senior Staff Engineer – Modeling to join our dynamic team in Synthetic Molecule Process Development (SMPD). As a key member of our Process Engineering & Technology Group, you will be responsible for designing, developing, optimizing, and scaling up manufacturing processes for...

OverviewTakeda Pharmaceutical is seeking a highly experienced Regulatory Affairs Director, CMC Small Molecules to lead global cross-functional teams and ensure compliance within the organization.Job SummaryThis role requires an advanced degree in a scientific discipline and 10+ years of pharmaceutical regulatory experience, including late-stage development...

Takeda Pharmaceutical is a leading global biopharmaceutical company driven by our commitment to patients, customers and employees. We strive to foster an inclusive and collaborative work environment that inspires innovation and excellence in everything we do.We are currently seeking a highly skilled Regulatory Affairs Director for our Small Molecules team....

Job Description:This is a remote position.Company OverviewRibbon Bio, a growth stage synthetic biology company, seeks an experienced Commercial Development Manager to join our expanding commercial team. We specialize in synthesizing long and highly complex DNA molecules.Key ResponsibilitiesOwning and managing customer relationships, serving as the primary...

Job DescriptionWe are seeking a Senior Scientist, Global DMPK Project Lead to join our team at Takeda Pharmaceutical. This role will be based in Cambridge, MA.About the RoleThe successful candidate will be responsible for overseeing and managing research activities within the DMPK department, developing and integrating the DMPK strategy to progress drug...

About the RoleWe are transforming patient care through novel specialty pharmaceuticals and patient support programs. Our Synthetic Molecule Process Development team is responsible for developing robust processes for new small molecule pharmaceuticals, with a focus on purity and quality.The successful candidate will be responsible for process safety...

We are seeking an Associate Director, Global Regulatory Affairs to lead our global regulatory strategy in Cambridge, MA.Takeda Development Center Americas, Inc. is a leading pharmaceutical company that prides itself on innovation and excellence in the field of immunology and inflammation therapeutic franchise.The ideal candidate will have a Master's degree...

Unlock Your Potential in Global Regulatory AffairsTakeda is a patient-focused company that transforms patient care through novel specialty pharmaceuticals and best-in-class patient support programs.As an Associate Director, Global Regulatory Project Management and Strategic Planning - GI2 TAU, you will be part of our Global Regulatory Affairs organization,...

Takeda Pharmaceutical is a world-class R&D organization driving innovation and delivering transformative therapies to patients globally. We are seeking a skilled Senior Process Safety Specialist to join our Synthetic Molecule Process Development (SMPD) team.The successful candidate will be responsible for all aspects of process safety evaluation during...

About the RoleWe are seeking a highly skilled Process Modeling Engineer to join our team at Takeda Pharmaceutical. In this role, you will be responsible for developing and implementing process models to improve the efficiency and effectiveness of synthetic molecule process development.The ideal candidate will have a strong background in chemical engineering...

Company OverviewTakeda Pharmaceutical is a leading global biopharmaceutical company committed to transforming patient care through innovative specialty pharmaceuticals and best-in-class patient support programs. Our vision is to deliver Better Health and a Brighter Future to people around the world.Salary and BenefitsThe estimated annual salary for this...

About the JobWe are seeking an experienced Associate Director to join our Global Regulatory Affairs team as a Global Regulatory Project Management Lead. This role will provide strategic leadership and guidance on global regulatory project management for moderately complex programs and submissions.The ideal candidate will have a minimum of 8 years of...

At Takeda Pharmaceutical, we are a world-class R&D organization dedicated to unlocking innovation and delivering transformative therapies to patients worldwide.We are seeking an experienced Pharmaceutical Regulatory CMC Lead to oversee the development and execution of regulatory CMC development and registration strategies. As part of our Global Regulatory...

About the Opportunity:We are seeking an experienced Manufacturing Safety Engineer to join our team at Takeda Pharmaceutical. In this critical role, you will play a vital part in ensuring the safe development and production of our life-changing therapies. As a Manufacturing Safety Engineer, you will be responsible for evaluating chemical processes for...