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 Description:
About the role:
As Associate Director, Drug Product Manufacturing Science & Technology, you will be Takeda's global subject matter expert for small-molecule drug product and packaging.
You will lead how tablets, capsules, and injectable products are industrialized, transferred to internal sites and CMOs, and continuously improved across our global network.
You will be at the interface of development, manufacturing, and regulatory, shaping robust, scalable processes and ensuring they are consistently applied worldwide to reliably supply medicines to patients.
How you will contribute:
Serve as the global expert for small-molecule oral solid dose (OSD) and/or parenteral drug product manufacturing technologies.
Lead drug product manufacturing process characterization, including definition of critical process parameters and control strategies.
Lead technology transfer of drug product and packaging processes to internal manufacturing sites and CMOs, ensuring smooth and compliant implementation.
Lead or oversee validation of drug product and packaging processes in line with regulatory and Takeda standards.Act as part of rapid response teams to resolve complex manufacturing issues across local Operating Units, using data-driven root cause analysis and sustainable corrective actions.
Drive strategies for continuous improvement of marketed (mature) drug products in the late phase of their lifecycle, improving robustness, yield, and efficiency.
Shape and implement manufacturing strategies for key Takeda products across the internal network and CMOs, in close collaboration with Pharmaceutical Sciences and Operations.
Ensure that process knowledge and best practices are systematically captured, shared, and leveraged across sites and functions within the Manufacturing Sciences and Technical Services network.
Partner effectively with local Technical Services, site leadership, Pharmaceutical Sciences, Global Quality, Regulatory CMC, and other key functions to align on technical decisions and manage cross-functional issues.
What you bring to Takeda:
At least a Bachelor's or degree in Chemistry, Chemical Engineering, or a closely related discipline.
Extensive industrial experience, including at least 5 years in pharmaceutical development and manufacturing.
Deep expertise in drug product manufacturing technologies for oral solid dosage forms and/or injectable products, including proven experience with tech transfer, process characterization, and validation.
Demonstrated experience acting as a subject matter expert in a matrix environment, influencing cross-functional and cross-site stakeholders.Strong analytical and problem-solving skills, with a track record of independently making high-impact technical and operational decisions for complex manufacturing processes.
Excellent communication skills, with the ability to explain complex technical concepts clearly and build alignment across technical and non-technical partners.
Ability to focus on critical priorities, deliver consistent, high-quality results, and proactively build capabilities for the future across the network.
Intellectual curiosity about technology and new ways of working, coupled with a collaborative and open mindset.Willingness to travel to our international manufacturing sites and work side-by-side with site teams on highly complex issues.
More about us :
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do.
We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Empowering our people to shine :
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
Locations:
Zurich, SwitzerlandAUT - Wien - Industriestrasse 67, BEL - Lessines, Bray, Ireland, Brooklyn Park, MN, CHE - Neuchatel, Grange Castle, Ireland, Hikari, Japan, IRL - Dublin - Baggot Street, Linz, Austria, Oranienburg, Germany, SGP - Singapore - Woodlands, USA - CA - Thousand Oaks - Rancho Conejo
Worker Type:
Employee
Worker Sub-Type:
Regular
Time Type:
Full time
Show more Show less
-
Hikari Takeda $120,000 - $160,000 per yearAs Associate Director, Drug Product Manufacturing Science & Technology, you will be Takeda's global subject matter expert for small-molecule drug product and packaging. You will lead how tablets, capsules, and injectable products are industrialized... · ...
-
Hikari Takeda Full time￥2,000,000 - ￥4,000,000 per yearAs Associate Director, Drug Product Manufacturing Science & Technology, you will be Takeda's global subject matter expert for small-molecule drug product and packaging. You will lead how tablets, capsules, and injectable products are industrialized, transferred to internal sites ...
-
Hikari, Yamaguchi TakedaAs Associate Director, Drug Product Manufacturing Science & Technology you will be Takeda's global subject matter expert for small-molecule drug product and packaging. · ...
-
Hikari Takeda ￥5,000,000 - ￥10,000,000 per yearAs Associate Director, Drug Product Manufacturing Science & Technology, you will be Takeda's global subject matter expert for small-molecule drug product and packaging. · You will lead how tablets, capsules, and injectable products are industrialized, transferred to internal site ...
-
Hikari Takeda $137,000 - $215,270Embedded in our Global Manufacturing Science (GMSci) team you will provide process science and manufacturing technology leadership for drug product manufacturing across Takeda's global network. · ...
-
Hikari Takeda ￥1,200,000 - ￥1,830,000 per yearAs Associate Director, API Process Engineering, you will be Takeda's global expert for small-molecule API manufacturing processes across batch and continuous platforms. · ...
-
Hikari Takeda ￥5,000,000 - ￥10,000,000 per yearAs Associate Director, API Process Engineering, you will be Takeda's global expert for small-molecule API manufacturing processes across batch and continuous platforms. · You will apply chemical engineering and process chemistry fundamentals to design, scale, and control API proc ...
-
Hikari, Yamaguchi TakedaAs Associate Director of API Process Engineering at Takeda you will lead the Small Molecules API Manufacturing Sciences activities within Global Process Science. You will apply chemical engineering and process chemistry fundamentals to design scale control API processes from clin ...
-
Hikari, Yamaguchi Takeda ￥10,000,000 - ￥15,000,000 per yearAs Associate Director API Process Engineering you will apply chemical engineering process chemistry fundamentals to design scale control API processes. · ...
-
Hikari Takeda ￥4,000,000 - ￥10,000,000 per yearExpertise in data science and numerical simulation modeling is required to drive digital twin model development. · ...
-
Hikari, Yamaguchi Takeda ￥120,000 - ￥180,000 per yearThe Head of Commercial Vaccines Quality is responsible for leading the quality organization at a manufacturing site in Hikari,JapandevelopinganddeployingthequalitystrategyandqualitysystemsbasedonglobalTakedaandsitequalitystandards. · ...
-
Yamaguchi Bristol Myers Squibb Full timeBMS seeks a seasoned government affairs leader to be Director, Government Affairs & Market Access Policy Lead. · Develop and execute the companies integrated government affairs & market access policy strategy in close partnership with cross-functional partners · Build and enact t ...
-
Yamaguchi Bristol Myers Squibb Full timeThis role provides leadership as a Senior Manager of Safety Quality Management activities. As a member of the Patient Safety Japan (PSJ) Extended Leadership Team or in an equivalent role, drives organization change and development of the team and represents PSJ across the organiz ...
-
Yamaguchi Bristol Myers Squibb Full timeThis position will oversee a team of APAC Operations Specialists and manage real-time operational issues while maintaining a positive team atmosphere and delivering on SCLT strategy.Directly oversee a team of APAC Operations Specialists and manage real-time operational issues whi ...
-
Yamaguchi Bristol Myers Squibb Full time￥5,000,000 - ￥10,000,000 per yearChallenging work that transforms the lives of patients and careers at Bristol Myers Squibb. · ...
-
Yamaguchi Bristol Myers Squibb Full timeAct as the Japan ePlan reporting representative ensuring accurate and consistent project and resource data reporting for portfolio analysis and governance decision-making Additionally extract insights from analysis that can be linked to strategy · ...
-
Yamaguchi Bristol Myers Squibb Full time￥5,000,000 - ￥10,000,000 per yearThe Clinical Research Associate is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SO ...
-
cyp training
2週間前
山口県 岩国市, U.S. Marine CorpsA T&C Specialist is assigned the responsibility of providing training to CYP professionals based on needs of the program. Marine Corps Community Services (MCCS) is looking for the best and brightest to join our Team MCCS. · ...
-
Yamaguchi Bristol Myers Squibb Full time￥4,000,000 - ￥8,000,000 per yearThe position of Associate, Therapeutic Area Specialist at Bristol Myers Squibb involves promoting the proper use and dissemination of prescription drugs by providing information to healthcare professionals. The role requires a deep understanding of company pharmaceuticals and con ...
-
Yamaguchi Bristol Myers Squibb Full timeThis role will lead the RCO Japan Clinical Operations team and is responsible for execution excellence in operational planning implementation trial management site management and monitoring of clinical trials conducted within Japan. · ...
-
山口県 岩国市, U.S. Marine Corps $120,000 - $180,000 per yearThe job is for a Director MCCS position at Marine Corps Air Station Iwakuni, Japan. The incumbent will serve as the executive manager of all MCCS programs and services located on MCAS Iwakuni, Japan. · ...