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Join us as a R&D Digital Health Product Manager in our Cambridge, MA office. The product manager will manage the quality, budget, on-time delivery to milestones, and compliance of the technology to the established regulations and guidelines. Accountable to the GPL for the delivery of the digital ...
Manager, Global Regulatory Affairs CMC in Cambridge, MA with the following requirements: Master’s degree in Regulatory Affairs or related field plus 2 years of related experience. ...
Provide project management support for TAU GRA department meetings and project management leadership for business critical projects and/or programs of very high complexity for TAU GRA specific initiatives and workstreams as required/requested. Consult, support, advise and contribute to Takeda’s b...
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How you will contribute:Vice President, Biologics and ATMP is a critical role within GRA, Takeda R&D, responsible for managing a complex organization that spans two critical modalities. ...
Manager, Statistical Programmer in Lexington, MA with the following requirements: Master’s degree in Math, Computer Science, or related field or foreign academic equivalent plus 6 years of related experience OR Bachelor’s degree in Math, Computer Science, or related field or foreign academic equi...
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Director, Global Regulatory Project Management, GI ² within our Global Regulatory Affairs organization, based remotely. ...
This role is crucial for the future of Takeda as it oversees the entire Takeda portfolio for biologics and ATMP, including cell and gene therapy products. ...
Join Takeda as an Associate Director, Global Labeling Lead where you will be responsible for the development, maintenance, and implementation of Company Core Data Sheets (CCDS) in line with international standards and guidelines. ...
Regulatory Authority) requirements and support audits/inspections as a labeling subject matter expertLiaise with US Labeling Operations and EU Labeling Operations to ensure labeling objectives and timelines are metAnalyze relevant competitor labeling to ensure Takeda products have competitive lab...
Join Takeda as a Director, GRA CMC Pharmaceuticals, Oligonucleotides where you will lead the GRA CMC Pharmaceuticals regulatory team in the development and implementation of global CMC regulatory strategies during development commercialization and post approval LCM stages. As part of the GRA CMC ...
Join Takeda as a Senior Director, GRA Pharmaceuticals- Small Molecule where you will establish collaboration with Global CMC teams and leadership through networks and enable CMC regulatory team’s success in meeting goals/objectives. As part of the Regulatory Affairs CMC team, you will report to t...
Prior experience must include: Develop the regulatory submission strategies for products in commercial and development phase by working in close coordination with the quality, manufacturing and global regulatory teams; Ensure the response to health authority queries are provided in a timely and e...
The Brink's name is a promise to respect the trust we've earned in over 150 years in business. Every employee honors that promise by offering the highest levels of service and support to our customers. We take pride in our work, and we share a passion about our future. Learn why so many people ha...
Candidates ideally live in Northern New Jersey area.Account Management experience selling IT solutions and services to large enterprise customers, preferrably in life science / pharmaceutical industry.Highly regarded at Technical levels.Ability to work independently and solve customer-facing prob...
The firm handles pharmaceutical, medical device, product liability, and personal injury litigation across the nation. We are seeking a dynamic and passionate Associate Litigator specializing in personal injury cases to join our legal team. The ideal candidate will have a strong background in liti...
Department/Discipline : ArtThe VP, Associate Creative Director/Art is responsible for ensuring that all Agency work is on strategy and meets or exceeds the highest level of creative accomplishment. Title : VP, Associate Creative Director (Art), pharmaceutical advertising experience. The VP, Assoc...
Director of Engineering needed to join a major Pharmaceutical company based in the Greater NYC area. In depth knowledge of one or more of the following areas:. This is a global role providing strategic process/equipment engineering guidance on projects and ongoing operations for key sterile injec...
Consultant, Technical Director - Construction, Pharmaceutical Summary Our client, a Fortune 500 Pharmaceutical Company , has engaged GForce Life Sciences to provide a Technical Director of Construction. This position will report to an Associate Director of Facilities Project Management or higher,...
A technology solutions firm based in Orlando, Florida; AssistRx focuses on connecting pharmaceutical and biotech manufacturers together with their patients, providers and pharmacies.Assist℠, AssistRx's flagship product is a state-of-the-art technology that simplifies the prescribing process of sp...