At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create,
About Us We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the
Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications. Influence the regulatory strategy
Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications. Influence the regulatory strategy
General Information Job Advert Title: 【アステラス製薬/焼津】経口製剤処方およびプロセス設計担当（主に低／中分子医薬品，グローバルCMC） Location: Yaizu, Shizuoka Division: Product Research & Development Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 アステラス製薬製剤研究所では患者さんの「価値」向上のため，患者さんに実際に投与し，最大限の効果を発揮できる製剤化研究を実施しています。治療手段，モダリティが多様化する中でも，経口製剤は治療手段として引き続き重要な位置を占めています。製剤開発研究室では，主に経口製剤の開発において，処方設計・プロセス設計あるいは生産サイトへの技術移転・商用生産等の経験を有し，斬新なアイデアとチャレンジ精神，熱意を持って製剤研究や新規技術開発を遂行し，プロジェクトをグローバルにリードできる人材を募集します。 【職務の内容 / Essential Job Responsibilities】 （雇入れ直後） チームリード，製剤リードの指示のもと，経口剤の開発を中心に下記の業務を遂行していただきます。 ・ 経口剤の処方設計 ・ 経口剤の治験薬製造 ・ 経口剤のプロセス開発（スケールアップ検討含む） ・
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Sr. Director,
This is a high impact position with great visibility across all levels of the Alkermes organization. This position will have critical responsibilities in the clinical department involved in the development of therapies for neuropsychiatric indications. Key trial
Build our future together: As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff,
Build our future together: As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff,
Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement.read on In 2015, we pioneered a “moneyball for biotech”
Job Description SummaryWe are seeking a highly motivated and detail-oriented Regulatory Affairs – CMC professional with a strong background in radiopharmacy or radiopharmaceutical development. The successful candidate will support global regulatory strategy and execution for both marketed and
About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Regulatory CMC Manager Cell and Gene Therapy Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
Regulatory Consultant - CMC (CMC with small molecule products) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping
About Cristcot We are in the business of addressing the problem within the problem. We focus on the details and connections that other, major pharma companies have left ignored for years. There are better ways, better drugs
If you are a current Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We
Let’s build the future of medicine - together. Join Enveda as a CMC Director – Drug Product and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation - are you
Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our
Department: 36112 Carolinas Medical Center - Forensic Nurse Examiners Program: SANE/SATC Status: Part time Benefits Eligible: No Hours Per Week: 0 Schedule Details/Additional Information: Varied, mostly nights and weekends; 100% remote Pay Range:$28.55 - $42.85 Essential