Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.
Life Science • Freelance • Remote Jobs • Healthcare • IT
51 - 200 employees
Founded 2020
🤖 Artificial Intelligence
🧬 Biotechnology
💊 Pharmaceuticals
💰 Pre Seed Round on 2022-03
March 7
Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.
Life Science • Freelance • Remote Jobs • Healthcare • IT
51 - 200 employees
Founded 2020
🤖 Artificial Intelligence
🧬 Biotechnology
💊 Pharmaceuticals
💰 Pre Seed Round on 2022-03
• The Director, CMC Drug Substance serves as the responsible leader with oversight of CMC Drug Substance. • This position will provide strategic guidance on planning and technical insight. • The role will involve significant collaboration within the CMC group and cross-functionally.
• Bachelor’s degree with 15 years; Master’s degree with 12 years; or PhD with 8 years experience. • Proven director-level/functional area management experience. • Ph.D. in organic chemistry (preferred) or chemical engineer with at least 7 years of related technical experience. • In-depth knowledge and experience in synthetic route development and large-scale manufacturing of drug substance. • Prior experience selecting and working with domestic and international CMOs and consultants. • Familiarity with analytical techniques and methods used to characterize small molecule APIs. • A broad understanding of cGLP/cGMP requirements, compendia testing, ICH, FDA, and EMA guidelines. • Direct experience in authoring of drug substance sections of NDA, MAA, IND, and IMPD. • Experience in developing a robust control strategy. • Excellent interpersonal and communication skills. • Strong ethical standards.
• competitive wages • medical • dental • vision • time off • retirement plan • other voluntary benefits
Apply NowMarch 7
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