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MS/BS in Molecular Biology, Biochemistry, Chemistry with 10+ years relevant industry experience; MS or BS with 15+ years of industry experience in Pharma / Biotech industry required. Designing, performing, and/or overseeing the execution of stability studies of critical materials, intermediates, drug substance and drug product related to the company's AAV gene therapy and RNA PMO product pipelines.
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Analytical Chemistry, Clinical Supply, Biotech, Pharmaceutical Supply Chain, Biologics, Formulation Development, Drug Delivery, Clinical Packaging, Dose Form Manufacturing, Gene Therapy, Vaccine Production, Pharmaceutical, Drug Development, Cell Therapy, Biopharmaceutical, and Innovation.
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Established as a Transformational Research Unit (TRU) following Novo Nordisk’s acquisition of Dicerna Pharmaceuticals, Inc. in December 2021, the Dicerna TRU is a unique new organization within Novo Nordisk that brings together the best of both worlds – the agility, collaborative pioneering spirit and calculated risk-taking profile of a biotech along with the scale, resources and capabilities of a global leader in drug development.
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We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally.
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BSc. /BEng. with a minimum of 10 years of direct biotech/pharma or related experience. Familiarity with biotech manufacturing cycle times, constraints, method development, and working with external CMOS.
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We provide unparalleled capabilities with our lab analysis, sample management and storage services, informatics software, and consumables, with the largest installed base managing over 1 billion samples globally.
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Minimum of seven years of experience in corporate compliance, preferably in life science (Device, Pharma, Biotech, or DME) required. Minimum of five years of experience in a global role covering Third party related risks, ideally with experience in other related areas, such as Healthcare Fraud and Abuse laws, durable medical equipment sales models, and global procurement processes required.
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Demonstrated experience in aseptic manufacturing and other pharmaceutical manufacturing activities (API, DP, Biotech, Oral Solid Dosage) applicable to the role. Advanced computer skills for MSOffice and enterprise systems such SAP, QTS, Vault, Documentum platforms, Minitab.
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We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation (PBC). Technical expertise in multiple cell biology techniques including quantitative polymerase chain reaction, fluorescence microscopy, flow cytometry and other immune-based assays are critical to this position.
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We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire & Contract Consultants) and Retained Executive Search.
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As a Biotech Manufacturing Associate, you will play a pivotal role in our mission by contributing to the production process of cutting-edge mRNA therapeutics and vaccines. Perform routine production activities such as upstream and downstream processing, purification, and formulation.
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Minimum of 7- 10 years of pharmaceutical/biotech and/or life science related digital marketing experience (Agency experience welcome). Design and implement governance process for modular content that allows for snackable, multi-purpose use and functionality in our omni channel customer engagement model.
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Proven experience (5+ years) as a Legal Operations professional or in another role with transferable skills, ideally within the Pharmaceutical/Biotech industry. Lantheus is seeking a legal operations professional with system, project and budget management experience to work with the Legal department to advance our operational excellence and provide critical insights relating to legal spend and portfolio management.
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Responsibilities: Oversight of the General Ledger & Month-End Review of journal entries and account reconciliations Preparation of Financial Statements for SEC Filing Work with the Corporate Controller in maintain SOX compliance Project Based Work Assist with managing a team of 5+ accountants Qualifications: B.S. in accounting or a related field CPA preferred 7+ years of accounting experience Biotech experience highly preferred Staff management experience.
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Are you ready to start your Biotech career with a groundbreaking company that's shaping the future of healthcare manufacturing as pioneers in harnessing the power of mRNA technology creating innovative medicines and vaccines.
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biotech job Company: Parexel in Billerica, MA
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