Project Coordinator, Cmc
Job DescriptionArrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them.
Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.
RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein.
Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease.
The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics.
Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI and San Diego, CA.
Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The PositionThe Project Coordinator will work with a core team to support a wide variety of tasks across the Chemistry Manufacturing and Controls (CMC) group including contracting with external vendors, managing the workflow of external projects, and generating purchase requisitions.
This individual will also work to support CMC project management staff by facilitating project logistics, documentation and communication. ResponsibilitiesRequest proposals and draft purchase orders from contract manufacturing/research organizations. Track and review vendor invoices; collaborate with finance department to process payments. Facilitate communication with external vendors and internal team members. Support project management staff by facilitating project logistics, documentation, and metrics. Record and follow up on project meeting agendas, minutes, and action items. Lead cross-organizational activities and ensure that team members are aware of and meet all expected deliverables and outcomes. Collaborate with Project Managers, vendor management, quality assurance, and technical teams to solve problems. Perform other related duties as assigned. Requirements:Bachelor's degree in a scientific field such as Chemistry, Chemical Engineering, Biochemistry, Biotechnology. 2 years' experience in a pharmaceutical company, contract manufacturing organization, or contract research organization. Excellent verbal and written communication skills. Excellent organizational skills and attention to detail. Excellent time management skills with a proven ability to meet deadlines. Ability to prioritize tasks and to delegate them when appropriate. Thorough understanding of or the ability to quickly learn about the project or product being developed. Proficient with Microsoft Office Suite or related software. Ability to work prolonged periods at a desk and working on a computer. Must be able to lift up to 20 pounds at times. Preferred Qualifications:GLP or GMP Laboratory or Manufacturing experience. Experience with Project Management Software such as Smart Sheet or MS Project. Experience with an ERP system such as Microsoft Dynamics (D365) or SAP. Willingness and ability to travel on a limited basis (
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Informazioni dettagliate sull'offerta di lavoro
Azienda: Buscojobs Località: Verona
Veneto, VeronaAggiunto: 13. 3. 2025
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