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The Bioproduct Research and Development (BR&D) organization strives to deliver creative medicines to patients through the development and commercialization of insulins, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, peptides and gene therapy systems.
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20+ years in the healthcare industry, including 5+ years in rare disease and/or gene therapy. The VP Commercial, Gene Therapy and Gene Editing will serve as the go-to-market lead for Lilly’s one-time genetic medicines portfolio, responsible for developing and implementing strategic and operational commercialization plans.
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This includes some of the traditional flagship Biologics, but Peptides, Gene Therapy, and as a result of a recent acquisition, includes Cell Therapy as well. Leading development of bioassays and potency assay for Cell Therapy Products, Proteins, Peptides, and Gene Tx.
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Experience of biologics development of therapeutics classes from mAbs, Antibody-conjugates, and cell or gene therapy. Develop and optimize assays to assess the biological activity of bioproducts such as antibodies, bispecific antibodies, multifunctional proteins, peptides as well as Cellular & Gene Therapy Products.
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Our research programs encompass a broad range of biomedical research activities and areas of study, focusing on various fields such as cardiovascular disease, alcoholism, hematopoietic cancer, behavioral research, aging, and gene therapy.
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In addition to its patient care and breadth of research that spans basic science, translational, computational, and clinical trial research, Medical and Molecular Genetics is notable for its clinical genetic testing laboratories, GMP cell and gene therapy facility, and biobanking expertise.
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The Sr Director will design and lead the implementation of the SEQS Quality System to support cell & gene therapy across Medical, Regulatory and Safety and ensure operation in a manner such that all GCP/GVP activities are followed.
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Conducts biologic and molecular analysis according to defined standard operating procedures for gene therapy vector products, transduced cells, and patient samples, and more. The person in this position will be part of a dedicated team working to support clinical gene therapy trials in the US and abroad.
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We provide biomanufacturing strategy and execution to start up and established gene and cell therapy, pharmaceutical, and biotechnology companies. Project Farma (PF) is the leading advanced therapy technical operations consulting company in the life science industry.
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Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities. Will you now or in the future require Precision Medicine Group to commence (sponsor) an immigration case in order to employ you (for example, work visa application or work visa transfer, or other-employment based immigration case.
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Support the overall development of pharmaceutical biomanufacturing programs Execute system and process validation protocols Continually develop technical aptitude of PF's core capabilities including but not limited to: Project Management Cell and Gene Therapy Capital Projects Facility Builds Tech Transfers Validation Life Cycle Commissioning and Qualification Quality, Regulatory, and Compliance Engineering Automation and Serialization Reliability, Maintenance, and Asset Management.
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To support cell and gene therapy projects. Knowledge of clinical laboratory automation platforms and/or NGS bioinformatics tools (bedtools, vcftools, python, perl, R, or equivalent) is desired.
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Cell and Gene Therapy. Project Farma is a wholly owned subsidiary of Precision Medicine Group, LLC, a leading global life sciences company with over 2,000 employees. Precision Medicine Group is an Equal Opportunity Employer.
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If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.
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Engineering Automation and Serialization. The Project Engineer will work collaboratively with partners, vendors, contractors, and other Project Farma (PF) Team Members to support projects related to biomanufacturing across the entire lifecycle to further our mission of accelerating market access for next-generation medicines.
$61,000 - $65,000 a yearFull-timeExpandApply NowActive JobUpdated Today
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