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This position will serve as a SME in environmental monitoring, ensuring the regulatory compliance of the GMP facility in collaboration with other functional groups. AbelZeta Inc is a biopharmaceutical company focusing on the development of novel cell therapy products for the treatment of advanced solid and hematological malignancies.
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Write, edit, and review analytical sections of CMC regulatory filings. Excellent record keeping abilities to adequately record, analyze, and document analytical data generated in support of regulatory requirements.
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All positions must strive to support wfm core values and goals, promote national, regional, and store programs and initiatives, and ensure adherence to all applicable health and safety regulations including food safety and regulatory duties required in the department.
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The Principal Investigator conducts comprehensive and timely investigations, including matters of various sizes and levels of complexity, where there is cause to believe violations exist of applicable rules and securities laws, under FINRA or Regulatory Service Agreement (RSA) jurisdiction, related to securities market regulation.
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The ideal candidate will have knowledge of the evolving fields of molecular biology, biochemistry, pharmacology, toxicology, and medicinal chemistry, and experience with GMP scale-up, large molecules, cell and gene therapy approaches, and regulatory affairs.
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Comfortable in a courtroom, projecting confidence and competence. Job Overview: A law firm in Rockville, MD, seeks a dedicated Family Law Litigation Attorney who will professionally manage cases, provide exceptional legal advice to clients, and uphold ethical standards in all legal proceedings.
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You are comfortable in a courtroom and know how to project confidence and competence when representing our clients. You are excellent at time management and know how to maximize the use of your calendar to ensure that your billable targets are met, your legal assistant and paralegal are clear on their tasks, and you deliver an incredible client experience.
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Secondarily, as requested by the Chief Administrative Judge of the Panel, and not inconsistent with his/her primary adjudicatory proceeding responsibilities, performs other assigned duties, including advising the Chief Administrative Judge and the Panel concerning regulatory, administrative, and procedural matters relating to the licensing process of the NRC.
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A minimum of two (2) years' experience in a pharmaceutical, biotechnology and/or clinical environment which includes medical and regulatory technical writing/editing (Desired) Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.
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Experience in cross-functional collaboration with clinical development, regulatory affairs, medical affairs, quality and legal counsel. Knowledge of regulatory guidance related to drug safety (FDA, EMA, MHRA, etc.
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Collaborate with internal and external legal and policy specialists on various gaming related law and regulatory issues, including privacy, accessibility and digital safety matters associated with the video gaming industry.
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They are accountable for execution of all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable Wells Fargo policies and procedures, appropriately fulfilling risk and compliance obligations, timely and effective escalation and remediation of issues, and making sound risk decisions.
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Knowledge of GLP and GMP requirements, with experience in regulatory submissions. Meet’s global biopharmaceutical client is looking for a Senior Scientist to spearhead their Formulation Development department.
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Assist in the preparation and review of bioanalytical data and reports suitable for regulatory submission. Background in molecular biology techniques such as cloning, site-directed mutagenesis, DNA and RNA isolation and purification, sequencing, RT-PCR, and qPCR.
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Provides labelling expertise for assigned products regarding language, placement and regulatory content detail for CPI and MPI in line with company procedures, regional labelling regulations and guidance.
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regulatory courtroom jobs in Gaithersburg, MD
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