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At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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As a Clinical Trial Specialist, you will coordinate the initiation and activation of all new clinical trial protocols, ensuring compliance with various oversight bodies such as the Scientific Review Board (SRB), Institutional Review Board (IRB), and Human Research Oversight Committee (HROC.
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As a Quality Assurance Specialist, you will engage in batch record review, assist in writing SOPs, and author Annual Product Review Reports. Actalent is a global leader in engineering and sciences services and talent solutions.
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Active Certification: Must have and/or acquire a certification as a Certified Recovery Specialist within 6 months of employment. Building a culture of care, engagement, and recognition with clear outcomes.
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Diversity, Equity & Inclusion. Your role will focus on part & machine design, maintenance, tooling, and troubleshooting of equipment and processes. You will also coordinate the delivery, installation, and ramp up of new equipment as needed while supporting improvements, optimizing processes, and applying lean manufacturing concepts.
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The ERP Data Specialist plays a pivotal role in ensuring the smooth and efficient functioning of manufacturing operations by managing the configuration and upkeep of items, routings, and bills of material (BOMs) within the ERP system across various production sites.
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This is a hybrid position requiring some days on-site in Basking Ridge, New Jersey and some days remote. This includes both internally sourced studies and those outsourced to CROs. Responsibilities include scheduling and coordinating meetings, preparing agendas and presentation materials, compiling study manuals, and managing the eTMF. Furthermore, the Specialist will track site activation, monitor updates, and assist with clinical trial registry postings.
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Performs documentation review, including but not limited to non-conformance events/deviations, data analysis with a high attention to detail, using working knowledge of cGMPs and internal procedures and controls.
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An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.
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Document Controller responsibilities include reviewing engineering drawings and ensuring all team members have access to necessary documentation. 2+ years experience as a Document Controller or similar role.
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A typical day includes managing the intake of complaints, monitoring pharmacovigilance, coordinating projects, and writing reports. The QA Complaints Specialist is primarily responsible for monitoring the safety, quality, and efficacy of radiopharmaceutical products by receiving, capturing and evaluating product feedback reports in accordance with current FDA and Health Canada regulations.
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As a Quality Specialist, your key role is to support the Quality Department in ensuring that all employees comprehend and adhere to Standard Operating Procedures (SOPs). Overseeing completeness and good documentation practices of in-process batch records is also a key part of your role.
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Lead and support a diverse and collaborative team environment with clear and concise communication to deliver high productivity and contribute to team goals. Assist with investigations, deviations, CAPA, validation documentation, change control, and other related controlled documents.
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Responsibilities will include conducting and supporting gowning training and associated structured on-the-job training (SOJTs), sampling to ensure sterility in the gowning process and collaborating with the Environmental Monitoring (EM) lab on results, assisting with training-related paperwork, and working cross-functionally with site training and EM teams.
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Tasks include soldering, stripping wires, crimping pins, heat shrinking of tubing, and applying labels. Performs builds of PCB's per blueprint standards and ensures they meet specifications.
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diversity and inclusion a jobs Title: specialist Company: Actalent in Sherwood, Oregon
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