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QA Document Control Specialist (Part Time) Our client, a global leader in biotechnology and innovation of therapies for rare and genetic diseases and life-threatening conditions is seeking a QA Documentation Control Specialist II that will be responsible for responsible for the maintenance of the cGMP controlled documentation system.
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Aside from mild weather year-round, Modesto allows for easy access to many major tourist attractions in California. The Service Specialist is an excellent entry level store position, with many opportunities for growth and learning within our Save Mart family of businesses in the grocery industry.
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Livelink and MS Access a plus. Bachelor of Science degree in Biology, Biochemistry, Chemistry, Biotechnology, Molecular Biology, and QA experience is desired. Understanding and familiarity with FDA and European regulatory requirements, guidelines.
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We're looking for a Trial Master File Specialist , working in Pharmaceuticals and Medical Products industry in San Rafael, California, United States. May enter new and updated records information accurately in a variety of records management databases, such as the Vault eTMF, Clinical Document Management Database, Access and LiveLink (via scan / index software.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Visit the IRS SPD Library to access the position descriptions. This experience may have been gained through work experience as a project/program manager, team lead or project/program lead, technical advisor, or senior specialist/analyst that included managing resources, providing support to managers, mentoring team members, providing day to day guidance training and/or oversight of peers or others.
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Quality Document Control Specialist. Proficiency in Microsoft Word and Excel; Livelink and Microsoft Access experience is a plus. Quality Document Control, EDMS, Word, Excel, Livelink, Access, regulatory.
ExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The Community Engagement Specialist is responsible for enhancing grant funded activities that support services and provide assistance and professional intervention to Alzheimer’s families and to foster cooperative relationships with the local community health and social service professionals.
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The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various BioMarin departments the documentation that is necessary to perform cGxP activities.
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Access to our dedicated Credentialing Specialist from the minute you join GO. Access to our dedicated Credentialing Specialist from the minute you join GO. From the first conversation with your Go Recruiter to your last day of your assignment, you can tell we are a different travel nurse company.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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STEP THREE: Connect with an account specialist to discuss available accounts (We’ll contact you at the number provided) Employees have access to AFLAC benefits (employee pay) STEP THREE: Connect with an account specialist to discuss available accounts (We’ll contact you at the number provided.
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The QA Technical Support Specialist is responsible for the maintenance of the cGMP controlled documentation system and for providing the various departments the documentation that is necessary to perform cGxP activities.
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Innova Solutions is immediately hiring for a Quality Document Control Specialist-. a Quality Document Control Specialist, you. Livelink and MS Access a plusAbility to communicate clearly and effectively through verbal and type-written correspondence Legible penmanshipOrganizational skills to coordinate multi-discipline projects Experience in participation in regulatory inspections a plusUnderstanding and familiarity with FDA and European regulatory requirements, guidelinesEducation:BA or BS in a related discipline Equivalent experience may be considered.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Onsite with Hybrid option after trainingThe QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various BioMarin departments the documentation that is necessary to perform cGxP activities.
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The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various. The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various.
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Required Certifications: Possession of valid ICC certification for Combination Inspector and California Certified Access Specialist (CASp) certification. The Supervising Building Inspector works as a first-line supervisor planning workload distribution and assigning, organizing, and directing the activities of building inspection program as well as providing performance planning, evaluation, and coaching.
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access specialist jobs in Novato, CA
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