Quality Assurance Specialist III
LeadStack Inc.
Job DescriptionJob DescriptionJob Titles: Quality Assurance Specialist III Location: Research Triangle Park, NC 27709 Duration: 6 months Payrate: $30/hr - $40/hr on W2 Job Description:This position is responsible for providing QA oversight and auditing of activities related to clinical and preclinical studies.Examples of activities within the scope of oversight and auditing include but are not limited to: preclinical animal studies, sample analysis from clinical (GCLP guidelines) and preclinical studies (GLP regulations), qualification and/or validation of methods, laboratory processes, etc.This role will assure corporate compliance with applicable GCP, GLP, GCLP national, international, and state regulations and guidelines. This position will report to the Quality Assurance Manager (GCP/GLP). Responsibilities & AccountabilitiesAssess and assure study, project, and process compliance with protocols, controlled documents, and applicable regulations and guidelines through audits of AskBio laboratoriesAudit studies, processes, reports, records, and data for accuracy and compliance with applicable regulations. Follow up on any audit findings.Perform in-process inspections of nonclinical study phases and assay methods.Based on knowledge of regulations, guidelines and relevant SOPs, support staff by acting as a technical resource for compliance related issues.Other duties, as assigned by Quality Assurance Management. Education/ Qualifications:Bachelor's degree, in a health care or relevant scientific field and 5 years of relevant industry experience.Knowledge of industry best practices and regulatory requirements (Good Clinical Laboratory Practice, Good Laboratory Practice, a solid understanding of 21 CFR Part 11, and laboratory standards relevant to clinical and preclinical laboratory research). Knowledge of GCPs a plus but not required. Experience, skills, and characteristics:Laboratory and/or Quality Assurance experience in a laboratory setting.Audit experience, requiredRobust knowledge of immunogenicity (NAb and TAb) and ddPCR assays, requiredStrong collaborative skills. Must be able to effectively collaborate cross-functionally with peers, scientific and technical staff; and be comfortable working in a matrixed team.Ability to identify and/or resolve quality issues/discrepancies with others in a proactive, diplomatic, flexible, and constructive manner.Ability to prioritize, organize, work independently, and multi-task among multiple projects and tasks simultaneously.Excellent interpersonal, verbal, and written communication skills.Proficiency in MS Word, Excel, PowerPoint, and other applicationsExcellent interpersonal, verbal, and written communication skills.Proficiency in MS Word, Excel, PowerPoint, and other applications If you have any questions, feel free to call me on View phone number on click.appcast.io or send an email on View email address on click.appcast.io Thanks and Regards Akarsh YathirajSenior Recruiter C.View phone number on click.appcast.ioD.View phone number on click.appcast.ioA.611 Gateway Blvd, Ste 120 South San Francisco, CA 94080W.
- ...unmet medical needs. We work to restore quality of life to those with debilitating... ...on via Science Foundry. The Quality Assurance Specialist will support efforts to ensure the quality... ...with implantable medical devices or Class III medical devices. Science...SuggestedLocal areaShift work
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- ...a Master’s Degree with 4+ years of relevant experience. Quality Assurance experience within a cGMP-regulated biopharmaceutical environment... ...of World cGMP guidelines. Job Description: The QA Specialist will perform compliance reviews of manufacturing...SuggestedFull timeShift work
$30 - $40 per hour
...We are seeking a QA Associates to support quality operations within a regulated pharmaceutical manufacturing environment. These roles... ...scientific discipline required. Minimum of 3 years of Quality Assurance experience in a biotechnology, biopharmaceutical, or...SuggestedFull time- ...external regulatory standards and expectations into appropriate quality standards and provide mentorship to project teams or functions... ...with a focus on GMP studies Demonstrated knowledge of Quality Assurance activities, ICH regulations, and FDA/EU GxP regulations as they...Suggested
- ...purpose of this role is to work together with global or regional Quality Management teams, functional teams, and other stakeholders in a... ...audits. \n Provide direct strategic and operational Quality Assurance support to CMC and Supply Chain. \n Partner cross-...Work at office
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- ...companies to reach diverse populations beyond traditional means of conducting clinical research POSITION OVERVIEW The Quality Assurance Specialist will participate in continuous improvement of the quality system framework at Science 37 by assisting with the creation...For contractorsWork at officeRemote work
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$88k - $105k
...experienced leaders and experts across the pharmaceutical and medical technology industries. What is the role? The Senior Quality Assurance Specialist provides laboratory-focused, risk-based Quality oversight of analytical testing, microbiology, stability programs,...Contract workTemporary work- ...Technical Source is currently in search of a Senior QA Operations Specialist for our biotechnology client in the Raleigh-Durham-Chapel... .... The qualified candidate should have experience supporting quality operations on the floor of a drug substance or cell/gene therapy...Full timeContract workVisa sponsorshipShift workAfternoon shift
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$43 - $80 per hour
...Band Level 3 Job Description Summary Quality is not just a checkpoint hereit is the promise we make to patients. As a Manufacturing Quality Assurance Specialist at Novartis you will be a hands-on partner to manufacturing teams ensuring every stage of production...Hourly payFull timeRelocation packageMonday to FridayShift workDay shift- ...experience, or Equivalent combination of education and regulatory, quality, compliance and/or industry experience. Skills and... ...Investigator and management promptly Issue accurate quality assurance statements for inclusion in final reports Become familiar with...Contract workTemporary workFor subcontractorWork at office
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- ...designation. For more information, visit . JOB SUMMARY: The Supplier Quality Specialist, is responsible for supporting the Supplier Quality function... ...execution of release activities. Perform other Quality Assurance responsibilities as assigned. EXPERIENCE & QUALIFICATIONS:...Temporary workWork at officeLocal areaVisa sponsorshipWeekend work
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- ...diseases, such as diabetes & obesity. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world.In NC, we operate three pharmaceutical manufacturing facilities that are...Local area
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- ...Technical Source is currently in search of a QA Operations Specialist for our biotechnology client in the Raleigh-Durham-Chapel Hill... ...work. The qualified candidate should have experience supporting quality operations on the floor of a drug substance or cell/gene...Full timeContract workVisa sponsorship
$26 - $29 per hour
...including Cubic Transportation Systems (CTS) and Cubic Defense (CD). Explore more on Cubic.com. Job Details: Provides direct support on quality and compliance to internal departments and programs while remaining aligned to company-wide strategic business objectives....For subcontractorWork at office- ...Description Job Description DEPARTMENT: Quality LOCATION: Durham, NC; Onsite/Not... ...JOB SUMMARY: The Supplier Quality Specialist, is responsible for supporting the Supplier... ...activities. Perform other Quality Assurance responsibilities as assigned. EXPERIENCE...Temporary workWork at officeLocal areaVisa sponsorshipWeekend work
$89.6k - $166.4k
...QC Specialist IIThe QC Specialist II is a highly skilled laboratory professional who will support the start-up and growth of Novartis' Small Molecules Quality Control laboratory in Morrisville, North Carolina. This role serves as a technical subject matter expert for complex...Work experience placement- ...Job Summary The QC Associate performs analytical testing and supports quality control activities within a cGMP-regulated pharmaceutical manufacturing environment, ensuring raw materials, in-process samples, and finished products meet established quality standards....
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- ...compliance activities within the warehouse Perform AQL sampling and inspection of hand-packaged materials Serve as a liaison between Quality and Operations teams Adhere to required gowning procedures Maintain accurate inventory and perform cycle counts Manage...Full timeRemote workAfternoon shift
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