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Reporting to the Assistant Clinical Director (ACD) of X-Ray, the Quality Assurance (QA) Specialist facilitates the X-Ray QA program and provides appropriate education and guidance to staff which includes assessing, planning, implementing, and evaluating both orientation and continuing education programs to enhance the quality of patient care services.
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The Good Clinical Practice (GCP) Senior Quality Assurance (QA) Auditor is crucial in ensuring that clinical trials are conducted ethically, with integrity, and in compliance with regulatory requirements and GCP guidelines.
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Proclinical is seeking a QA Specialist - Equipment and Computer Systems to join a global biopharmaceutical company. QA Specialist - Contract - Onsite. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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Provide support and contribute to other QA activities as needed. Prior experience working in a QA environment. Working knowledge of applicable business systems including: Veeva, Maximo, LIMS, and Smartsheet.
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Walker Cole International is searching for a QA/RA Specialist to join a Global Medical Device business in Massachusetts, Boston. Lead the complaint management and post-market surveillance activities and maintain compliance to the systems for change controls and Corrective & Preventive Actions (CAPA's) to ensure product safety.
$100,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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In collaboration with the CPD Quality & Compliance Educator and CPD Ambulatory Training Specialist & QA Officer, must create, edit, and implement CPD training curriculums and complete yearly competency assessments as required.
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The Complaint Resolution Specialist will be responsible for working collaboratively with MBTA staff and service providers to categorize, catalogue, maintain , investigate, and resolve customer complaints to the standard set forth by the MBTA.
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The role will oversee compliance and program related activities on behalf of PDx QRA with a focus on GCP and R&D functions including to but not limited to CROs, Investigator sites, Centralised Labs and specialist Non Clinical Labs. In this role insights and industry trends are to be proactively shared within PDx to ensure continued compliance and early identification of areas for continuous improvement.
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The GMP Operational Quality Specialist works with a high degree of independence to provide QA Analytical support for release and stability program for commercial products. The GMP Operational Quality Specialist executes routine tasks and activities in support of QA Analytical function.
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We are looking for a highly motivated Instrument Support Specialist to provide critical, on-site, scientific and operational support as part of a dynamic PerkinElmer lab service team. Perform general and routine on FACS equipment maintenance, timely instrument start-up/shutdown, QC/QA of cytometers following documented Standard Operating Procedures (SOPs.
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Author, maintain, update, QA, and publish website content through Sitecore CMS (Content Management System) and Digital Asset Management (DAM) The Web Content Production Specialist will be responsible for timely and accurate execution of content production on ptc.com and mathcad.com. As a member of our web production team, they will work on content authoring, updates, and edits as well as content quality assurance under the direction of Web Content Lead and in collaboration with internal web team members of other functions.
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Job Title: Associate Scientific Services Specialist/ Instrument Support Specialist. The role is mainly responsible for supporting Flow Cytometry and FACS equipment and scientists' operators as requested by our pharmaceutical customer.
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A highly qualified candidate will have experience with flow cytometry systems. Duties may include identifying, handling, generating, accumulating, storing and labeling hazardous waste. Potential risk to lab-based hazards including but not limited to extreme temperature, biological materials, hazardous chemicals.
$25 - $30.41 an hourExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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The QA Specialist-Equipment and Computerized Systems will approve documents created as part of the validation/ qualification of computerized systems and equipment (e.g. reports/protocols.
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The Senior QA Contractor will assist with batch record review and will provide a thorough review and analysis of mission critical data focused on QMS trending and reporting and will assist with audit functions.
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qa specialist jobs in Malden, MA
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