Excellent employment opportunity for a Documentation Specialist I in the Fremont, CA area. Collaborates within Manufacturing to resolve batch record discrepancies or errors as it relates to Good Documentation Practices or Manufacturing Execution System (MES) inventory. Required skills: BATCH RECORD ...
As a Clinical Documentation Improvement Specialist, you will be responsible for improving the overall quality and completeness of clinical documentation by expediting clarification to clinical documentation. Clinical Documentation Improvement Specialist. We are seeking an experienced and detail-orie...
Quality Assurance in a pharmaceutical, medical device or drug manufacturing company. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. Authors or approves procedures, work instructions and othe...
Reporting to the Sr Manager of Global Quality Assurance for Raw Materials and Reagents Center of Excellence, you will assist with managing the activities of the Quality Assurance department and supervise quality assurance efforts to ensure conformance to Company Pharmaceutical quality standards and ...
The Quality Assurance (QA) Specialist - Supplier Quality will play a pivotal role in ensuring that all external suppliers and third-party vendors adhere to Vaxcyte’s quality standards and regulatory requirements. Supplier Quality Agreements: maintain quality agreements with key suppliers to define q...
Work with the QA Document Control Manager to manage document training when new documents are approved or existing documents are revised. At Freenome, we are looking for a Document Control Specialist II to help expand our growing Quality team. This position focuses on all aspects of Document Control ...
Quality Assurance (QA) Specialist, External Manufacturing will play a pivotal role in ensuring that all external batch records adhere to Vaxcyte’s quality standards and regulatory requirements. Minimum of 5+ years of experience in quality assurance, batch record review, manufacture, or quality syste...
As a Compliance Program Specialist on TikTok's USDS Trust & Safety (T&S) Operations team, your main objective is to support the compliance program, which focuses on core T&S operations and BPO vendor compliance. Content that the Compliance Specialist interacts with includes images, video...
USDS Financial Crime Compliance is responsible for overseeing and operationalizing all aspects related to Anti-Money Laundering (AML) and Sanctions Compliance activities related to TikTok USDS's operations. As a Financial Crimes Compliance Specialist, you will be responsible for risk mitigation acro...
Mytra's Systems Engineering team is looking for a Technical Writer Lead to build and own our technical documentation infrastructure. As Technical Writer Lead, you will work across disciplines to distill interdisciplinary information for system-level components into documentation for internal and ext...
Slalom Flex (Project Based) - Customer Support Content Writer - Technical Writer. Proven experience in content writing, technical writing, or process documentation. ...
In collaboration with the Director of Accreditation, The Accreditation and Regulatory Compliance Specialist manages all aspects of accreditation, regulatory and hospital licensure compliance across the healthcare enterprise. Identifies opportunities for improvements based on evidence based practices...
Supplemental Health Care is seeking a travel nurse RN Clinical Document Improvement Specialist for a travel nursing job in San Mateo, California. Clinical Document Improvement Specialist. ...
Our diverse backgrounds and experiences enrich the way we work together to explore novel ideas, have fun, and grow as individuals and technical writers. Rubrik seeks a technical writer who enjoys mastering the latest technologies. As a member of our technical writing team, you will get the chance to...
The resource should have a combination of experience in the Quality Assurance area along with knowledge of Facilities/Utilities design, maintenance, and validation. The metrics tracked will be validation document turnaround, Quality System records turnaround, and other group throughput data. Perform...
The ideal candidate will be responsible for improving the current processes and bringing in new systems for process improvement as a part of the Quality Assurance team. Continues to build on professional concepts toward culture of quality in compliance with ISO 9001:2015 standards and FDA regulation...
Client is looking for consultant who can join Risk, Compliance & Integrity organization and can brings together critical compliance, assurance, risk and governance functions across and help the company meet compliance needs and enable our businesses to innovate. Assess and advise stakeholders on com...
Administrative Assistant / Receptionist. The Administrative Assistant / Receptionist will be responsible for being the face of Hammon Plating, Palo Alto. Respond professionally and amiably to requests for administrative support or assistance. Assist other staff in administrative tasks, as requested....
TEG Clinical Specialist for our Los Angeles market. Support sales process through clinical education and ongoing value demonstration of the TEG line. Increase product usage at existing accounts and expand customer base through clinical education of new users. Train new and existing customers on all ...
The Technical Writer is responsible for writing, editing, formatting, and managing the publication and translation of customer-facing documents for in vitro diagnostic Xpert tests and GeneXpert instrument systems. This position is part of the Technical Publications Team within Regulatory Affairs New...
Blue chip medical device manufacturer is looking to fill a "clinical specialist" position. Clinical Specialists from other medical device companies. You will provide clinical, teaching, educational, technical and product knowledge support to existing and potential customers during surgical procedure...
Document Imaging specialist is also responsible work using automated workflows for point of care scanning This position is responsible for providing basic, routine maintenance of the scanning equipment The DI Specialist resolves problems with documents such as missing Medical Record Numbers, account...
The Quality Assurance Compliance Specialist is responsible for ensuring that products and processes meet established quality standards and regulatory requirements. This role involves conducting audits, implementing quality control procedures, and collaborating with cross-functional teams to enhance ...
We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what’s possible, to improve people’s lives around the world. Provides on-site clinical support during procedures while maintaining a “hands off”...
Performs all the duties of the Clinical Laboratory Scientist I and II. Interact regularly with clinical services to ensure open communication. Contribute to content of clinical policies and laboratory procedures. Expert knowledge of all aspects of clinical sample testing in specific area(s) of exper...