CAD Manager / Document Control Specialist. CM & Engineering Document Control Assistance. Drawing & Engineering Document Checking with high GD&T proficiency. ...
The Document Control Specialist is responsible for collecting, maintaining, archiving and retrieving all documents necessary to ensure compliance with the company's Procedures and FDA regulations. The Document Control Specialist monitors production operations to ensure that all users have the l...
Document Control or Quality experience for Document Control Specialist 3 – 5 years of Document Control or Quality experience for Document Control Specialist II. Administration of the document control system to include: Administering and maintaining changes to documents in accordance with company req...
Irvine based Medical Device Company is looking for a Document Control Specialist. Administration of the document control system to include:. Ensuring new documents and records are consistent with company procedures; reviewing all documentation for accuracy, completeness and consistency in content, f...
Immediate Entry Level Document Control Specialist Opportunity!**. Will start off with very basic document control and administrative tasks performing reviewing of Job Travelers, scanning documents in preparation for reviews and audits, entering engineering or production drawings into the MRP system ...
Irvine based Medical Device Company is looking for a Document Control Specialist. Administration of the document control system to include:. Ensuring new documents and records are consistent with company procedures; reviewing all documentation for accuracy, completeness and consistency in content, f...
TURION) is seeking a CAD Manager / Document Control Specialist to join our team in Irvine, CA. CM & Engineering Document Control Assistance. Drawing & Engineering Document Checking with high GD&T proficiency. ...
A company is looking for a Technical Writer....
A company is looking for a Quality Assurance Specialist. Key Responsibilities:Prepare and execute test plans for various types of testing during the CI/CD pipelineIdentify and track software defects, collaborating with development teams for resolutionDevelop and maintain test automation frameworks a...
A company is looking for a Document Cloud Sales Specialist. ...
A company is looking for a Document Management Support Specialist. ...
A company is looking for a Quality Improvement Specialist. Key Responsibilities:Coordinate and support HEDIS projects through medical record retrieval and abstractionsHandle data entry and validation of HEDIS Supplemental dataProvide administrative support for health care correspondences and conduct...
A company is looking for a Quality Control Specialist. ...
A company is looking for a Clinical Laboratory Quality Management Specialist. ...
A company is looking for a Junior Document Review Specialist. ...
A company is looking for a Quality Audit Specialist. ...
A company is looking for an Administrative Assistant for remote work within Washington State. ...
A company is looking for a Legal Quality Assurance Specialist for a remote IME position in the United States. ...
A company is looking for a Senior Clinical Documentation Specialist (RN required) for a remote position. ...
The Quality Control Clinical Laboratory Specialist position supports the testing and documentation needs of the Quality ControlDepartment during the manufacture and release of company control products. Quality Control Clinical Laboratory Specialist. Job requires working side by side with the Quality...
Looking for a full time, Quality Control and booking Keeping back ground. ...
Clinical Quality Specialist, GCP, Medical Device/Pharmaceuticals. Our client, a global medical device company, has engaged GForce Life Sciences to provide a Clinical Quality Specialist (GCP). This position will report to the Associate Director, Clinical Quality. Support inspection readiness activiti...
The Senior Specialist, Clinical Quality ensures GCP compliance with standard operating procedures, ICH and US FDA regulations and guidelines, and clinical study protocols. Participate in solving GCP compliance issues within Quality Assurance, Clinical Operations, Regulatory Affairs, Medical Affairs,...
Our client, a research-based biopharmaceutical company delivering life-saving therapies to patients in need, has engaged GForce to identify a Quality Engineer to implement Design Controls and Risk Management activities for combination devices to integrate in with the existing Quality Management Syst...
The Documentation Specialist who will be responsible for supporting the manufacturing of products by creating, processing and reviewing production batch records. Complete required documentation in an accurate and timely manner following Good Documentation Practices (GDP). The Doc Specialist will fol...