The Regulatory Affairs & Documentation Specialist is responsible for formatting, assembling, and timely preparation of documents for domestic and international regulatory submissions and ensuring compliance with applicable regulations. Manages and prepares documentation for all international pro...
QA Documentation Specialist III. QA Documentation Specialist III. Maintains documentation manuals to ensure accuracy and current information. Supports the distribution and maintenance of GXP documentation. ...
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...
Legal Support seeks a Production Specialist that has a keen eye for detail, communicates effectively, and is problem solver. Production Specialist Key Responsibilities:. Burn CDs as well as copies and binds the produced documents to be mailed to the client. Quality check all documents before going o...
Clinical Marketing Specialist. Develop molecular testing methods/workflow for clinical research applications. ...
Safeguards the clinical samples, clinical data and records, ensuring that the confidentiality, integrity and security of the clinical samples and clinical records are maintained, and PHI information is protected. R&D and Operations personnel and external clinical research organizations (CROs) on...
The Field Clinical Specialist works using independent judgement, partners with local Account Managers to increase clinical support, education resulting in clinical acumen. Candidates must have 3 years of medical experience in a clinical capacity either as a clinical specialist or cath lab provider. ...
Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing required. ...
The Technical Writer (Environmental Science, Wildlife & Natural Resources) specializes in producing professional biological and environmental reports. The Technical Writer will collaborate closely with a team of scientists, biologists, GIS analysts, data managers, technicians, and administrative sta...
Collect, organize, summarize, write, and revise extensive, complex technical information in a concise manner for various audiences, assisting in the preparation of developed materials for reports, articles, manuals, specifications, presentation materials, illustrations and other technical and non- t...
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...
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...
As our first Quality Specialist, you will be tasked with the unique challenge of both inspecting machined parts and creating new quality processes to support production and engineering teams. This role will be the first dedicated quality person in the machining and development operations group, and ...
They are seeking a detail-oriented and experienced Compliance Specialist to join the compliance team. This role is critical in supporting the firm's compliance framework and maintaining a robust culture of compliance. Conduct regular compliance audits and risk assessments, identifying and mitigating...
Compliance Specialist I maintains Quality Compliance by being aware of quality requirements; preparing standards, metrics, standard operating procedure (SOP) management; supporting audits, Quality Investigations and Corrective and Preventive Actions (CAPA); analyzing and verifying documentation; and...
Join our expanding compliance team as a Compliance specialist! We are seeking a detail-oriented, proactive, and self-starting individual who is eager to grow and advance in the field of audits and corporate compliance. In this role, you'll play a crucial part in maintaining our company’s compliance ...
Senior Specialist, Clinical Quality Assurance - Hybrid (Los Angeles, California). The Senior Specialist, Clinical Quality ensures GCP compliance with SOPs, ICH and US FDA regulations, guidelines, and clinical study protocols. Maintain and update Clinical Trial Quality Management system. ...
CMC Regulatory Technical Writer, Associate Director/Director. CMC technical document review and writing, authoring and compiling the CMC sections for global regulatory filings by working closely with the cross-functional teams including CMC, Quality, Clinical and Regulatory Affairs to ensure all CMC...
The Environmental Planning and Historic Preservation Cadre (EHP) announces the hiring of EHP Environmental Compliance Review Specialist (ECSP) position under FEMA's Reservist Program. Assist in the fulfillment of the Agency’s compliance with a range of federal environmental/historic regulations gove...
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,...
Supports Quality Assurance, and Quality Control activities to ensure operations are conducted in compliance with applicable regulations and standard operating procedures to ensure product quality is consistent with the specifications and facilitate batch disposition for commercial purposes. ...
Provide administrative and organizational support to the radiologists and clients. ...
Environmental Permitting and Compliance Specialist). Environmental Permitting and Compliance Specialist). Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our missio...
Located in Moorpark, CAMore Information about this Job: Ventura County- Moorpark, CA Clinical Education Service Specialist (CES Specialist) - Exempt We invite you to join a team of highly skilled emergency medical professionals! Our mission of providing care to the world at a moment's notice is at t...
The Specialist, Quality Control is a customer facing role, working in close collaboration with Quality Control (QC), Quality Assurance, Manufacturing, and Information Technology (IT) teams. The Specialist, Quality Control is a customer facing role, working in close collaboration with Quality Control...