Data Managers assist and support the Project team in planning, preparing, organizing, controlling, and submitting contractually required data, as well as manage the release and control of a wide variety of program related documentation. ...
You will also be responsible for establishing, monitoring and providing oversight or acting as a liaison for compliance programs, processes and department of insurance examinations, as well as making recommendations to leadership on compliance matters that affect the product portfolio, forms, system...
The Senior Quality Assurance Compliance Specialist is crucial in ensuring the integrity and compliance of documentation processes. As the most senior Compliance Specialist, this individual will provide exceptional customer service to internal teams, mentor less experienced specialists, and act as a ...
Mortgage Loan Processor/Closer is responsible for processing loan applications to closing (includes new loan applications, and construction loans). Establishes loan files and orders documentation required to process loans. Is accountable for the accuracy and completeness of all loan documentation an...
Our Technical Writers are responsible for documenting processes, procedures, training manuals and other necessary documents to ensure we meet or exceed our customer’s requirements and expectations. LDRM, a joint venture comprised of Lockwood Hills Federal, an Akima company, and DTSV, is not ju...
In the coming months, Sequel will be hiring Clinical Diabetes Specialists across the country to deliver unparalleled clinical education and product training for people with diabetes and healthcare providers to drive product adoption and persistent use. Are you a passionate and experienced Clinical D...
Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do. Releases product based on Quality Assurance record review and approval by QA Manager. Works closely with Manufacturing and Quality Control to resolve open issues resulting from record reviews, i...
Works closely with Manufacturing and Quality Control to resolve open issues resulting from record reviews, walk through audits of the facility, and deviation issues. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. ...
Clinical Science Specialist, Liver, Manchester. In this field-based role as a Rare Disease Clinical Science Specialist – Cholestatic Liver, you will be accountable for achieving or exceeding regional performance targets/metrics in the Manchester, NH region and for contributing to the overall perform...
Releases product based on Quality Assurance record review and approval by Manager, Quality Assurance. A minimum of three (3) years of GMP-related experience in a pharmaceutical or biotechnology company with one (1) year direct Quality Assurance experience. Works closely with Manufacturing and Qualit...
Interfaces with technical writers at other sites & in Manufacturing Development. This could be a great opportunity for someone who has technical writing or other professional writing experience OUTSIDE of the Life Science industry, who is interested in applying their skills to help us supply med...
The ATF Compliance Specialist performs a wide range of tasks relating to the Compliance and Legal Group and assuring the company operates within the Federal Firearms regulations. Problem Solving - Identify areas of compliance vulnerability and risks: develop and implement corrective action plans for...
Ability to review new and existing systems design projects, or outsourcing plans for compliance with PCI security standards and overall architectural plans. Be a champion of PCI compliance; educate other team members through both formal and informal methods. Collaborate with and support Retail IT te...
Clinical Support Specialist [Data Entry]**. Our IT Team is seeking a **Clinical Support Specialist** who will oversee the management of our WITS system. ...
Releases product based on Quality Assurance record review and approval by QA Manager. Work Experience: A minimum of five (5) years of GMP-related experience in a pharmaceutical or biotechnology company, with three (3) years of direct QA experience Experience in a licensed drug or biologic facility r...
Clinical Oncology Specialist (COS). They must also demonstrate oncology clinical & medical expertise. ...
The Administrative Assistant will provide support to key members of the Sophia Institute team, including marketing, accounts and billing, fundraising, and other areas. ...
To coordinate and perform a wide variety of department/program activities that will increase department/program efficiency, expedite/coordinate the work of others, and ensure the smooth operation of the department/program.Description Required Qualifications - Education and Yrs Exp Associates or equi...
Writing and editing deliverables in Global English for non-technical and technical users. You will manage installation guides, help systems, Web services guides, technical white papers, and knowledgebase articles, to name a few. Learning complex, technical products and explain them in clear, concise...
The Senior Quality Assurance Compliance Specialist is crucial in ensuring the integrity and compliance of documentation processes. The Specialist will identify and resolve quality issues within documents, ensuring compliance with regulatory standards while balancing efficiency. As the most senior Co...
ATF Compliance Specialist (SEC). The ATF Compliance Specialist (SEC) is responsible for ensuring the company's operations adhere to Federal Firearms regulations. This role involves a wide range of tasks within the Compliance and Legal Group, requiring meticulous attention to detail, problem-solving ...
Interfaces with technical writers at other sites & in Manufacturing Development. This could be a great opportunity for someone who has technical writing or other professional writing experience OUTSIDE of the Life Science industry, who is interested in applying their skills to help us supply medicin...
Our Technical Writers are responsible for documenting processes, procedures, training manuals and other necessary documents to ensure we meet or exceed our customer's requirements and expectations. LDRM, a joint venture comprised of Lockwood Hills Federal, an Akima company, and DTSV, is not just ano...
Releases product based on Quality Assurance record review and approval by Manager, Quality Assurance. Works closely with Manufacturing and Quality Control to resolve open issues resulting from record reviews, walk through audits of the facility, and deviation issues. A minimum of three (3) years of ...
Claims Clinical Specialist – Medical Review Team. The Claims Clinical Specialist role is an excellent opportunity for a Registered Nurse seeking a career change. ...