We are looking for a GMP Operations Documentation Specialist. Job Title: GMP Operations Documentation Specialist (Entry Level). ...
The Clinical Documentation Specialist (CDS) responsibilities include assisting in clarifying documentation regarding the patient s diagnoses and/or procedures, co-morbid conditions, complications, and other reportable data elements. The Clinical Document Specialist is responsible for ensuring accura...
QA Clinical Supplies Specialist. Responsibilities for the QA Clinical Supplies Specialist:. Electronic batch record review of finished clinical goods to ensure clinical supplies are incompliance with cGMP and SOPs. Qualifications for the QA Clinical Supplies Specialist:. ...
The Technical Writer III is responsible for the development, creation, and revision of controlled documentation in accordance with policies and procedures, current GMP, 21CFR820, ISO 13485 and AATB Standards. Technical Writing in a GMP or medical device manufacturing environment. ...
Experience in Quality Assurance testing process and best practices. ...
Minimum 1 year related pharmacuetical quality assurance experience. This role will provide critical quality support to process to ensure compliant receipt, inspection and release of materials used in cGMP manufacturing operations. You will be essential to Quality floor support of the warehouse, aidi...
The QA Specialist shall assist in the management and implementation of the Quality Management System (QMS). The QA specialist shall also oversee inspection and testing of incoming and outgoing products to confirm quality conformance to prescribed regulatory and customer specifications. The QA Specia...
Sr Specialist, Document Control. Author or update documents identified in both Document Framework. Review/edit documents for compliance with the IT-SOP-100 documentation requirements. The purpose of this role is to develop and deliver a Document Framework for the overall Autodesk Construction Cloud ...
Reviews quality events, deviations, investigations, and change controls. Supports Trackwise Digital Quality R&D Division process improvement projects (UAM/UAT testing). Experience in quality oversight of R&D/Clinical product manufacturing and packaging. ...
Senior Specialist, Document Control. Maintains accurate training documentation and employee record keeping. Performs administrative tasks such as scheduling training sessions, ordering training supplies, coordinating enrollment, and completing documentation. ...
We are looking for a talent who is proficient in quality management to help the business department with incoming material control, on-site quality monitoring, quality data analysis and product release. Responsible for quality-related data collection and statistical work, timely feedback on quality ...
JOB TITLE: Sr Specialist, Document Control. Author or update documents identified in both Document Framework. Review/edit documents for compliance with the IT-SOP-100 documentation requirements. The purpose of this role is to develop and deliver a Document Framework for the overall Autodesk Construc...
Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concerns. Collaborates with center management when viewing the Quality Management System...
Global Document Management Specialist. Our client, a growing, mid-sized pharmaceutical client is seeking a Global Document Management Specialist to manage medical affairs Veeva Vault submissions and approvals. Complete all resource development/approval tracking & documentation. ...
Clinical Science Specialist, Liver, Southwest. In this field-based role as a Rare Disease Clinical Science Specialist - Cholestatic Liver, you will be accountable for achieving or exceeding your territory performance targets, for the Rare Disease Cholestatic Liver franchise, and contributing to the ...
The Specialist, QA Engineering is responsible for ensuring quality, integrity, and compliance of site Information Technology (IT) systems, review of validation and qualification documents for all equipment and facility activities. Previous experience as a computer system validation / quality assuran...
In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical documents throughout the department. CMC Regulatory Technical Writer II. The technical writer contributes to various US, EU and rest of world (ROW) dossiers such as NDA, MAA, IND, IMPD, CTA...
Clinical Science Specialist, Liver, Northwest. In this field-based role as a Rare Disease Clinical Science Specialist - Cholestatic Liver, you will be accountable for achieving or exceeding your territory performance targets, for the Rare Disease Cholestatic Liver franchise, and contributing to the ...
This position is responsible for second shift quality compliance support of manufacturing operations. This position will interact with the manufacturing, engineering, validation, quality control and regulatory departments. The Quality Professional works within Lilly cross-functional groups, anticipa...
Clinical Risk and Loss Prevention Specialist. Collaborate with Executive, Regional, Local, Nursing and Clinical Leadership to create a sustainable culture of risk prevention to reduce harm for both patients and team members (inclusive of all caregivers); improve the human experience and reduce expos...
Regional Chief Quality & Safety Officer, HMH Vice President Clinical & Nursing Quality, HMH Patient Safety Officer and local Director of Patient Safety & Quality to provide leadership for quality & safety improvement initiatives. The Quality Improvement Specialist collaborates with HMH initiative-fo...
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Administrative/Clerical:** Provide administrative/clerical support including answering and routing phone calls to appropriate parties; coordinate conference room requests; schedule necessary office vendor inspections/repairs; office and field supply ordering as authorized by management. A minimum ...
Our team within our Research & Development Division's Quality Assurance, Global Development Quality organization is responsible for oversight of manufacturing activities for the Clinical Supply Chain. Specialist, Clinical Supplies Quality Operations & Technology, plays a critical role supporting the...
This role will provide critical quality support to process to ensure compliant receipt, inspection and release of materials used in cGMP manufacturing operations. You will be essential to Quality floor support of the warehouse, aiding the effective resolution of deviations and nonconformances associ...