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...
Specialist I, Clinical Applications (NY or NJ). We currently have a great opportunity for a Clinical Applications Specialist I. The Clinical Applications Specialist (CAS) is part of a multidisciplinary team that supports the equipment and middleware integration process from order to go-live in the l...
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. ...
We have openings for call center representative, warehouse, assembly, production, forklift, machine operators, medical receptionist, maintenance mechanics, assistant teacher, medical receptionist, medical call center representative, medical case manager, receptionist, data entry, medical case manage...
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. Requires understanding of GMP manufacturi...
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...
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. ...
Experience in Quality Assurance testing process and best practices. ...
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 ...
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...
Clinical Science Specialist, Liver, Central. 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 ov...
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. ...
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...
The Clinical Supplies Specialist works collaboratively on multi-disciplinary work groups and projects, supporting staff within Clinical Supplies to execute the activities necessary to produce clinical trial study supplies. The Specialist will work with Clinical Supplies Managers to ensure vendors fo...
Clinical Science Specialist, Liver, Southeast. 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 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 ...
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The qualified individual will be responsible for managing assigned tasks as part of the DEA Compliance Group as they relate to the Drug Enforcement Administration (DEA), the New Jersey Department of Health and the State of New Jersey Controlled Dangerous Substances (CDS), as well as ensure complianc...
Clinical Donation SpecialistStatus: Full Time positionPlease ensure your cover letter and resume are attachedGeneral Summary:The Clinical Donation Specialist is responsible for facilitating the organ and tissue donor process through assessment, authorization, donor management, organ allocation, and ...
Sr Specialist, Document Control. The purpose of this role is to develop and deliver a Document Framework for the overall Autodesk Construction Cloud (Client) application and for the Capital Project Realization and Information Management (CPRIM) configuration project. Advanced Level Experience with I...
As a member of the Regulatory Compliance NERC Team, the Senior NERC Compliance Specialist provides essential support for NRG’s NERC Compliance Program under the direction of the Sr. Director Regulatory Compliance. In addition to supporting the Regulatory Compliance NERC Team, you will be working wit...
The Regulatory Compliance Specialist will contribute to our organization success by ensuring the organization adheres to legal and relevant regulatory requirements by partnering cross-functionally with internal and external partners. Review labeling to ensure compliance for international standards a...