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... Myers Squibb Clinical Trial Result Specialist in Princeton New Jersey Bristol-Myers ... The Clinical Trial Results Reporting Specialist is responsible for creation of ... the databases. The Results Reporting..
... strategic direction of the data quality programs necessary to achieve and ... achieve and maintain high data quality in GRS systems Oversees and ... guidances with impact to BMS..
... Preventive Actions (CAPA), Vendor Certification, Quality Agreements, Annual Product Review/Report for ... Inspection. Assists the Associate Director Compliance and Auditing during regulatory agencies ... and discuss reports of assigned..
... role as a **Sr Principal Compliance/Audit Specialist** you will have responsibility to ... to determine the state of compliance to appropriate regulations and standards, ... risk assessments and/or audits/assessments..
... join the Alliance as a Compliance Specialist II in the Compliance Department. We are filling one ... RESPONSIBLE FOR Reporting to the Compliance Supervisor, you will: Conduct regular .....
SENIOR REGULATORY AFFAIRS SPECIALIST Aortic Business Unit The Aortic ... Lives The Senior Regulatory Affairs Specialist is responsible for developing strategies ... at reviewer level. Support regulatory compliance activities, including..
... Record of Processing Activities (RoPA) Compliance Specialist will be responsible for assisting ... (IRM) instance of ServiceNow The Specialist will respond to RoPA program ... team of privacy professionals,..
... finance, legal, human resources, corporate compliance and ethics, and information technology. ... role in executing BioMarinu2019s GxP Compliance Audit Program.u00A0 The overall purpose ... program is to ensure continuous..
Job Summary:The Quality Compliance Project Manager will be responsible ... the oversight and/or management of quality systems at all Lannett Company, ... Inc. (LCI) sites. Additionally, the Quality Compliance Specialist..
... RESPONSIBLE FOR Working as a Compliance Specialist (Temporary) you will be conducting ... questions from staff regarding regulatory compliance and respond to external requests ... external audit processes to..
REGULATORY AFFAIRS SPECIALIST - Peripheral Vascular Health Peripheral ... Change Lives: The Regulatory Affairs Specialist is responsible for worldwide regulatory ... regulatory requirements. The Regulatory Affairs Specialist is responsible for..
... exciting role as a Customer Quality Compliance/Audit Specialist you will have responsibility to ... and product hold order (PHO) quality assurance process to demonstrate process ... improvement opportunities for..
... Cycle processes including design controls, quality planning, risk assessments/analysis/management, design reviews, ... teams Support DMR and DHF compliance assessments to ensure quality and regulatory requirements are successfully ... standards..
... Alliance as a Regulatory Affairs Specialist in the Compliance Department. This role can be ... functions. ABOUT THE TEAM The Compliance Department promotes a culture of ... Department promotes..
**SENIOR REGULATORY AFFAIRS SPECIALIST** Our vision is to become ... Lives** The **Senior Regulatory Affairs Specialist** is responsible for managing regulatory ... Ensure personal understanding of all quality policy/system items..
... Astellas Pharma Inc. is a pharmaceutical company conducting business in more ... & Facilities team, the Senior Compliance Specialist is responsible for delivering compliant ... effective and compliant; participating..
SENIOR REGULATORY AFFAIRS SPECIALIST - INTERNATIONAL Join us in ... Lives The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for ... cross-functionally, while ensuring timely and high-quality execution of..
... grow, and succeed. The Research Compliance Specialist will be responsible for providing ... for providing organizational integrity and compliance guidance, developing and implementing proactive ... the areas assigned. The..
PRINCIPAL REGULATORY AFFAIRS SPECIALIST - CYBERSECURITY Transforming diabetes care ... as a Principal Regulatory Affairs Specialist in Cybersecurity, you will develop ... industry expectations to ensure regulatory compliance with new..
... PRINCIPAL OBJECTIVE OF POSITION Global Quality, Quality Laboratory Practices (GQ-QLP) is responsible ... preclinical research processes to determine compliance with regulatory requirements, guidelines and ... technical expertise, regulatory risk,..
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and ..