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About Fresenius Kabi
Fresenius Kabi is a global health care company that specializes in lifesaving medicines ..
nThis position will assist with the preparation and submission of ANDAs, Amendments, Supplements and Annual Reports to appropriate regulatory agencies. This position will also provide support of the regulatory function through ..
nShift: Part time, Daysn n28 Hrs/WeeknnReporting to the Point of Service Manager interacts with patients and/or their representatives to greet, pre-register and schedule appointments in order to ensure patient satisfaction, claim ..
... pre-registration data for changes and compliance with payer requirements for medical ... physician orders for completeness and compliance with regulatory agencies and NCH ... arrival. Reviews physician's orders for..
nMedline Industries has an immediate expansion opportunity for a Regulatory Affairs Specialist-Technical files for CE marked medical device products located in the Northfield, IL headquarters. Regulatory Specialist will evaluate new medical ..
Medline Industries has animmediate expansion opportunity for a Regulatory Affairs Specialist-Technicalfiles for CE marked medical device products located in the Northfield,IL headquarters. Regulatory Specialist will evaluate new medical devices and create ..
... Status:Full time Job Function:Professional Department:406001 Compliance-Mgmt Shift Hours / Days: Hours ... Days: Hours / Pay Period:DIRECTOR COMPLIANCE & PRIVACYOpportunity in Zion, IL, ... the Mother Standard®.Overview:The Director of..
Ensures that regulatory and compliance guidelines are followed * Make Possibilities Real: * Must ... biotech industry SDL2017..
... and biotech studies. May involve all phases of development and a variety of therapeutic areas ... We provide innovative, GCP-compliant services for biopharmaceutical and medical device companies by .....
... compliance and regulatory counsel to Lundbeck's US business units which are growing rapidly ... biotech industries. * Demonstrated experience drafting and negotiating contracts for the Life .....
... biotech, pharmaceutical, academia or hospital setting is acceptable. * Familiar with clinical ... Understands or experience with internal/external audits and compliance requirements with clinical .....
Minimum of 5-8 years of experience in compliance, quality operations, or related field within a biotechnology, biologics, or pharmaceutical manufacturing facility..
... compliance for the Manufacturing and Engineering Services division of the company. This role will ... Minimum of 15 years of Technical experience with 10 years of Pharmaceutical/Biotech. A technical .....
... and biotech studies. May involve all phases of development and a variety of therapeutic areas ... Train and manage Country Coordinators in their roles for specific studies to ensure compliance ..
Responsible for assuring compliance to all regulatory requirements – FDA, OSHA, OFCCP, EPA, etc ... biotechnology, or comparable environment. * Ability to manage activities of departments through .....