We are seeking a skilled Regulatory Specialist to join our team at Sol-Millennium. Lead, develop and communicate regulatory strategies for new products or changes to existing products to ensure compliance with applicable regulatory agencies (e. Be a steward of ownership and collaboration within glob...
The Regulatory Affairs Specialist will ensure global compliance with all cosmetic and OTC regulatory requirements by performing a wide range of tasks. Regulatory Affairs Specialist – Onsite - Ottawa, Illinois. This role involves supporting and selectively managing regulatory affairs matters, collabo...
Compile regulatory documents for FDA submission (eCTD experience preferred), including: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulato...
Support teams to develop regulatory submissions strategy and update strategy based upon regulatory changes. Support regulatory submissions for Food, FSMP, Enteral Nutrition, IF & FUF, Drug for global. Partnership with affiliates to support regulatory agency interactions to expedite approval of p...
The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips' Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...
Sr Specialist, Regulatory Affairs is responsible for the coordination and preparation of regulatory documents/deliverables/packages to support Establishment Registrations and Listings for Drugs for the US market. Compile and submit, in a timely manner regulatory deliverables in support of Structured...
The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips’ Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...
Regulatory Government Affairs Specialist. Regulatory Government Affairs Specialist. How does a Regulatory Government Affairs Specialist make an impact?. COUNTRY Financial, you will have the opportunity to work with colleagues across the enterprise on legislative and regulatory items of impact to the...
Senior Regulatory Affairs Specialist. Master’s degree in regulatory affairs may be considered in lieu of direct regulatory experience. Participate as the regulatory functional product team member for the organization’s Transfusion Medicine regulatory team. Work with Regulatory and CFT to improve eff...
Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Acts as core team member providing review and analysis of applicable regulatory guidelines and project regulatory assessments as needed. Reviews an...
The Regulatory Affairs Specialist will ensure global compliance with all cosmetic and OTC regulatory requirements by performing a wide range of tasks. Regulatory Affairs Specialist – Onsite - Ottawa, Illinois. This role involves supporting and selectively managing regulatory affairs matters, collabo...
Title: Regulatory Affairs Ops Specialist I. Managing the preparation of regulatory submissions for IND, ANDA, NDA, K, Clientrom, and other electronic submission types. Creating timelines for regulatory filings. Overseeing authoring and reviewing of regulatory documents. ...
Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements as well as staying awa...
Title: Regulatory Affairs Ops Specialist II. Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Client’s products. Compile and submit, ...
The Regulatory Affairs Specialist will ensure global compliance with all cosmetic and OTC regulatory requirements by performing a wide range of tasks. Regulatory Affairs Specialist – Onsite - Ottawa, Illinois. This role involves supporting and selectively managing regulatory affairs matters, ...
Confer routinely with Technical Program Manager and Technical Operations Manager to ensure preventative maintenance program for routine machine maintenance, to ensure the timely repair of disabled machines, to coordinate infection control measures, routine culturing, water testing, logging of result...
The Qualification & Training Specialist is responsible for administrating the Operator Qualification Program, as well as, coordinating, implementing, and documenting employee training for various regulatory programs (OQ, Emergency Response, HAZMAT, Control Room, Integrity Management, etc. Serve as T...
The Qualification & Training Specialist is responsible for administrating the Operator Qualification Program, as well as, coordinating, implementing, and documenting employee training for various regulatory programs (OQ, Emergency Response, HAZMAT, Control Room, Integrity Management, etc. Serve as T...
We are currently seeking a Compliance Testing Analyst that will be responsible for performing testing activities for various regulatory compliance requirements applicable to Old National lines of business. This position will report to the Compliance Testing Manager and is part of the Corporate Compl...
Accounting Policy and Project Manager. We are currently have an open position for a Manager of Accounting Policy and Projects. The Accounting Policy team is seeking a Manager to serve as a valued business partner, providing timely and accurate financial consultation on emerging, existing and complex...
The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. ...
Full Time - Grants Compliance Specialist III (GCS III). The Grants Compliance Specialist I will be responsible for monitoring and ensuring adherence to federal regulations and reporting requirements related to the grant programs supporting broadband expansion in our state. Develop and implement comp...
Manager, Regulatory Affairs - Labeling. Independently ensuring all project timelines and regulatory commitments are met for labeling at all stages of the product lifecycle, and with no disruptions to commercial availability of marketed products, driving measurable efficiencies and continuous improve...
Regulatory Affairs Associate Director/Director. Director)/ 7 – 9 (Associate Director). Regulatory Affairs (strong preference for experience in oncology). This role provides leadership in the strategic guidance and execution of regulatory concepts within cross-functional project teams and. ...
The Regulatory Specialist will support the Legal and Regulatory Departments with monitoring and assessing the implications of existing and pending laws and regulations on RCP products and advocating for RCP's interests. Beacon Hill is seek a Regulatory Specialist for a Hybrid role in Lake Forest, IL...