A company is looking for a Senior Regulatory Compliance Specialist to assist with the implementation and maintenance of its Compliance Software Program. ...
Kitsch is looking for a highly skilled and knowledgeable Regulatory Compliance Specialist to become an integral part of our enthusiastic Quality team. The role is expected to work closely with our team of product development, production, purchasing, marketing, sales and vendors to conduct prod...
A company is looking for a Regulatory Affairs Specialist to support US and OUS regulatory activities for Class II and III products. CFR 820, MDR)Experience in regulatory affairs, clinical affairs, Quality, or Engineering is required. ...
The Southern California Natural Resources Team is looking for a an experienced Regulatory Specialist to support permitting needs, including preparing permit applications for individual, general, and programmatic permitting efforts with the U. You will join an existing team of Natural Resources profe...
A company is looking for an R&D Regulatory Specialist to develop and implement regulatory strategies for products in the biotechnology and pharmaceutical industry. ...
Biological Regulatory Specialist/Project Manager. Serving as Rincon's primary Project point of contact for the client and regulatory agencies. Regulatory compliance oversight and monitoring. ...
Regulatory Compliance Specialist. The role is expected to work closely with our team of product development, production, purchasing, marketing, sales and vendors to conduct product evaluation and specify regulatory compliance requirements, ensure current and new products comply with regulatory requi...
Regulatory Affairs Operations Specialist II. This new team member will perform specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agency specif...
Regulatory Affairs Operations Specialist II. This new team member will perform specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agency specif...
Seeking a Principal Regulatory Affairs Specialist to support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global basis by:. Managing regulatory compliance activities for Kindeva and existing customer products and registrations as requ...
R&D Regulatory Specialist (Remote). Your main responsibilities as a R&D Regulatory Specialist (Remote):. What we are looking for in a R&D Regulatory Specialist (Remote):. Develops and implements worldwide regulatory strategies for projects and issues affecting development of new products...
Regulatory Affairs Specialist II. As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agenc...
To help grow and maintain the regulatory and quality standards, we are seeking a Regulatory Affairs (RA) and Quality Assurance (QA) specialist to provide RA-QA support and leadership to ensure compliance with FDA QSR, ISO 13485, and MDSAP for all SprintRay products as well as implement and maintain ...
Regulatory Affairs Specialist II. As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agenc...
Maintain or create technical/regulatory documentation such as IL, QIL, QF and SDS. Review artwork for fill weight claims, ingredients and regulatory issues. Assist with developing technical documents for new/existing products to meet regulatory and customer needs. High school Diploma or GED and 1-3 ...
Senior Regulatory Affairs Specialist. Acts as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to the development team. Provides mentoring and leadership to Regulatory Specialist I and II team members. Master’s Degree in Re...
Conducts regulatory audits and surveys by consulting on the interpretation and interaction of current regulatory policies and requirements in preparation for surveys. Identifies and recommends improvements to processes of responding to regulatory audits and survey preparedness efforts by: independen...
Regulatory Affairs Specialist/Manager will oversee medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. The specialist will also support government interactions regarding device registrations, manage regulatory assessment...
Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving moderately complex conflicts between those requirements and development issues; also keeps...
Regulatory Affairs Specialist/Manager will oversee medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. The specialist will also support government interactions regarding device registrations, manage regulatory assessment...
The Role Kitsch is looking for a highly skilled and knowledgeable Regulatory Compliance Specialist to become an integral part of our enthusiastic Quality team. The role is expected to work closely with our team of product development, production, purchasing, marketing, sales and vendors to con...
The Sr Regulatory Affairs Specialist is responsible for ensuring digital medical device regulatory clearance to enable market access by demonstrating compliance to applicable regulations through a registration dossier. Provides regulatory guidance and defines regulatory strategy for digital products...
Regulatory Affairs Specialist II. Regulatory Affairs Specialist II:. Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review. Regulatory Affairs Specialist II:. ...
Participate in the preparation and review of regulatory submissions to the US FDA and international (outside the US) regulatory authorities. Participate in the development of regional regulatory strategy and update strategy based on regulatory changes. A minimum of 5 years of experience in medical d...
R&D Regulatory Specialist (Remote). R&D Regulatory Specialist (Remote):. R&D Regulatory Specialist (Remote):. Develops and implements worldwide regulatory strategies for projects and issues affecting development of new products or medical devices or new indications for existing products. ...