Regulatory Relations Liaison is responsible for filing necessary applications and handling all government interactions pertaining to the regulation and certification process for a plant or other facility. Develops procedures to ensure regulatory compliance. Being a Regulatory Relations Liaison prepares reports for top management detailing projects that may impact the organization's regulation status. May represent the organization before federal or state legislations. Additionally, Regulatory Relations Liaison requires a bachelor's degree. Typically reports to a manager or head of a unit/department. The Regulatory Relations Liaison typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. To be a Regulatory Relations Liaison typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. (Copyright 2024 Salary.com)
Join the OSR Team to transform Regulatory submissions publishing and the way you work.
About OneSource Regulatory
OneSource Regulatory™ helps companies implement the correct solutions, processes, standards, systems, templates, and best practices for effective Regulatory Operations. With the right Regulatory Operations group, our clients can achieve high quality document management, data management, and regulatory agency submissions.
Today we provide the following exemplary operations services:
5 years of experience in pharmaceutical, biotechnology, medical device, nutritional supplements, animal health and cosmetic products
Collaborative professionals who file applications for new brands as well as maintain growth and legacy products in eCTD format.
We hire the best, most experienced and collaborative experts in the industry and ensure that they have the latest resources and technology solutions.
What You’ll Do
Do you want the opportunity to work with a diverse group of pharmaceutical companies and provide publishing support for some of the most innovative products in the industry - from the comfort of your home?
OneSource Regulatory (OSR), is seeking qualified Regulatory Operations Submission Publishing professionals based in the US. You should be a collaborative team member who provides routine and non-routine submission activities including publishing, scheduling, scanning documents, making documents submission ready, quality checking electronic submissions, and document archiving.
You should have a strong ability to work independently, with flexibility and a strong ability to connect and collaborate with clients and team members while working remotely.
The OneSource Regulatory team is comprised of the top experts in Regulatory Operations. OSR team members have an average of 15 years of industry experience in large, mid-size and small companies across every therapeutic area.
At OSR, you will be offered interesting and challenging work, and your position will come with a competitive salary, a flexible schedule and innovative incentive programs that reward your contributions and innovations. You will have the opportunity for personal and professional development through internal coaching and mentoring, in addition to the opportunity to attend key external events.
Learn more about OSR by visiting our website: www.OneSourceRegulatory.com
Questions? Email us at info@OneSourceRegulatory.com
Interested in joining the OSR Team?
Provide your information through the BambooHR form below.
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