Regulatory Specialist: Average Salary in Modesto, CA in 2024

Our client, a large healthcare company is seeking a Regulatory Affairs Specialist to join their team! As the Regulatory Affairs Specialist you would provide regulatory support and expertise by developing global regulatory strategies, identifying needed registration data, obtaining this data and ensu...

Senior Regulatory Affairs Specialist - (Medical Device) - ONSITE position in. Engage with regulatory authorities and agencies to facilitate product approvals and resolve regulatory issues. If you would like to learn more about this Regulatory Affairs Specialist opportunity, apply directly or reach o...

This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. Provides guidance on regulatory requirements necessary for strategic an...

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...

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...

The ideal candidate, within a short period of time, is responsible to provide Regulatory Compliance documentation plant wide (air water, sewer, BOD's, Environmental Regulations and any newly regulations. Authoring and submitting findings for regulatory agencies. Recent experience with regulatory law...

As a Quality Assurance Specialist at Bell Brothers, you will play a crucial role in identifying and qualifying potential customers, driving lead generation, and contributing to the sales pipeline. Achieve productivity standards and goals set by the company while maintaining high-quality calls. ...

Proficient in conducting research and fact-checking to ensure quality. The review process will include but not limited to provide feedback on observed opportunities, edit audited products to ensure accuracy and quality expectations are achieved. ...

Licensing & Compliance Specialist. Licensing & Compliance Specialist. The Licensing and Compliance Specialist plays a critical role in supporting Finance Operations by managing all aspects of business and security agency licensing across the various jurisdictions where the company operates. The Kais...

CMC Regulatory Technical Writer, Associate Director/Director. CMC technical document review and writing, authoring and compiling the CMC sections for global regulatory filings by working closely with the cross-functional teams including CMC, Quality, Clinical and Regulatory Affairs to ensure all CMC...

Cybersecurity & Compliance Analyst (CMMC). Five or more years' experience working in Information Security or Cybersecurity Analyst role with a strong focus on compliance and auditing. Assists in planning, implementing, upgrading, and monitoring security measures and compliance for the protection of ...

Bay Area Senior Manager/Associate Director Regulatory Affairs Opportunity. One of our key mid-sized biotech clients is seeking a dynamic Senior Manager/Associate Director of Regulatory Affairs to become an integral part of their team. This pivotal role will have you steering regulatory strategies in...

Manager of Regulatory Affairs to play a part in their early and late stage clinical trials. Provide leadership to the regulatory therapy area team. Manage regulatory interface with domestic and international health authorities. Develop and deploy regulatory programs for product approval. ...

As the Senior Manager of Regulatory Operations, you will oversee the planning, coordination, and execution of regulatory IND submissions and maintenance activities to ensure compliance with global regulatory requirements. Your role will involve developing and implementing regulatory strategies, main...

Provide high level strategic and operational regulatory leadership and mentorship on projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approval in domestic and international markets, regulatory strategic development plans...

The Program / Project Manager will be assigned to cross-functional projects or to projects where initial requirements will need further elaboration. Experience managing junior project managers to manage smaller aspects of the larger program. Under the leadership of the Senior Manager, Project Manage...

Our client is a well-known Fortune 500 company in the technology industry and is looking for a Senior Program Manager to join their Developer Programs team. The Senior Program Manager will work closely with event vendors and cross-functional teams to deliver high-quality events and projects. Maintai...

The new Global Regulatory Affairs Director is a critical hire to this organization leading PMA regulatory negotiations as the FDA point person as well as guiding clinical affairs, quality management, R&D, and all company team leaders toward successful pre-market approval. In collaboration with the V...

As a Chartered Project Management company, my client provides full cost, procurement, and/or project management services which provide essential ingredients for the development and implementation of a successful project. Senior Project Manager - Los Angeles CA. You must have a strong Project Managem...

Orion Group is hiring a remote Senior Program Manager-Supply Chain who will be responsible for achieving successful implementation of regional and global programs, and managing all activities required to define, design, develop and deliver new products or therapies for our medical device client in C...

RBW is partnering with an innovative late clinical-stage, oncology Biotech (140 FTE) in their urgent and business-critical search for a new Director/AD, Regulatory Affairs. The client is seeking an autonomous, results-driven candidate who can lead cross-functionally, work well in a multicultural tea...

The Senior Compliance Analyst will be a member of Via LA’s Global Compliance team and will support the Licensee audit process. The position will be accountable for identifying, preparing, and supporting the execution of license compliance reviews and initiatives within Via LA. This hybrid role repor...

A growing immuno-oncology company is seeking a Senior/Executive Director of Regulatory Affairs to join the team in executing regulatory strategies and supporting the development of their product pipeline with an emphasis on early stage development. Senior/Executive Director Regulatory Affairs. The S...

Serve as a resource on regulatory affairs, providing training and guidance to team members as needed. You have a proven track record of successful regulatory submissions and interactions with regulatory agencies (FDA, Notified Bodies, etc. This individual will join our client's regulatory team and c...

The Compliance Analyst will be responsible for day-to-day tasks related to regulatory compliance, including analyzing and interpreting regulations, conducting audits, and ensuring adherence to industry standards. This is a full-time hybrid role for an entry level Compliance Analyst at Kingswood U. E...