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...
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 II. Regulatory Affairs Specialist II:. Regulatory Affairs Specialist II:. Works in close collaboration with internal customers and supports multiple projects to align on regulatory strategy to achieve business objectives. ...
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...
Under the general direction of the Executive Director, the Senior Project Manager (SPM) of the Capital Program will provide leadership and oversight for day-to-day management of the Capital Program Delivery function by directing the activities of staff and high-level consultants who are responsible ...
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. ...
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...
Senior Director/Executive Director, Regulatory Affairs. Meet has partnered with a pre-IPO biotech that is looking for a Head of Regulatory Affairs to join their team. Develop and execute regulatory strategies to streamline the development and approval of innovative medicines. Lead the preparation of...
As the Regulatory Affairs Director, you will have the opportunity to lead Allogeneic trials – the most innovative in history! This role allows you to bring past Regulatory knowledge to the table, while also be creative in strategic discussions and decisions. Regulatory Affairs experience within a ph...
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...
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...
A growing medical device company based in San Diego county is hiring a Regulatory Affairs Manager for their QA/RA department. The RA Manager will be responsible for leading the regulatory strategy and managing submissions for new product launches. Prepare, review, and submit regulatory documentation...
We are seeking a highly skilled Financial Manager with a robust financial background, ideally within academic environments. ...
Kleinfelder's NorCal Area is looking for a Geotechnical Project Manager to join our team. Are you ready to be challenged, make a difference, and experience professional growth in your career? Kleinfelder's Geotechnical team is looking for you! From earthquake and seismic engineering to the latest tr...
Business Intelligence Developer & Analyst - Compliance. Business Intelligence Developer to join our Compliance Operations team to lead compliance focused analytics on multiple campaigns. Fully manage multiple campaigns and clients by serving as the lead for all compliance and operational reporting; ...
The Cybersecurity & Compliance Analyst will play a key role in driving the strategy, planning, implementing, monitoring, and managing security measures and compliance for the protection of controlled unclassified information (CUI), federal contract information (FCI), computer networks, and IT infras...
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...
As the Lead Technical Program Manager (TPM) at a pioneering company in AI compute systems and infrastructure, you will play a pivotal role in driving the execution of complex hardware/software co-development projects. Proven track record as a Technical Program Manager with 10+ years of experience in...
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...
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...
Job responsibilities will include leading and supporting project origination, opportunity analysis, and project development activities across the development lifecycle of greenfield, co-development and acquired projects. AMPYR Energy USA (AMPYR) is seeking Senior Manager, Project Development - BESS ...
We are representing a reputable General Contractor in their search for a Senior Project Manager to oversee their portfolio of Life Sciences and Commercial construction projects. Lead and mentor other Project Managers. The ideal candidate will have prior experience managing commercial new build and/ ...
The Associate Director / Director, Regulatory Affairs will work closely with the Regulatory Affairs team and other departments to develop and implement regulatory strategies for the company's rare disease development programs. Assist in the development and implementation of strategies for early regu...
Email Quality Assurance Specialist. Conduct quality assurance reviews and other activities to ensure the accuracy and timeliness of email deployments. ...
The Senior Specialist, Clinical Quality ensures GCP compliance with standard operating procedures, ICH and US FDA regulations and guidelines, and clinical study protocols. Participate in solving GCP compliance issues within Quality Assurance, Clinical Operations, Regulatory Affairs, Medical Affairs,...