Associate Director Regulatory Affairs (Temp to Perm). Oversee regulatory submissions and approvals, ensuring alignment with global regulatory standards. Lead regulatory strategy development and execution for both U. Collaborate with stakeholders to establish project timelines and regulatory goals. ...
As a Senior Associate of Regulatory Affairs, you will support Regulatory Affairs management in the day-to-day operational aspect of the department and support interactions with global regulatory authorities. Senior Associate, Regulatory Affairs. Represent Regulatory Affairs on project teams and clos...
This Associate Director of Regulatory CMC will directly report to the Senior Director of Regulatory Affairs, CMC, and will be responsible for representing regulatory CMC on cell therapy pipeline + products. Associate Director, Regulatory Affairs CMC. Regulatory Affairs CMC experience in a pharma/bio...
As an Associate Director of Regulatory Affairs, you will represent regulatory affairs on cross-functional teams and provide regulatory advice on clinical development matters. Associate Director, Regulatory Affairs. Regulatory Affairs, regulatory submissions, drug development, oncology, FDA, EMA. The...
Corporate/Regulatory Associate. Our corporate/commercial health practice offers general counsel, health regulatory and governance advice to healthcare organizations, associations and professionals. We provide strategic advice and regulatory opinions on a wide variety of issues. ...
As a Regulatory Affairs manager, you will provide project teams with regulatory advice, manage and coordinate various Regulatory Affairs activities within and between departments, and obtain and maintain National Health Authority approvals for investigational products. Regulatory Affairs, FDA, regul...
Job Description: Regulatory Affairs Specialist - On-site 5x a week in Alameda, CA. Provide consultation and advice to regulatory specialists regarding change control and product development. Experience with Japanese and Chinese regulatory submissions. Ability to interpret and apply regulatory requir...
As the Director of Regulatory Affairs, you will be a pivotal leader within the company, driving strategic regulatory decisions across the entire portfolio. Director of Regulatory Affairs. You’ll co-lead a growing regulatory team, and play a key role within regulatory submission and strategy. Regulat...
Regulatory Affairs Manager - Permanent - Remote. Proclinical is seeking a Manager, Regulatory Affairs for a global medical device company. The Manager, Regulatory Affairs will:. Leads regulatory resources to ensure timely product registrations, regulatory planning for new product introductions and p...
A leading provider in the health care and digital health space is seeking a Senior Regulatory Affairs Specialist to join their regulatory team. Minimum of 5 years of experience in medical device Regulatory Affairs with a deep understanding of regulatory frameworks. As a key player in regulatory over...
The Senior Manager in Regulatory Affairs is responsible for developing and managing regulatory strategies to ensure compliance with U. Extensive knowledge of regulatory requirements, including ICH and regional guidelines, and an understanding of current global and regional trends in regulatory affai...
Seeking an experienced Director of Regulatory Affairs to join a dynamic Regulatory Affairs team in a hybrid role, with some onsite presence required at our Redwood City, CA offices. Offer strategic regulatory guidance across teams (R&D, clinical, operations, legal, marketing) to align with regulator...
Vice President or Senior Vice President, Regulatory Affairs & Quality Assurance. Lead Regulatory Affairs and Quality Assurance functions. Meet has engaged on a search for a confidential search for a VP/SVP of Regulatory and Quality with one of our biotech clients. Manage all aspects of Regulatory su...
They are looking to bring on a Senior Director, Regulatory Affairs to the team. Provide strategic and operational leadership in regulatory affairs, including regulatory strategies, clinical study requirements, and marketing approvals in various regions. Utilize deep knowledge of regulatory requireme...
Director of Regulatory Affairs, you’ll take the helm of regulatory submissions and strategic planning for successful drug approvals across key markets, including the FDA, EMA, and other regulatory agencies worldwide. Are you ready to lead regulatory strategies that bring innovative therapeutics from...
Director of Regulatory Affairs - Full Time - Onsite/Hybrid/Remote. The Director will work closely and report to the Head of Regulatory Affairs. Work closely with the Head of Regulatory Affairs to achieve company goals. Any other regulatory affairs tasks assigned or required as per the business needs...
Liaise with colleagues in Regulatory Affairs therapeutics teams, local Affiliates, Regulatory Operations, Regulatory Project Management and third-party local agents to develop filing plans and deliver submissions to agreed priorities and timelines. Senior Manager, CMC Regulatory Affairs, Biologics. ...
This Senior Director/Director of Regulatory Affairs will also oversee the preparation of all regulatory documents and submissions, mentor junior team members, and stay updated on changes in FDA and EU regulations. Senior Director/Director of Regulatory Affairs. Regulatory Affairs experience in a pha...
Our partner, a leader in innovative biopharma resources and patented ingredients, is seeking a Regulatory Affairs Specialist to join their Los Angeles team. This role offers a chance to contribute to groundbreaking developments and regulatory processes with a global impact. Develop and support regul...
Apex Systems is looking for an Environmental Compliance Specialist for one of our largest government clients! This position is going to be 100% on site in El Centro, CA and will be a permanent/direct hire. Title: Environmental Compliance Specialist. Monitor and track implementation of environmental ...
The Regulatory Specialist is a part of Research and Development, this team is responsible for assessing ingredient safety and regulatory compliance, coordinating safety, micro, stability, compatibility and claims testing, ensuring product compliance with international cosmetic regulations, and advis...
Environmental Permitting and Compliance Specialist). Environmental Permitting and Compliance Specialist). Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our missio...
Utilize MS Project and other project management tools to monitor project budgets and timelines, ensuring projects are delivered on time and within budget. We seek an experienced Senior HVAC Project Manager to oversee large-scale commercial HVAC projects in Orange, CA. Job Title: Senior HVAC Project ...
Assist the Plumbing Project Manager in all phases of commercial plumbing projects, from inception to completion, ensuring adherence to project scope, timelines, and budget. We are seeking an organized and motivated Assistant Plumbing Project Manager to support the successful execution of commercial ...
Business Affairs Manager to our team in either NC, NY or LA. Provide business affairs support for CYLNDR internal productions, issue contracts, purchase orders and handle any other business affairs needs. Manage business affairs needs for assigned accounts for integrated commercial, promotional, exp...