Regulatory Affairs Leader (Associate Director). Create regulatory compliance / project plan with Product RA to ensure all requirements are met for country Regulatory market clearance submissions. Bachelor's Degree (or internationally recognized equivalent) & minimum of 3 years experience in the ...
The Director of Quality Assurance and Regulatory Affairs (QA/RA) is responsible for ensuring that Precision Optics Corporation's products meet applicable regulatory requirements and quality standards. Responsible for all quality assurance and regulatory functions across POC's Portland & Gardner site...
In this role, you will work in collaboration with other talented engineers and project managers to provide professional assistance on complex fire and life safety issues through code consulting, fire protection design, and fire & life safety special inspections and testing services for designers...
The construction project manager oversees and coordinates all aspects of construction projects, from estimating to execution and completion. Construction project managers are primarily responsible for ensuring the successful execution of construction projects. Do note that a construction project man...
The Project Controls Manager is responsible for managing and overseeing all aspects of project controls for complex construction projects, with a strong commitment to safety and quality. Reporting directly to the Business Unit Leader, the Project Controls Manager will develop and implement project c...
The Senior Building Project Manager will provide knowledge, leadership, and management to complete building construction projects safely, profitability and in accordance with the contract documents. Must be experienced in industrial life sciences and manufacturing building construction, with proven ...
The Principal, Global Compliance Audit & Monitoring position reports directly to the Associate Director, Global Compliance Audit & Monitoring and is responsible for supporting program/project planning, execution, implementation, and reporting across a variety of Global Compliance programs. Obtain an...
Principal Regulatory Affairs Specialist - EndoscopyAbout the role:At Boston Scientific, this is a place where you can find meaningful purpose, improving lives through your life's work. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new busine...
Press Tab to Move to Skip to Content LinkSelect how often (in days) to receive an alert: Create AlertPrincipal Regulatory Affairs Specialist - Endoscopy Onsite Location(s): Marlborough, MA, US, 01752Additional Locations: N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - Hi...
Senior Director of Quality, Regulatory and Clinical Affairs. The role will be responsible to work through multiple levels within the organization and external stakeholders to influence and drive Waters Quality, Regulatory & Clinical Affairs strategy to support Waters business growth and success ...
Berkley Accident and Health team (BAH)! You will be responsible for the collaboration of design, development, implementation, and support for all compliance programs, both at the corporate and business unit level for the company. Collaborate with business partners on drafting compliance policies, pr...
The Lead Compliance Specialist will perform critical QA compliance tasks in support of GMP manufacturing programs as AIRM moves through clinical trials and commercialization. The successful candidate will foster compliance across a broad range of Quality Assurance areas and will work closely with ta...
Regulatory Manager, Regulatory Affairs - CMC (Gene Therapy). Plans and prepares CMC regulatory packages, assesses changes for potential regulatory impact, responds to action letters, and maintains filings and approvals. Acts as CMC regulatory lead or deputy for complex projects/products, requiring a...
Regulatory Manager, Regulatory Affairs - CMC (Gene Therapy). Plans and prepares CMC regulatory packages, assesses changes for potential regulatory impact, responds to action letters, and maintains filings and approvals. Acts as CMC regulatory lead or deputy for complex projects/products, requiring a...
Delivery & Execution - Establishes and executes effective communication with Project Stakeholders; Partners with stakeholders to lead the project planning effort, including the formulation of the project scope, definition of the project deliverables and the required delivery dates, creation of a log...
We expect the Manager, Regulatory Affairs CMC to join a growing team and provide support to interpret the current, approved and planned clinical regulatory landscape by contributing to the regulatory submission form process. May act as a submission compliance liaison with other areas of Regulatory A...
What is the Compliance Analyst responsible for?. Create summary reports to Compliance and Business Management that detail compliance findings and corrective actions. What is the Compliance group responsible for?. Franklin Templeton’s Global Compliance team provides oversight and guidance to the vari...
Compliance Specialist – Rate Filing. Be sure to include your preferred contact information as one of our Qualification Specialists will connect with you promptly. ...
Supports global regulatory strategy and execution on development programs, including maintaining strong relationships with cross-functional internal colleagues, regulatory agencies, CROs, consulting groups, and other third parties. Significant regulatory affairs experience is required. Provides stra...
The Regulatory Affairs Specialist will work closely with the Director of Regulatory Affairs to obtain and maintain global regulatory approvals to allow IPG to market its state of the art devices worldwide. Regulatory affairs experience in generating applications and experience in collaboration with ...
This includes developing and implementing regulatory strategies for product approvals, leading the registration of products, ensuring compliance with global regulatory requirements, and managing the regulatory affairs team. Title: Regulatory Affairs Manager. The Regulatory Affairs Manager will be re...
Tetra Tech has an immediate opening in our Boston, Massachusetts office for an Engineering Project Manager with experience in solid waste management and engineering. This position includes participation in advanced gas modeling projects, development concepts, and operational and design strategies fo...
Provide overall company leadership and direction for worldwide Tecomet Quality Assurance and Regulatory Affairs Systems, encompassing both improvements and sustaining activities. ...
Senior Manager of Regulatory Affairs and Quality Assurance - (Medical Device) - Hybrid in MA. Our client is a growing boutique IVD and Medical Device company and they are seeking a Senior Manager of Regulatory Affairs and Quality Assurance to lead a small international team to ensure compliance with...
The senior analyst will also draft, maintain, and communicate guidance documents on product compliance and other issues for target audiences, and review documentation for compliance with laws and regulations. Product Compliance Risk Analyst. They will work on projects relating to compliance with sta...