Search Results: 12,037 vacancies
Takeda Development Center Americas, Inc. is seeking a Manager, Regulatory Affairs
CMC in Cambridge, MA to Develop the Global Regulatory Strategy for products in commercial and development phase; ensure timely submission of new submissions (IND, NDA, BLA, JNDA) to various...
Suggested
...Vice President, Regulatory Affairs
About the Company
Clinical-stage biotechnology (BioTech... ...support global approvals and maintain product licenses across multiple regions. This... ...essential for this position.
Hiring Manager Title
Senior Vice President of Regulatory...
Suggested
Innovative Chemical Products Group (ICP Group) is a leading formulator and manufacturer of... ...looking to identify a Product Safety & Regulatory Affairs Specialist. The PSRA Specialist... ...manufacturing facilities and product lines.
Manage product registrations as mandated by...
Suggested
Local area
...more equitable future.
Position Summary
As the Senior Manager of Regulatory Affairs, you will play a critical role in ensuring... ...successful development, registration, and commercialization of our products.
Key Responsibilities:
As the Senior Manager, Regulatory...
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Flexible hours
...This Role
This role is responsible for Regulatory CMC expertise into the development and... ...for the CMC aspects of assigned projects/products. Responsibilities include preparation... ...activities in the assigned regions and managing of routine and non-routine Health Authority...
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Local area
Remote job
...addition to QINLOCK, we have identified and advanced multiple product candidates from our platform into clinical studies,... ...more details on our portfolio.
Job Description
The Manager, Regulatory Affairs provides regulatory support for oncology products in...
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Temporary work
Summer work
Summer holiday
Flexible hours
...personal and professional ambitions.
Viridian Therapeutics is seeking a Manager of Regulatory Affairs to provide strategic and operational leadership to the development and commercialization of products within the Thyroid Eye Disease (TED) and Autoimmune portfolios....
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Holiday work
Temporary work
Local area
Immediate start
Remote job
...Description
We're looking for a Manager of Regulatory Affairs , working in Biotechnology/Medical Devices industry in Cambridge, Massachusetts... ...regulatory activities relating to specific portfolio of products/projects.
Participates as an active team member of the...
Suggested
...Collaborate with engineering, data science, data engineering, and other product teams to deliver models that are efficient, scalable and... ..., driving progress and communicate results to stakeholders
Manage trade-offs, risks and dependencies across multiple projects and...
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Worldwide
...Job Description
Job Description The Technical Product Manager is expected to possess a comprehensive understanding of the products... ...applications in the biological industry.
Familiarity with relevant regulatory requirements and standards in the biological industry,...
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...application is true to the best of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA with the following requirements: Bachelor's degree in a scientific...
Suggested
Full time
Remote job
Worldwide
...direction and guidance, review and remediate regulatory documentation in support of market... ...documentation in local PLM system and corresponding product registrations with FDA and EU Notified... ....
Trains to and executes document management within local Product Lifecycle...
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Local area
...Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA to establish global submission activities and timelines in partnership with global and cross-functional stakeholders in Pharmaceutical...
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Full time
Remote job
...with us at ZoomInfo.
This role will own our Unified profile product, the AI-powered real-time data and entity resolution that... ...in what you are trying to solve. You have 10+ years of product management experience, and are comfortable setting a product strategy, roadmap...
Suggested
Worldwide
...health and empower life science researchers with easy access to target proteins.
Nuclera is seeking a motivated and high energy product manager to manage a new and exciting product in the market. In this role, you will be contributing to our customer success by...
Suggested
Holiday work
Temporary work
Summer work
Work alone
...develop new medicines for patients.
The Position
Manage and oversee all assigned projects/products/processes. Assist the Director/Associate Director in... ...and submission of any required documents to regulatory agencies.
Relationships
Report to a Director...
Local area
Night shift
...lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions... ...of the position are to drive improvements in regulatory affairs processes, systems and infrastructure...
Night shift
3 days per week
1 day per week
...physicians enhance patient care with its broad product portfolio.
Lantheus is an... ...products while maintaining compliance with all regulatory requirements and commitments. Evaluates... ...this level, the incumbent independently manages a major segment of the Company’s...
Contract work
Local area
Night shift
...Position Summary:
As part of the MSAT team, the Senior Manager of Drug Product Manufacturing Science and Technology, will manage tech transfer... ...process controls, risk mitigation and suitability for regulatory filings.
Bring deep technical expertise in areas such...
Contract work
Work experience placement
Local area
...is currently seeking a Pharmacy Operations, Credentialing and Regulatory Specialist. Under the direction of the Pharmacy Director, supports... ...for inventory reporting, co-pays, compliance audits, management of the contract process and support for inventory management of...
Contract work
Local area
