Search Results: 1,207 vacancies
$62.5 - $83.33 per hour
...to the best of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC in Cambridge, MA with the following requirements: Master’s degree in Regulatory Affairs or related field plus 2 years of...
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...prepared align with company goals, submission requirements, legal, & regulatory requirements.
Perform in depth quality reviews of labeling &... ...industry experience required, specifically in Regulatory Affairs & US NDA 505(b)(2) / ANDABe able to multi-task in a fast paced...
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...updated on all country requirements and changes.
* Participate in change control meetings. Review and approve requests. Notify Regulatory Bodies of changes that impact clearances, licenses, etc.
* Perform labeling reviews/approvals as required.
* Researching and...
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...career aspirations while making a direct impact on the lives of patients we serve.
About the Role
The Regulatory Associate will be part of the Regulatory Affairs team reporting to the Director of Regulatory Affairs. The associate will be responsible for supporting...
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The CMC Regulatory Affairs Specialist is responsible for for a subset of programs at the IOPS facility. Evaluate proposed changes to IOPS documents and procedures to determine regulatory impact.E ssential Duties and Responsibilities include, but are not limited to, the...
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...as other research areas centered around rare diseases and immune disorders.SummaryResponsible for leading and developing global regulatory strategy for assigned development projects. Represents Daiichi Sankyo's regulatory group in internal and external development project...
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Overview:
The Associate Director/Director, Regulatory Affairs - GDP, provides essential support to the Senior Director in overseeing regulatory activities related to Quality of Life (QOL) initiatives on a regional and/or global scale. This role involves assisting in...
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The Senior Director, Regulatory Affairs- GDP provides strategic oversight and direction for regulatory activities on a regional and/or global scale. This role entails leading a multidisciplinary team in developing and executing regulatory strategies to advance...
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...partnering with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development... ...pharmaceutical industry required.
~8 or More Years in regulatory affairs
~ Experience in providing regulatory strategic input into...
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...personal lives. Read more: careers.bms.com/working-with-us.We are seeking a highly skilled and experienced US Regulatory Lead to join our dynamic regulatory affairs team. This pivotal role offers a unique opportunity to lead and drive the regulatory strategy for an...
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...saving lives. We are looking for individuals who share this passion to join our team.
We currently have an opening for a Sr. Regulatory Affairs Specialist supporting the Cardiac Surgery product area. This position is responsible for activities which lead to and...
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Overview:
The Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior Director in overseeing regulatory activities related to QOL initiatives. This role involves actively contributing to the development and execution...
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...therapies to help people build families, stay healthy, and stand up to the world's oldest enemy: disease.
As the Director, Regulatory Affairs - Advertising, Promotion and Regulatory Compliance you will be responsible for leading a group of US Regulatory Affairs...
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...Position: CONTRACTORUS Regulatory Affairs- GDP, RA, Associate
Location: Remote (East or Central Time Zone)
Contract: 12mns
Pay Rate: 25/hr - 35/hr
This Regulatory Affairs CONTRACTOR will assist the department with completing regulatory correspondence and...
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...related master data for submission to UDI databases.
Complete UDI database submissions (e.g. US GUDID)
Support and advise on regulatory requirements for UDI direct part marking compliance
Assign and maintain the EU Basic UDI for Client portfolio
Provide the...
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$32 - $34 per hour
...A Regulatory Affairs (hybrid) position based out of Morris Plains, NJ is now available through Adecco Medical and Science. In this role, you will support and review formulas in R&D for the cosmetics industry. This is a 6-month+ temp/contract position starting in April...
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...Job Details
The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area...
Local area
$32 - $34 per hour
Adecco Medical & Science is assisting a local client in recruiting for a Regulatory Affairs Specialist/ Data Entry in Morris Planes, NJ.
Location: Morris Planes, NJ
Type : 6+ Month contract
Schedule: Mon- Fri 8am-5pm( Hybrid schedule in office 2-days a week...
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...Communications, and Real-World Evidence.
We are seeking a life-sciences professional with healthcare regulatory experience to serve as the Director of Regulatory Affairs within our Clinical and Regulatory team. This role sits within our wider Global Strategic Consulting...
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...Role DescriptionOverall Objective: Create and drive the regional regulatory strategy for a product / project and ensure there is a sound... ...and/or regional cross-functional stakeholders (e.g., medical affairs, marketing, market access) where required to ensure alignment...
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