Government Affairs Specialist - Phoenix

The Government Affairs Specialist will be a key player in shaping policy and advocating for the interests of the AAA Mountain West Group (MWG). As the government affairs contact for this region, you will help develop and implement advocacy strategies, effectively build relationsh ...

We have an exciting opportunity for a skilled and experienced FDA Regulatory Affairs Specialist to join our team This position reports to the Sr. · Director, FDA Regulatory Affairs & Food Safety and will support Central animal food facilities. · The position includes interacting ...

Prepares regulatory applications and reviews communications to ensure they adhere to applicable regulatory standards. Maintains medical device regulations and supports product release process. · ...

Central has an exciting opportunity for a skilled and experienced FDA Regulatory Affairs Specialist to join their team. · ...

The Regulatory Affairs (RA) Specialist will provide primary RA support for one or more product lines and/or region(s), including independent participation on new product development teams and continued RA support through the lifecycle of the product. · We are seeking a highly mot ...

The Regulatory Affairs (RA) Specialist will provide primary RA support for one or more product lines and/or region(s), including independent participation on new product development teams and continued RA support through the lifecycle of the product. · ...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions. · ...

+Job summary · The Regulatory Affairs Specialist role is responsible for preparing and submitting documentation for FDA 510(k) submissions.++•Ability to work in a fast paced collaborative team environment+•Ability to handle multiple projects and coordinate cross functional teams+ ...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies. This position requires a minimum of five years medical device regulatory experi ...

This role will proactively engage with state economic development agencies, governors' offices, legislators and federal agencies to identify pursue and negotiate grants tax credits and incentive programs. · ...

The Regulatory Affairs Document Specialist provides support in various projects including formulas labels product materials and records review product registration and help support the work associated with obtaining government approval for product imports into global markets. Thi ...

The Regulatory Affairs Document Specialist provides support in various projects including formulas labels product materials and records review product registration and help support the work associated with obtaining government approval for product imports into global markets.The ...

Lead day-to-day efforts securing state and federal funding for large-scale manufacturing and energy projects. · Coordinate funding applications · Develop incentive strategies · ...

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week at our Exton PA. · The Sr. Specialist, Regulatory Affairs, Medical is responsible for influencing department regulatory processes and procedures, · developing strategies, · authoring, · ...

The Regulatory Affairs Document Specialist provides support in various projects including formulas labels product materials and records review product registration and helps support the work associated with obtaining government approval for product imports into global markets. · ...

This role will proactively engage with state economic development agencies, governors' offices, legislators, and federal agencies to identify, pursue, and negotiate grants, tax credits, and incentive programs. · Coordinate funding applications. · Develop incentive strategies. · < ...

BioLab Holdings is seeking an accomplished Regulatory Affairs leader with hands-on regulatory experience to architect and drive regulatory strategy for complex products. · ...

The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical device and IVD products. · This role will assist in managing regulatory projects ensuring compliance with FDA ISO 13485 and other global regulatory requ ...

You will report to the Plasma Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to support plasma center operations. · ...

Every day at Takeda we feel good knowing that what we do helps improve the lives of patients with rare diseases. · At BioLife while you focus on our donors we will support you. · We offer a purpose you can believe in a team you can count on opportunities for career growth and a c ...