Director, US Regulatory Affairs Pharmaceuticals - Duluth, GA

The Director US Regulatory Affairs Pharmaceuticals leads the US Regulatory Affairs RA Pre and Post approval organization responsible for the Animal health portfolio of Pharmaceutical nutraceutical pesticide New Innovative products in close collaboration with Global RA Global Inno ...

+The Director, US Regulatory Affairs Pharmaceuticals leads the US Regulatory Affairs (RA) Pre and Post approval organization responsible for the Animal health portfolio of Pharmaceutical, nutraceutical, pesticide & New Innovative products; in close collaboration with Global RA, G ...

The Manager, · Associate Director, Regulatory Affairs Pharma Safety & Efficacy will represent the US regulatory safety and efficacy function in global development projects and provide regulatory strategy for assigned projects that leads to a reliable and efficient timeline for pr ...

The Regulatory Affairs Manager will represent the US regulatory safety function in global development projects providing regulatory strategy for assigned projects leading to a reliable timeline for product approval they will ensure project teams meet US requirements through activ ...

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. · ...

We are seeking a Medical Support Specialist (Plasma Center Nurse) to support plasma center operations. As a Medical Support Specialist, you will determine donor eligibility to donate plasma and work under the guidance of the Center Manager for operational guidance and under the m ...

BioLife Plasma Services is seeking a Medical Support Specialist (Plasma Center Nurse) to support plasma center operations in Duluth. · ...

Plasma Center Nurse – LPN position at BioLife Plasma Services in Duluth, USA. The role involves determining donor eligibility and managing adverse events. · Determine donor eligibility to donate plasma · Management of donor adverse events · ...

We are not a staffing firm or agency and we promote jobs on LinkedIn on behalf of its direct clients, · Biolife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. · ...

We are seeking a Plasma Center Nurse to join our team at BioLife Plasma Services in Duluth, GA. As a Medical Support Specialist (Plasma Center Nurse), you will be responsible for determining donor eligibility and managing donor adverse events. · Determine donor eligibility; to in ...

The Director, Scientific Expert CMC is responsible for providing new product and marketed product regulatory strategy in the Global Regulatory Affairs (RA) Chemistry, Manufacturing and Controls (CMC) function for pharmaceutical biotech and vaccine products in line with Company po ...

The Senior Associate Director of US Regulatory Affairs Animal Health Intelligence and External Engagement provides technical regulatory expertise to our operations in the respective scope of their responsibilities: Global Innovation, Global Supply, Global Strategic Marketing, US ...

The Senior Associate Director of US Regulatory Affairs Animal Health Intelligence and External Engagement is responsible for advancing Boehringer Ingelheim's (BI) regulatory intelligenceand engagement strategies for US Animal Health. · ...

Every day at Takeda, we feel good knowing that what we do helps improve the lives of patients with rare diseases. · About BioLife: Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. · ...

The job of Plasma Center Nurse is to support plasma center operations and provide medical support to donors. The nurse will determine donor eligibility, manage adverse events, review laboratory test results, and notify donors of unsuitable test results. · ...

As an employee of Boehringer Ingelheim, · You will actively contribute to the discovery, development and delivery of our products to our patients and customers. · ...

The Senior Associate Director of US Regulatory Affairs Animal Health Intelligence is responsible for advancing Boehringer Ingelheim's regulatory intelligence and engagement strategies for US Animal Health. · ...

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the development manufacturing and distribution of Class II IVD devices. · The ideal candidate will have at least 7 years of experience in the IVD industry with a strong background in qua ...

In this role, you will own and execute the Raw Material Quality Assurance program, focusing on supplier qualification, compliance, and continuous improvement. · Raw Material Assessment: define and oversee the evaluation and approval of suppliers and raw materials, · , ensure that ...

At Avanos Medical, they passionately believe in three things: making a difference in their products and services, · Making a difference in how they work and collaborate for innovation,Having an impact on the healthcare challenges people face worldwide. · We strive to be independe ...