Regulatory Affairs Specialist - Billerica, MA

Rapiscan Systems is seeking a Regulatory Affairs Specialist based out of Billerica MA to support global regulatory compliance for security screening products. · ...

The Specialist role is responsible for collection review analysis and management of data in support of product regulatory compliance with Federal and State laws. · ...

+The Regulatory Affairs Specialist role is responsible for collection, review, analysis, and management of data in support of product regulatory compliance with Federal and State laws. · +BA/BS degree in biology, chemistry, food science or related scientific field, · 2-5 years of ...

We have an exciting challenge for you and your future.Our culture is built on value commitments to innovation, · quality results integrity community people and collaboration that fosters strong employee engagement teamwork safety and wellness. · ...

The Regulatory Affairs Specialist role is responsible for collection, review, analysis and management of data in support of product regulatory compliance with Federal and State laws. · Leads technical review of ingredients. · Develops nutrition facts and ingredient statements. · ...

The Regulatory Affairs Specialist supports the activities of the Regulatory Affairs Department in ensuring compliance with accreditation, licensing, and regulatory requirements. · Bachelor's degree in clinical/ healthcare management or related field; Master's degree preferred. · ...

The Regulatory Affairs Specialist role is responsible for collection, review, analysis and management of data in support of product regulatory compliance with Federal and State laws. · ...

The Regulatory Affairs Specialist supports the activities of the Regulatory Affairs Department in ensuring compliance with accreditation, licensing, and regulatory requirements. · This position assists with survey readiness, documentation management, · performance tracking, · and ...

+Develop regulatory regional strategy for ZOLL Resuscitation products and features. · +, Develop and implement regional regulatory strategies for new and sustaining products/features that result in device approval. · ...

The Regulatory Affairs Specialist II supports the company's regulatory initiatives to meet strategic short- and long-term objectives. · ...

We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. · The Acute Care Technol ...

+Introduction · Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. · We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, · Acutecare Diagnostics, · Transfusion, · Autoimmunity, · and Transplant.In our OEM busine ...

Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy. · Assist in the implementation of comprehensive regulatory strategies by ...

In this role you be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy. · ...

We are a growing family-owned innovative company founded in 1966. We operate directly in over 30 countries and have a workforce of more than 7, · 000 strong. · Participates as regulatory design team member for new products providing early input on analytical test requirements. · ...

+Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy.+Assist in the implementation of comprehensive regulatory strategies by ...

This job involves preparing regulatory submissions while ensuring compliance with current regulations. The specialist will maintain meticulous regulatory documentation. · Proficiency in Regulatory Documentation. · Strong understanding of Regulatory Compliance. · ...

We are seeking a Regulatory Affairs Specialist to support the Life Cycle Management (LCM) Regulatory Affairs team in the creation,maintenance,and review of technical documentation.This role ensures compliance with European and U.S.medical device regulations,includingsuch as EU MD ...

We believe there is a smarter, more data-driven way to make decisions in healthcare and our cloud-native AI powered SOPHiA DDM Platform makes that vision a reality on a daily basis.You will have direct input to our mission to democratize data-driven medicine for the ultimate bene ...

We are looking for a Regulatory Affairs Specialist to develop and deploy innovative and compliant regulatory strategies across business and markets. · Assist in implementing comprehensive regulatory strategies by collaborating with regulatory subject matter experts (SMEs). · Coor ...