Regulatory

A leading medical device company is seeking a Regulatory Affairs Specialist to lead the regulatory strategy and manage submissions for new product launches.This is a hands-on role that requires a deep understanding of regulatory requirements and processes, particularly in premarket submissions.The ideal candidate will have a blend of hands-on regulatory...

A growing medical device company based in North San Diego county is hiring a Regulatory Affairs Manager for their QA/RA department. The company is developing breakthrough products for the treatment of cardiac arrhythmias and will be commercializing several new products by the end of this year and early next.The RA Manager will be responsible for leading the...

Job Title: Regulatory Affairs DirectorJob Summary:The Regulatory Affairs Director at Carlsmed is responsible for leading the company's regulatory submissions and ensuring successful interactions with regulatory agencies. This role requires a strong understanding of US and international regulatory pathways and the ability to create effective and efficient...

About the RoleWe are seeking a highly skilled Clinical Laboratory Scientist, Generalist to join our team at Novartis Group Companies. As a key member of our laboratory team, you will be responsible for designing, creating, executing, and troubleshooting new procedures and assays. You will work independently on multiple projects, contributing to the launch of...

Job SummaryThis position is responsible for leading the Quality team to ensure compliant processes, team management, and oversight of the Quality compliance and Quality operations in support of EU, FDA, Clinical Trial, CLIA/CAP, state, and ISO compliance requirements.Key ResponsibilitiesManage personnel and compliance for assay validation, clinical study...

About the Role As the Senior Director of Clinical Affairs you will spearhead clinical collaboration programs driving forward innovative oncologyfocused research. You will be responsible for building and managing relationships with academic institutions research groups and community practices to execute impactful clinical studies. This role requires a strong...

About the Role As the Senior Director of Clinical Affairs you will spearhead clinical collaboration programs driving forward innovative oncologyfocused research. You will be responsible for building and managing relationships with academic institutions research groups and community practices to execute impactful clinical studies. This role requires a strong...

About the RoleWe are seeking a highly experienced Senior Director of Clinical Affairs to lead our clinical collaboration programs, driving forward innovative oncology-focused research. As a key member of our team, you will be responsible for building and managing relationships with academic institutions, research groups, and community practices to execute...

The Document Control Specialist manages and maintains quality-related documentation, including SOPs and work instructions. This role ensures compliance with regulatory standards, oversees version control, and facilitates communication and training on document changes. The Specialist supports internal and external audits, utilizes Electronic Document...

Job SummaryA leading orthopedic manufacturing company is seeking an experienced Senior Design Transfer Engineer to oversee the seamless transition of innovative medical devices from R&D to large-scale manufacturing. This role plays a crucial part in ensuring products meet the highest standards for regulatory and quality compliance and are launched...

About the RoleWe are seeking a highly experienced Senior Director of Clinical Affairs to lead our clinical collaboration programs and drive forward innovative oncology-focused research. As a key member of our team, you will be responsible for building and managing relationships with academic institutions, research groups, and community practices to execute...

Job SummaryThe Environmental Scientist is a key member of our team, responsible for assisting in the execution of environmental compliance and permitting responsibilities. This role requires a strong analytical mindset, attention to detail, and effective communication skills.Key ResponsibilitiesCompliance Inspections: Assist with air, water, and waste...

Job DescriptionWe are seeking a Health and Food Safety Manager to support Aramark food and beverage operations at LEGOLAND California Resort. The successful candidate will coordinate efforts to implement safety and risk control programs, processes, and procedures to protect people, property, environment, and company assets. This role will function as a...

Join our cardiovascular electrophysiology client's rapidly growing team and help as they embark on an exciting phase of their development! The company is eager to find a talented Quality Engineer to facilitate quality activities. This person will provide engineering support to new product development teams and sustaining manufacturing/operation teams. This...

Job SummaryK2 Staffing is seeking a highly skilled Civil Construction Safety Manager to join our team. As a key member of our organization, you will play a pivotal role in ensuring the safety of our workforce and compliance with all relevant safety regulations and standards.Key Responsibilities:Develop and Implement Safety Policies and Procedures: Design and...

Job DescriptionJob Title: Staff AccountantDepartment: Accounting Reports To: EVP Controller SUMMARYThe Staff Accountant at CNB Bank is responsible for supporting the bank's financial operations by performing essential accounting duties, including account reconciliation, journal entries, and maintaining financial records. This role ensures accuracy,...

About the Job Our mission at ClearPoint Neuro is to improve and restore quality of life to patients and their families by enabling therapies for the most complex neurological disorders. We are seeking a Quality Engineer to support our quality management system and regulatory requirements at our Carlsbad, CA facility. The ideal candidate is highly organized...

As a Quality Engineer in New Product Development, you will utilize quality engineering principles and methodologies to ensure compliance with regulatory standards, enhancing product development, manufacturing, and distribution processes for internal and external medical devices.Key ResponsibilitiesDeliver engineering expertise in Quality Assurance, Design...

Work schedule must be flexible based on time zones for project needs. This Remote contract position is part of the Regulatory and Clinical Affairs organization. This position ensures that the internal and external work performed to develop our in vitro diagnostics is in compliance with Good Clinical Practice, applicable regulatory requirements (domestically...

Seeking a CRA to join our exciting Medical Device client in CA! This individual must have at least 2 years of proven experience as a clinical CRA in Medical Device industry. (Open to indication experience).**National Travel is required**Key Qualifications:Clinical Experience: Hands-on involvement in clinical evaluations, working directly with medical...