Regulatory Affairs Senior Associate

Immediate opportunity for a REMOTE Regulatory Affairs Senior Associate within the Regulatory Information Management & Systems (RIMS) team with one of the world's leading biotechnnology companies located in Thousand Oaks, CA.Schedule/Shift: 1st shift, Mon.-Fri., EST time zone preferredPosition type: 1 year contrat (through November 2025); extension...

Immediate opportunity for a REMOTE Regulatory Affairs Senior Associate within the Regulatory Information Management & Systems (RIMS) team with one of the world's leading biotechnnology companies located in Thousand Oaks, CA.Schedule/Shift: 1st shift, Mon.-Fri., EST time zone preferredPosition type: 1 year contrat (through November 2025); extension...

Immediate opportunity for a REMOTE Regulatory Affairs Senior Associate within the Regulatory Information Management & Systems (RIMS) team with one of the world's leading biotechnnology companies located in Thousand Oaks, CA.Schedule/Shift: 1st shift, Mon.-Fri., EST time zone preferredPosition type: 1 year contrat (through November 2025); extension...

Job Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Accordance Search Group. As a key member of our regulatory team, you will be responsible for providing comprehensive regulatory support for new product launches and existing product lines.Key Responsibilities:Develop and implement global regulatory strategies for...

About the RoleAmgen is seeking a highly skilled Regulatory Affairs Director to lead the development and execution of strategy for the CMC and Device Regulatory Affairs team. This role will ensure strategic alignment across programs and geographies, representing the CMC and Device Regulatory Affairs team with Amgen leadership, governance bodies, regulatory...

Job SummaryAmgen is seeking a highly skilled Regulatory Affairs Director to lead the development and execution of strategy for the CMC and Device Regulatory Affairs team. This role will oversee the development of regulatory strategies, decisions, and implementation plans for the Obesity portfolio.Key ResponsibilitiesDevelop and execute regulatory strategies...

Job Title: Regulatory SpecialistJob Summary:We are seeking a highly skilled Regulatory Specialist to join our team at Accordance Search Group. The successful candidate will provide comprehensive regulatory support for new product launches and existing product lines, collaborating with cross-functional teams to ensure compliance with regulatory...

The Opportunity Our location in Irving, TX or Abbott Park, IL currently has an opportunity for a Senior Regulatory Affairs Specialist. What You’ll Work On Participate as the regulatory functional product team member for the organization’s Transfusion Medicine regulatory team. Supports necessary regulatory activities required for...

The Opportunity This position works out of our Lake Bluff, IL (Abbott Park) location in the Transfusion Medicine Division . Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision...

The Opportunity This position works out of our Lake Bluff, IL (Abbott Park) location in the Transfusion Medicine Division . Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision...

The OpportunityAt Abbott, we are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team in Irving, TX or Abbott Park, IL.What You'll Work OnParticipate as the regulatory functional product team member for the organization's Transfusion Medicine regulatory team.Support necessary regulatory activities required for product market entry...

Job SummaryAs a member of the BioSpace, Inc. team, you will play a key role in shaping the company's regulatory strategy and ensuring compliance with global regulations. The ideal candidate will have a strong background in CMC regulatory affairs and experience in leading cross-functional teams.Key ResponsibilitiesDevelop and execute CMC regulatory strategies...

Job Title: Senior Director, Regulatory Risk ServicesAmgen is seeking a highly skilled Senior Director, Regulatory Risk Services to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring the quality and compliance of our products and processes.Key Responsibilities:Develop and implement regulatory strategies...

Position Overview:Collaborate with a cross-functional team to provide comprehensive regulatory support for both new product launches and existing product lines. Engage with quality teams, engineers, and technical experts to address and resolve regulatory issues and inquiries from regulatory agencies.Key Responsibilities:Offer regulatory guidance and input to...

Role SummaryWe are seeking a highly skilled Senior Associate, Security Systems Administrator to join our team at Amgen. As a key member of our Global Security team, you will be responsible for the design, implementation, and maintenance of our security systems.Key ResponsibilitiesDevelop and implement security systems and protocols to protect Amgen's assets...

Transform Your Career with AmgenWe are seeking a Senior Associate, Security Systems Administrator to join our team at Amgen. As a key member of our Global Security team, you will be responsible for ensuring the security and integrity of our systems and data.Key Responsibilities:Develop and implement security policies and procedures to protect Amgen's systems...

HOW MIGHT YOU DEFY IMAGINATION?Youve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge youve worked hard to acquire and the passion you already have. At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over...

The Opportunity Manage within the Medical Affairs Sub-Function. Focus is on synthesizing and advancing scientific and clinical knowledge within diabetes for both internal and external stakeholders. What You'll Work On • The Medical Affairs Manager will be responsible for advancing and maintaining scientific and clinical knowledge, with a...

615531Our client, a leading Pharmaceutical company in Thousand Oaks, CA, is looking for a Process Development Senior Associate to be responsible for executing small molecule formulation experiments to support the development of oral solid dosage forms for early-stage clinical studies. Required Skills:0+ Years w/ Relevant BS OR equivalent 2+ Years w/ Relevant...

615531Our client, a leading Pharmaceutical company in Thousand Oaks, CA, is looking for a Process Development Senior Associate to be responsible for executing small molecule formulation experiments to support the development of oral solid dosage forms for early-stage clinical studies. Required Skills:0+ Years w/ Relevant BS OR equivalent 2+ Years w/ Relevant...