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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...

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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...

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📑 Vice President or Senior Vice President, Regulatory Affairs & Quality AssuranceHybrid Role - San Francisco Bay AreaMeet has engaged on a search for a confidential search for a VP/SVP of Regulatory and Quality with one of our biotech clients. Our client is focused in the Heme/Onc space - you'll be reporting into C-Suite and will be heading up Reg an ...

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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercializatio ...

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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercializatio ...

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📑 A clinical-stage biotech focused on Rare Diseases. This company utilizes antibodies to harness the bodies immune system to fight off disease.The RoleThis person ill serve as the GRL for the company's early stage proprietary pipeline as well as supporting partnered programs with large pharma , reporting into the SVP of Regulatory Affairs.Main Respon ...

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📑 This clinical-stage biotech company is revolutionizing the treatment of cancer. They are seeking a Vice President of Regulatory Affairs to oversee all regulatory activities including serving as the primary contact with FDA and other regulatory agencies. You will develop and implement regulatory strategies, lead Health Authority interactions, and ov ...

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📑 Clinical Development Leader (Medical Director to Senior Director level)San Francisco (remote/hybrid) **MUST reside on the West Coast or willing to relocate**Full-timeSciPro is working with one of the most exciting names in Oncology. This position holds high visability and will report directly to the CMO.My client is on the verge of going public due ...

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📑 Becoming a part of MAA is exciting and rewarding for those who enjoy working with a dynamic team. Join us as we exceed our residents’ expectations of a place to call home. Apartment Maintenance Technician Do you pride yourself on a job well done? Are you a natural problem solver while maintaining high standards of work? ...

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📑 This is a stellar opportunity responsible for leading upstream mammalian cell culture process development and tech transfer activities for the generation of complex molecules including monoclonal antibodies, Antibody Drug Conjugates, Bispecific Antibodies and Fusion Proteins. This is a once-in-a-lifetime Global Expat leadership opportunity within t ...

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📑 Job Title: Tech Transfer Project LeadLocation: San Francisco CA 94107 Remote Job Description:The Tech Transfer Project Lead, Drug Substance Development and Manufacturing will oversee key scientific, regulatory, and business functions pertaining to process chemistry for the organization. Responsibilities include oversight of late development/launc ...

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📑 Senior Manager, Regulatory Project Management - Contract - Cambridge, MAProclinical is seeking a Sr. Manager, Regulatory Project Manager for a leading pharmaceutical company. This is a contract position located in Cambridge, MA.Primary Responsibilities:The role is focused on R&D project management for late-stage global regulatory filings. The succe ...

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📑 Senior Manager, Regulatory Project Management - Contract - Cambridge, MAProclinical is seeking a Sr. Manager, Regulatory Project Manager for a leading pharmaceutical company. This is a contract position located in Cambridge, MA.Primary Responsibilities:The role is focused on R& ...

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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...

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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...

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📑 Title: Quality Assurance Manager (Medical Device)Location: Billerica, MAA pharma/med device company is seeking a Quality Manager to spearhead Quality activities related to their combination products. The Quality Manager will be responsible for all aspects of QA for medical devices manufactured on site or through third party contractors.Responsibili ...

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📑 Job title: Regulatory Strategist (RS)Report to: Global Regulatory Lead (Anu Mahashabde)Knowledge, Skills & Competencies:Proactively contribute with curiosity and openness to diverse perspectivesUnderstanding of clinical development of drugs and/or innovative biologics productsDemonstrated experience with driving the preparation of regulatory docume ...

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📑 Job title: Regulatory Strategist (RS)Report to: Global Regulatory Lead (Anu Mahashabde)Knowledge, Skills & Competencies:Proactively contribute with curiosity and openness to diverse perspectivesUnderstanding of clinical development of drugs and/or innovative biologics productsDemonstrated experience with driving the preparation of regulatory docume ...

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📑 Job title: Regulatory Strategist (RS)Report to: Global Regulatory Lead (Anu Mahashabde)Knowledge, Skills & Competencies:Proactively contribute with curiosity and openness to diverse perspectivesUnderstanding of clinical development of drugs and/or innovative biologics productsDemonstrated experience with driving the preparation of regulatory docume ...

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📑 Job title: Regulatory Strategist (RS)Report to: Global Regulatory Lead (Anu Mahashabde)Knowledge, Skills & Competencies:Proactively contribute with curiosity and openness to diverse perspectivesUnderstanding of clinical development of drugs and/or innovative biologics productsDemonstrated experience with driving the preparation of regulatory docume ...

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📑 Senior Director, Regulatory Affairs CMCHybrid - Philadelphia, PAMeet has partnered with a very well-established pharma with hundreds of approved products. They are looking for a Senior Director of Regulatory CMC (small molecule) to join their team. This position will be working across the company's mid-stage, new development pipeline and will be re ...

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📑 Description:Under the supervision of the site Practice Manager, provides administrative support to physicians in a high-volume ambulatory clinic setting, functioning as the primary interface between patients and providers. Emphasis is placed on the ability to stay organized and prioritize administrative tasks related ...

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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and lead ...

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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercializatio ...

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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and lead ...

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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercializatio ...

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📑 Our client is looking to fill the role of Executive Director, Head of Safety/Pharmacovigilance. This position is hybrid and based out of the Carlsbad office.Responsibilities:Position will lead as Deputy to Head of Safety and Pharmacovigilance Department with full oversight of Drug Safety Physicians teamProvide strategic oversight and guidance for s ...

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📑 Our client is seeking a Sr. Director, Clinical Regulatory Affairs to develop regulatory strategies for both non-clinical and clinical programs and lead interactions with regulatory authorities. Reporting to the SVP, Head of Regulatory Affairs, this role will have significant strategic oversight of various submissions and will be the global regulato ...

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📑 Senior Director, Regulatory Affairs CMCHybrid - Philadelphia, PAMeet has partnered with a very well-established pharma with hundreds of approved products. They are looking for a Senior Director of Regulatory CMC (small molecule) to join their team. This position will be working across the compan ...

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📑 Main responsibilities:Leads the US regulatory activities.As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Specialist leverages their regulatory expertise to contribute to the definition of the global regulatory strategy, to enable and drive the execution of aligned US, EU ...

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📑 Main responsibilities:Leads the US regulatory activities.As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Specialist leverages their regulatory expertise to contribute to the definition of the global regulatory strategy, to enable and drive the execution of aligned US, EU ...

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📑 Main responsibilities:Leads the US regulatory activities.As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Specialist leverages their regulatory expertise to contribute to the definition of the global regulatory strategy, to enable and drive the execution of aligned US, EU ...

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📑 Main responsibilities:Leads the US regulatory activities.As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Specialist leverages their regulatory expertise to contribute to the definition of the global regulatory strategy, to enable and drive the execution of aligned US, EU ...

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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lea ...

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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lea ...

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📑 As a pivotal member of the Corbus Product Development Team(s) (PDT) supports Corbus’ drug development by developing and overseeing the execution of regulatory strategy in the US/EU and other territories deemed applicable.Qualifications and Experience:Bachelor’s Degree in life sciences</li ...

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📑 Our client is seeking a Sr. Director, Clinical Regulatory Affairs to develop regulatory strategies for both non-clinical and clinical programs and lead interactions with regulatory authorities. Reporting to the SVP, Head of Regulatory Affairs, this role will have significant strategic oversight of various submissions and will be the global regul ...

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📑 Our client is looking to fill the role of Executive Director, Head of Safety/Pharmacovigilance. This position is hybrid and based out of the Carlsbad office.Responsibilities:Position will lead as Deputy to Head of Safety and Pharmacovigilance Department with full oversight of Drug Safety ...

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📑 Responsibilities: Responsible to communicate new regulatory guidelines. Lead the strategic efforts in the interpretation of relevant and new quality guidelines to ensure that the current and phase appropriate requirements and standards are properly and timely implemented. Provide support to Regulat ...

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📑 Job Description Job Description Come make your mark with Watermark!FOUNDED BY USAF VETERANS in 2007, we are proud to be a Service-Disabled Veteran Owned Small Business.SUBJECT MATTER EXPERTS specializing in security and risk management. We’re intimately familiar with DOD security programs and mission requirements.OUR CORE VALUES drive e ...

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📑 GENERAL SUMMARYThe Medical Assistant is a multi-skilled individual that works in a healthcare setting to support the non-clinical and clinical functions of the service area. Functions under the direction and continuous supervision of a licensed healthcare provider (MD, NP, RN, LPN) during performance of uncomplicated clinical services and tasks. Re ...

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📑 Remote - Candidates must be located in the United States - Ideally Southern California The Sr. Director/Director of CMC Regulatory Affairs will be responsible for developing, leading and executing CMC regulatory strategies and activities for the organization, including the preparation and filing of BLA submissions. This position is a hands-on role, ...

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📑 Responsibilities: Prepare and review CMC submission documents, registration dossiers, health authority briefing packages and responses to health authorities through collaborations with relevant line functions and with minimal supervision. Responsible for the global regulatory evaluation of CMC ch ...

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📑 About the jobOur teamThe team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages and post marketing to support the Diabetes Franchise business, driving the growth of the General Medicines Global Business Unit. In our team, you will manage the US post-marketing activities for TZIELD. You will al ...

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📑 About the jobOur teamThe team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages and post marketing to support the Diabetes Franchise business, driving the growth of the General Medicines Global Business Unit. In our team, you will manage the US post-marketing activities for TZIELD. You will al ...

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📑 About the jobOur teamThe team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages and post marketing to support the Diabetes Franchise business, driving the growth of the General Medicines Global Business Unit. In our team, you will manage the US post-marketing activities for TZIELD. You will al ...

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📑 About the jobOur teamThe team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages and post marketing to support the Diabetes Franchise business, driving the growth of the General Medicines Global Business Unit. In our team, you will manage the US post-marketing activities for TZIELD. You will al ...

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📑 BS/BA degree in Scientific Discipline with3 years in the pharmaceutical industry, preferably with 1 year CMC regulatory experienceResponsibilities will include, but are not limited to, the following:1. Participate in the development of the CMC regulatory strategy for biologics submissions. ...

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📑 Associate Director, Regulatory Affairs - Boston, MA - PermanentProclinical is seeking a strategic regulatory leader to join a renowned biotech. This is a permanent position located in Boston, MA.Primary Responsibilities:The primary focus of this role is to work with internal and external stakeholders to ensure the timely release of finished product ...

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📑 Summary GENERAL SUMMARY The Medical Assistant is a multi-skilled individual that works in a healthcare setting to support the non-clinical and clinical functions of the service area. Functions under the direction and continuous supervision of a licensed healthcare provider (MD, NP, RN, LPN) during performance of un ...

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