Regulatory Affairs CMC Associate

Job DescriptionJob DescriptionFoster City, CAContract Duration: 6-18 monthsRate: NegotiableResponsibilities:Excellent employment opportunity for a Regulatory Affairs CMC Associate in the Foster City, CA area. Bay area candidates ONLYProvide Regulatory CMC support for biologic and small molecule drugs being evaluated or marketed for the treatment of oncology,...

Position Overview:We are seeking a qualified candidate with expertise in Pharmaceutical Regulatory CMC to join our team. While preference is given to local candidates in the Bay Area, we are open to considering individuals located within the Pacific time zone who possess relevant experience.Key Responsibilities:Prepare and manage moderately complex...

Description Home Search Jobs Job Description Regulatory Affairs Associate - II Contract: Foster City, California, US Salary: $60.00 Per Hour Job Code: 352568 End Date: 2024-09-08 Days Left: 28 days, 3 hours left Apply Pay range: $55 to $50/hr.Responsibilities: Collaborate with the RA CMC team to meet deliverables and timelines Ensure data...

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap –...

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap –...

Position Overview:We are seeking a qualified candidate with expertise in Pharmaceutical Regulatory CMC to join our team. While preference is given to local candidates, we are open to considering individuals located within the Pacific time zone who possess the necessary experience.Key Responsibilities:Prepare and manage moderately complex regulatory...

Job DescriptionJob DescriptionFoster City, CAContract Duration: 12-18 monthsRate: NegotiableResponsibilities:Excellent employment opportunity for a Regulatory Affairs Associate II in the Foster City, CA area. (Onsite Role)Contractor must meet the company site requirements for the COVID Vaccination PRIOR to starting roleResponsible for the preparation of Drug...

Director Regulatory Affairs CMCSan Francisco, CA (Hybrid)6 month initial contract (likely extension and conversion to FTE)This client is a clinical-stage precision oncology biotech focused on creating cutting-edge therapies to target cancer treatments. Responsibilities:Develop and implement CMC regulatory strategies to facilitate the clinical development and...

The Regulatory Affairs CMC (Chemistry, Manufacturing, and Controls) – Data Administrator Contractor will play a key role in supporting the RA CMC team by managing product information within Gilead Information Systems. This position involves routine data entry, quality control, and report generation to ensure the completeness, correctness, and consistency...

**General** **Description:** BeiGene is seeking an experienced and energetic regulatory professional to manage, evaluate, and complete regulatory projects consistent with company goals. This individual will be responsible for development of strategies, planning, drafting, and managing CMC-related regulatory submissions and HA interactions to meet the...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Pharmatech Associates. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our clients' projects with global regulatory requirements.Key ResponsibilitiesCMC and Clinical Regulatory Expertise: You will...

Job Description Job Title: Regulatory Affairs Specialist Company: US Tech Solutions Job type: Contract Duration: 12 months ID: 5175 Department: Regulatory Affairs Prerequisites: BS/BA degree in Scientific Discipline (Masters or higher preferred) A minimum of 7 years in the pharmaceutical industry A minimum of 5 years CMC regulatory (biologics preferred)...

Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease.At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients. Our work is rewarding – both professionally and personally – because...

Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease.At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients. Our work is rewarding – both professionally and personally – because...

Position Title: Regulatory Affairs SpecialistCompany: Katalyst HealthCares & Life SciencesEmployment Type: ContractDuration: 12 monthsDepartment: Regulatory AffairsQualifications: Bachelor’s or Master’s degree in a relevant Scientific Discipline At least 7 years of experience in the pharmaceutical sector Minimum of 5 years of experience in CMC regulatory...

Job SummaryORIC Pharmaceuticals, Inc. is seeking a highly motivated and experienced Director/Associate Director to lead our Regulatory Affairs and Compliance team. As a key member of our organization, you will be responsible for ensuring compliance with global regulatory requirements and developing strategies to support our clinical development programs.Key...

Job Title: Regulatory Affairs CMC – Data Administrator ContractorLocation: Foster City CADuration: 12 MonthsDescription:Specific Job Responsibilities Perform data entry using Gilead Information Systems to enter and maintain relevant product information to support cross-functional stakeholders. Work collaboratively to support the RA CMC team to meet...

DescriptionAbout PaciraPacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients.    Each of our 3 marketed products, both in pharmaceutical and medical device, represent cutting edge technologies for pain...

Job DescriptionOverviewCodera, a leading life sciences-focused investment company, is seeking a highly skilled Regulatory Affairs Director to support the development and execution of domestic and international regulatory strategy.Key ResponsibilitiesRegulatory Strategy Development: Provide strategic advice and support the development and execution of...

DescriptionAbout PaciraPacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients.    Each of our 3 marketed products, both in pharmaceutical and medical device, represent cutting edge technologies for pain...