Cmc regulatory affairs in San Francisco, CA

CMC Quality Control Writer / Reviewer
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A California-based biopharmaceutical company is looking to add an experienced professional to their CMC Quality Control Department as a Writer / Reviewer. In this role, the CMC Quality Control Writer / Reviewer will be responsible for authoring,...

Regulatory Specialist
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Candidates located in the US/Canada (where we have clinic locations) are welcome to apply. Seize the opportunity to work in a role that offers the flexibility of remote work, with occasional travel to our vibrant headquarters in...

Regulatory Affairs Manager
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Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation; manages requirements for certifications and licensure from...

Regulatory Specialist
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Regulatory Affairs Specialist II On-site in Alameda, CA Qualifications BS in Life Sciences or Medical Engineering/Technology5+ years of professional experience (not internship...

Regulatory Specialist
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Regulatory Affairs Specialist II On-site in Alameda, CA Qualifications BS in Life Sciences or Medical Engineering/Technology5+ years of professional experience (not internship...

Regulatory Affairs Manager
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Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining...

CMC Quality Control Writer / Reviewer
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A California-based biopharmaceutical company is looking to add an experienced professional to their CMC Quality Control Department as a Writer / Reviewer. In this role, the CMC Quality Control Writer / Reviewer will be responsible for authoring,...

Head of CMC Regulatory Affairs - Small Molecules
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For Current Gilead Employees and Contractors: Please log onto your Internal Career Site ( to apply for this job. At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled...

Regulatory Affairs Specialist Digital Health Technologies
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Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices,...

Regulatory Affairs Associate
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SUMMARY/JOB PURPOSE: Responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and preparing amendments in compliance with guidelines and regulations.

Regulatory Affairs Manager
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Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining...

Regulatory Affairs Specialist II APAC - Diabetes Care
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Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices,...

Senior Regulatory Affairs Specialist - Lingo (on-site)
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Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices,...

Regulatory Affairs Manager
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Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining...

Regulatory Affairs Specialist
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Position Summary The primary responsibility of the Regulatory Affairs Specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies. The RAS is also responsible for ensuring products...

Regulatory Affairs Associate
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SUMMARY/JOB PURPOSE: Responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and preparing amendments in compliance with guidelines and regulations.

Regulatory Consultant/CMC, Cell/Gene Therapy
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Pharmatech is proud to be an equal opportunity employer. Together we are committed to fostering an environment that is professional, inclusive and diverse. Explore the exciting opportunities currently available in the US and around the...

Head of CMC Regulatory Affairs Small Molecules
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Head of CMC Regulatory Affairs Small Molecules page is loaded Head of CMC Regulatory Affairs Small Molecules Bewerben locations United States - California - Foster City time type Full time posted on Vor 18 Tagen ausgeschrieben job...

Manager/Senior Manager, CMC Quality Control
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Innova Solutions is immediately hiring for a Manager/Senior Manager, CMC Quality Control. Manager/Senior Manager, CMC Quality Control This is a hybrid role requiring 2 days onsite in Brisbane, CA and 3 days remote work. Position...

Data Regulatory Reporting
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Innova Solutions is immediately hiring for Data Expert with Regulatory ReportingPosition type: ContractDuration- 9+ MonthsLocation: Concord, CAAs a Business Execution Lead you would:Act as a key data expert for Financial & Risk Regulatory...

CMC Regulatory Technical Writer, Associate Director/Director
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THE COMPANY 89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product...

Regulatory Associate II
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Clinical Trials Regulatory Research Associate - Remote Pay: $34.78 - $55.92/hour Hours: 8:00am - 4:30pm PST *This is a 6-month contract position Department...

Regulatory Affairs Associate
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Role: Regulatory Affairs Associate Location: Alameda, CA - 94502 Duration: 12 Months Job Description Responsible for filing...

Medical Assistant - 40 hours per week - San Francisco
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Job Summary: Assists in examination and treatment of patients under the direction of the Physician and/or Designee. Essential Responsibilities: ...

Regulatory Affairs Manager
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Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining...

Medical Documentation Auditor
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Must live in Northern California Job Summary: The EIO Medical Documentation Auditor ensures accurate and complete documentation through compliance and...

Director, CMC Regulatory Affairs
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Director, CMC Regulatory Affairs Direct Hire Fulltime Role Salary Range: $208,000 - $235,000 per year Location: Redwood City, CA - Hybrid Role Job...

Specialist, Regulatory Affairs
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About Pendulum Pendulum is on a mission to help people improve physical and mental health by creating a new category of products that target the microbiome. We are researching, developing and commercializing a novel class of...

Regulatory Specialist II
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Job Title: Regulatory Specialist II Location: Alameda, CA (94502) Duration: 12 Months Shift: 8 AM to 5 PM Experience...

Manager/Senior Manager, CMC Quality Control
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A recognized biopharmaceutical company in California is currently seeking an experienced professional to join their CMC Quality Control Department as their new Manager or Senor Manager. In this role, the Manager / Senior Manager will be...