Job Description Job Description Regulatory Affairs Specialist II - Temporary Summary : Able to work with minimal supervision. Strong customer orientation and focus Able to work independently and with others. Requirements: Education: Bachelor’s degree or equivalent in Biology, Chemistry,
Role: Regulatory Specialist II Location: Alameda, CA - 94502 Duration : 12 Months Experience Background (Any): Medical Device, Pharmaceutical, Regulatory Affairs, Quality Assurance, SW Engineering, APAC regulatory submission, or APAC-related work under Quality Assurance/Engineering. Job Description (Expectation) Responsible for regulatory activities, including
Description: Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function Skills: Knowledge of regulations and standards affecting IVDs and/or biologics Education: BS preferred in a technical discipline
For further information please contact our Talent Specialist: Divya | (224) 369-2969 Rashi | 630 847 1027 Title: RA Specialist II Location: Alameda, CA Duration: 12 Months ( with possible extensions) 100% Onsite Description: Preferred/Optional: Bilingual (Japanese or
For further information please contact our Talent Specialist: Rakesh | 630 847 0275 Title: Clinical Research Associate (CRA) - B Location: Alameda, CA Duration: 6 Months with possible extension Description: This position is Non-Exempt. Hours over 40
Your work days are brighter here. At Workday, it all began with a conversation over breakfast. When our founders met at a sunny California diner, they came up with an idea to revolutionize the enterprise software
Heluna Health and the Infant Botulism Treatment and Prevention Program (IBTPP) of the California Department of Public Health (CDPH) invite applications for the position of GXP Compliance and Biologics Development Specialist (GCBDS). IBTPP is a unique public
Twist Bioscience is looking for a Communications Generalist focused on Internal Communications responsible for providing communications support across the organization for all divisions of the company. Reporting to the Sr VP, Corporate Affairs, the Communications Generalist will
Are you interested in working with the World’s leading AI-powered Quality Engineering Company? Ready to advance your career, team up with global thought leaders across industries and make a difference every day? Join us at Qualitest!
Job Description Job Description Santa Monica, CA Contract Duration: 12-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Quality Assurance Specialist III in the Santa Monica, CA area. Reporting to the Sr Manager of Global Quality
Help us change lives At Exact Sciences, were helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most.
One of our largest pharmaceutical clients is looking for a Global Regulatory Documentation Specialist to join their team. The Regulatory Affairs (RA) Associate is a key role of the Global RA Transition project who will assist with the coordination and/or
Primary Duties and Responsibilities: Providing regulatory and quality consultation as a subject matter expert. Providing both Regulatory and Quality training to Investigators, CTP team members, and at large training. Understanding regional, provincial, and federal laws that apply to