Associate/Associate II, Regulatory Affairs - Yorba Linda

Join the Clean Energy Revolution · Become a Regulatory Affairs & Compliance Advisor at Southern California Edison (SCE) and build a better tomorrow. In this job, you'll experience a variety of challenges from supporting complex compliance operations to assuming leadership roles i ...

Join the Clean Energy Revolution · Become a · Regulatory Affairs & Compliance Advisor · at Southern California Edison (SCE) and build a better tomorrow. In this job, you'll experience a variety of challenges from supporting complex compliance operations to assuming leadership rol ...

The Regulatory Affairs Project Manager (RAPM) is responsible for directing and coordinating all regulatory activities associated with global Legal Manufacturer (LM) transitions across the organization. · This role oversees a defined 12-month program timeline, ensures cross-functi ...

Career-defining. Life-changing. · iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. · ...

+The Regulatory Affairs Project Manager (RAPM) is responsible for directing and coordinating all regulatory activities associated with global Legal Manufacturer (LM) transitions across the organization. · +Lead the end-to-end regulatory workstream for Legal Manufacturer changes a ...

· Company Description · eTeam was formed in 1999 with the goal of becoming the supplier of choice for clients, employees and contingent workers. Today, we're one of the fastest-growing companies in New Jersey and ranked as one of the best companies to work for by Staffing Indust ...

Develop and execute global regulatory strategies for new and existing products (e.g., dietary supplements, herbal extracts, TCM). · ...

Regulatory Affairs Manager · Santa Ana, CA · Part-time Employee · Salary depending on experience. · About Huisong: · Founded in 1998, Huisong Pharmaceuticals specializes in the R&D and manufacturing of premium-quality natural ingredients for world-leading companies in the pharmac ...

· At HYCOR we believe you should LOVE WHAT YOU DO. · We're looking for innovators who strive to make a difference. We care about our people and our industry of improving the health, well-being and quality of life of individuals with allergic conditions. So, come join us if you d ...

Job Title: · Regulatory Affairs Specialist II · Join our client's Regulatory Affairs team to support the transition to the EU's In Vitro Diagnostic Regulation (IVDR), impacting all CE-marked IVD products. · ...

Become a Regulatory Affairs Advisor at Southern California Edison (SCE) and build a better tomorrow. · Lead portions of the General Rate Case (GRC) · ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions.This role will support execution of global regulatory strategies, ensure compliance with FDA, EU, and international requirements, and collabor ...

Responsible for establishing preparing and leading the strategy for worldwide product approval submission activities As a recognized expert manage multiple large projects or processes Responsible for submission activities focused on USEUCanada and for ensuring compliance to FDA a ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partne ...

The Manager provides regulatory guidance and strategic direction for Biological and Pharmaceutical Advertising initiatives. · ...

Regulatory Affairs Specialist II · Location: Irvine, CA (Hybrid – Core onsite days Tuesday & Thursday; third onsite day flexible) · Duration: 12-month contract · Pay Rate: $45–$50/hour or about $102,000 a year · Only accepting local candidates · Position Overview · This role sup ...

We are searching for a Director of Regulatory Affairs with deep expertise in invasive electromechanical medical devices and extensive experience preparing and submitting · 510(k) notifications. This individual will lead regulatory strategy and submissions for · devices requiring ...

We are a high-growth company with an entrepreneurial spirit that produces reliable products supported by proven clinical data. · - Familiarize with the design manufacture and clinical use of Terumo Neuro products · - Perform specific regulatory tasks for new/modifified product · ...

· We are searching for a Director of Regulatory Affairs with deep expertise in invasive electromechanical medical devices and extensive experience preparing and submitting 510(k) notifications. · Leads the preparation, submission, and negotiation of 510(k) premarket notification ...

Job Summary · The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and ...