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The Associate Director, Medical Writing, is responsible for the efficient preparation of high-quality, strategically aligned medical writing deliverables within one or more program. Possible oversight of contract medical writers to ensure efficient preparation of medical writing deliverables for ass
Material HandlerAs a Material Handler, you will be responsible for receiving and auditing incoming materials, conducting daily cycle counts of inventory, and processing jobs via computer systems. You
Freezer, Cooler and Deli Stocker AssociateWhy do people love shopping for fresh food at Sam's Club? Our members tell us one of the biggest reasons is our hard-working and happy-to-help fresh food asso
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Candidates should possess strong healthcare regulatory compliance experience, project management capabilities, and exemplary communication skills. A prestigious healthcare organization in San Diego is seeking a Director of Licensing to oversee systemwide licensing and compliance for various healthca
Role Overview We are seeking a high-caliber Director of Business Development to lead our expansion into the 503A, 503B compounding, medical wellness sectors. You will be responsible for building stra
Easy apply, no experience needed. Steady hours and a calm workspace. USPS roles fill fast.
Administrative AssistantProvide administrative assistance to the Transportation Department and Site Manager as required.Primary Responsibilities:Assist in the preparation of shipping documentation for
This pivotal role involves coordinating with cross-functional teams to ensure compliance and successful submissions to regulatory authorities. The ideal candidate will have extensive experience in CMC regulatory affairs, particularly in small molecule drug development, and will thrive in a fast-pace
Provide oversight for global regulatory affairs in all major regions (North America, Europe, Asia Pacific, Latin America) for all regulatory functions, including Clinical, Non‑clinical, Regulatory Operations, and broad oversight for Regulatory CMC and Regulatory Diagnostics. This position involves
Serve as the clinical pharmacology Lead at cross function teams, and responsible for the dose selection and rationale in phase 1 studies and contribute to dose selections in clinical studies beyond phase 1. Contribute to the timely publication and/or presentation of clinical pharmacology and pharmac
Look for hospital Jobs Listings Full/Part Time + Benefits $20-$35+ / Hour. (APPLY HERE)
Job PostingEmployment OpportunityInter-Con is searching for aspiring individuals to join our thriving team of Security Officers. You'll work as a member of a close team to form the backbone of the bro
Join Thermo Fisher ScientificBill: BR/hr Pay: BR/hr When you join us, you'll be part of a smart, driven team that shares your passion for exploration and discovery.
A leading pharmaceutical company in San Diego seeks a Director, Quality Assurance (GCP) to oversee GCP QA systems, ensuring compliance with regulatory requirements.
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Night Stock AssociateThe Retail Associate is responsible for ensuring our customers have a positive shopping experience. The Associate makes eye contact, smiles, and greets all customers in a courteou
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To qualify for the Regulatory Affairs Specialist III role, candidates must have a Bachelor's degree in life sciences, engineering, or a related field, along with at least 6 years of experience in a regulated environment, including 4 years of direct experience in Regulatory Affairs. The Regulatory Af
Must be willing to work between 6am to 4:30pm PST.