Overview Who We Are: At Dendreon, we’re transforming the battle against cancer with personalized immunotherapy. Our flagship product, PROVENGE® (sipuleucel-T), was the first FDA-approved immunotherapy for metastatic castrate-resistant prostate cancer, utilizing a patient’s own immune cells
Perform proper handling of incoming product to insure accurate and available inventory. Perform all tasks according to best practice procedures. ESSENTIAL JOB FUNCTIONS Maintain safety standards while operating and identify unsafe practices and situations. Unload various
MAIN JOB RESPONSIBILITIES / COMPETENCIES As a Sr. Business Analyst IT – Sales & Commerce Applications within STAAR Surgicals Information Technology team, this individual plays a critical role working closely with the business and across the
Shift: Wednesday - Sunday Key Responsibilities Advanced Production & Laboratory Operations Manufacture biological indicator components in accordance with cGMP procedures, including but not limited to: Spore seeding and inoculation; Agar pour plate preparation and testing; Preparation
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and
Position Overview We are hiring a Liquid Prep Technician. The Liquid Prep Technician will be responsible for controlled room disinfection/prep and set up, assist with Product Inspection, Labeling, Case Packaging, Accountability and Quarantine of Sterile Filled
Company Description JAVA Developer (CCDI Operations / Backend) (Mid-Level) On-site role (Mandatory) Contract position (Start: July, Minimum 1 year) Compensation: $100K+ DOE Position Overview We are seeking Mid-Level Backend Developers to support CCDI operations and development.
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from
Company Description As a leading healthcare education organization, Unitek Learning’s family of schools helps thousands of students launch and accelerate their careers every year. As a rapidly growing and highly successful company, Unitek is also a
Summary Our client, a first-in-class biopharmaceutical client located in Southern California, is seeking an Associate Director, R&D Quality Assurance (Early-Stage Development) to support their expanding pipeline. This individual will lead quality assurance activities for early-phase clinical
Responsibilities: * Review executed batch records and supporting documentation for completeness, accuracy, and compliance * Support product release activities and ensure adherence to cGMP, GDP, and ALCOA+ principles * Review deviations impacting batch quality and assist with CAPA activities
Title: Biologist II Location: Irvine, CA Contract: 6+ months - possible extension - based on performance and business needs What are the top 3-5 skills, experience or education required for this position: Cell therapy and gene
Quality Manager Gummy Dietary Supplement For over 60 years, MeriCal has been at the forefront of innovation in the dietary supplement industry, delivering custom manufacturing and packaging solutions with passion and precision. With state-of-the-art facilities in
Engineering Manager The Engineering Manager leads the team that builds CoreVests lending technology both Salesforce solutions and custom full-stack applications across origination, underwriting, pricing, and servicing. This is a player-coach role: approximately 80% hands-on engineering leadership
Product Manager (Hybrid) Anaheim, CA Parsec Automation, LLC (Parsec) is a trailblazing creator and provider of manufacturing operations management software. Consistently recognized by organizations like Gartner and IDC and a winner of numerous awards, including the
About Forma Life Sciences Forma Life Sciences is a next-generation CDMO headquartered in Irvine, California, where molecules become medicine. Forma supports oral solid dosage programs from early clinical development through commercial manufacturing, with deep formulation expertise
Job Title: Quality Engineer Manager Department: Quality & Compliance Reporting To: Head of Quality Classification: Exempt Compensation Range: $110,000-$160,000 What We Do Forma is a next-generation Contract Development and Manufacturing Organization (CDMO) based in Irvine, California.
Company Description JAVA Developer (CCDI Operations / Backend) (Mid-Level) On-site role (Mandatory) Contract position (Start: July, Minimum 1 year) Compensation: $100K+ DOE Position Overview We are seeking Mid-Level Backend Developers to support CCDI operations and development.