Director of Quality Kalon Executive SearchDirector of QualityLos Angeles, CA$140,000–$180,000 / yearThis executive will play a critical role in ensuring regulatory compliance, driving continuous improvement initiatives, maintaining audit readiness, and supporting the successful development and commercialization of high-quality nutritional supplement products. Kalon Executive Search is partnering with a leading contract manufacturing organization in the nutritional supplement industry to identify a highly accomplished Director of Quality & Regulatory Affairs .
Regulatory Affairs Specialist Nihon Kohden Orange MedRegulatory Affairs SpecialistSanta Ana, CA$80,000–$95,000 / yearCoordinates regulatory requests from Sales Offices and internal stakeholders, including Certificates to Foreign Governments (CFGs), Certificates of Free Sale, authentications, and other regulatory certificates or documentation. Ensures regulatory information for assigned products and markets is current and supports timely retrieval and presentation of documentation for internal stakeholders, regulatory authorities, audits, inspections, and other authorized requests.
Sr. Medical Affairs Specialist LancesoftSr. Medical Affairs SpecialistLos Angeles, CA$85Develop and execute data dissemination plans to effectively communicate the clinical value of ***’s line of products to both internal and external audiences, including healthcare providers, people with diabetes, investors, and regulatory bodies, to emphasize the value of ***’s line of products and inform clinical care. ·Responsible for collaborating with cross-functional teams to ensure the clinical value of the Omnipod line of products is communicated internally and externally in a manner that is scientifically accurate, solves unmet needs, and meets global regulatory requirements.
KMO Director, Clinical Affairs (Brea, CA) EnvistaKMO Director, Clinical Affairs (Brea, CA)Pomona, CA$177,300–$216,700 / yearEnvista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.
KMO Director, Clinical Affairs (Brea, CA) Envista Holdings CorpKMO Director, Clinical Affairs (Brea, CA)Brea, CA$177,300–$216,700 / yearEnvista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.
Regulatory Affairs Manager Huisong PharmaceuticalsRegulatory Affairs ManagerSanta Ana, California$38–$48Position Overview Huisong Inc. is seeking an experienced Regulatory Affairs Manager to support regulatory strategy and compliance for dietary supplements, botanical ingredients, herbal extracts, and Traditional Chinese Medicine products. Founded in 1998, Huisong Pharmaceuticals specializes in the research, development, and manufacturing of premium-quality natural ingredients for leading companies in the pharmaceutical, nutraceutical, food and beverage, and personal care industries.
Medical Affairs LancesoftMedical AffairsSanta Monica, CA$30–$36.72 / hourThe individual contributes to the operational execution of treatment-use and clinical support activities by coordinating study- and program-related deliverables, managing vendors and external partners, supporting site and investigator communications, tracking key milestones and risks, and helping ensure activities are conducted in alignment with applicable regulations, internal procedures, and program requirements.\. May assist in the review of study-related and essential start-up documents, as delegated by the study manager, including clinical protocols, informed consent forms, investigator brochures, pharmacy manuals, monitoring plans, case report forms, CRF completion guidelines, and other relevant study plans and charters.
Microbiologist Integrated Resources, IncMicrobiologistIrwindale, CaliforniaContractorMinimum a 4 year degree in the sciences (preferential in Microbiology/Engineering/Chemistry/Biochemistry) with 3-5 years' work experience with a proven track record in Equipment Validation and general laboratory techniques within the medical device and/or pharmaceutical industry or master's degree in engineering and 2-3 years of experience in the field or in a related area. Following SOPs and special test designs; analyzes test data and completes required documentation, initiates and manages QA test method improvements, equipment, and process validations.
Sr Quality Engineer LanceSoft IncSr Quality EngineerNorthridge, CA$50–$55 / hourThe Quality Engineer will partner closely with Quality, Manufacturing, Regulatory Affairs, R&D, Operations, Supplier Quality, and Customer Service teams to investigate quality issues, drive corrective and preventive actions (CAPA), maintain risk management documentation, and support post-market surveillance activities. Bachelor’s degree in Engineering, Quality, Biomedical Engineering, Mechanical Engineering, Industrial Engineering, Chemical Engineering, or related technical discipline.
NewSr. Mechanical Design Engineer Nihon Kohden Orange MedSr. Mechanical Design EngineerSanta Ana, CA$120,000–$150,000 / yearIndependently develop and maintain mechanical engineering documentation throughout the product lifecycle, including design specifications, drawings, engineering analyses, design reviews, change orders, and Design History File (DHF) records, in accordance with established design controls, FDA requirements, and applicable quality system procedures. Collaborate with Quality Assurance, Regulatory Affairs, Manufacturing, suppliers, and other cross-functional teams to ensure mechanical designs and supporting documentation meet applicable regulatory and quality requirements and support regulatory submissions, including 510(k) submissions where applicable.
KMO Director, Clinical Affairs (Brea, CA) Envista DentistryKMO Director, Clinical Affairs (Brea, CA)Brea, CaliforniaEnvista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.
NewBilingual Korean/English Senior Regulatory Affairs Manager - Cosmetics, OTC & Supplements (FDA Compliance Macpower Digital Assets Edge Private LimitedBilingual Korean/English Senior Regulatory Affairs Manager - Cosmetics, OTC & Supplements (FDA ComplianceLos Angeles, CA$90,000–$140,000 / yearGuided by the core values of Beautiful, Healthy, and Refreshing , they innovate beyond traditional cosmetics and household products, delivering creative solutions tailored to evolving consumer needs. As the Senior Regulatory Affairs Manager , you will ensure regulatory compliance for cosmetic, OTC, dietary supplement, and medical device products in North America—from concept to market launch.
Chemist - II Integrated Resources, IncChemist - IILos Angeles, CaliforniaContractorThe Scientist must be familiar with using the following pieces of equipment: viscometer, pH meter, densitometer, potentiometric titrator, Karl Fischer, FT-IR, Conductivity meter, TOC Analyzer, HPLC and GC. The Scientist will perform routine laboratory testing, non-routine testing, and compendia testing independently and with minimal direction.
Senior R&D Project Engineer Karwell TechnologiesSenior R&D Project EngineerIrvine, CAJob Description: We are seeking a highly motivated Senior R&D Project Engineer to lead Cost Improvement Projects (CIP), design changes, supplier change initiatives, and product lifecycle management activities within a regulated medical device environment. The ideal candidate will possess strong project management skills, medical device product development experience, regulatory knowledge, and the ability to collaborate effectively with cross-functional teams and external suppliers.
Research & Development Manager (Nutraceuticals) Keystone & Golden, Inc.Research & Development Manager (Nutraceuticals)Los Angeles, CAThe role will support both new product development and existing portfolio optimization , working closely with the VP of R&D and cross-functional partners to move concepts from research through launch. A fast-growing, Los Angeles-based women’s health company is seeking an R&D Manager to help develop and commercialize innovative products across women’s health, wellness, supplements, and personal care.
Quality Control Manager - Food Manufacturing Industry Michael Page InternationalQuality Control Manager - Food Manufacturing IndustryEl Monte, California$110,000–$135,000 / yearFull timeIf you are ready to take your career to the next level as a QA Manager in Los Angeles, apply today and join a company dedicated to excellence in the food and beverage manufacturing industry! A successful QA Manager should have: Strong knowledge of quality assurance principles and practices within the food and beverage manufacturing industry.
Senior R&D Project Engineer Katalyst Healthcares & Life SciencesSenior R&D Project EngineerIrvine, CAJob Summary: We are seeking a highly motivated Senior R&D Project Engineer to lead Cost Improvement Projects (CIP), design changes, supplier change initiatives, and product lifecycle management activities within a regulated medical device environment. The ideal candidate will possess strong project management skills, medical device product development experience, regulatory knowledge, and the ability to collaborate effectively with cross-functional teams and external suppliers.
Principal Quality Engineer Katalyst Healthcares & Life SciencesPrincipal Quality EngineerIrvine, CAThe Principal Quality Engineer serves as a subject matter expert, partnering with cross-functional teams to ensure products meet customer, regulatory, and business requirements while driving continuous improvement and operational excellence. This role provides technical leadership for quality systems, product quality improvements, risk management, CAPA activities, process validation, and compliance programs.
Chemist II LancesoftChemist IINorthridge, CA$40In this role, you will support analytical testing, method development, validation, and troubleshooting activities for pharmaceutical and/or medical device products. Required Qualifications Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
NewDownstream Pilot Plant Associate Stark Pharma Solutions IncDownstream Pilot Plant AssociateLos Angeles, CAWe provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success. We are seeking a Downstream Pilot Plant Associate with hands-on experience in downstream purification of viral vector gene therapies at pilot or production scale.