Jobs at Good Samaritan Hospital, Los Angeles

The Clinical/Health Care Research Nurse serves as a key coordinator within the Institute for Clinical and Translational Science, supporting the design and execution of clinical trials. Key responsibilities include screening and enrolling patients, obtaining informed consent, managing regulatory documentation, and assisting with data collection and budget administration. This role appeals to nursing professionals seeking to accelerate translational science and foster innovation in healthcare. The position offers a hybrid work arrangement within Iowa, combining on-campus and remote duties, and provides a comprehensive benefits package including retirement contributions and paid leave.

This six-month onsite role in Irving, Texas, serves as an entry-level quality assurance position within Abbott's manufacturing and testing operations. The technician supports production schedules by performing incoming dimensional and visual inspections on medical device components such as cable harnesses and printed circuit boards using hand tools and advanced measuring instruments. Key responsibilities include maintaining accurate GMP and GLP compliant records, accepting or rejecting supplier lots, and documenting non-conformances to support regulatory initiatives. The position appeals to candidates seeking to work in a global healthcare environment where quality and safety are paramount, offering exposure to FDA and ISO standards while contributing to life-changing medical breakthroughs.

This full-time Pharmacy Technician role within the clinical trials department supports the execution of regulated medical studies. The position involves maintaining organized study files, dispensing medications and devices, calculating dosages, and managing inventory to ensure patient safety. Key responsibilities include monitoring compliance with federal and state regulations, preparing for quality assurance audits, and coordinating with trial sites and sponsors to resolve protocol issues. The role offers a stable 40-hour work week with opportunities to contribute to medical advancements through rigorous adherence to good clinical practices. While primarily based on-site, the position may require some travel for study-related activities.

The Clinical Trial Monitor II role within the Clinical Trials Office at Dana-Farber Cancer Institute ensures research compliance with federal regulations and institutional policies. Key responsibilities include conducting remote data reviews and onsite monitoring visits to verify data accuracy, developing monitoring plans, and mentoring new team members. The position requires managing multiple projects simultaneously while promoting a culture of regulatory awareness. This opportunity appeals to professionals seeking to contribute to groundbreaking cancer research within an inclusive, mission-driven academic environment. The role is based in Boston with occasional travel required for onsite visits.

The Clinical Research Coordinator role at Huntsman Cancer Institute supports the Principal Investigator in managing the implementation and quality control of cancer research studies across the Intermountain West region. Key responsibilities include ensuring regulatory compliance with FDA and IRB guidelines, managing study budgets and participant enrollment, and coordinating all aspects of patient interactions from screening to informed consent. The position also involves supervising junior staff and maintaining detailed research documentation. This opportunity appeals to professionals seeking to contribute to a mission-driven organization dedicated to reducing the global cancer burden. The role offers a collaborative environment with opportunities for professional growth, requiring a blend of administrative precision and patient-centered care within a hybrid work setting.

This full-time Clinical Research Associate role is dedicated to a single sponsor and requires candidates to reside in the US near major hub airports in the Southeast, Northeast, Central, or West regions. The position involves performing site monitoring visits, including selection, initiation, and close-out, while ensuring adherence to Good Clinical Practice and international guidelines. Key responsibilities include managing subject recruitment plans, overseeing regulatory submissions and data integrity, and maintaining accurate Trial Master Files. The role offers the opportunity to work with a leading global provider of clinical research services, contributing to the development of innovative medical treatments. This position is travel-intensive, requiring approximately 65-70% nationwide travel to support diverse study sites.

The Production Associate role at Tennessee Foam supports manufacturing operations in Knoxville for diverse industries including medical and bedding. The position involves operating machinery in compliance with GMP and ISO13485 standards, maintaining a clean and safe work environment, and ensuring products meet strict customer specifications. Key responsibilities include troubleshooting equipment issues, adhering to standard operating procedures, and participating in ongoing training for professional development. This opportunity appeals to candidates seeking a dynamic, growth-oriented career within a global company that values innovation and strong team collaboration. The role offers a casual yet productive culture with access to comprehensive benefits and career advancement pathways, requiring no travel and based entirely on-site.

The Packaging Quality Supervisor role is a full-time position within the Quality department at a beverage facility in Rochester, NY. This leader oversees packaging quality functions, manages a team of analysts, and ensures compliance with FDA and TTB regulations. Key responsibilities include directing product safety testing, leading root cause investigations for quality issues, maintaining laboratory operations, and facilitating new product commercialization. The position offers a collaborative culture focused on continuous improvement and community involvement, supported by flexible scheduling, generous paid time off, and comprehensive benefits. While primarily based on-site, the role includes occasional travel to suppliers and customers for technical support and audits.

This full-time Packer role supports 80 Acres Farms' mission to revolutionize sustainable agriculture by packaging pesticide-free produce in advanced vertical farming facilities. The position involves operating packaging machinery, ensuring products meet strict specifications, and maintaining a sanitized work environment through rigorous cleaning and adherence to good manufacturing practices. Employees are responsible for lifting items up to 50 pounds and standing throughout shifts in temperature-controlled settings. The role appeals to individuals passionate about food sustainability and offers comprehensive benefits including immediate health coverage, paid time off, and a 401(k) match. The company provides extensive on-the-job training in a collaborative culture that values diversity and purpose-driven work across multiple locations.

This full-time role serves as a Press Floor B-Operator within the Press Department at the TPT Plant, focusing on third-shift production from 3:30pm to 5:30am. The position involves operating machinery to remove quality products, adhering to strict food safety and manufacturing standards, and maintaining high productivity levels to meet daily quotas. Key responsibilities include ensuring safe work practices, managing machine output, and performing necessary cleaning and product changeovers. The role appeals to individuals seeking a stable position within a collaborative team environment that values integrity, continuous improvement, and customer focus. While the work requires physical stamina for lifting and maneuvering heavy loads, it offers the opportunity to contribute directly to the company's mission of producing pet treats in a fast-paced setting.

This Lab Technician role supports Manufacturing Operations within a leading pharmaceutical organization based in Pearl River, New York. The position involves executing production activities using process equipment, assisting with operational qualification training, and ensuring strict compliance with standard operating procedures and global regulatory guidelines. Key responsibilities also include troubleshooting, technology transfer, and applying analytical tools to optimize production start-ups. The role appeals to candidates seeking to contribute to projects that impact global health while working in a dynamic, innovative environment. The company fosters a collaborative culture that values integrity and continuous improvement, offering opportunities for professional development and skill enhancement through ongoing training.

This on-site Buyer Associate role at Ferguson Industrial supports procurement and customer service functions within the La Porte, Indiana facility. The position involves managing MRO procurement activities, monitoring inventory levels, and leading supplier negotiations to secure favorable terms. Key responsibilities include drafting procurement reports, expediting orders, reconciling billing discrepancies, and assisting with warehouse operations as needed. The role appeals to candidates seeking a collaborative environment within a Fortune 500 company that values continuous process improvement and professional growth. The position offers a supportive culture focused on holistic well-being and includes opportunities for career development within a fast-paced, team-oriented setting.

This full-time second-shift Production Team Member role supports the packaging operations for a leading coffee manufacturer. The position involves collaborating with the production team to meet daily quotas while strictly adhering to safety and food quality standards. Key responsibilities include operating packaging lines, performing case filling and pallet stacking, maintaining equipment, and executing sanitation tasks. The role appeals to candidates seeking a stable career with opportunities for growth and advancement within a supportive company culture. Benefits include comprehensive health coverage, a 401(k) plan, paid time off, and employee perks. The position requires physical stamina for standing and lifting in an on-site industrial environment.

This senior-level Tool Room Supervisor role leads daily operations within the tooling department, overseeing injection molding maintenance, repair, and optimization. Key responsibilities include managing the full lifecycle of proprietary and customer-owned tooling, supervising and mentoring a team of mold mechanics, and ensuring strict compliance with ISO 13485 quality standards. The position involves coordinating preventative maintenance schedules, managing external vendors for major repairs, and collaborating with engineering teams to improve manufacturing efficiency. The role is appealing for its opportunity to drive continuous improvement in a medical molding environment, offering a collaborative culture that values technical growth and safety. The position is based on-site within the tool room facility.

This onsite Manager role at Varian Medical Systems leads Quality Control testing operations for the Interventional Oncology business in Austin, Texas. The position involves overseeing daily laboratory activities, managing and developing QC staff, and ensuring all medical devices meet strict regulatory specifications before release. Key responsibilities include driving compliance with Quality System Regulations, applying Statistical Process Control to monitor performance, and supporting sterilization and biocompatibility testing initiatives. The role appeals to professionals seeking to lead a diverse global team within a culture that values innovation, sustainability, and individual growth. It offers the opportunity to directly impact patient safety while collaborating cross-functionally to advance medical technology breakthroughs.

This senior clinical research associate role at ICON plc focuses on ophthalmology trials within a global healthcare intelligence organization. The position involves overseeing clinical trial activities to ensure strict adherence to protocols, regulatory requirements, and Good Clinical Practice standards. Key responsibilities include conducting site visits to assess performance, resolving operational issues, collaborating with cross-functional teams for accurate data reporting, and providing mentorship to junior staff. The role appeals to professionals seeking a culture that values inclusion, innovation, and talent development. It offers a flexible benefits package focused on well-being and work-life balance, with a work arrangement requiring approximately 60% travel to manage multiple sites.

The Internal Loan Originator role at AnnieMac Home Mortgage involves managing a steady flow of loan volume from real estate brokers, referrals, and company-provided leads. Key responsibilities include processing qualified inbound inquiries, completing loan applications, and analyzing borrower financial data to determine affordability. The position requires counseling clients through the home buying process, explaining loan products and costs, and maintaining communication with borrowers and lenders throughout the closing phase. This opportunity appeals to sales-oriented professionals seeking to leverage their mortgage industry expertise in a supportive environment. The role offers a comprehensive benefits package including medical, dental, vision, and 401K options, along with opportunities for professional growth within a collaborative team.

This senior clinical research associate role at ICON plc focuses on ophthalmology trials within a global healthcare intelligence organization. The position involves leading complex monitoring tasks to ensure sites adhere to protocols, regulatory standards, and Good Clinical Practice. Key responsibilities include conducting site visits to assess performance, collaborating with cross-functional teams for accurate data reporting, and providing mentorship to junior staff. The role appeals to professionals seeking a diverse, inclusive culture that rewards high performance and supports work-life balance through comprehensive benefits. While the position requires approximately 60% travel, it offers significant opportunities for professional growth and the chance to shape the future of clinical development.

This full-time Machine Operator I role is based in Reading, Pennsylvania, operating on a weekday day shift schedule. The position involves safely operating machinery to produce parts that meet strict customer specifications, including reading work orders, assisting with material feeding, and monitoring for defects. Key responsibilities also encompass inspecting finished products, measuring characteristics, packaging items, and maintaining accurate production records within a computer system. The role appeals to candidates seeking professional growth within a supportive team environment that values innovation and individual development. The company offers a pleasant workplace culture with opportunities to work alongside industry professionals on diverse projects. The position requires physical capability to lift up to 35 pounds and adapt to varying environmental conditions.

This 1099 independent contractor role as a Principal Investigator in Neurology focuses on leading objective clinical research to enhance client quality of life. The position involves managing the full lifecycle of research projects, ensuring strict adherence to federal regulations and Good Clinical Practice guidelines, and overseeing subject safety and informed consent processes. Key responsibilities include designing study protocols, monitoring data integrity, and coordinating with internal teams to maintain compliance. The role appeals to experienced medical professionals seeking to apply their leadership skills in a dynamic, client-focused environment. It offers the opportunity to drive clinical continuous improvement while working with a collaborative team dedicated to making a meaningful impact in the field of neurology.

The Quality Control Inspector role at Orchid Orthopedic Solutions involves performing receiving, in-process, and final inspections on medical device components within a Swiss-style turning manufacturing environment. Key responsibilities include utilizing precision metrology tools for dimensional and visual testing, maintaining accurate documentation in compliance with FDA and ISO standards, and conducting First Article Inspections. The position offers the appeal of working for a world-leading medical device company with a mission to improve patient lives, providing opportunities for professional growth, comprehensive benefits, and a collaborative culture that values integrity and teamwork. This on-site position in California requires adherence to modified production schedules and supports a diverse, inclusive workplace.

This full-time seasonal role involves operating the palletizing station within Bolthouse Fresh Foods' carrot production facility. The position requires manually stacking finished bags, cartons, and trays onto pallets while adhering to strict safety and quality standards. Key responsibilities include rotating through various line stations, assembling IFCO trays, applying product codes, and maintaining a clean work environment. The role offers the opportunity to join a century-old industry leader with a strong commitment to food quality and employee development. The position is based on-site in a fast-paced environment with potential for overtime and rotating schedules.