- Danaher Corporation (West Sacramento, CA)
- …(PLC, LabX, C++, etc.). + Computer Aided Design + Experience with ISO13485, FDA , and IVDR manufacturing systems. Join our winning team today. Together, we'll ... accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit… more
- Abbott (Alameda, CA)
- …+ Extensive Knowledge of regulations for medical device development (ISO134851, ISO13485, FDA ) is a plus. Extensive understanding of processes and materials used in ... the development and manufacturing of medical devices, particularly handheld devices. + Extensive experience in all of the following: + Performing complex engineering calculations and relating results to controlled tests, including statistical analysis,… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …pre-market and post-market development activities + Experience in regulated industries ( FDA , Automotive, Industrial, etc.) At BD, we prioritize on-site collaboration ... because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence… more
- Gilead Sciences, Inc. (Foster City, CA)
- …(eg, Docker, Kubernetes). + Knowledge of AI-related regulatory frameworks (eg, HIPAA, GDPR, FDA , EU AI Act). + Strong grasp of ML algorithms and tuning techniques. ... + Working knowledge of BI tools (eg, Tableau, QuickSight) and pharma data types (eg, RWE, EMR, claims). **Non-technical skills:** + Recognized as a credible data science expert and partner to commercial and cross-functional teams. + Skilled in enabling teams… more
- VTI Life Sciences (Los Angeles, CA)
- …(Mechanical Eng., Chemical Eng., Chemistry, Biology, etc.). + 5+ years of relevant FDA -regulated industry experience. + Candidates must be local to the LA area as ... travel expenses are not allowed. + Knowledge of cGMP and other regulatory standards. + Proficiency in Project Engineering and construction-related activities + Experience with pharmaceutical process equipment and instrumentation. + Proficiency in Equipment,… more
- Abbott (Temecula, CA)
- …compliance of the Quality System. (eg compliance with internal procedures and FDA , BSI regulations etc). + Interacts with internal and external customers, by ... meeting regularly, responding to requests and explaining procedures. + Interprets and executes policies that affect work processes and personnel within the assigned organizational unit. + Contributes to the development of operational policies and procedures… more
- AbbVie (Irvine, CA)
- …computerized systems, used within the R&D laboratory function associated with FDA Good Manufacturing Practices (GMP) testing for biological and small molecule ... projects. + Responsible for the planning, design and implementation of validation projects, coordination of validation activities, and preparation of validation documentation within Pharmaceutical Development, with established guidelines for pharmaceutical… more
- Schwan's Company (La Palma, CA)
- …industry standards of quality and food safety, GMPs, HACCP, food labeling and FDA /USDA regulations + General culinary knowledge and passion for global food is ... beneficial Compensation and Benefits: The base salary range for this position is $73,500 to $122,500 annually with eligibility for a 10% annual incentive bonus, that is based on organizational performance. The pay range represents the numerous factors… more
- Abbott (Sylmar, CA)
- …requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes, ... and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. + Performs other related duties and responsibilities, on occasion, as assigned. **Required… more
- Terumo Neuro (Aliso Viejo, CA)
- …test method validation and data analysis. 3. Demonstrated command and knowledge of FDA and ISO medical device quality system requirements. 4. Proven experience in ... statistical analysis (statistical analysis tools). 5. Proficient computer skills including MS Word, Excel, and statistical software (eg, MiniTab, Statgraphics, Design of Experiment DOE, etc.). 6. Solid written and verbal communication skills. **Desired… more