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Principal Design Quality Engineer – Class III Implantable Medical Device San Francisco Bay Area | Full-Time | Hybrid A fast-growing medical device company developing next generation implantable technology is expanding its engineering team and hiring a Staff Design Quality Engineer to support the development of a highly innovative Class III medical device platform. This is a highly technical, hands-on role embedded directly with R&D, focused on ensuring quality is built into product development from early feasibility through clinical and commercial stages. You will play a key role in helping bring a breakthrough therapy to market while working alongside experienced engineers and cross-functional leaders in a collaborative development environment. Responsibilities • Partner closely with R&D and systems engineering teams to integrate design quality into product development, • Lead and support design control activities throughout the product lifecycle, • Drive risk management efforts (ISO 14971) including hazard analysis, FMEAs, and risk mitigation strategies, • Support verification and validation planning and execution, • Ensure compliance with FDA design control requirements and global quality standards, • Participate in cross-functional design reviews and technical decision making, • Help translate regulatory and quality requirements into practical engineering processes Qualifications • BS or MS in Engineering (Biomedical, Mechanical, Electrical, or related), • 7+ years of experience in medical device product development or design quality, • Strong experience with design controls and risk management, • Experience supporting Class II or Class III medical devices, • Ability to collaborate closely with R&D in early-stage product development, • Experience supporting IDE, PMA, or complex regulatory pathways is highly valued What Makes This Opportunity Unique • Work on cutting-edge implantable technology, • Join a highly technical engineering-driven team, • Be involved early in the development lifecycle, • Significant opportunity for technical ownership and influence, • Competitive compensation, bonus, and equity package If you are interested in learning more, feel free to reach out directly.

Job Description Predicine is a Silicon Valley-based global precision medicine company that is committed to developing the first- and best-in-class liquid biopsy cancer diagnostics and precision medicine portfolio to address the unmet medical needs in global drug development. We have developed an innovative liquid biopsy technology that is empowering biopharma partners in clinical drug development and oncology medicine research. Our international business services provide molecular insights to the top 10 MNC BioPharma’s to support biomarker-driven clinical trials in US, EU, APAC including China. We believe our most important asset is our people and are dedicated to maintaining a thriving workplace. We value a culture of Integrity, Innovation, Quality, Respect, Courage, Collaboration, Caring, and Communication. We are seeking a highly skilled and motivated Sr. Automation Engineer ( Laboratory) with expertise in Next-Generation Sequencing (NGS) to join our dynamic team. In this role, you will play a critical part in developing, optimizing, and automating workflows to advance our NGS capabilities. As an integral member of our team, you will work closely with cross-functional groups to enhance the efficiency, scalability, and precision of our sequencing technologies. If you have a passion for automation, NGS, and cutting-edge technology, we invite you to contribute to our innovative and fast-paced environment. Key Responsibilities: • Design, develop, and implement automated liquid handling systems for NGS assays, • Translate and optimize manual processes onto automated platforms, • Provide training and technical support for operations during deployment of new methods, • Author and update SOPs (Standard Operating Procedures) and quality documentation to ensure compliance with industry standards., • Maintain and manage instrument configuration documentation (IQ/OQ/PQ and SOP)., • Bachelor’s degree in Engineering, Biotechnology, Biology or related field., • 3+ years of laboratory automation engineering experience required., • Strong Experience in programming and developing automated systems for assay development on Hamilton using Venus Software, experience with scheduling software., • Familiarity with lab automation tools, instrumentation (e.g., Agilent, Bio-Rad, Thermofisher), and software (e.g., BIOlims)., • Familiarity with barcoding, labware management, and traceability tools., • Experience in process development and scaling in a laboratory and/or manufacturing environment., • Ability to work cross-functionally with IT, Facilities, and Operations teams., • Strong problem-solving and troubleshooting skills., • Excellent communication skills and the ability to document technical processes clearly., • Experience with technology transfer and vendor management. Employee benefits include comprehensive medical, dental and, vision, for eligible employees and their dependents. Other benefits include stock allocation and 401k matching benefits, 4 weeks of sabbatical after 5 years of service, lunch provided daily for onsite employees. Predicine is a global molecular insights company that is committed to advancing precision medicine in oncology. Predicine has developed a breakthrough cell-free DNA- and cell-free RNA-based liquid biopsy technology enabling minimally invasive molecular diagnosis for treatment selection, therapy monitoring, and minimal residual disease and early cancer detection. The company has launched a portfolio of blood-urine- and tissue-based diagnostic assays for oncology. We are proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities, and perspectives. Inclusive collaboration benefits our employees, our community, and our patients, and is critical to our mission of changing the management of disease worldwide. All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, location where the role is to be performed, internal equity, and alignment with market data. All job offers are contingent upon successful completion of background verification. Applicants must be legally authorized to work in the USA without sponsorship. *

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Remote Work From Home Administrative Assistant Admin - Part Time Market Research Panelists Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Market Research assignments.

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