Gilead Sciences, Inc.
Senior Quality Engineer II – Combination Product Development
Gilead Sciences, Inc., Foster City, California, United States, 94420
Senior Quality Engineer II – Combination Product Development
Overview
Gilead Sciences is looking to hire a
Sr Quality Engineer
for the Combination Product Development team. Responsibilities
Serve as a lead quality engineer for medical device combination product development projects, with a strong emphasis on design control and risk management activities. Collaborate with device engineering on new combination product development, supporting design verification, validation, and transfer activities. Contribute to quality improvement initiatives and ensure compliance with relevant regulations and standards, including FDA 21 CFR Part 820, 21 CFR Part 4, ISO 13485, ISO 14971, and Gilead’s quality system requirements. Plan and implement approved quality improvement action items and deliverables. Interface with internal stakeholders, contract manufacturers, and suppliers to resolve complex technical issues related to drug-device combination products, processes, and quality. Act as an escalation point for complex and high-impact quality issues, concerns, and decisions. Support strategic relationships with internal cross-functional teams and contract manufacturing organizations (CMOs). Provide guidance and impact assessments for change controls, including Design History File (DHF) and Risk Management File (RMF) assessments. Develop and/or review controlled documents (e.g., protocols, reports, plans, risk analyses, specifications, test methods). Qualifications
Bachelor's degree in engineering or a scientific discipline with 8+ years of relevant experience, OR a Master's degree in a relevant field with 6+ years of relevant experience. Demonstrated knowledge and experience in quality assurance for the development of medical devices and/or drug-device combination products. Prior experience with combination products (e.g., autoinjectors, co-packed kits, pre-filled syringes) is preferred. Strong project management and process improvement skills. Understanding of domestic and international quality system regulations and the ability to drive continuous improvement. Possess a strong foundation in statistical techniques (e.g., normality tests, capability analysis, tolerance intervals), test method validation (MSA, Gage R&R), and risk management principles per ISO 14971, including FMEA and systems analysis. Expertise in one of these areas is required. Ability to develop and improve complex concepts, techniques, standards, and new applications based on quality principles and theories. Strong knowledge of medical devices and/or combination products manufacturing. Excellent verbal, written, and interpersonal communication skills.
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Overview
Gilead Sciences is looking to hire a
Sr Quality Engineer
for the Combination Product Development team. Responsibilities
Serve as a lead quality engineer for medical device combination product development projects, with a strong emphasis on design control and risk management activities. Collaborate with device engineering on new combination product development, supporting design verification, validation, and transfer activities. Contribute to quality improvement initiatives and ensure compliance with relevant regulations and standards, including FDA 21 CFR Part 820, 21 CFR Part 4, ISO 13485, ISO 14971, and Gilead’s quality system requirements. Plan and implement approved quality improvement action items and deliverables. Interface with internal stakeholders, contract manufacturers, and suppliers to resolve complex technical issues related to drug-device combination products, processes, and quality. Act as an escalation point for complex and high-impact quality issues, concerns, and decisions. Support strategic relationships with internal cross-functional teams and contract manufacturing organizations (CMOs). Provide guidance and impact assessments for change controls, including Design History File (DHF) and Risk Management File (RMF) assessments. Develop and/or review controlled documents (e.g., protocols, reports, plans, risk analyses, specifications, test methods). Qualifications
Bachelor's degree in engineering or a scientific discipline with 8+ years of relevant experience, OR a Master's degree in a relevant field with 6+ years of relevant experience. Demonstrated knowledge and experience in quality assurance for the development of medical devices and/or drug-device combination products. Prior experience with combination products (e.g., autoinjectors, co-packed kits, pre-filled syringes) is preferred. Strong project management and process improvement skills. Understanding of domestic and international quality system regulations and the ability to drive continuous improvement. Possess a strong foundation in statistical techniques (e.g., normality tests, capability analysis, tolerance intervals), test method validation (MSA, Gage R&R), and risk management principles per ISO 14971, including FMEA and systems analysis. Expertise in one of these areas is required. Ability to develop and improve complex concepts, techniques, standards, and new applications based on quality principles and theories. Strong knowledge of medical devices and/or combination products manufacturing. Excellent verbal, written, and interpersonal communication skills.
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