Sr. Quality Engineer I- Combination Products
Foster, CA - USA
Job Summary
At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference.
Every member of Gileads team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions and were looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future you are the key driver in evolving our culture and creating an environment where every employee feels included developed and empowered to fulfil their aspirations. Join Gilead and help create possible together.
Job Description
Key Responsibilities
- Serve as a Lead Quality Engineer for medical device combination product development programs with a strong focus on design controls risk management and lifecycle quality oversight.
- Partner closely with Device Engineering on new combination product development supporting design verification design validation and technology transfer activities.
- Ensure compliance with applicable regulatory requirements and standards including FDA 21 CFR Part 820 21 CFR Part 4 ISO 13485 ISO 14971 and Gilead Quality System requirements.
- Plan implement and track approved quality improvement initiatives ensuring timely execution of action items and deliverables.
- Interface with internal crossfunctional teams contract manufacturers and suppliers to resolve complex technical and quality issues related to drugdevice combination products processes and manufacturing.
- Act as an escalation point for complex highimpact quality issues risks and decisions.
- Support and strengthen strategic relationships with internal stakeholders and Contract Manufacturing Organizations (CMOs).
- Provide quality guidance and impact assessments for change controls including evaluations of Design History Files (DHF) and Risk Management Files (RMF).
- Develop review and approve controlled documentation including protocols plans reports risk analyses specifications and test methods.
Basic Qualifications
- Bachelors degree in Engineering or a scientific discipline with at least 6 years of relevant experience OR
- Masters degree in a related field with at least 4 years of relevant experience.
- Demonstrated experience in Quality Assurance for medical devices and/or drugdevice combination products.
- Excellent verbal written and interpersonal communication skills with the ability to influence across functions.
Preferred Qualifications
- At least 8 years of experience supporting combination products (e.g. autoinjectors prefilled syringes copackaged kits) with deep expertise in design controls and risk management.
- Strong project management and process improvement capabilities.
- Working knowledge of domestic and international quality system regulations and the ability to drive continuous improvement in regulated environments.
- Strong foundation in statistical methods including normality testing capability analysis tolerance intervals and test method validation (MSA Gage R&R).
- Advanced proficiency in risk management per ISO 14971 including FMEA systemlevel risk analysis and hazard analysis (expertise in at least one area required).
- Ability to develop and evolve complex quality concepts standards and methodologies based on sound quality engineering principles.
- Strong knowledge of medical device and/or combination product manufacturing operations.
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Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment and is dedicated to fostering an inclusive work environment comprised of diverse perspectives backgrounds and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race color religion national origin sex age sexual orientation physical or mental disabilitygenetic information or characteristic gender identity and expression veteran status or other non-job related characteristics or other prohibited grounds specified in applicable federal state and local order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973 the Vietnam Era Veterans Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990 applicants who require accommodation in the job application process may contact for assistance.
For more information about equal employment opportunity protections please view theKnow Your Rights poster.
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YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
For Current Gilead Employees and Contractors:
Please apply via the Internal Career Opportunities portal in Workday.
Required Experience:
Senior IC
About Company
Gilead Sciences is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensu ... View more