- Monitor external medical device standards for QMS updates to ensure compliance with all applicable global regulations.
- Monitors external device/combination product enforcement trends and provides recommendations and action plans for continuous improvement of QMS.
- Actively communicate and collaborate with stakeholders across various functions when creating/revising QMS processes.
- Manage the development and rollout of device standards lists by product types/families and ensures these are kept up to date.
- Actively participates on relevant external industry committees and ensures that existing policies are in compliance with all applicable medical device and combination product regulations.
- Lead gap assessments against new regulations and relevant inspectional observations as required and performs impact assessments.
- Supports medical device and combination product inspectional readiness activities and regulatory inspection responses as needed.
- Support combination product complaints process and investigations. Coordinate and lead root cause analyses and identification, ensuring effective corrective actions for mitigations are documented.
- Perform MDR evaluations and document written justification to support reportable and non‐reportable regulatory decisions.
- Evaluate information from a technical perspective to ensure appropriate analysis and investigations/ MDR's are accurately assessed for risk prioritization and performed per procedures, standards, and regulations.
- Strong collaboration with Safety team, and manufacturing sites/CMOs for effective complaint handling/MDR assessments and adverse events with potential product quality issues.
- Compile and analyze data, metrics, and trends associated with combination product processes.
- Support internal and external audits and inspections; ability to communicate regulatory and process positions as an SME during regulatory inspections and provide follow-up support as required.
- Coordinate and lead the process mapping and change for the development, revision, and/or maintenance of applicable department SOP's, job aids, and WI's.
- May manage Quality personnel (contract or FTE), including organizing and prioritizing daily tasks, conducting training, and writing performance reviews.
- Support complaints investigations and filter information back to the design and development team.
Knowledge, Experience, and Skills: - Must have 8+ years of relevant experience and a Bachelor's degree in a Science or Engineering related field; or 6+ years of relevant experience with a Master's degree in a Science or Engineering related field.
- Medical device experience preferred.
- Demonstrated in-depth knowledge of Quality principles, concepts, industry practices, and standards.
- Previous experience with combination devices is preferred (i.e., Autoinjectors, co-packaged kits, pre-filled syringes).
- Familiarity with end-to-end lifecycle QMS management.
- Strong project management and process improvement skills.
- Demonstrates keen understanding of U.S. and international quality systems regulations to adopt best in class systems/processes and drive continuous improvement initiatives.
- Knowledge of applicable standards, such as 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, IEC 62366, etc.
- Knowledge of Six Sigma, Define-Measure-Analyze-Improve-Control (DMAIC) methodology, performance measures and quality improvement statistics is preferred.
- Knowledge of ISO 14971 Risk Management tools (e.g., Hazard Analysis and Critical Control Points (HACCP) and/or FMEA is preferred.
- Certification by ASQ (such as CQA, CQE, or CQM) or other industry-recognized professional organizations is preferred.
,
The salary range for this position is: $154, $199, Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
For jobs in the United States:
As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic 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 laws. In 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 the 'Know Your Rights' poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
PAY TRANSPARENCY NONDISCRIMINATION PROVISION
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 log onto your Internal Career Site to apply for this job.
jeid-f6b2583affcdba459194d203ebaa23fb -
Gilead Sciences Foster City, United States RegularJob Description · At Gilead, we're creating a healthier world for all people. For more than 35 years, we've 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 therap ...
-
Gilead Sciences, Inc. Foster City, United States Full timeDescription · Sr. Manager Quality – Combination Products, Compliance · This opportunity is an exciting and challenging role that will be key to Gilead's success as we work towards bringing new combination products, such as vial kits and pre-filled syringes, to market. You will ...
-
Product Marketing Manager, Product Compliance
3 weeks ago
Meta San Francisco, United StatesWe believe in the endless power of people when they come together. But we also believe strongly in our responsibility to minimize harm and keep people safe. In this role, you will be responsible for helping to shape roadmaps and develop and execute against launch plans for the in ...
-
Security and Compliance Product(Privacy)
1 week ago
ByteDance San Jose, United StatesAbout ByteDance · Founded in 2012, ByteDance's mission is to inspire creativity and enrich life. With a suite of more than a dozen products, including TikTok, as well as platforms specific to the China market, including Toutiao, Douyin, and Xigua, ByteDance has made it easier and ...
-
Gilead Sciences San Mateo, United StatesThis opportunity is an exciting and challenging role that will be key to Gilead's success as we work towards bringing new combination products, such as vial kits and pre-filled syringes, to market. You will be a key Quality person managing Gilead com Manager, Quality, Compliance, ...
-
Snowflake Computing San Mateo, United StatesBuild the future of data. Join the Snowflake team. · AS A SENIOR / PRINCIPAL PRODUCT MANAGER AT SNOWFLAKE, YOU WILL: · Lead and build out Snowflake's compliance and product security solutions for our global business including regulated industries across numerous strategic vertic ...
-
Product Marketing Manager, Product Compliance
3 weeks ago
META Menlo Park, United StatesWe believe in the endless power of people when they come together. But we also believe strongly in our responsibility to minimize harm and keep people safe. In this role, you will be responsible for helping to shape roadmaps and develop and execute against launch plans for the in ...
-
Qualys Foster City, United StatesCome work at a place where innovation and teamwork come together to support the most exciting missions in the world · The Position · Qualys seeks an experienced product leader and technical practitioner with excellent written and speaking communication skills to lead the federal ...
-
Product Compliance Manager, FedRAMP
5 days ago
Five9 San Ramon, United States Full timeJoin us in bringing joy to customer experience. Five9 is a leading provider of cloud contact center software, bringing the power of cloud innovation to customers worldwide. · Living our values everyday results in our team-first culture and enables us to innovate, grow, and thriv ...
-
Global Hardware Product Compliance Lawyer
3 weeks ago
Entrusted Advisors Palo Alto, United StatesEntrusted Advisors is actively seeking a Hardware Product Compliance attorney to work with our client a Big Tech company**. The ideal candidate must have expertise in dealing with European Union (EU) Hardware Compliance matters. The candidate must be experienced in advising on ha ...
-
Product Compliance Manager, FedRAMP
8 hours ago
Five9 San Ramon, United States· Apply fast, check the full description by scrolling below to find out the full requirements for this role. · Join us in bringing joy to customer experience. Five9 is a leading provider of cloud contact center software, bringing the power of cloud innovation to customers world ...
-
Global Hardware Product Compliance Lawyer
3 weeks ago
Entrusted Advisors Palo Alto, United StatesEntrusted Advisors is actively seeking a Hardware Product Compliance attorney to work with our client a Big Tech company**. The ideal candidate must have expertise in dealing with European Union (EU) Hardware Compliance matters. The candidate must be experienced in advising on ha ...
-
Director, Quality Assurance Compliance/auditor
2 weeks ago
Gilead Sciences Foster City, United StatesFor Current Gilead Employees and Contractors: · Please log onto your · Internal Career Site · At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to dev ...
-
Sumo Logic Redwood City, United StatesSenior/Principal Product Manager, FedRAMP and Compliance · Sumo Logic · is a cloud-native SaaS data analytics platform that solves complex observability and security problems. Customers choose our product because it allows them to easily monitor, optimize, and secure their appl ...
-
Director, Revenue
2 weeks ago
Qualys Foster City, United StatesCome work at a place where innovation and teamwork come together to support the most exciting missions in the world · Director, Revenue Accounting · The Director, Revenue Accounting will be responsible for managing the month-end close process for revenue. · Key Responsibilities i ...
-
Research Scientist
2 weeks ago
Gilead Sciences Foster City, United StatesFor Current Gilead Employees and Contractors: · Please log onto your · Internal Career Site · At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to dev ...
-
Director, L4p Hcp Lead
2 weeks ago
Gilead Sciences Foster City, United StatesFor Current Gilead Employees and Contractors: · Please log onto your · Internal Career Site · At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to dev ...
-
Resident Area Manager
2 weeks ago
ISS Foster City, United StatesThe **Resident Area Manager** is responsible for ensuring all functions, initiatives, and priorities support the customer's overall business strategy. This position is responsible for the effective and efficient functioning of the operation(s) within the guidelines established by ...
-
Warehouse Specialist
2 weeks ago
Stericycle Foster City, United States**Starting pay: $20.13/hr + OT** · **About Us**: · Stericycle is a U.S. based business-to-business services company and leading provider of compliance-based solutions that protects people and brands, promotes health and well-being, and safeguards the environment. Since our foundi ...
-
Product Compliance Associate
2 weeks ago
Vouch San Francisco, United States[Full Time] Product Compliance Associate at Vouch (United States) | BEAMSTART Jobs · Product Compliance Associate · Vouch United States · Date Posted · 31 Mar, 2023 · Work Location · San Francisco, United States · Salary Offered · $55000 — $65000 yearly · Job Type · Full Time · ...
Sr. Manager Quality Combination Products, Compliance - Foster City, United States - Gilead Sciences, Inc.
Description
Sr. Manager Quality Combination Products, ComplianceUnited States - California - Foster City
Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead's therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.
Making an impact on a global scale
Inclusion is one of the company's five core values. That's because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide.
When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible
For Current Gilead Employees and Contractors:
Please log onto your Internal Career Site to apply for this job.
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've 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 world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
We empower our leaders to step up, share ideas, listen, learn, and lead. We're welcoming bright, diverse, and imaginative minds; we're nurturing them to foster an environment of inclusion and growth where innovation is encouraged. We expect our people leaders to model that environment, and to focus on creating inclusion, developing talent, and enabling teams.
Every member of Gilead's 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 we're looking for the next wave of passionate and ambitious people ready to make a direct impact. Join Gilead and help create possible, together.
Job Description
Sr. Manager Quality - Combination Products, Compliance
This opportunity is an exciting and challenging role that will be key to Gilead's success as we work towards bringing new combination products, such as vial kits and pre-filled syringes, to market. You will be a key Quality person managing Gilead combination products compliance. We are looking for an experienced Quality professional to ensure that we have a QMS that enables end-to-end Quality support of our combination products.
Roles/Responsibilities:
