LeadStack
Associate Director*
LeadStack, Foster City, California, United States, 94420
LeadStack Inc. is an award-winning, one of the nation's fastest-growing, certified minority-owned (MBE) staffing services provider of contingent workforce. As a recognized industry leader in contingent workforce solutions and Certified as a Great Place to Work, we're proud to partner with some of the most admired Fortune 500 brands in the world.
Job Title: Associate Director
Location: Foster City, CA 94404
Duration: 12 months Contract
Payrange: $80/hr - $100/hr on W2Description:
Associate Director, Functional Quality Business Partners, Medical Devices, R&D Quality (Foster City, CA). We are looking for an expert Quality Assurance Professional with experience advising development teams in IVD and Combination Product quality strategy within a pharmaceutical organization. As a member of the Functional Quality Business Partner Team you will be the medical device subject matter expert within R&D Quality, and key functional development leaders. Specifically, you will partner with Regulatory, Safety, Clinical Operations, and Device Manufacturing to set the quality management system strategy for R&D for medical devices.This role is suited to candidates who possess strong communication, leadership, and strategic risk-based thinking skills. Utilizing expert knowledge in this role you will be a trusted business partner effectively communicating and collaborating with senior stakeholders and leadership teams across the global organization.Primary Responsibilities
Advance the understanding of medical device quality requirements in support of clinical development programs and the regulatory framework to ensure data integrity and patient safety.Support key functions such as Regulatory, Safety, Clinical Operations, and Device Manufacturing on medical device R&D quality strategy.Act as subject matter expert for Quality & Compliance Audit in supporting risk assessments and audit strategy for medical devices.Advise business stakeholders and study teams as needed on quality oversight of outsourced IVD assays for all products; including development of Quality Agreements.Advise Diagnostic Sub-Teams on matters related to R&D device Quality.Partner with study teams, including Therapeutic Area quality leads on management of medical device quality issues, vendor oversight and CAPAs.Provide guidance to functions on procedural development and review to assure alignment with internal processes and regulatory requirements for medical devices.Gain insights from metrics and other mechanisms to uncover trends and/or gaps in medical device quality at a portfolio level and advise business on any mitigation requirements.Partner with relevant functional areas to gap assess, investigate and problem solve cross portfolio medical device quality issues; Support functions such as Patient Safety, Clinical Operations and Diagnostics on implementation of Quality Improvement plans.Provide timely risk-based compliance advice that facilitates decision making.Partner/advise key functional areas in the development & investigation of internal deviations or CAPAs.Participate in quality and/or cross functional process improvements initiatives as assigned.Support key functions and study teams as needed during regulatory inspections.Education & Qualifications:
BA or BS and 10-12+ years of relevant experience (10+ years of relevant experience with an MS).Significant experience working to or advising R&D business on medical device quality strategy.Understand the use and application of IVD assays in clinical trials.Experience in GCP regulations and guidance, such as ICH E6 R2.Expert in IVD regulations, such as IVDR.GCLP experience is a plus.Understanding of FDA + Global regulations and Guidance for medical devices, and how to apply them in an R&D setting.Must have experience advising business in a compliance related role.Recognized as an expert resource on a range of med device compliance topics.Bio-pharma or Diagnostics Sponsor experience required.Is a strategic problem solver with a deep understanding of drug development.Exceptional verbal, written, interpersonal skills to include delivering presentations to senior leaders of the organization.Experience with CAPA management programs preferred.Excellent organization and project management skills.About Gilead R&D Quality Gilead R&D Quality is a phenomenal place to develop your skills and expertise. Our strong pipeline of therapies will provide you opportunities to be challenged and stretched while supported and developed by our diverse and expert team.To know more about current opportunities at LeadStack, please visit us at
https://leadstackinc.com/careers/
.Should you have any questions, feel free to call me on
(415) 322-5419
or send an email on
akarsh.yathiraj@leadstackinc.com
.Thanks and RegardsAkarsh YathirajSenior RecruiterC. (510) 500-5003D. (510) 500-5003A. 611 Gateway Blvd, Ste 120South San Francisco, CA 94080W.
www.leadstackinc.com
#J-18808-Ljbffr
Job Title: Associate Director
Location: Foster City, CA 94404
Duration: 12 months Contract
Payrange: $80/hr - $100/hr on W2Description:
Associate Director, Functional Quality Business Partners, Medical Devices, R&D Quality (Foster City, CA). We are looking for an expert Quality Assurance Professional with experience advising development teams in IVD and Combination Product quality strategy within a pharmaceutical organization. As a member of the Functional Quality Business Partner Team you will be the medical device subject matter expert within R&D Quality, and key functional development leaders. Specifically, you will partner with Regulatory, Safety, Clinical Operations, and Device Manufacturing to set the quality management system strategy for R&D for medical devices.This role is suited to candidates who possess strong communication, leadership, and strategic risk-based thinking skills. Utilizing expert knowledge in this role you will be a trusted business partner effectively communicating and collaborating with senior stakeholders and leadership teams across the global organization.Primary Responsibilities
Advance the understanding of medical device quality requirements in support of clinical development programs and the regulatory framework to ensure data integrity and patient safety.Support key functions such as Regulatory, Safety, Clinical Operations, and Device Manufacturing on medical device R&D quality strategy.Act as subject matter expert for Quality & Compliance Audit in supporting risk assessments and audit strategy for medical devices.Advise business stakeholders and study teams as needed on quality oversight of outsourced IVD assays for all products; including development of Quality Agreements.Advise Diagnostic Sub-Teams on matters related to R&D device Quality.Partner with study teams, including Therapeutic Area quality leads on management of medical device quality issues, vendor oversight and CAPAs.Provide guidance to functions on procedural development and review to assure alignment with internal processes and regulatory requirements for medical devices.Gain insights from metrics and other mechanisms to uncover trends and/or gaps in medical device quality at a portfolio level and advise business on any mitigation requirements.Partner with relevant functional areas to gap assess, investigate and problem solve cross portfolio medical device quality issues; Support functions such as Patient Safety, Clinical Operations and Diagnostics on implementation of Quality Improvement plans.Provide timely risk-based compliance advice that facilitates decision making.Partner/advise key functional areas in the development & investigation of internal deviations or CAPAs.Participate in quality and/or cross functional process improvements initiatives as assigned.Support key functions and study teams as needed during regulatory inspections.Education & Qualifications:
BA or BS and 10-12+ years of relevant experience (10+ years of relevant experience with an MS).Significant experience working to or advising R&D business on medical device quality strategy.Understand the use and application of IVD assays in clinical trials.Experience in GCP regulations and guidance, such as ICH E6 R2.Expert in IVD regulations, such as IVDR.GCLP experience is a plus.Understanding of FDA + Global regulations and Guidance for medical devices, and how to apply them in an R&D setting.Must have experience advising business in a compliance related role.Recognized as an expert resource on a range of med device compliance topics.Bio-pharma or Diagnostics Sponsor experience required.Is a strategic problem solver with a deep understanding of drug development.Exceptional verbal, written, interpersonal skills to include delivering presentations to senior leaders of the organization.Experience with CAPA management programs preferred.Excellent organization and project management skills.About Gilead R&D Quality Gilead R&D Quality is a phenomenal place to develop your skills and expertise. Our strong pipeline of therapies will provide you opportunities to be challenged and stretched while supported and developed by our diverse and expert team.To know more about current opportunities at LeadStack, please visit us at
https://leadstackinc.com/careers/
.Should you have any questions, feel free to call me on
(415) 322-5419
or send an email on
akarsh.yathiraj@leadstackinc.com
.Thanks and RegardsAkarsh YathirajSenior RecruiterC. (510) 500-5003D. (510) 500-5003A. 611 Gateway Blvd, Ste 120South San Francisco, CA 94080W.
www.leadstackinc.com
#J-18808-Ljbffr