Exelixis

SUMMARY/JOB PURPOSEThe Associate QA Operations Director Systems and Process is accountable for providing QA lead support for Quality Systems (Deviations Change Control CAPA etc.) As a Partner responsible for guiding the organization in the successful thorough and timely execution of

SUMMARY/JOB PURPOSEThe Associate QA Operations Director Systems and Process is accountable for providing QA lead support for Quality Systems (Deviations Change Control CAPA etc.) As a Partner responsible for guiding the organization in the successful thorough and timely execution of

COMPANY DESCRIPTION:Every Exelixis employee is united in an ambitious cause: to launch innovative medicines that give patients and their families hope for the this pursuit we know our employees are our most valuable asset. After operating in the challenging biotech sector for 25 year

COMPANY DESCRIPTION:Every Exelixis employee is united in an ambitious cause: to launch innovative medicines that give patients and their families hope for the this pursuit we know our employees are our most valuable asset. After operating in the challenging biotech sector for 25 year

SUMMARY/JOB PURPOSE (Basic purpose of the job):The Compliance QA Director leads the companys GxP inspection readiness ensuring ongoing preparedness for global health authority inspections. This role manages regulatory inspections and responses directs internal audits and mock inspecti

SUMMARY/JOB PURPOSE (Basic purpose of the job):The Compliance QA Director leads the companys GxP inspection readiness ensuring ongoing preparedness for global health authority inspections. This role manages regulatory inspections and responses directs internal audits and mock inspecti

SUMMARY/JOB PURPOSE: The Senior Corporate Counsel Contracts takes a supporting role in setting the material terms of the many business transactions undertaken by the company the drafting and negotiation of definitive and ancillary agreements reflecting those terms and the organization

SUMMARY/JOB PURPOSE: The Senior Corporate Counsel Contracts takes a supporting role in setting the material terms of the many business transactions undertaken by the company the drafting and negotiation of definitive and ancillary agreements reflecting those terms and the organization

SUMMARY/JOB PURPOSE:Designs plans and executes biostatistical components of plans for research and development projects that establish the conditions essential for determining safety efficacy and marketability of compounds. Projects prepares the statistical component of protocols whic

SUMMARY/JOB PURPOSE:Designs plans and executes biostatistical components of plans for research and development projects that establish the conditions essential for determining safety efficacy and marketability of compounds. Projects prepares the statistical component of protocols whic

SUMMARY/JOB PURPOSE:The Executive Director Scientific Publications leads the publication planning and execution functions at Exelixis. Responsibilities include management of the Publications team oversight of publication planning for each Exelixis development compound coordination of

SUMMARY/JOB PURPOSE:The Executive Director Scientific Publications leads the publication planning and execution functions at Exelixis. Responsibilities include management of the Publications team oversight of publication planning for each Exelixis development compound coordination of

SUMMARY/JOB PURPOSE:The Clinical Trials Manager (CTM) Clinical Operations coordinates the activities associated with the evaluation initiation and management of solid tumor oncology clinical trials. This position is responsible for overseeing the execution of clinical trials collabora

SUMMARY/JOB PURPOSE:The Clinical Trials Manager (CTM) Clinical Operations coordinates the activities associated with the evaluation initiation and management of solid tumor oncology clinical trials. This position is responsible for overseeing the execution of clinical trials collabora

SUMMARY/JOB PURPOSE: The Executive Medical Director PVRM is responsible for the development and execution of the global product safety strategy for complex clinical development program(s) as well as post-marketing pharmacovigilance activities for Exelixis products. This role leads and

SUMMARY/JOB PURPOSE: The Executive Medical Director PVRM is responsible for the development and execution of the global product safety strategy for complex clinical development program(s) as well as post-marketing pharmacovigilance activities for Exelixis products. This role leads and

SUMMARY/JOB PURPOSE:The Compliance QA Manager QA Core is responsible for coordinating and maintaining inspection readiness activities and provides support for assessing proposed corrective and preventive actions in response to inspection findings. This role supports continuous improve

SUMMARY/JOB PURPOSE:The Compliance QA Manager QA Core is responsible for coordinating and maintaining inspection readiness activities and provides support for assessing proposed corrective and preventive actions in response to inspection findings. This role supports continuous improve

SUMMARY/JOB PURPOSE:The Associate Director Stability Management is responsible for the establishment and management of the stability group withing Exelixis CMC department. This role oversees the overall strategy and oversight of Exelixis stability and reference standard programs for d

SUMMARY/JOB PURPOSE:The Associate Director Stability Management is responsible for the establishment and management of the stability group withing Exelixis CMC department. This role oversees the overall strategy and oversight of Exelixis stability and reference standard programs for d

JOB DESCRIPTION DETAILS:The position will be an integral part of the Corporate Legal Affairs team with respect to all aspects of its securities and corporate governance practice including the management of all corporate legal records. Some support of SEC filings contracts business tra

JOB DESCRIPTION DETAILS:The position will be an integral part of the Corporate Legal Affairs team with respect to all aspects of its securities and corporate governance practice including the management of all corporate legal records. Some support of SEC filings contracts business tra

SUMMARY/JOB PURPOSE: Responsible for the development and implementation of global regulatory strategies that align with asset and corporate goals as well as health authority requirements. Ensures timely preparation of organized consistent and scientifically valid submissions. Provides

SUMMARY/JOB PURPOSE: Responsible for the development and implementation of global regulatory strategies that align with asset and corporate goals as well as health authority requirements. Ensures timely preparation of organized consistent and scientifically valid submissions. Provides

SUMMARY/JOB PURPOSE: Responsible for driving the development and implementation of global regulatory strategies that align with asset and corporate goals as well as health authority requirements. Ensures timely preparation of organized consistent and scientifically valid submissions.

SUMMARY/JOB PURPOSE: Responsible for driving the development and implementation of global regulatory strategies that align with asset and corporate goals as well as health authority requirements. Ensures timely preparation of organized consistent and scientifically valid submissions.

SUMMARY/JOB PURPOSE:This key role drives consistency across QA systems and processes for the Clinical QA team identifying issues and risks escalating in a timely fashion and aligning metrics that provide input into a compliance scorecard for Clinical programs. This leader provides ins

SUMMARY/JOB PURPOSE:This key role drives consistency across QA systems and processes for the Clinical QA team identifying issues and risks escalating in a timely fashion and aligning metrics that provide input into a compliance scorecard for Clinical programs. This leader provides ins

The GCP/GVP QA Director is accountable for Good Clinical Practices (GCP) and Good Pharmacovigilance Practices (GVP) systems and activities drives compliance and continuous improvement ensures that Quality is integrated throughout GCP/GVP processes supports internal/external audits imp

The GCP/GVP QA Director is accountable for Good Clinical Practices (GCP) and Good Pharmacovigilance Practices (GVP) systems and activities drives compliance and continuous improvement ensures that Quality is integrated throughout GCP/GVP processes supports internal/external audits imp

SUMMARY/JOB PURPOSE (Basic purpose of the job):The Senior GCP/GVP QA Manager is accountable for assisting with the development implementation and maintenance of end-to-end QA systems and activities for GCP/GLP operations including planning and supporting vendor audits and associated d

SUMMARY/JOB PURPOSE (Basic purpose of the job):The Senior GCP/GVP QA Manager is accountable for assisting with the development implementation and maintenance of end-to-end QA systems and activities for GCP/GLP operations including planning and supporting vendor audits and associated d