drjobs Assoc Director Quality Assurance GCP contract

Assoc Director Quality Assurance GCP contract

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

San Diego, CA - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Erascais a clinicalstage precision oncology company focused on discovering developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancersmost commonly mutated signaling cascades the RAS/MAPK pathway which affects approximately 5.5 million lives each year worldwide. The name Erasca has an important embedded meaning: it is a contraction of our audacious hope to erase cancer that drives our mission and everything that we do on behalf of patients with cancer.

Position Summary:

This position will be responsible for the and oversight of vendor audit policies plans and quality system elements related to GxP audit activities in support of clinical programs & studies along with external GxP qualifications and inspection readiness. In addition the role facilitates quality contractual reviews and obligations (such as Quality Agreements) oversees supplier scorecards performance and quality and supports GDPR compliance and serious breach assessment. This person will sit on clinical study teams and work closely with crossfunctional stakeholders in clinical operations clinical development data management and other functions involved in the conduct of Erasca clinical trials.

Note this is a part time contract position 20 hours per week and can be based anywhere in the United States.

Responsibilities:

  • Establish maintain and ensure effectiveness of quality programs and documentation to assure compliance in international regulatory environment and provide guidance in clinical Quality related areas.
  • Represent Quality Assurance on crossfunctional study teams.
  • Support GCP QA in the conduct and oversight of GxP vendor audits (GMP GCP GLP and & GVP) including IT systems.
  • Maintain risk based GxP supplier/vendor audit schedule and performance overview in compliance with procedures. Author (or ensure authorship for outsourced audits) review and approve internal and external audit reports.
  • Review audit findings and other potential compliance risks to subject safety data integrity and business operations and escalate risks to QA management.
  • Ensure audit reports and corrective actions are developed and completed within timelines mandated in internal procedures as well as ensuring appropriate effectiveness checks through subsequent vendor audits.
  • Author review and facilitate contractual agreements (Quality Agreements Pharmacovigilance Agreements (PVA) etc..
  • Perform all duties in keeping with the Companys core values policies and all applicable regulations.

Requirements:

  • Undergraduate degree in in Biology Chemistry Physical Sciences or related discipline or comparable experience.
  • 10 years of experience including management of GxP Quality/Compliance audits in a pharmaceutical or biotech environment required.
  • Extensive knowledge of ICH Guidelines US European and ROW regulatory requirements regarding applicable drug development regulations.
  • Experience with transition from Phase 13 to commercial quality systems preferred.
  • Previous experience working with FDA and participating in regulatory agency inspections of clinical research activities.
  • Excellent interpersonal and influencing skills.
  • Must have good written and verbal communication skills with the ability to tailor communication to all levels and prepare and present appropriate updates to functional groups and leaders.
  • Demonstrated ability to achieve high performance goals and meet deadlines in a fastpaced environment.
  • Strong learning orientation curiosity and commitment to science and patients.

Along with our casual collaborative and fun work and the chance to make your mark in our mission to erase cancer Erasca offers a comprehensive and competitive benefits package that includes: Paid Time Off Holiday and Sick Leave Medical Dental and Vision Plans Short and LongTerm Disability Basic and Voluntary Life/AD&D Coverage Flexible Spending Accounts (FSA HSA and Commute Critical Illness and Accident Coverage Pet Insurance Employee Assistance Program 401(k) Plan with Erasca contribution and the opportunity to participate in an Employee Stock Purchase Program.

Erasca Inc. is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment hiring training promotion or other employment practices for reasons of sex race religion national origin ancestry physical or mental disability protected medical condition genetic information marital status registered domestic partner status age sexual orientation military and veteran status or any other basis protected by federal state or local law or ordinance or regulation.


Required Experience:

Director

Employment Type

Contract

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.