Director, GxP Quality Assurance and Compliance New York; Cambridge, MA
: Job Details :


Director, GxP Quality Assurance and Compliance New York; Cambridge, MA

Tbwa Chiat/Day

Location: New York,NY, USA

Date: 2024-12-18T08:13:28Z

Job Description:
Director, GxP Quality Assurance and ComplianceNew York; Cambridge, MAWe are looking to hire a Director, GxP Quality Assurance and Compliance to join us in our mission to discover and develop drugs that improve human health through the use of breakthrough computational methods. We are seeking outstanding individuals to join our drug discovery group and contribute to our rapidly expanding portfolio of drug discovery programs and collaborations.Our drug discovery and early clinical development team includes a cross-functional group of scientists and drug developers with experience working on all common target classes and therapeutic areas. The group is supported by more than 100 software developers and engineers, as well as a large-scale compute infrastructure to apply our proprietary physics-based drug design and optimization platform. Several programs we have worked on have achieved developmental candidate status and have progressed into clinical development after IND approval.Who will love this job:
  • A strategic subject matter expert who's ready to partner with cross-functional teams as an experienced Quality technical resource
  • A solutions-oriented and collaborative coach to internal partners
  • An excellent verbal and written communicator with robust project management skills
  • A goal-oriented team player who can bring excellent leadership skills to the oversight of cross-functional teams, including members of our toxicology, bioanalytical, CMC, and clinical teamsWhat you will do:
    • Overall GxP Responsibilities:
    • Design, develop and implement overall GxP Quality Assurance strategy and vision for Schr--dinger's Therapeutics Group
    • Develop, implement, and manage the continuous improvement of robust quality management systems, including vendor management, deviation management, change control, CAPAs, product label review, risk management, and eQMS (MasterControl)
    • Ensure compliance, in collaboration with relevant SMEs and senior leaders, with all applicable GxP regulations, including GMP, GCP, and GLP
    • Establish key quality system metrics and process indicators to proactively identify and address quality systems or product issues
    • Oversee the development and implementation of all relevant training programs to ensure staff are knowledgeable about GxP requirements and quality standards
    • Provide leadership and guidance to teams on inspection readiness, including hosting and participating in regulatory inspections (GMP, BIMO, etc.)
    • Account for appropriate oversight of all vendors, including CDMOs and CROs, to ensure regulatory compliance
    • GMP Responsibilities:
    • Serve as spokesperson and technical subject matter quality expert for all matters governed by GMP-related regulations/guidelines and industry best practices (e.g., FDA, EMA, PMDA, etc.)
    • Perform and manage day-to-day GMP QA activities
    • Author, review, and approve all relevant GMP quality documentsWhat you should have:
      • Bachelor's degree in life sciences (Master's degree in life sciences preferred)
      • Twelve to fifteen years of Quality Assurance experience in the pharmaceutical or biotech industry, with at least five years in a leadership role
      • Technical quality experience preferred
      • Experience in manufacturing operations preferred
      • Expert level knowledge of GMP regulations and FDA requirements, Guidance documents, and industry best practices, with a focus on Analytical/QC testing
      • Good working knowledge of global GxP standards, including USP/Ph., FDA/EMA, and ICH
      • History of success with the management of inspections performed by the FDA and other regulatory bodies
      • Excellent written and oral communication skills
      • Ability to travel domestically and internationally on occasionPay and perks:Schr--dinger understands it's people that make a company great. Because of this, we're prepared to offer a competitive salary, stock options, and a wide range of benefits that include healthcare (with dental and vision), a 401k, pre-tax commuter benefits, a flexible work schedule, and a parental leave program. We have regular catered meals in the office, a company culture that is relaxed but engaged, and over a month of paid vacation time. Our Administrative and Human Resources departments also plan a myriad of fun company-wide events. New York is home to our largest office, but we have teams all over the world. Schr--dinger is honored to have been selected as one of Crain's New York Best Places to Work for the past three years running.Estimated base salary range: $185,000 - $235,000. Actual compensation package is dependent on a number of factors, including experience, education, degrees held, market data, and business needs.Sound exciting? Apply today and join us! #J-18808-Ljbffr
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