Job Information
Palantir Technologies Quality Compliance Manager in New York, New York
- Continue to develop a Palantir-wide QMS that lives under ISO 9001 and drives consolidation of process documentation and promotes process consistency at Palantir.
- Author and ensure implementation of approved procedures across the organization, setup non-conformance and CAPA processes to monitor deviations and management reporting.
- Establish inter-departmental relationships to achieve key results.
- Be the champion and advocate for ingrained QMS across Palantir, work with product development and product reliability teams to implement GxP processes.
- Enhance quality culture at Palantir.
- Support life sciences sales cycle, support customer and FDA audits regarding Palantir's Quality Management System, and complete assessment questionnaires for Life Sciences clients.
- Support Implementation of internal applications/systems supporting QMS processes like Document Management System and Learning Management System.
- Develop a Palantir-wide QMS that lives under 9001 and drives consolidation of process documentation and promotes process consistency at Palantir.
- Collaborate with software development teams to integrate quality and compliance considerations into product design and development processes.
- Develop and deliver training programs on quality management and ISO 9001 compliance to all relevant employees.
- Experience documenting SOPs and coordinating cross-functionally to maintain adherence to documented process.
- Experienced in building and running a Quality Management System and process areas within a QMS (e.g. Doc Control, Training, Supplier Management CAPA, SDLC, Change Control, etc.).
- Thrives in a fluid, dynamic and fast-paced environment, specifically a modern SaaS company.
- Ability to connect and develop positive relationships with employees across cross-functional teams (engineering, compliance, product reliability, product development, among others).
- Experience in demonstrating value proposition of a Quality System to internal stakeholders without experience/buy-in.
- A visionary who has no problem getting their hands dirty and doing the work necessary to create and improve the state of the world.
- You have at least 5+ years of relevant work experience.
- Strong understanding of ISO 9001 standards and experience in managing or implementing quality management systems in a software development environment.
- Knowledge of FDA and EU regulatory requirements and other guidelines related to GxP activities, including 21 CFR Part 11 / GAMP 5.
- Experience in defending organization's QMS in internal/external /regulatory/customer audits, especially as a SaaS provider.
- Bachelor's degree in Computer Science, Information Systems, Management Information Systems, or related.
- Familiarity with agile development methodologies and tools used in software development.
- Medical, dental, and vision insurance
- Life and disability coverage
- Paid leave for new parents and emergency back-up care for all parents
- Family planning support, including fertility, adoption, and surrogacy assistance
- Stipend to help with expenses that come with a new child
- Commuter benefits
- Unlimited paid time off
- 2 weeks paid time off built into the end of each year
Palantir is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. Please see the United States Department of Labor's EEO poster and EEO poster supplement for additional information. We will also make all reasonable accommodations to meet our obligations under the Americans with Disabilities Act (ADA) and state disability laws.
Minimum Salary: 90000.00 Maximum Salary: 150000.00 Salary Unit: Yearly