Executive Director, Quality Operations chez Ardelyx
Ardelyx · Waltham, États-Unis d'Amérique · Hybrid
- Senior
 - Bureau à Waltham
 
- Demonstrate a primary commitment to patient safety and product quality by maintaining compliance to Ardelyx Quality Policies and procedures
 - Support the development of a proactive quality systems culture throughout the business
 - Establish a high-performing team to drive organizational goals & objectives and instill a robust quality culture. Drive engagement to ensure personnel have clear expectations, appropriate tools and information, and opportunity to share, grow and develop and team members are recognized for their contributions
 - Ensure adequate and compliant investigations into OOT/OOS results generated at contract test labs
 - Ensure compliance with applicable post market requirements for annual stability testing of designated batches as per commitment to regulatory agency
 - Partner with Technical Operations and Regulatory Affairs on development projects, method and process transfer/optimization and validation program requirements
 - Establish data trending programs across products to proactively identify and investigate trends and report trending outcomes at Quality Management Review and other forums
 - Drive systemic process change as a result of deviations/investigations and other quality trends
 - Help define department objectives to align with corporate goals
 - Keep management informed on product quality and other concerns such as supplier Quality issues, deviations
 - Assure appropriate systems and processes are in place for assessing product impact, investigation, follow up and closure of deviations and audit observations
 - Sponsors quality and technical projects with third party suppliers; collaborating with internal stakeholders and GxP partners to facilitate resolution of quality and technical issues.
 - Evaluate and approve compliance documentation including regulatory filings for Ardelyx products
 - Collaborate with Ardelyx international business partners as needed
 - Develop budget forecasts and track QA expenses
 
- Bachelor’s degree with 15+ years of related experience in life sciences, with a minimum of ten years of Quality Assurance and Quality Control experience in development and commercial programs or equivalent experience
 - Must have strong expertise in US FDA regulations and guidance with a strong emphasis on compliance and direct experience with regulatory submissions
 - Experience with hosting, leading and managing US regulatory agency inspections preferred
 - Strong analytical skills including trend and statistical analysis
 - Demonstrated ability to communicate and interact with all levels of the organization including Executive Leadership
 - Strong interpersonal skills to provide coaching, training, and direction
 - Proven experience influencing across the organization to improve product or processes
 - Proven ability to identify Quality issues/discrepancies through a risk-based approach and effectively and proactively resolve the issues/discrepancies in a diplomatic, flexible and constructive manner
 - Regulations, 21CFR 210/211, ICH Guidelines
 - Must be able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic environment
 - Must have strong written and communication skills
 - Ability to travel domestically and internationally up to 15%
 
- East Coast Hybrid or local to Waltham, MA