Site Quality Head

Curia

4d • Onsite

About The Position

Build your future at Curia, where our work has the power to save lives. The Site Quality Head is directly responsible for oversight of total quality and compliance operations at the assigned site. This role uses leadership and experience to instill the highest caliber of operational excellence and guides department leadership teams in the execution of quality goals, with a focus on continuous improvement, high-quality standards, and the best-in-class customer satisfaction. The Site Quality Head works closely with global teams in developing, implementing and maintaining corporate quality standards, policies, procedures, and processes, and control tests ensuring that the quality in site operations meet all legal, corporate, and FDA quality requirements. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.

Requirements

• Bachelor’s degree in science or a relevant field and a minimum of 10 years of relevant related work experience in aseptic production/processing cleaning practices within a regulatory environment, plus 5 years in professional management role
• Ability to create and maintain strong working relationships with multiple organizations, both on-site and externally
• Ability to enable and empower managers and hold them accountable for results
• Ability to provide strategic leadership to the organization in terms of strategy development, and provide resources and execution of defined strategy
• Ability to read, analyze and interpret financial reports, common scientific and technical journals and legal documents
• Ability to respond to common inquiries or complaints from customers, regulatory agencies or members of the business community
• Ability to effectively present information to all levels throughout the organization, government agencies, boards of directors and customers
• Must pass a background check
• Must pass a drug screen
• May be required to pass Occupational Health Screening

Responsibilities

• Supervise, coach and develop Quality staff
• Oversee day-to-day operations for Quality Systems
• Collaborate with others to avoid potential obstacles and to resolve exceptions and/or deviations resulting from process, equipment, or environmental excursions
• Ensure that all exception reports are triaged, investigated, and resolved with the appropriate CAPAs within clearly defined timeframes
• Oversee Validation, Change Control, Work Orders, training, planned deviations and Environmental Monitoring activities as they apply to manufacturing operations
• Own change requests
• Develop, write, review and/or approve Change Controls, protocols, summary reports, memorandums, action plans, etc., and oversee training and execution of related activities
• Ensure business process needs and deliverables are met and that the group’s routine business process functions are executed in conjunction with Curia policies and cGMP

Benefits

• Generous benefit options (eligible first day of employment)
• Paid training, vacation and holidays (vacation accrual begins on first day of employment)
• Career advancement opportunities
• Education reimbursement
• 401K program with matching contributions
• Learning platform

What This Job Offers

• Job Type: Full-time
• Career Level: Senior