C

Curia

End-to-end drug development and manufacturing

Site Quality Head

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeHopkinton, MA, USA$206.1k - $251.3k /yrIn-person

About the Job

Requirements

  • A bachelor's degree in science or a relevant field and at least 10 years of relevant related work experience in aseptic production/processing cleaning practices within a regulatory environment, including 5 years in a 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 strategy development and provide resources and execution of the 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 resolve exceptions or deviations resulting from process, equipment, or environmental excursions.
  • Ensure that all exception reports are triaged, investigated, and resolved with appropriate corrective and preventive actions 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, and action plans, 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 current Good Manufacturing Practices.

About the Company

Curia

End-to-end drug development and manufacturing

Curia is a contract development and manufacturing organization (CDMO) that partners with pharmaceutical and biotech companies to move medical breakthroughs from concept to market. It provides end-to-end services across the drug development lifecycle, including early research, method development and validation, preformulation, material science, solid-state chemistry, and package device testing. Revenue comes from service contracts for specialized capabilities and expertise, with clients ranging from small startups to large pharma. Curia also collaborates with industry leaders to advance continuous flow development and manufacturing programs. The company differentiates itself through flexible and scalable solutions, deep scientific expertise, and state-of-the-art technology that help clients accelerate development timelines while navigating discovery to commercialization. Its goal is to enable efficient, reliable progression of drug candidates from conception through to market approval.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Albany, NY
Founded
1991

Recently Posted Jobs

Explore more opportunities at Curia

See more jobs