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Curia

End-to-end drug development and manufacturing

Supervisor - Production Operations, Nights

Translational Research & Bench BiologyConfirmed live in the last 24 hours
Full-timeAlbuquerque, NM, USANo salary listedIn-person

About the Job

Requirements

  • High school diploma or general education degree (GED), required
  • Enrollment in an accredited Associate’s or Bachelor’s degree program in science, business, engineering, or a related field, preferred
  • Minimum of five (5) years’ experience in relevant related work in a pharmaceutical manufacturing environment or relevant industry, required
  • Minimum of one (1) year leadership experience in a pharmaceutical manufacturing or relevant industry, required
  • Associate’s degree in Science, Business, Engineering, or a related field, with three (3) years of relevant experience in pharmaceutical manufacturing or a related industry, including at least one (1) year in a leadership role, preferred
  • Bachelor’s degree in Science, Business, Engineering, or a related field, with one (1) year of relevant experience in pharmaceutical manufacturing or a related industry, including at least one (1) year in a leadership role, preferred
  • Must pass a background check
  • Must pass a drug screen
  • May be required to pass Occupational Health Screening
  • May be required to obtain and maintain media qualification
  • May be required to wear a respirator

Responsibilities

  • Manage and coordinate personnel and room activities for assigned shifts
  • Compile area-specific shift information and line status data on time accurately conveying information to support groups and oncoming shift management team
  • Ensure compliance with cGMPs, corporate and site-specific policies and procedures
  • Maintain and report metrics to evaluate the performance of the assigned production unit
  • Mentor, develop, and guide direct reports in succession planning and cross-functional training.
  • Schedule adherence and material consumption rates relative to specific areas
  • Manage operational and preventive maintenance of area-specific processing equipment
  • Report and investigate safety incidents and quality deviations
  • Become fluent in all functional areas and provide leadership in the absence of manager(s)
  • Share resources with other production units as needed and when available
  • Lead and/or conduct investigations, document revisions, protocol creation, and CAPA projects
  • Read/interpret SOPs to ensure compliance
  • Maintain up to date trainings
  • Other duties as assigned

Desired Qualifications

  • Enrollment in an accredited Associate’s or Bachelor’s degree program in science, business, engineering, or a related field, preferred
  • Bachelor’s degree in Science, Business, Engineering, or a related field, with one (1) year of relevant experience in pharmaceutical manufacturing or a related industry, including at least one (1) year in a leadership role, preferred
  • Associate’s degree in Science, Business, Engineering, or a related field, with three (3) years of relevant experience in pharmaceutical manufacturing or a related industry, including at least one (1) year in a leadership role, preferred
  • May be required to obtain and maintain media qualification
  • May be required to wear a respirator

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

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