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Curia

End-to-end drug development and manufacturing

Production Operations Supervisor - Nights

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeAlbuquerque, NM, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or general education degree (GED) is required.
  • A minimum of five years of relevant experience in a pharmaceutical manufacturing environment or relevant industry is required, including at least one year of leadership experience.
  • The employee must be able to read and interpret safety instructions, standard operating procedures, technical procedures, and governmental regulations.
  • The employee must have written, verbal, and presentation communication skills.
  • The employee must be proficient in arithmetic operations, units of measurement, fractions, decimals, percentages, algebra, and geometry.
  • The employee must be able to define problems, collect data, establish facts, draw valid conclusions, and interpret technical instructions in mathematical or diagram form.
  • The employee must be proficient in manufacturing and internet software and Microsoft Office tools, including PowerPoint, Excel, Word, and Outlook.
  • The employee must pass a background check and drug screen, including random drug screens.
  • The employee may be required to pass an occupational health screening.
  • The employee must obtain and maintain gowning certification and media qualification.
  • The employee must be able to wear a respirator.
  • The employee must be willing to work nights.
  • The employee must be able to perform the physical demands of the role, including lifting, pushing, pulling, sitting, standing, reaching, and other position-specific movements.
  • The employee must comply with aseptic gowning and use required personal protective equipment in sterile manufacturing environments.

Responsibilities

  • Manage and coordinate personnel and room activities for assigned shifts.
  • Compile area-specific shift information and line-status data accurately and on time for support groups and the oncoming shift management team.
  • Ensure compliance with current Good Manufacturing Practices, corporate policies, and site-specific policies and procedures.
  • Maintain and report metrics used to evaluate the performance of the assigned production unit.
  • Mentor, develop, and guide direct reports in succession planning and cross-functional training.
  • Monitor schedule adherence and material consumption rates for 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 managers.
  • Share resources with other production units as needed and when available.
  • Lead or conduct investigations, document revisions, protocol creation, and corrective and preventive action projects.
  • Read and interpret standard operating procedures to ensure compliance.
  • Maintain up-to-date training records and qualifications.
  • Supervise the setup of sterile filling equipment, operation of dehydrogenation equipment, filling and capping processes, and formulation tasks.
  • Ensure current Good Documentation Practices for production activities.
  • Supervise sanitation of aseptic and controlled areas using specialized solutions and equipment.
  • Follow sanitization protocols for sterile equipment processing and standard operating procedures for sanitation and documentation activities.
  • Evaluate team-member performance and support team development to achieve departmental and organizational objectives.
  • Promote a safe and healthy work environment by identifying and addressing hazards, following safety protocols, participating in safety training, and fostering safety awareness.
  • Perform 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.
  • An Associate’s degree in science, business, engineering, or a related field with three years of relevant pharmaceutical manufacturing experience, including at least one year in a leadership role.
  • A Bachelor’s degree in science, business, engineering, or a related field with one year of relevant pharmaceutical manufacturing experience, including at least one year in a leadership role.

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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