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Curia

End-to-end drug development and manufacturing

Manager of Analytical Chemistry

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeAlbuquerque, NM, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Science, Chemistry, Biology, or a related field of study.
  • At least five years of experience in Analytical Chemistry, Quality Assurance, or Regulatory Compliance Management.
  • At least two years of experience in a leadership role.
  • Read and interpret safety instructions, standard operating procedures, technical procedures, and governmental regulations.
  • Use arithmetic operations across units of measurement, including whole numbers, fractions, decimals, and percentages, and apply algebraic and geometric principles.
  • Define problems, collect data, establish facts, draw valid conclusions, and interpret technical instructions in mathematical or diagram form while handling abstract and concrete variables.
  • Use manufacturing and internet software and Microsoft Office tools, including PowerPoint, Excel, Word, and Outlook.
  • Pass a background check and drug screen; occupational health screening may also be required.
  • Meet role-dependent physical demands, including lifting, pushing, pulling, sitting, standing, reaching, visual acuity, and hand and finger dexterity; some roles may also involve stooping, kneeling, twisting, crouching, crawling, balancing, climbing, or working at heights.
  • Work in an office, manufacturing, or warehouse environment as applicable; sterile manufacturing work requires aseptic gowning and task-appropriate personal protective equipment, and work may involve cleaning agents, wet or humid conditions, confined areas, cold temperatures, or other listed workplace hazards.

Responsibilities

  • Oversee all operations within the Analytical Chemistry Laboratory, including personnel management, hiring, performance reviews, performance management, and scheduling.
  • Prepare and manage budgets, maintain departmental metrics, and represent the department in internal and external meetings.
  • Ensure the laboratory is audit-ready for regulatory bodies and customers.
  • Collaborate with internal stakeholders and external customers to deliver service and define project objectives; provide written and verbal progress reports.
  • Foster continuous improvement, ensure compliance with Good Laboratory Practices and Good Manufacturing Practices, and lead initiatives to improve laboratory efficiency and effectiveness.
  • Complete assigned tasks in a timely manner and in compliance with current Good Manufacturing Practice, regulatory, corporate, and health, safety, and environmental requirements.
  • Mentor chemists and analysts.
  • Write, review, revise, and approve standard operating procedures, project progress reports, project timelines, acceptance methods, and test data summaries.
  • Conduct and document laboratory investigations.
  • Write, review, and direct the execution of analytical protocols.
  • Analyze data using scientific and statistical tools; troubleshoot and resolve complex issues.
  • Observe and communicate trends and develop continuous-improvement plans.
  • Use analytical instrument troubleshooting and repair knowledge to address instrument issues.
  • Read and interpret standard operating procedures to ensure compliance and maintain up-to-date training.
  • Lead and support the team, oversee day-to-day operations, manage departmental goals, and ensure adherence to organizational policies and procedures.
  • Foster a positive work environment, guide and support team members, and evaluate performance to drive improvement and 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 awareness and responsibility among team members.
  • Perform other duties as assigned.

Desired Qualifications

  • Five years of experience in a chemistry leadership role.
  • Five years of chemistry experience in an aseptic or sterile environment and a Good Manufacturing Practices-regulated setting.
  • Obtain and maintain media qualification if required.
  • Wear a respirator if required.

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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