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Quality Control Manager

AMRI Springfield Full-Time
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Quality Control Manager in Springfield, MO

AMRI provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries.
The Quality Control Manager is an integral part of the AMRI team, contributing to our success by ensuring our Quality Control Laboratory is running effectively and efficiently so we can meet our operational activities and the attainment of Quality department goals for our clients.
Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture.
In this role, you will:                                                                                           
  • Provide leadership and supervision to the QC Laboratory staff including work assignments and ensuring staffing at all times by coordinating overtime and schedules to meet production priorities.
  • Assist the Quality Director, maintaining records of material specifications, test methods, laboratory procedures, analytical raw data, QC staff training, and other GMP QC requirements in a manner consistent with regulatory requirements
  • Ensure departmental SOP’s are in conformance with QA and FDA requirements
  • Work with Analytical to transfer and adopt new analytical methods and material specifications
  • Provide oversight of the daily supply and maintenance purchases
  • Assure compliance with laboratory CHP and laboratory waste handling procedures.

Qualifications and background to be successful in this role:


  • Minimum of a Bachelor’s degree in Chemistry

  • 5 – 10 years of experience as analyst in QC/Analytical Development with 2 years minimum experience in analytical development

Strongly Desired

  • Highly proficient with common pharmaceutical analytical equipment and methodology including HPLC, GC, Empower, titration, Karl Fisher, refractive index, melting point analysis, particle size analysis, etc. techniques

  • Proven Supervisory/Management

  • Experience as a bench analyst in a Quality Control Laboratory

  • Excellent communication skills, both written and verbal, problem solving skills, and project management skill

  • Excellent ability to multi-task

  • Solid understanding of LIMS software from the user perspective and must know Quality department goals

  • A mechanical aptitude for analytical instrumentation troubleshooting and repairs

  • Strong attention to detail and a capability to handle diverse functions simultaneously by establishing priorities

All interested applicants must apply online.  AMRI is an Equal Opportunity Employer, we value diversity and inclusiveness.  Minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity are encouraged to apply.


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Albany Molecular Research, Inc. (AMRI) is a global contract research and manufacturing organization with more than twenty years’ experience in providing customers with fully integrated drug discovery, development, and manufacturing partnerships. AMRI builds its expert knowledge and advice into customers’ programs to deliver a complete range of value-added services with more informed decision-making, resulting in enhanced efficiency and more successful outcomes at all stages of the pipeline. AMRI’s smarter options for insourcing and outsourcing support discovery and development of pharmaceutical products, manufacturing of API and drug product for existing and experimental new drugs. With unrivalled project management and locations in the United States, Europe, and Asia, AMRI maintains geographic proximity and seamless delivery across multiple sites. AMRI has historically leveraged its drug discovery expertise to progress several internal programs to the development candidate stage and, in some cases, into Phase I clinical development. AMRI has successfully partnered certain programs and is actively seeking to out-license its remaining programs to strategic partners for further development.

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