PAI II

ALIRIColorado Springs, CO
$100,000 - $130,000Onsite

About The Position

Provide leadership that ensures efficient production that is scientifically sound and regulatory compliant. Responsible for helping implement efficiency improvements in overall productivity.

Requirements

  • Bachelor's Degree in Chemistry or related Scientific field with 8-10+ years experience is required -OR- Master's Degree or equivalent in Chemistry or related Scientific field with 7+ years experience is required -OR- Ph.D. or equivalent in Chemistry or related Scientific field with 5+ years experience is required
  • Significant work experience will be considered as a substitution for education
  • Strong understanding of the technical knowledge to ensure operational efficiency of Laboratory Operations within the business program
  • Proficient knowledge of instrumental analysis, including mass spectrometry and chromatography
  • General knowledge of current industry guidance and regulations
  • Ability to build lasting client relationships and support marketing and sales activities
  • Strong oral and written communication skills, including very strong bias toward calling and talking with customers on the telephone, when in-person interactions are not possible
  • Very strong attention to detail; the ability to manage large numbers of competing requirements is absolutely mandatory
  • Understanding of customer perspective for bioanalytical regulatory development programs
  • Technical expertise to ensure technical quality, suitability of data for the intended purpose, and operational efficiency of projects execution
  • GLP regulatory and experimental design experience
  • Forecasting, planning, and interdepartmental facilitation skills
  • Integrating the commercial and technical aspects of laboratory operations

Nice To Haves

  • Mass spectrometry or HPLC experience.
  • Advanced knowledge of Watson LIMS.
  • Advanced knowledge of Excel.
  • Current experience with industry and regulatory guidance

Responsibilities

  • Planning, coordinating and organizing, including efficient productivity, scheduling, and forecasting resources (e.g., liaising with different departments to working on allocation, utilization and direction of company resources cross-functionally)
  • Maintaining knowledge of status/progress for projects across different departments
  • Monitoring productivity to help meet monthly revenue goals and overall goals of the organization
  • Ensure incoming projects are feasible from an overall organizational standpoint so that Aliri Labs Inc. can successfully meet client deliverables
  • Acting as the interface between Laboratory Operations, QA, and Reporting
  • Scheduling and coordinating, including directing others, to ensure overall successful completion of studies
  • Communicating frequently and effectively as the main point of contact with the client, providing updates on ongoing programs
  • Engaging Laboratory Operations throughout the entire productivity process; planning, developing and implementing, as well as sharing impact of efforts, including helping distribute risk evenly between all projects
  • Advocating for both the internal and external clients
  • Completely understanding and managing clients’ expectations
  • Including the entire project team in communications throughout project
  • Ensuring that all results meet internal and/or protocol specifications
  • Ensuring that the study design, results, and interpretation address changing stakeholder needs
  • Manage studies; project initiation planning; helps both customers and laboratory staff to interpret data and adjusts the bioanalytical development approach.
  • Support internal resources and customers by applying current scientific, regulatory, and project management expertise to establish experimental design and support execution: a) Relating analytical data to study objectives as the study progresses, in “real time” b) Reviewing technical data
  • Managing studies to meet GLP, CDER, CVM, ICH, FIFRA, VICH, or applicable regulatory guidance
  • Writing content for technical-regulatory study protocols, plans, and reports
  • Reconciling data and report reviews, as well as archival approval
  • Applying data evaluation techniques and tools (e.g., Analyst®, JMP®, Microsoft Excel, etc.) to assess analytical phase data
  • Understand the business need for each project and make on-going decisions based on what’s best for the organization—even if that means challenging senior stakeholders on critical success factors.
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