Now Hiring!

Now Hiring!

LexaMed is hiring for at least one full time microbiologist for out Toledo, OH laboratory.  Qualified aplicants can email their resume or CV to  [email protected]  

Position Summary

Responsible for coordination and execution of client sponsored studies related to the pharmaceutical and medical device industry in compliance with FDA 21 CFR Part 820 cGMPs.Includes design of experiments, authoring protocols, executing projects, including coordination of project work schedule with Laboratory. Interfaces with clients outlining cost proposals, project status and issues final report.

Duties and Responsibilities

Primary duties and responsibilities include performance of the following:

  • Be capable of proper operation, maintenance, and performance of laboratory instrumentation.
  • Prepare and maintain proper records and documentation.
  • Data acquisition, analysis, and reporting.
  • Provide rapid, accurate, and technically correct response to client request.
  • Advise supervisory personnel of non-functioning equipment, non- compliant situations, and potential problems.
  • Perform procedures and tasks assigned by supervisor.
  • Perform design of experiments, author protocols, executing projects, issuing final reports for client sponsored projects.
  • Interacting with clients.
  • Remain current in field of expertise.
  • Promote safety and innovation with coworkers.
  • Other duties and responsibilities as assigned.

Organizational Responsibilities

  • Complies with and helps to enforce LexaMed’s standard policies and procedures.
  • Suggests areas for improvement in internal processes along with possible solutions.
  • Seeks and participates in development opportunities.

Education/ Experience Requirements

  • Bachelor’s or advanced degree in Microbiology or closely related field.
  • Minimum of 3 years of microbiology laboratory experience including conducting and/or coordinating custom R&D projects and routine microbiology testing.
  • Working knowledge of FDA GMP/GLP requirements.
  • Capable of working autonomously at a high technical level and possess high skills in area of expertise.
  • Excellent writing and verbal communication skills. Experience with protocol authoring, execution and final report generation.
  • Knowledge of appropriate AAMI/ISO/PDA/USP guidelines and standards.
  • Ability to effectively interact with individuals at all levels both internally and externally.
  • Excellent computer and documentation skills.
  • Willingness to travel.
Adam Parton