Research & Development

QC Microbiology Laboratory Technician

The person filling this position will provide Analytical Quality Control (QC) functions in the Microbiology and Analytical Laboratory. The primary goals of this position are to maintain accurate and efficient microbiological and analytical laboratory operations with adherence to Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP).

Additionally, is to ensure timely and appropriate release of Raw Material (RM) lots, Bulk Formula (BF) batches, and Work-in-Process (WIP) and Finished Goods (FG) lots.

Department: Quality Control

Reports to: Director of Quality Control

We are proud to be an EEO employer, maintain a drug-free workplace and perform pre-employment substance abuse testing.

All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

 

Apply Now

Please email your resume to: CPrice@mcp-mail.com

 

Duties & Responsibilities:

  • Working knowledge of analytical and instrumental testing methods (specifically micro testing)

  • Laboratory record-keeping requirements, best practices, and Good Documentation Practices

  • The use of personal protective equipment

  • Core Competencies

  • Team Oriented

  • Flexible to change and open to constructive feedback

  • Solid written and verbal communication skills

  • Math skills and computer literate

  • Proficient in organizing and filing documents

  • The Analytical QC Micro Technician will be responsible for:

  • Main responsibility: Perform all micro analysis on bulk, finished goods and raw materials

  • Help provide Certificates of Analysis (COAs) for FG lots whenever possible

  • Ensuring that all analytical testing and testing reviews/second checks required are carried out in an accurate and efficient manner.

  • Reviewing testing data and authorizing release of RM lots, BF batches, and FG lots

  • Reviewing Lab Technicians’ notebooks for adherence to Good Laboratory and Good Documentation Practices

  • Maintaining analytical laboratory operations with adherence to GLP principles

  • Maintaining samples (testing and retain) and records of Analytical QC work with adherence to Good Documentation Practices and cGMP

  • Assist with archiving of retains, bulk batches (samples and paperwork) and PLR packets

  • Responsible for releasing of finished goods in Syspro ( MCP’s system)

  • Assist Analytical Supervisor and other duties as assigned


Education & Experience:

  • Two- or four-year degree preferred in the field of experimental research, or working knowledge of micro testing or equivalent

  • Preferably some knowledge of chemistry

  • Must have worked in a Quality Control Laboratory environment

  • Working familiarity with Good Laboratory Practices and current Good Manufacturing Practices preferred

  • Math skills and computer skills (e.g. MS Office including Excel and Word) are essential

Physical Requirements:

  • Prolonged periods of standing

  • Must be detailed oriented, hand eye coordination  

  • Must be able to lift to 10 pounds