TN/QUALITY TECHNICIAN/00050 Position Available In Shelby, Tennessee
Tallo's Job Summary: The Quality Technician position, reporting to the Quality Supervisor, involves supporting production processes such as inventory maintenance, label verification, and final product checks. Responsibilities include assisting with DEA reporting, ensuring facility compliance, and participating in SOP reviews. Requirements include the ability to work independently, good communication skills, and the ability to lift up to 25 lbs. Pharmaceutical industry experience is preferred but not required.
Job Description
Job Description:
QUALITY TECHNICIAN. ADDITIONAL INFORMATION
JOB TITLE
QualityTechnician STATUS:
Non-Exempt
REPORTS TO
Quality Supervisor GENERAL:
Under the supervision of the Quality Supervisor, theQuality Technician will support all production processes.
RESPONSIBILITIES
1. Assistance with maintenance of the finished product and rawmaterial inventory, receiving and inspection, label verifications,batch reconciliation and environmental monitoring. 2. Responsible for performing final checks for all compoundedproduct. The final checks will include checking the integrity ofall compounded product for items such as leakage, visible PM,discoloration and the legibility of the labels. 3. Assist the DEA Officer (Quality Manager) with the compilation ofdata for quarterly reporting to the Drug Enforcement Administrationusing the ARCOS system. 4. Assist in maintaining facility compliance with the GMPs and allstandard operating procedures. 5. Participate in the training of new personnel and assumeadditional duties as required and assigned by the QualitySupervisor. 6. Participate in the ongoing review of existing SOPs.
Job Requirements:
1. Must have the ability to work independently 2. Must have good communication skills 3. Must be able to make routine decisions while followingguidelines and/or procedures. 4. Must be able to lift up to 25 lbs and stand for long periods oftime. 5. Must have H.S. Diploma (or GED) with 1 or 2 years applicableexperience (in a GMP and FDA regulated facility preferred). 6. Pharmaceutical industry experience preferred but notrequired.
