Jupiter, FL
As a Quality Control/Lab Technician, you will be responsible for ensuring the quality and safety of our animal health products through testing and analysis. You will work closely with our Quality Control team to perform laboratory tests and maintain accurate records of all testing procedures. This is a full-time, permanent position with opportunities for growth and advancement within the company.
Key Responsibilities:
• Evaluate in- process, Finished goods, R&D and Stability samples for physicals analysis.
• Provide in-process batch adjustments by performing analysis and lab trails as instructed per the master batch record.
• Record all evaluations in the laboratory notebook and report test results in the appropriate forms and analysis sheets according to cGMP, SOP, and current industry practices.
• Clean and maintain a clean work area which includes cleaning glassware, counters, and equipment.
• Ensuring Packaging / Filling Line Equipment is cleared and cleaned before all production runs begin.
• Responsible for ensuring the Packaging / Filling lines have the correct and appropriate documentation for Packaging material and product before and during packaging runs.
• Pulling the correct labels for the production run from the label room.
• Responsible for completeness and accuracy of Packaging Pages during and at the completion of production runs. This includes Lot number, packaging size, expiration date, expected yield and so forth.
• Responsible for completing in-process fill checks throughout the packaging run in accordance with SOP and management instruction. Checks include: labels, Date code, lot numbers, heat seals / leakers and overall quality and free from defects. Checking cases for case codes, Case labels and correct palletization patterns.
• Responsible for collecting Retain and Laboratory evaluation samples as per SOP or Packaging page or Management instruction.
• Responsible for Finished Product counts including Date, Number of pallets, number of cases and performing the appropriate calculations to document accurate counts.
• Back-flushing product as pallets complete. This is done in the BEAS system which is an interface to the SAP system.
• Responsible for Printing / verifying accuracy and attaching Pallet count sheets to the Pallets.
• Responsible for completeness of label reconciliation sheets and returning unused labels to the label room.
• Responsible for verifying that equipment logbooks have been completely and accurately filled out by Quality and the production associates at the beginning and end of packaging runs.
• Responsible for reporting and Quality non-conformances to the Quality Management.
• Responsible for ensuring all documentation is reported utilizing cGMP / Good documentation practices and all applicable SOP as well as industry best practices.
Qualifications:
• Preferred degree in Chemistry or Related Scientific field
• Minimum 2 years in a Lab setting (Pharmaceutical Manufacturing)
• Experience and skill with analytical weighing, pipetting, general analytical lab skills including related calculations.
• Experience with GMP / FDA regulated industry preferred
• Read, Write, Comprehend SOP, Compendia, Technical documents in English
• Proficient with Microsoft Office Suite, including Outlook, Word, Excel
• High level of attention to detail
$20 - $22