Quality Control Technician II - First Shift
Full-timeMasters
Description
<p style="text-align:left"><b>Work Schedule</b></p>First Shift (Days)<p style="text-align:inherit"></p><p style="text-align:left"><b>Environmental Conditions</b></p>Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting<p style="text-align:inherit"></p><p style="text-align:left"><b><u>Job Description</u></b></p><p style="text-align:inherit"></p><p><b>Job Title: </b>Quality Control Technician II</p><p>Day/Shift: Mon - Fri 08:00 AM to 04:30 PM</p><p></p><p><b>Position Summary: </b></p><p>Responsible for the evaluation of quality control samples through physical evaluation and microbial load testing of plated and non-plated media, control of documents, and maintaining good general laboratory practices.</p><p></p><p><b>Key Responsibilities: </b> </p><ul><li>Review and maintain product compliance specifications, documentation control.</li><li>Gain proficiency on all testing areas.</li><li>Documentation of testing results and determination of aesthetic quality on finished product.</li><li>Maintain consistency for training tasks in Master Control.</li><li>Maintain SOP criteria for inspection/testing.</li><li>Responsible for maintaining department equipment and ordering consumable stock supplies when necessary.</li><li>Exercise GMP and GLP compliance in work environment.</li><li>Work well in a high volume fast paced environment.</li><li>Work closely with Quality Assurance department as a quality team.</li><li>Work with the continuous improvement program within the department.</li><li>Understand and exercise all safety requirements and procedures.</li><li>Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations.</li><li>Accomplish department goals.</li><li>Support all company policies.</li><li>Performs other duties as assigned.</li></ul><p></p><p><b>Minimum Requirements/Qualifications: </b></p><p><b>Education:</b></p><ul><li>High School Diploma OR GED Required</li></ul><p></p><p><b>Experience:</b></p><ul><li>Some laboratory experience in a biological sciences laboratory is preferred.</li><li>A minimum combined 1-2 years of experience of in related QC/QA, microbiology laboratory work in a laboratory setting, or an equivalent combination of education and experience is a plus.</li><li>Some familiarity with FDA regulations for medical devices.</li><li>Possess the ability to manage many tasks and in an organized fashion.</li><li>Possess intermediate computer skills, preferably with experience in Microsoft word to include Word, Excel and PowerPoint programs. Experience working in SAP is a plus.</li><li>Listen to, and follow, written and verbal instructions in English.</li><li>Able to adapt and to learn new procedures and to maintain a scientific and objective approach.</li><li>Must be available to work alternate shifts when needed.</li><li>Must maintain a professional workplace attitude.</li><li>Self-motivated, highly responsible and possess a good teamwork spirit.</li></ul><p></p><p></p><p></p><p></p>
Pipeline
Retrospective Cohort EnrollmentN/A
Technical Evaluation of Brahms PCT DirectN/A
Blood sample collectionN/A
Blood samplingN/A
RimegepantN/A