Quality Control Associate II - 2nd Shift QC

Mightyworks       |    Location:CA       |    Country:United States Of America

<p>Now hiring multiple experienced QC Associates to assist a growing biotech company on the forefront of the COVID-19 response. Second&nbsp;shift: 3 pm to 11:30 pm.<br /> &nbsp;</p> <p>Great opportunity for a full-time position that breaks into biotech if you have basic lab experience, including pipetting. Positions will fill quickly! APPLY NOW!<br /> &nbsp;</p> <p><strong>MUST&nbsp;</strong>have: high school diploma, awesome Microsoft Excel and Word&nbsp;skills, great written and oral communication, high energy,&nbsp;&nbsp;experience in biotech manufacturing,&nbsp;experience as a QC for raw materials, understanding of Good Lab Practices (GLP) and Good Documentation Practices (GDP)<br /> &nbsp;</p> <p>Responsibilities (training provided):</p> <p>&middot; Perform incoming inspections of all raw materials.</p> <p>&middot; Operate all equipment safely, as trained and directed, in accordance with established practices.</p> <p>&middot; Maintain material identification and status control.</p> <p>&middot; Execute test and inspection procedures in compliance with written and approved standard operating procedures.</p> <p>&middot; Collect, process, and analyze data.</p> <p>&middot; Summarize data to monitor/trend product performance.</p> <p>&middot; Supports weekly, monthly, and quarterly metrics.</p> <p>&middot; Supports process and product improvement projects.</p> <p>&middot; Supports troubleshooting and lab investigations.</p> <p>&middot; Create and own low to medium risk Non-Conformances/ Deviations / CAPAs.</p> <p>&middot; Recommend and execute test procedure updates.</p> <p>&middot; Performs tasks related to QC functional responsibilities such as, stability, validations, sample retention program, customer complaints, inventory maintenance, and continuous improvement efforts.</p> <p>&middot; Provides training to other QC personnel.</p> <p>&middot; Reviews manufacturing batch records for accuracy, completeness, and GDP.</p> <p>&middot; Always complies with Good Lab Practices (GLP) and Good Documentation Practices (GDP).</p> <p>&middot; Embodies cultural values and aligns daily actions with department goals and company culture.</p> <p>&middot; Other activities as deemed necessary by the QC management team.<br /> &nbsp;</p> <p>PHYSICAL DEMANDS:</p> <p>&middot; Ability to work long hours and execute under pressure with short turnaround times.</p> <p>&middot; Ability to speak, write, and use all office equipment including scanner and printer, phone, computer, etc.</p> <p>&middot; Regular use of fine motor skills.</p> <p>&middot; Ability to lift and/or move objects that weigh more than 30 pounds.</p> <p>&middot; Regularly required to stand, walk, stoop, kneel, crouch or crawl.</p> <p>&middot; Specific vision abilities required for this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust and focus.</p> <p>&middot; Available weekends, and holidays when needed.</p>