Supply Chain Quality Assurance Inspector - 2nd Shift
Full-timeOncology
Description
<p style="text-align:left"><b>Work Schedule</b></p>Second Shift (Afternoons)<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, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse, Will work with hazardous/toxic materials<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>Second Shift: Monday-Friday 2pm-10:30pm</p><p></p><p>As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.</p><p></p><div><div><p><b><span>How will you get here?</span></b><span> </span></p></div><div><p><b><span>Responsibilities</span></b><span> </span></p></div><div><ul><li><p><span><span>Applies Good Manufacturing Practices (cGMP) in all areas of responsibility.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrates and promotes the<span> </span></span><span>company</span><span><span> </span>vision.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Performs approval of specifications and incoming inspections on material (</span><span>i.e.</span><span><span> </span>drug, components) and<span> </span></span><span>distribution</span><span><span> </span>shipments.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Performs<span> </span></span><span>material and<span> </span></span><span>process inspections</span><span><span> </span>and<span> </span></span><span>samplings</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Review and<span> </span></span><span>approve</span><span><span> </span>Packaging Electronic Production Orders. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Participates in continuous improvement initiatives and<span> </span></span><span>assists</span><span><span> </span>with root cause investigations for nonconforming issues.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Author’s</span><span>, revises, and<span> </span></span><span>complies with</span><span><span> </span>all relevant SOP’s and Work Instructions and properly<span> </span></span><span>documents</span><span><span> </span>activities when necessary.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Resolve and<span> </span></span><span>a</span><span>ssure that issues potentially affecting product quality/compliance are escalated to the attention of the Team Leader and/or Management. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Assures that issues are resolved in a timely<span> </span></span><span>manner</span><span><span> </span>and corrective actions are implemented accordingly.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Performs all activities in a safe and efficient manner.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Other duties may be assigned to meet business needs.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p><div><p><b><span>Education</span></b><span> </span></p></div><div><ul><li><p>High School Diploma OR GED Required</p></li></ul></div></div><div><p><span> </span></p></div><div><p><b><span>Knowledge, Skills, Abilities</span></b><span> </span></p></div><div><ul><li><p><span><span>3+ years of experience in Pharmaceutical<span> </span></span><span>or of a</span><span><span> </span>related, regulated industry.</span></span></p></li></ul></div><div><ul><li><p><span><span>Familiar</span><span><span> </span>with Quality Systems (Change Control, deviations, complaint management, documentation management, among others).</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Must be able to work in a refrigerated environment (35F to 46F) with provided protective wear.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Must be able to work in a freezer</span><span><span> </span>(-20F)</span><span><span> </span>environment with provided protective wear.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Must be able to work in potent compound suites with provided protective wear (PPE).</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Good reasoning and problem-solving skills, basic math skills, good communication skills</span><span>, basic</span><span><span> </span>computer skills.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Must be willing to work various shifts and overtime depending on business needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Must</span><span><span> </span>be able to work independently.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Mastery of skills<span> </span></span><span>required</span><span><span> </span>to read, understand, and adhere to the SOPs and policies of a GMP environment.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><b><span>Physical Requirements</span></b><span> </span></p></div><div><ul><li><p><span><span>Must not</span><span><span> </span>be allergic to penicillin or cephalosporin products.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Extensive standing and walking on<span> </span></span><span>packaging</span><span><span> </span>floor<span> </span></span><span>in order to</span><span><span> </span></span><span>monitor</span><span><span> </span>room activities.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Work schedule, Monday through Friday, 8 hours per day.<span> </span></span><span>Additional</span><span><span> </span>overtime and weekend (Saturday or Sunday) work may be<span> </span></span><span>required</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>This position requires standing,<span> </span></span><span>bending</span><span><span> </span>and liftin</span><span>g.<span> </span></span><span>Exerting and lifting up to 25</span><span>lbs of materials occasionally, and 10lbs of materials regularly.</span><span> </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>The position is exposed to cold temperatures for more than one hour at a time. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>The position is exposed to -20F temperatures for at least 15 minutes at a time.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>The position will be exposed to atmospheric<span> </span></span><span>conditions</span><span><span> </span>could require special personal protection equipment. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Incumbent must meet applicable visual acuity/color blindness standards to perform visual inspections in a cGMP environment</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div></div><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