Specialist QAWe at Kelly ® Science & Engineering hear you, and we're here for you! We're seeking a Specialist QA to work at a premier biotechnology client in Juncos, PR. Sound good? Take a closer look below. You owe it to yourself to consider this great new opportunity.
Compensation: $38.00 HR (W2) Shift: Administrative 8hrs shift – with work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours coverageWhy You Should Apply To Be Specialist QACompetitive pay rate and robust workplace safety cultureOpportunity to contribute to industry-leading quality assurance and compliance programsWork with a highly respected organization in the biopharmaceutical sectorGain valuable experience in regulatory audits, process validation, and manufacturing qualityBi-Weekly pay by W-2Vacations, Sick & Holidays paid*Christmas bonus *This Job Might Be An Outstanding Fit If You Have The Following Qualifications:Bachelor's degree in Sciences (Engineering, Biology, Chemistry, Physics, Computer Science, etc.)Experience of at least 10 years in the biopharmaceutical industry, including a minimum of 5 years in QualityStrong experience in Quality and Compliance, regulatory audits, validation, characterization and automation reportsStrong experience in reviewing and approving deviations, critical utilities, and environmental monitoring trend reportsAdvanced communication, facilitation, and presentation abilities in Spanish and EnglishExpertise in data trending, evaluation, and working independently across various levelsCan effectively interact with regulatory agencies and collaborate with cross-functional teamsWhat's A Typical Day As Specialist QA? You'll Be:Reviewing and approving product manufacturing procedures (MPs) and validation protocolsApproving process validation reports for manufacturing processesParticipating on incident triage teams and approving environmental characterization reportsLeading investigations, site audits, and representing QA on new product introduction teamsOwning site quality program procedures and acting as designee for the QA managerReviewing risk assessments and supporting automation, facilities, and environmental programsApproving work orders, EMS/BMS alarms, non-conformance investigations, and CAPA recordsApproving change controls, providing lot disposition, and authorizing lots for shipmentHelping you discover what's next in your career is what we're all about, so let's get to work. Apply to be Specialist QA today!