Job Description: This position is a lead role in the QC Bioanalytical laboratory and may have direct reports. Experience with ELISA and/or PCR is preferred. Lead will be responsible for ensuring the routine testing is scheduled and authorization is performed to meet timelines needed for manufacturing to maintain schedules or the QA disposition group to disposition batches. Lead should be able to help troubleshoot assays within the group and provide testing support, as needed and be willing to have direct reports. Job Responsibilities: ability to identify issues, presents complex problems with possible solutions, and actively takes leadership role to resolve or independently resolves complex issues applies discipline’s principles, appropriate procedures, and leadership skills to develop action plans and contributes to executing toward individual, team, and project goals expertly solving highly complex mathematical problems and solving situation dependent multifaceted problems using even only ambiguous information at least method 1, yellow belt certified and/or applies method 1 tools to solve complex issues, implements unique approaches to problem solving, and may coach others to become method 1 certified receives feedback well from management and other colleagues, grows self utilizing feedback and takes accountability for actions and personal development Job Requirements: 8 -10 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry with a BS/BA Degree in Science/related field 5 -7 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry with a MS Degree in Science/related field 2-4 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry with a Ph. D in Science/related field Job Details: Company: Pfizer Vacancy Type: Full Time Job Location: Fayetteville, NC, US Application Deadline: N/A Apply Here getyourvacancy.com
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