QA & QC Investigator

This QA & QC Investigator Position Features:Location: Rensselaer, NY 12144?? Pay Rate: $30-35/hrDuration: 3 MonthsPosition OverviewWe are seeking Quality Control Analyst I professionals to support laboratory investigations, deviation handling, and compliance activities in a pharmaceutical GMP environment. This role will focus on executing and supporting QC investigations, ensuring data integrity, and maintaining compliance with regulatory and quality standards.Key ResponsibilitiesPerform laboratory-based investigations related to QC deviations and out-of-specification (OOS) resultsConduct initial impact assessments and support full investigation lifecycleApply root cause analysis tools (e.g., Fishbone, 5 Whys) to identify true root causesDocument investigations in compliance with:GMP (Good Manufacturing Practices)GDP (Good Documentation Practices)Internal SOPs and regulatory standardsSupport CAPA development and implementation to prevent recurrenceEnsure timely initiation and closure of investigations within defined timelinesCollaborate with cross-functional teams (QA, Manufacturing, etc.)Assist in backlog reduction efforts by managing ongoing and aged investigationsMaintain accurate and audit-ready documentationIdentify opportunities for improvements in:Analytical methodsEquipment reliabilityLaboratory processesParticipate in audits and customer interactions as neededQualificationsBachelor's degree in Chemistry or related scientific disciplineMinimum 6+ years of experience in a QC laboratory or equivalent combination of education and experiencePrior experience in pharmaceutical or regulated industry (required)Strong knowledge of:GMP & GDP standardsDeviation investigations & OOS handlingCAPA processesProven experience in technical writing and documentationPreferred SkillsExperience with investigation tracking systemsFamiliarity with FDA regulationsStrong analytical and problem-solving skillsAbility to manage multiple priorities in a fast-paced environmentKey Success FactorsStrong attention to detail and complianceAbility to identify true root cause vs. symptomsEffective communication and cross-functional collaborationAbility to work under tight timelinesNotes for SuppliersMust have hands-on QC investigation experience (not just theoretical)Pharma/GMP experience is mandatoryCandidates with root cause analysis + CAPA exposure will be prioritizedShort-term contract - candidates should be available for the full durationEqual Opportunity Employer / Disabled / Protected VeteransThe Know Your Rights poster is available here:https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdfThe pay transparency policy is available here:https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdfFor temporary assignments lasting 13 weeks or longer, AppleOne is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team.AppleOne participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program.https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf