Quality Control Inspector

Primary Job TitleQuality Control Inspector IILocationNewark, DEContract DetailsPosition Type: ContractContract Duration: 6 monthsStart: Upon hirePay Rate: $25.00$31.00 / Hour (USD)Shift / Schedule: Second shift, 2:30 PM to 11:00 PM, MondayFriday. Initial training required on first shift (6:00 AM to 2:30 PM) for approximately 34 weeks before transitioning to second shift. Second shift differential applies per site policy.Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.Role Environment and ScopeQC Inspector II role within a regulated medical device manufacturing environment. Work is 100 percent on site. Responsibilities include device history record review, documentation verification, physical inspection, and final quality signoff. Three total openings. Contingent staff augmentation assignment.Job SummaryPerforms inspections, testing, and sampling procedures for product manufacturing in a regulated medical device manufacturing environment. Work includes packaging line and incoming material checks, device history record review and release, and may include assistance with validation or troubleshooting of testing methods. Routine assignments with limited judgment; works under moderate supervision while acquiring job skills and following company procedures.Key ResponsibilitiesMaintain and promote a safe work environmentConduct inspections of in-process and finished goodsRecord and maintain quality control documentationSupport investigations into non-conforming productsSupport process audits for SOP and WI adherenceInitiate Non-Conforming Events (NCEs)Review device history records and sales ordersParticipate in Kaizen and continuous improvement initiativesComplete training requirements and maintain recordsEnsure regular, punctual attendance and ability to work overtimeRequired QualificationsHigh school diploma or GEDAbility to lift and move up to 40 poundsPrior manufacturing or quality experience appropriate for a Level II roleStrong attention to detailAbility to follow SOPs and controlled documentationReliability and consistent attendanceWillingness and ability to work second shiftRequired SkillsAbility to follow written procedures and controlled documentationStrong attention to detailEffective written and verbal communicationTeamwork and independent work capabilityAbility to read schematics and blueprintsBasic Microsoft Office (Excel, Word, SharePoint, OneDrive)Familiarity with GMP and GDPPreferred QualificationsOne to two years of quality or manufacturing experienceMedical device industry experienceGDP and GMP experienceExperience in other regulated industries such as aerospace or pharmaceuticalFamiliarity with Oracle ERP or Agile PLMEducation RequirementsHigh school diploma or GED (required)Associate degree (preferred)Work Environment / Physical RequirementsSit, stand, walk, reach, stoop, kneel, crouch, crawlLift and move up to 40 poundsExposure to mechanical parts, vibration, and moderate noiseSafety shoes required in designated areasMay work with high voltage electronics, radiation, clean rooms, controlled environments, or dark roomsStandard manufacturing and quality PPE as required on siteInterview ProcessInitial phone interviewOn site interview with hiring teamResume Screening SignalsPositive Signals:Experience in regulated manufacturing or quality environmentsExperience with documentation review and inspection activitiesDemonstrated attention to detail and compliance mindsetRed Flags:No exposure to regulated environmentsNo manufacturing or quality related experienceInability to meet second shift requirementsExperience Level GuidanceTarget profile is early career to mid level quality or manufacturing professionals. Candidates with less experience may be considered if background is relevant. Candidates with more experience may be considered if interested in the role scope.BenefitsMedical, Vision, and Dental Insurance Plans401k Retirement FundAbout the ClientInnovative medical technology firm focused on women's health.About GTTGTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.Job Number: 26-05196#gttic #LI-GTT #LI-Onsite