GMP Training Specialist Synerfac Technical StaffingGMP Training SpecialistWhippany, NJ$35–$38.50 / hourTemporaryContractorManufacturing Practice (cGMP) training programs across the site's manufacturing operations, including solid oral dosage (tablet and capsule) production and aseptic fill-finish operations, as well. * Design and deliver training curricula for solid oral dosage manufacturing operations, including granulation, blending, compression, encapsulation, coating, and packaging.
Technology Rigor Controls Specialist-AVP BarclaysTechnology Rigor Controls Specialist-AVPWhippany, NJIdentifying and evaluating technology and AI-related control weaknesses across the USCB technology stack and performing detailed evaluation and investigation to support continuous improvement and risk mitigation aligned to the Barclays Controls Framework. Identification and investigation of potential weaknesses and issues within internal controls to promote continuous improvement and risk mitigation aligned to the bank’s control framework, prioritised by its severity to disrupt bank operations.
NewRegulatory and Quality Specialist - Labware - Millville, NJ Michael Page USARegulatory and Quality Specialist - Labware - Millville, NJVineland, NJ$70,000–$80,000 / yearFull timeThis role is responsible for maintaining quality systems, supporting audits and certifications, managing documentation, ensuring compliance with applicable regulatory requirements, and driving continuous improvement initiatives. With a legacy spanning over 100 years, they are committed to enabling scientific discovery and innovation through high-quality products, robust quality systems, and customer-focused solutions.
NewRCM Product Specialist SOFIERCM Product SpecialistTotowa, NJRemoteThe RCM Product Specialist will lead the development, implementation, and validation of manufacturing and analytical methods of new diagnostic and therapeutic radiopharmaceuticals for SOFIE within the itheranostic / FAPI Division. Working closely with SOFIE’s pharmaceutical partners and internal staff, they will ensure that these radiopharmaceuticals are in full compliance with all regulatory requirements (specifically, 21 CFR 211and 212).
Digital Marketing Specialist ECLARODigital Marketing SpecialistLawrence Township, NJ$81.74–$86.69 / hourIf needed, lead internal MLR review processes and work with external partners to ensure timely and accurate preparation of digital programs (e.g., CRM, third-party programs, HCP media, websites, mobile, email, social media, SEO / SEM, IVA, Field-Trigger e-mails, etc.). Position Overview: The Omnichannel Strategist serves as a dedicated point-of-contact for a brand, their creative, digital and media agencies, ensuring seamless planning and execution of omni-channel campaigns / tactics aligned to the brand strategy.
Commercial Loan Operations Specialist Vaco LLCCommercial Loan Operations SpecialistFairfield, NJRemote$50–$75 / hourDetermining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: the individual’s skill sets, experience and training; licensure and certification requirements; office location and other geographic considerations; other business and organizational needs. Determining compensation for this role (and others) at Vaco/Highspring depends upon a wide array of factors including but not limited to the individual’s skill sets, experience and training, licensure and certifications, office location and other geographic considerations, as well as other business and organizational needs.
NewEnvironmental Health, Safety, and Security Specialist JouléEnvironmental Health, Safety, and Security SpecialistSouth Brunswick Township, New Jersey$65,000–$75,000 / yearIdeal for candidates with EHS experience in cosmetics manufacturing, food production, pharmaceutical, or industrial environments seeking growth within a hands-on EHSS role - warehouse and distribution center experience translates. This role is responsible for ensuring regulatory compliance, promoting a strong safety culture, supporting environmental and security initiatives, and partnering with site leadership to maintain a safe and secure workplace.
Claims Specialist Medical Malpractice Diedre Moire Corp.Claims Specialist Medical MalpracticeUnion, NJ$100,000–$140,000 / yearFull timeCONSIDERED EXPERIENCE INCLUDES: Insurance Claims Examiner Adjuster Specialist Professional Liability Medical Malpractice MedMal Allied Healthcare #DiedreMoire #JobSearch #JobHunt #JobOpening #Hiring #Job #Jobs #Careers #Employment #jobposting #InsuranceJobs #UnderwriterJobs. Manage total claim costs for highly complex or severe injury medical malpractice claims while negotiating to resolution and providing high levels of customer service.
Quality Control Specialist (Weekend) WuXi Biologics Cayman IncQuality Control Specialist (Weekend)Cranbury, NJ$60,200–$96,300 / yearTechnical Skills / Knowledge: Candidate must possess willingness to learn analytical and QC operations of pharmaceutical industry, understand current regulations and industry trends of biologics product development, characterization and manufacturing testing requirement including cGMP, ICH, EMA, FDA, and other global compendia regulations and guidance. Job Summary: The QC specialist (Weekend Shift) is responsible for the quality and on-time testing/collection of samples, EM (Environmental sampling), Water and Gas system sampling (when required) with raw material sampling to the various testing sections.
Quality Control Specialist Zp Group LlcQuality Control SpecialistNJ$40–$48 / hourResponsibilities for the Quality Control Specialist include: Perform analytical testing (cell-based function, flow cytometry, and PCR-based assays) under cGMP in collaboration with QC Utilize knowledge of aseptic techniques using a BSC Track and trend analytical methods and assist in troubleshooting activities Maintain, calibrate, and operate analytical equipment Maintain laboratory material and reagent inventory Document testing in accordance with cGMP requirements Perform OOS/ Deviation investigations and carry out experiments in support of these investigations. Qualifications for the Quality Control Specialist include: A minimum of 4+ years' experience within quality control Hands-on experience conducting Flow Cytometry and PCR testing within a GMP laboratory environment Ability to conduct a deviation or OOS investigation Hands on experience within cell therapy or biologics manufacturing Technical writing experience preferred Bachelor's degree in chemistry or related field.
Seasonal Quality Control Specialist (REHIRES) Third PartySeasonal Quality Control Specialist (REHIRES)Mount Laurel, New JerseySeeking a video Quality Control Specialist for a 7-month seasonal position at NFL Films, a world-class professional sports media company and producer of Emmy Award-winning series such as HBO NFL Hard Knocks, NFL Films Presents and Inside the NFL. The Specialist is primarily responsible for receiving and watching finished shows and media and recognizing mistakes, spelling errors, technical issues, and content problems while working in person at our 200,000 square-foot facility and studios in Mt.
Quality Control Specialist (V2), NJ (temp-to-hire) Collaborative SolutionsQuality Control Specialist (V2), NJ (temp-to-hire)Jersey City, New JerseyWe grade, authenticate, vault, and sell millions of record-setting collectibles, all while modernizing and digitalizing the process to further our mission of helping collectors pursue their passions. We grade, authenticate, vault and sell millions of record-setting collectibles, all while modernizing and digitalizing the process to further our mission of helping collectors pursue their passions.
Centralized Governance & Control Specialist-Remediation Quality Assurance Testing The Toronto-Dominion BankCentralized Governance & Control Specialist-Remediation Quality Assurance TestingMount Laurel, NJ$91,000–$136,240 / yearJob Description: The Centralized Governance & Control - Remediation Quality Assurance Testing team performs in-flight Assurance Testing Activities throughout the Issue Remediation Lifecycle to ensure Management Action Plans (MAPs) are designed to sufficiently mitigate and manage risk drivers of the issues and operate effectively. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition.
Specialist, Quality Document Control Rocket Pharmaceuticals IncSpecialist, Quality Document ControlCranbury, NJ$56,000–$68,000 / yearWe are committed to compensating employees equitably based on several factors, including responsibilities and level of the position, depth and types of the employee's experience, location of the position and availability of similar talent in a competitive market. Degree in science related field preferredWork with documents, pushing carts to transport batch records and large sets of documents/binders.
Specialist, Quality Document Control Rocket PharmaceuticalsSpecialist, Quality Document ControlCranbury, New Jersey$56,000–$68,000 / yearFull timeWe are committed to compensating employees equitably based on several factors, including responsibilities and level of the position, depth and types of the employee’s experience, location of the position and availability of similar talent in a competitive market. Position Summary: The Specialist, Quality Document Control will provide support for the management and control of documentation at Rocket including within the ZenQMS electronic quality system.
NewSenior Quality Control Specialist Novartis AGSenior Quality Control SpecialistEast Hanover, NJ$85,400–$158,600 / yearExpected Annual Base Salary Range for role: 85,400 - 158,600 CHF.The salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. Ensure all activities comply with cGxP, data integrity, Quality, and HSE requirements, including equipment maintenance, calibration planning, training, risk identification, and safe working practices.
Paratransit Quality Control Specialist First Student IncParatransit Quality Control SpecialistHasbrouck Heights, NJIn the state of Washington, all technician and driving positions, including but not limited to van drivers and any other position requiring employees to drive a company-owned vehicle, are considered safety-sensitive and are therefore subject to drug and alcohol testing, including cannabis. As a Utility Service / Fueling Associate, you will play an important role in preparing vehicles and supporting the daily flow of para-transit operations.
Quality System Specialist II - Document Control Becton Dickinson and CoQuality System Specialist II - Document ControlFranklin Lakes, NJ$110,200–$176,400 / yearPerforming tasks, of moderate complexity, within planned schedules and timelines, supporting document retreival for audits, actively leading or participating on project teams and ensuring documentation compliance. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs.
Warehouse Quality Control Specilist 1st Shift B&H Foto & Electronics CorpWarehouse Quality Control Specilist 1st ShiftNJLong known as "The Professional's Source", B&H is recognized by savvy consumers worldwide for its honest, knowledgeable guidance, expert tips and articles… and always-great prices. At over 50 years old and counting, B&H has built a reputation as the trusted resource for photography and videography enthusiasts via its NYC SuperStore and its award-winning website.
Specialist I, QA Quality Management System Tris Pharma IncSpecialist I, QA Quality Management SystemMonmouth Junction, NJAlso requires skills (2 yrs exp) in: cGMPs in the pharmaceutical industry; Issuing, tracking and closing Investigations, CAPAs, CPIs, Planned Deviations and Product Quality Complaint Investigations; conducting investigations leading to root cause and closure of investigations within defined timelines; conducting investigations, root cause analysis, CAPA or CPI in accordance with Quality System; and tracking and trending quality metrics for open Investigations: lab OOS/OOT/Lab Event, CAPAs/CPIs, planned deviations, and product quality complaints. Report metrics pertaining to investigations of lab OOS/OOT/Lab Event, CAPAs/CPIs, planned deviations + product quality complaints to Quality Department Head or other appropriate company personnel.
Quality Assurance Documentation Specialist - Supplier Quality Innophos Holdings IncQuality Assurance Documentation Specialist - Supplier QualityCranbury, NJ$63,000–$93,000 / yearThe ideal candidate is a detail-oriented quality professional with a degree in Food Science, chemistry, or a related life science and at least three years of quality assurance experience, ideally within the food or dietary supplement industry. The benefits set forth in this posting reflect Innophos' current benefits for similarly situated employees, are subject in all respects to the terms and conditions of the applicable program policies and may be modified or discontinued by Innophos in the future (subject to applicable law).
Quality Assurance Documentation Specialist – Supplier Quality InnophosQuality Assurance Documentation Specialist – Supplier QualityCranbury, New JerseyThe ideal candidate is a detail-oriented quality professional with a degree in Food Science, chemistry, or a related life science and at least three years of quality assurance experience, ideally within the food or dietary supplement industry. The benefits set forth in this posting reflect Innophos’ current benefits for similarly situated employees, are subject in all respects to the terms and conditions of the applicable program policies and may be modified or discontinued by Innophos in the future (subject to applicable law).
Quality Specialist, Incoming Quality Novartis AGQuality Specialist, Incoming QualityEast Hanover, NJ$43.08–$80 / hourAs a Quality Specialist, Incoming Quality Assurance, you will play a critical role in safeguarding product integrity from the very first point of entry, ensuring that incoming materials meet the highest quality and compliance expectations. You will partner closely with operations, suppliers, and quality systems teams to drive excellence, support continuous improvement, and maintain a strong state of control across incoming quality processes.
Manager, Quality Control - Analytical RevanceManager, Quality Control - AnalyticalNewark, New JerseyThe Manager, Quality Control (QC) - Analytical is responsible for leading and overseeing the analytical testing program supporting both clinical and commercial drug substance (DS) and drug product( DP) manufacturing in a GMP-regulated facility and registered under the Federal Select Agent Program (FSAP). This position combines leadership, technical expertise, regulatory compliance, and biosecurity oversight to support product release, stability, method lifecycle management, and ensure laboratory readiness for inspections.
Director, Quality (Contamination Control and Microbial Excellence) Thermo Fisher Scientific IncDirector, Quality (Contamination Control and Microbial Excellence)NJ$145,500–$218,250 / yearProvide subject matter expertise (SME) in microbiology, microbiological methods, contamination control, aseptic processing, Environmental Monitoring, cleanroom design, cleaning and disinfection and other relevant areas required by site CCME teams and corporate quality management. 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.
Quality Specialist JouléQuality SpecialistParsippany, NJRemote$60,000–$85,000 / yearSupport and administer the Electronic Quality Management System (Veeva), including user access, reports, system configuration, validation, and end-user support. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
NewQuality / Regulatory Specialist-Millville, NJ Michael Page InternationalQuality / Regulatory Specialist-Millville, NJVineland, New Jersey$70,000–$80,000 / yearFull timeThe successful Quality & Regulatory Specialist will have:Bachelor's degree in Quality Assurance, Chemistry, Biology, Engineering, Regulatory Affairs, or a related scientific discipline. Relevant work experience will also be considered.1-5 years of experience in quality assurance, regulatory affairs, manufacturing quality, or a related role.
Project Controls Specialist DEPCOM PowerProject Controls SpecialistBedminster, NJFull timeAs a Koch Engineered Solutions company, DEPCOM Power is a leading energy solutions partner for the utility solar and broader energy industries, providing project development support, engineering, procurement and construction, energy storage, repowering and operations and maintenance services. This role plays a critical part in supporting the financial and operational success of utility-scale solar and energy projects by maintaining accurate forecasts, tracking productivity, and ensuring strong cash flow performance.
NewProject Controls Specialist Michael Page InternationalProject Controls SpecialistTrenton, New Jersey$135,000–$165,000 / yearFull timeOpportunity to support large-scale grid modernization and utility infrastructure programsStrong project backlog and long-term growth potentialCollaborative and technically focused environmentCompetitive compensation package with bonus potentialComprehensive benefits including medical, dental, vision, and retirement plansFlexible work environment depending on project needsCareer advancement opportunities into technical leadership and project management pathsJob SummarySector: ConstructionSub Sector: Construction PlanningIndustry: Energy & Natural ResourcesWhere: TrentonContract Type: PermanentConsultant name: Cullen SheridanJob Reference: JN-052026-7025683Job Nature: Hybrid working Using a variety of industry and proprietary software tools, including Primavera P6, you will perform the following tasks:Implement project controls tools and methodologyDevelop and support project schedule requirements per client procedures and best practicesPerform critical path analysis, provide schedule insights and corrective actions when requiredSupport schedule contingency management, and work with key stakeholders to identify and manage project risksProvide regular project updates and report deviations from the approved project baseline to the project team.
Payment Controls Specialist ApolisPayment Controls SpecialistWhippany, NJ$32–$37 / hourExecute and provide senior support in the payment control activities within the Payment Control Gateway. - Collaborate with Operations, Technology and Front Office stakeholders to resolve complex scenarios, verifying if.
Inventory Control Specialist -Parsippany, NJ CoreWeave IncInventory Control Specialist -Parsippany, NJParsippany, NJ$65,000–$85,000 / yearTo conform to U.S. Government export regulations applicable to that information, applicant must either be (A) a U.S. person, defined as a (i) U.S. citizen or national, (ii) U.S. lawful permanent resident (green card holder), (iii) refugee under 8 U.S.C. § 1157, or (iv) asylee under 8 U.S.C. § 1158, (B) eligible to access the export controlled information without a required export authorization, or (C) eligible and reasonably likely to obtain the required export authorization from the applicable U.S. government agency. In this role, you will: Asset Tracking: Maintain an accurate inventory of all hardware and other IT assets within the data center region, including servers, networking equipment, and other hardware and materials.
Loss Control and Risk Management Specialist W. R. Berkley CorpLoss Control and Risk Management SpecialistParsippany, NJ$125,000–$195,000 / yearThe company offers a competitive compensation plan and robust benefits package for full time regular employees which for this role includes: Base Salary Range: $125,000 - $195,000 The actual salary for this position will be determined by a number of factors, including the scope, complexity and location of the role; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. This individual will be instrumental in leveraging emerging technologies, delivering enhanced value to our insureds and broker partners, and strengthening collaboration across underwriting, loss control, and claims to drive improved loss performance.
NewDocument Control Specialist Delva Tool & MachineDocument Control SpecialistCinnaminson, NJFull timeIf you thrive in a fast-paced manufacturing environment and take pride in delivering high-quality, precision work, this is your opportunity to grow with a company that values craftsmanship, accountability, and continuous improvement. Delva Tool & Machine (DTM) and its 4 locations specialize in precision machining, fabrication, and assembly highly engineered components.
NewGroup Risk Specialist - Quality Assurance The Toronto-Dominion BankGroup Risk Specialist - Quality AssuranceMount Laurel, NJ$91,000–$145,600 / yearAdditional Responsibilities: The Group Risk Manager is an enterprise role which works with various stakeholders across Risk Management and Technology, including but not limited to, Non-Financial Risk Management, Compliance, Financial Crimes, Audit, Enterprise Protect, and Platforms and Technology teams that support Risk. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition.
Quality Specialist (Space Systems) Marotta Controls, Inc.Quality Specialist (Space Systems)NJ$25–$35 / hourUse inspection planning tools and perform a product audit, determine sample size for lots, pull random samples, check lot quality by sampling according to acceptable quality levels (AQL), may perform 100 inspection, visual or dimensional as required. Check one or more specified surfaces on similar work pieces for adherence to dimensional tolerances, geometric relationships, and/or configurations, appearance, workmanship, surface defects, cleanliness, marking, omissions, or improperly installed parts.
Senior Specialist, Quality Assurance Validation Bristol-Myers Squibb CoSenior Specialist, Quality Assurance ValidationNew Brunswick, NJ$78,980–$95,708 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Senior Document Control Specialist Platinum Global Talent Solutions Ltd.Senior Document Control SpecialistNew Jersey, New Jersey$90,000–$125,000 / yearThe busiest rail connection between New York, New Jersey, and the Northeast Corridor, the Hudson Tunnel Project will improve capacity, reliability, and resiliency of commuter and intercity rail transit serving 800,000 daily passengers from Washington, D.C. to New York and New England. Oversee document workflows within PMIS applications, identify and address system-related issues, and ensure project personnel are fully capable of working within the required software tools.
QA Specialist I WuXi Biologics Cayman IncQA Specialist ICranbury, NJ$60,200–$96,300 / yearQualifications: • Bachelors/Masters in relevant field (e.g., Life Sciences, Pharmacy) • 1-2 years in QA/project management, preferably in pharma/biotech • GMP regulations, project management methodologies • Strong communication, problem-solving, and organizational skills • Tools such as Project management: Jira, Aspera, MS Project, Document control: SharePoint, Document Vault (any skill would be a plus). Responsibilities: • Oversee QA projects, ensuring timely completion and quality • Coordinate cross-functional teams (QC, Regulatory and other relevant departments etc.) • Develop and execute project plans, timelines • Ensure compliance with GMP, regulatory requirements • Identify and mitigate project risks, track progress • Collaborate with stakeholders on project scope, changes.
Sr Quality Specialist, Global Contract Manufacturing Balchem CorporationSr Quality Specialist, Global Contract ManufacturingMontvale, NJ$70,000–$90,000 / yearThe role works closely with cross-functional teams - including R&D, Operations Quality, Commercial, Operations, and Procurement to select, qualify, manage, and support comanufacturing sites, and serves as the central hub for comanufacturing quality activities. Act as the primary authority ensuring quality and product safety for global comanufacturing partners, supporting both strategic (comanufacturer development, program deployment) and tactical (audits, issue resolution) activities.
Group Risk Specialist - 2LoD Controls Testing and Oversight The Toronto-Dominion BankGroup Risk Specialist - 2LoD Controls Testing and OversightMount Laurel, NJ$91,000–$145,600 / yearThe role requires hands-on experience and knowledge of leading industry practices pertaining to controls testing, operational risk management, regulatory reporting requirements, liquidity and capital risk management, and risk data aggregation and reporting, as well as capabilities to lead a team of testing professionals and influence senior stakeholders across business, risk, finance, technology, and data management functions. Lead the execution of independent testing in the following areas: Control Design & Operating Effectiveness, Transactions Testing, Data Reconciliations, Logic Reperformance, Data Profiling/Analytics, End-User Computing (EUC) Review, Policy & Procedure Review, Governance/Oversight, and Regulatory Rule Compliance.
NewQA Specialist Aurobindo Pharma LtdQA SpecialistEast Windsor, NJCompile, consolidate and review documents to prepare for and/or release product, including: Certificates of Analysis, Certificates of Conformance, Test and Batch Record Review Forms, Executed Batch Records, specifications, investigations and change controls. The Specialist will also help ensure that proposed changes consider the impact to other processes, documents, budget items and external partners through a full understanding of Acrotech's processes.
Senior Specialist, Project Controls Aecon Group IncSenior Specialist, Project ControlsNJ$120,000–$150,000 / yearAre committed to supporting and investing in inclusive work environments, through initiatives like Diversity, Equity, Inclusion, & Accessibility training, our Aecon Women in Trades and Aecon Diversity in Trades programs, and our Employee Resource Groups (ERGs) to ensure we are building inclusion into every aspect of our culture at Aecon. Reporting to the Project Controls Director, the Senior Project Controls Specialist will be responsible for providing project controls support to Aecons ongoing mega-projects in the Nuclear sector.
Quality Specialist - Final Inspection Marotta Controls, Inc.Quality Specialist - Final InspectionNJ$25–$35 / hourPosition Profile: A Quality Specialist (Final Inspection) is responsible for visual and dimensional inspections on manufactured parts, assemblies, and/or sub-assemblies using engineering drawings, specifications and contract/purchase order information to validate compliance with Internal and external requirements. Your employment, both initially and continually thereafter, is conditioned on production of such proof of citizenship and/or any export license that may be required to comply with any and all applicable laws, regulations, or executive orders, or required by Federal, State, or local government contracts.
AIR TRAFFIC CONTROL SPECIALIST (TERMINAL) United States ArmyAIR TRAFFIC CONTROL SPECIALIST (TERMINAL)Newark, NJ$79,744–$103,673 / yearFormer NG T32 Dual Status employees receiving an Honorable or a General Discharge under Honorable Conditions are eligible for reinstatement provided they have been separated for at least one year before applying for reinstatement and received a rating of record of their most recent permanent position of a least fully successful (or equivalent). Incumbent is responsible for the utilization of training materials that ensure controller-trainees are adequately trained and tested with the goal of creating a cohesive ATC team that provides multi-level ATC services to the aviation customer.
Senior Specialist, Quality Engineer 1 L3Harris Technologies IncSenior Specialist, Quality Engineer 1NJ$96,000–$178,000 / yearWith customers' mission-critical needs always in mind, our employees deliver end-to-end technology solutions connecting the space, air, land, sea and cyber domains in the interest of national security. By submitting your resume for this position, you understand and agree that L3Harris Technologies may share your resume, as well as any other related personal information or documentation you provide, with its subsidiaries and affiliated companies for the purpose of considering you for other available positions.
Specialist, Quality Engineering (Supplier) L3Harris Technologies IncSpecialist, Quality Engineering (Supplier)Camden, NJ$82,500–$141,500 / yearTrain suppliers as required and ensure effective containment plans are defined and implemented, that the that root cause corrective action (RCCA) is robust and effectively implemented in the timeframe required. The SQE will communicate and ensure our Suppliers and Subcontractors understand stated requirements, have the capability to consistently and predictively meet, and provide conforming products and services.
Senior Quality Validation Specialist Cellares CorpSenior Quality Validation SpecialistBridgewater, NJ$90,000–$210,000 / yearThe Quality Validation team at our IDMO Bridgewater facility will be responsible for providing Quality Assurance oversight of environmental, equipment (analytical and production), facility & utility, site automation, process validation & engineering documents, test protocols, CAPAs, deviations, change control records, and additional site based technical documentation and activities. Provide oversight of cleanroom lifecycle programs including aseptic process simulations, environmental monitoring performance qualification, cleanroom certification & recertification, cleaning & sanitization, and facility controls.
Life Science Quality Assurance Specialist III The Cooper Companies IncLife Science Quality Assurance Specialist IIILivingston, NJ$90,000–$115,000 / yearJob Summary: The Life Science Quality Assurance Specialist III is primarily responsible for establishing, developing, implementing, maintaining and improving Quality System processes and programs to include: Quality Event Reporting (Deviations, Nonconformance, Change Management, CAPA, Complaint), Document Control Program, Supplier Qualification, Validations, and Product Transfer. The candidate should have strong written and verbal communication skills to foster cross-functional collaboration and partnerships, lead by positive influence, maintain a high level of integrity, and possess a strong continuous improvement mindset.
Specialist I, QA QMS TRIS PHARMA, INCSpecialist I, QA QMSMonmouth Junction, NJAlso requires skills (2 yrs exp) in: cGMPs in the pharmaceutical industry; Issuing, tracking and closing Investigations, CAPAs, CPIs, Planned Deviations and Product Quality Complaint Investigations; conducting investigations leading to root cause and closure of investigations within defined timelines; conducting investigations, root cause analysis, CAPA or CPI in accordance with Quality System; and tracking and trending quality metrics for open Investigations: lab OOS/OOT/Lab Event, CAPAs/CPIs, planned deviations, and product quality complaints. ### Experience Required 2 years ### Minimum Education Required Bachelors ### Compensation $81,037.00 - $81,037.00 / Yearly ### Hours Per Week 40 ### Number Of Positions 1 ### Job Description Specialist I, QA QMS for Tris Pharma, Inc to work at our Monmouth Junction, NJ loc.
NewQuality Assurance Specialist Integrated Resources, IncQuality Assurance SpecialistPlainsboro Township, New JerseyFull timeJob Description• Coordinating efforts for the control of new and updated procedures for the manufacturing plant and supporting functions• Tracking, follow-up and implementation of, including but not limited to, ECOs, validation records, batch records and notebooks• Capable of both written and verbal effective communication skills• Proficient in the Microsoft Office suite and Adobe products. Qualifications• High School diploma at the minimum; business degree or related acceptable relevant experience• 1+ years relevant GMP/GLP experience required