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Global Brand Manager – Makeup (Hybrid | Summit, NJ) 📍 Summit, NJ (Hybrid) | 💼 Full-Time Join a globally recognized skincare and beauty leader, and help shape the future of its Makeup portfolio on a global scale. We’re looking for a strategic, creative, and data-driven Global Brand Manager to drive innovation, communications, and growth across the makeup category. This is a high-visibility role where you’ll collaborate with global teams, influence product pipelines, and lead campaigns that reach millions of consumers worldwide. No Sponsorship or C2C Global Consumer Health Company Global Brand Manager - Makeup Summit, NJ (Hybrid 2-3 days in office) Contract: 6-9 months with a possible extension Hourly Rate: $47.08 per hour / W2 Why This Role Stands Out • Own and shape global brand strategy for a major beauty platform, • Drive innovation + go-to-market execution across international markets, • Partner with R&D, creative agencies, influencers, and global stakeholders, • Work at the intersection of beauty, science, and digital marketing, • Highly collaborative, high-impact role with real visibility What You’ll Do • Support and help define the global makeup strategy, • Identify growth opportunities using consumer insights, data, and trends, • Lead development of product innovations and brand storytelling, • Partner with cross-functional teams to deliver end-to-end product launches, • Drive execution of integrated marketing campaigns (digital, social, eComm, media), • Collaborate with R&D and Regulatory to develop compelling product claims, • Manage creative development across packaging, content, and campaigns, • Partner with global markets to ensure strong launch adoption and sell-in success, • Manage and forecast global marketing budgets What You Bring • 5+ years of experience in brand marketing, product marketing, or related fields, • Makeup/beauty industry experience (required), • Proven success leading cross-functional teams and agency partners, • Strong experience in consumer-driven product innovation, • Expertise in digital marketing and integrated campaigns, • Exceptional communication, storytelling, and leadership skills, • Analytical mindset with strong data-driven decision-making ability, • Experience managing budgets and forecasting, • 📍 Hybrid role based in Summit, NJ, • Flexible in-office collaboration with global teams

🚨 Contract Opportunity – Treasury Administrative Assistant (Hybrid | Summit, NJ) We are currently seeking a highly organized and detail-oriented Treasury Administrative Assistant to support a dynamic Finance organization at a global consumer health company based in Summit, NJ. No sponsorship or C2C 📍 Location: Summit, NJ (Hybrid – 2–3 days onsite per week) ⏳ Duration: 7-month contract (with likely extension) 🕒 Schedule: 40 hours/week, Monday–Friday (onsite required per hybrid schedule) 💰 Rate: $47.45/hr About the Role: The Treasury Administrative Assistant will provide high-level administrative and operational support to the Treasury team within the Finance organization. This role plays a key part in ensuring smooth daily operations, strong executive support, and accurate financial administrative processes. Key Responsibilities: • Process headquarters mail, checks, and finance documentation, • Handle outgoing checks and route to appropriate requestors, • Manage purchase requisitions, invoices, contracts, and payment requests, • Track departmental spending against budgets, • Prepare and submit expense reports for treasury leadership, • Manage executive calendars and coordinate meetings, • Book conference rooms, handle visitor logistics, and support onsite meetings, • Coordinate domestic and international travel for treasury executives, • Provide broad administrative support to the Treasury team Stakeholder Interaction: • Internal: Finance, Procurement, IT, Security, Legal, • External: Banks, credit rating agencies, insurance partners, brokers, and service providers What We’re Looking For: • Bachelor’s degree required, • 8+ years of administrative or corporate finance support experience, • Strong proficiency in Microsoft Excel, Word, PowerPoint, Teams, and SharePoint, • Exceptional attention to detail and accuracy, • Strong communication skills (written and verbal), • Proven ability to collaborate in a corporate, cross-functional environment, • Experience in corporate finance is strongly preferred

Job Description Your Next Chapter Starts Now: Join Us! Master Your Craft, Mentor Others: Lead HVAC Installer Opportunity We are a trusted plumbing, electrical, heating, and air conditioning company with a legacy spanning over three generations. We take pride in being deeply rooted in the communities we serve, employing residents of the towns we call home. Success as a Lead HVAC Installer requires overseeing the installation of generators, gas lines, and HVAC units in residential settings. Your role extends to designing and installing advanced HVAC equipment, ductwork, and piping for optimal performance and efficiency, ensuring homes reach new levels of comfort. What We Offer: • Earn competitive wages starting at $35/hour, • Benefits Include major medical, prescription drug, optical, dental, orthodontia, long-term disability, and life insurance., • 401-K with Match with company match., • Access 100+ hours of training every year., • Participate in events like ball games, comedy clubs, dinners, awards, and more every quarter., • Company-provided uniforms., • Provide Stability - We have over 55 years in business., • Work with a fun, professional, and caring management team., • As we expand, so do the opportunities for career advancement., • Take pride in working for a company that makes a positive difference in the community. Responsibilities for the Lead HVAC Installer: • Install generator and related equipment, including gas lines used in a residential setting, successfully without supervision., • Replace heating, air conditioning, refrigeration equipment, or complete systems., • Test electrical circuits and components for continuity, using electrical test equipment., • Test pipe or tubing joints and connections for leaks, using a pressure gauge or soap-and-water solution., • Assemble and install heating and air-conditioning units used in homes., • Design and install HVAC equipment, ductwork, and piping., • Maintain accurate logs of all work performed., • Ensure our reputation for superior service is maintained during all interactions with customers., • Complete special projects and additional duties as assigned/required. Requirements for the Lead HVAC Installer: • Must have an EPA certification with a solid understanding of applicable installation and venting codes., • Minimum of 5 years experience, including hands-on training or work., • Proven expertise in heating and cooling systems, with the ability to draw simple diagrams and interpret blueprints., • Service experience is beneficial but not mandatory., • Trade School graduate preferred., • A Driver’s License is required., • Knowledgeable in HVAC codes, proper application, and electrical/HVAC safety., • Strong mathematical skills and the ability to produce routine reports., • Thrives in a dynamic, customer-focused environment., • Effective communication skills with both internal and external customers. Our staff is regarded with a sense of pride and familial connection, reflecting our commitment to treating everyone as an extension of our family. With a dedicated focus on making homes and businesses safe, comfortable, and efficient, we uphold a strong commitment to quality service and community well-being. Powered by JazzHR QDv9g3IWXi

Title: Veeva PromoMats & PMR Operations Specialist Pay Rate: $45-52/hour Location: Rahway, NJ (Hybrid) Duration: Contract until December 2026 (Possibility of extension) Position Overview This contractor role supports Promotional Material Review (PMR) operations and the Veeva Vault PromoMats platform, enabling the end-to-end promotional review process within our client's Animal Health business. The position partners closely with the Director of Content Excellence to ensure the promotional review ecosystem remains compliant, scalable, and continuously improving. This role focuses on translating business and compliance requirements into effective system capabilities and optimized workflows. The contractor collaborates cross-functionally with Marketing, Regulatory, Legal, Technical Services, IT, and external agencies to drive adoption of platform enhancements, streamline review processes, and improve cycle times and quality outcomes. This is a hands-on, execution-focused role with strategic influence across the promotional review landscape. Key Responsibilities Veeva Vault PromoMats Platform Support • Support day-to-day platform performance, configuration inputs, and enhancement prioritization. • Translate business needs into system requirements and recommendations., • Partner with IT on releases, upgrades, and new capabilities; assess impact and drive readiness. • Monitor industry trends and platform roadmap to improve compliance, efficiency, and scalability. Promotional Material Review (PMR) Operations • Enable efficient, compliant review workflows by optimizing submissions, routing, and approvals. • Support policy improvements and consistent application of review standards., • Troubleshoot workflow issues and drive continuous improvement., • Maintain audit-ready practices across the content lifecycle. Stakeholder & Agency Enablement • Serve as a subject matter expert on PromoMats, guiding internal teams and agencies., • Support training, documentation, and communication on system/process updates., • Partner on change management initiatives and governance updates., • Improve submission quality, metadata, and content reuse strategies. Metrics, Reporting & Continuous Improvement • Develop dashboards to track performance, cycle times, and bottlenecks., • Use data insights to improve speed-to-market while maintaining compliance., • Support PMR governance forums and identify enhancement opportunities. Required Qualifications & Experience • Bachelor’s degree or equivalent experience., • Extensive hands-on experience with Veeva Vault PromoMats in pharma or biotech., • Strong knowledge of PMR/MLR/PRC processes in regulated environments., • Experience translating business needs into system solutions., • Proven cross-functional collaboration skills., • Strong problem-solving, communication, and stakeholder management abilities. Preferred Experience • Experience supporting global or regional review models., • Familiarity with content lifecycle management, DAM, modular content, or reuse strategies. • Experience with system upgrades, releases, or transformation initiatives.

Position – Planning & Supply Management III Location – Millburn, NJ Shift & Timing: Wed - Sat, 3:30 PM - 1:00 AM Contract – 6 Months with a possibility of extension Job Summary Seeking a Planning & Logistics Specialist responsible for managing material planning, ERP master data, purchasing processes, and logistics coordination to ensure smooth supply chain operations and production support in a GxP environment. Key Responsibilities • Manage and maintain accurate master data in ERP systems in compliance with local and global standards., • Perform daily MRP review for BOM materials and manage Purchase Orders., • Ensure timely material availability based on approved production plans., • Maintain MRP-related data, material specifications, and supplier records in ERP., • Coordinate incoming material dispatch with Warehouse and Quality teams., • Monitor supplier performance metrics including OTIF, lead time, and quality compliance., • Handle supplier complaints, returns, rebates, and credit/debit notes., • Support KPI reporting, inventory management, and gap analysis activities., • Drive continuous improvement initiatives across logistics and supply chain operations., • Collaborate with cross-functional teams to resolve supply and system-related issues., • Ensure compliance with supply chain policies, procedures, and regulatory requirements. Required Qualifications • 2–3 years of experience in Supply Chain, Logistics, Material Planning, or Operations., • Experience with ERP systems; Microsoft Dynamics 365 (D365) preferred., • Strong knowledge of:, • Inventory Management, • Demand & Supply Planning, • Order Management, • Transportation & Logistics, • Customer Relationship Management, • Excellent analytical, coordination, and problem-solving skills., • Ability to collaborate across multiple teams and manage priorities effectively. Key Performance Indicators (KPIs) • Inventory accuracy and cost efficiency., • Master data completeness and consistency., • Supplier delivery performance (OTIF)., • On-time material availability and supply execution., • Compliance with quality and operational standards.

Position: Global Brand Manager Location: Summit NJ- 07901 Duration: 06 months contract with possible extension Job Description: The Brand Manager for Global Makeup is responsible for identifying and executing innovation, claims and communications required to drive global growth on the Makeup platform. This role will be highly collaborative as you will partner with cross-functional teams and global partners to shape, test and execute opportunities. You will play a critical role in shaping the brand’s innovation, comms and claims strategies to drive its success globally. Key responsibilities include but are not limited to: • Support the Marketing Director in shaping Client's Global Makeup strategy, • Identify opportunities for innovation and non-innovation-led growth, leveraging data and outside-in thinking to develop strategic recommendations, • Collaborate with global partners, HCPs, MUPA, CBI, Creative agencies and influencers to craft, & test innovations, • Drive relationship with key manufacturers to develop breakthrough innovations and always remain ahead of makeup trends, • Work closely with cross-functional teams to ensure launch timing accuracy of all new product innovations, • Support the shaping and lead the execution of Client's Makeup communication campaigns, partnering with multifunctional teams and leading creative and influencer agencies to deliver campaigns that drive mental availability for the brand and platform, • Lead the briefing and ongoing development of innovation and non-innovation o Packaging/ artwork o Ecom product page o Media assets o Social assets etc • Partner with R&D and Legal/ Regulatory affairs to create compelling claims list per new product innovation, continuously elevating and advancing brand superiority, • Support local market to develop compelling stories for NPIs, ensuring optimal sell-in volume, • Collaborate with global partners to ensure global fit of all innovations and communication strategies, • Manage Global budget for Makeup Required Qualifications • A minimum of a BA/BS degree is required; a master’s in business or marketing specialization preferred, • A minimum of 5 years of marketing, sales or related experience is required Desired Qualifications • Makeup industry experience required, • Experience leading cross-functionals to develop consumer-centric product innovation, • Experience leading cross-functionals and agencies to develop a communications strategy for multiple brands or priorities, • You should possess excellent creative instincts and strong leadership skills, • Excellent written and oral communication skills, with an ability to bring out the best in others., • Strategy and data are the core of everything we do, so strong critical thinking and analytical skills are required., • Digital marketing experience is critical., • Budget management and forecasting experience.

Job Description Summary CCCC is currently recruiting talented and motivated individuals to join our team as Eligibility Specialists. As an Eligibility Specialist, you will provide technical assistance to applicants enrolled in childcare assistance programs (CCAP), review eligibility in accordance with NJ DFD regulations, and ensure that all CCAP agreements are for eligible providers and periods. Duties Job Duties • Maintain records and files proving eligibility for childcare assistance payment for applicants., • ReviewApplicationsand other documents submitted by applicants and verify information for compliance with NJ DFD Instructions as outlined in policy., • Process requests for Change in Providers, • Process requests for initial and annual Child Abuse Record Investigations and Home Inspections, • Educate parent of other childcare options (RFCC, child care centers, etc.), • Maintain spreadsheets of applicants whose periods of subsidy are ending each month or whose agreements can be extended if proof of license extension is received. Requirements • BA preferred but not required, • Detail oriented, • Excellent customer service skills, • Good at calculating numbers, • Working knowledge of Microsoft Teams, Outlook, SharePoint, • Must know how to scan. Nice To Haves Bilingual preferred Benefits • 403(b), • Dental insurance, • Health insurance, • Life insurance, • Paid time off, • Professional development assistance, • Vision insurance

Leaf Home Stairlift is the nation’s fastest growing safety company and we are looking for new installers in your area NOW. Start out as an installer and you can even work your way up to becoming a trainer, an installation manager or regional manager in no time. Stop wasting your time and effort searching for and bidding on jobs only to lose out to another contractor. Spend your time doing what you do best … using your professional craftsmanship skills to help seniors age in the homes they love. We are looking for individuals with strong mechanical / carpentry skills that possess a strong attention to detail. You will be primarily providing installation of stairlifts both inside and outside of the home. Requirements: • Prefer 1 year of carpentry / construction skills including electrical skills (the ability to add or move outlets)., • A box truck, cargo van, full size pickup or full size SUV w/trailer., • Current or ability to obtain general liability insurance and workers compensation insurance or exemption depending on the state (we can assist)., • Must be willing to travel. Required overnight stays from Monday - Friday. Both in state and out of state., • Must have all necessary tools for the job including:, • Box wrenches, Allen wrenches, 12” Miter Saw, Nut Driver Set and Drill Driver Extension What’s in it for me: • This is a 1099 contractors position, • Stairlift installation compensation averages around $250-$1000., • All jobs are presold … no sales involved, just the installation., • Flexible Schedule, • No out of pocket expenses … We purchase and stage all jobs for you so no wasted time or reimbursements needed., • Weekly Pay – We pay per job each week by direct deposit.

Key Carriers alternate their role based on store needs, predominantly performing the role of Coordinator and occasionally acting as Key Carrier, taking on a leadership role in maintaining all aspects of the store. The Key Carrier role is an elevated extension of the Coordinator role. Key Carriers mu

Job DescriptionBA or Technical Payroll Analyst Other titles: Business analyst, Technical analyst, Payroll analyst, Payroll Systems analyst, etc. Hybrid 50% Location: NY,NY Contract: 9 months (possible extension based on client need) The initiative for this project is to modernize and maintain payroll systems to ensure accurate and compliant processing of employee compensation and tax documentation. The Business Analyst will support key HR Payroll applications, focusing on implementing tax updates and regulatory changes, improving system reliability and data accuracy through rigorous testing and simulation, and translating business needs into actionable technical solutions. The role also ensures compliance with labor laws and contractual obligations, contributing to data integrity, transparency, and accountability in payroll operations. Additionally, the initiative promotes interoperability across related HR and timekeeping systems. Top skills: • Business Analysis - experience analyzing and documenting business requirements, authoring functional and technical specifications, and translating them into actionable development tasks., • Payroll Systems - experience supporting Payroll (PMS) and W2 Amendment (W2AM) applications, • Testing/QA - experience support both system and user acceptance testing Additional Skills & Qualifications Previous experience working with an enterprise wide, large-scale environment. Experience Implementing Tax updates in a government or civil service environment. Excellent understanding of systems development lifecycle methodologies. Excellent communication (oral and written), interpersonal, and organizational skills required. Strong MS Office 2010 and later; including Visio, Excel, Project, and Access required. Preferred Qualifications: Experience and knowledge of PMS and PPMS (payroll processes), NYCAPS (personnel), CityTime (timekeeping) and CHRMS canned reports and Ad Hoc facility. Extensive knowledge of Fair Labor and Standards Act (FLSA) Overtime processing rules. Extensive knowledge of contractual overtime processing rules. Experience with application configuration design and set-up. Knowledge and experience in IBM Mainframe environments, QMF, SQL, MS SQL Server. Understanding of relational databases (e.g. DB2). Proficiency running back-end/database queries for data analysis (DB2 on Mainframe). Clearly document and explain problems and to work with others to resolve software defects while ensuring technical compatibility and end user satisfaction. Ability to demonstrate the ability to plan, manage time according to schedules, and status reporting. Flexible work from home options available.

Job Description SOKOL GxP Services is seeking a Scientist/Engineer to join our client site in Summit, New Jersey, supporting CAR-T manufacturing and Quality Control operations. This role is integral to driving robust investigation processes, ensuring timely resolution of deviations, and maintaining the highest standards of compliance and product integrity. Key responsibilities include: • Lead manufacturing and Quality Control investigation reports supporting CAR-T operations;, • Execute thorough root cause investigations, including interviewing personnel, hypothesis testing, and interpreting results;, • Author detailed investigation reports and identify corrective and preventive actions (CAPA), verifying their effectiveness;, • Troubleshoot complex problems and lead cross-functional investigation teams to ensure timely closure of reports;, • Conduct investigations (OOS, OOT, environmental monitoring, deviations) using root cause analysis tools;, • Perform GEMBA walks and propose CAPAs, developing comprehensive CAPA plans;, • Assess impact and risk, develop mitigation strategies, and initiate change control documentation;, • Coordinate impact assessments and provide technical support for investigations, CAPAs, and change controls;, • Support audit and inspection responses, including deviation defense, and train new team members;, • Author or review departmental procedures and support manufacturing and QC testing of CAR-T products as needed;, • Apply lean manufacturing and six sigma principles for continuous improvement;, • Bachelor’s degree in Science or Engineering;, • 3+ years of relevant experience in a regulated environment (e.g., GMP/cGMP);, • Experience conducting deviation investigations using root cause analysis tools;, • Experience managing CAPA processes, including defining corrective actions and verifying effectiveness;, • Hands-on experience using TrackWise and Veeva QMS;, • Experience working under global regulatory and cGMP requirements in a life sciences manufacturing or Quality Control context;, • Experience supporting health authority inspections (e.g., FDA) and responding to audit or inspection observations;, • Authorization to work in the United States.Preferred Qualifications:, • Experience initiating and managing change controls, including coordinating impact assessments;, • Experience working in a biopharmaceutical manufacturing facility; Work schedule: 100% on-site. Monday - Friday, regular business hours 6-month contract with possible extension Pay rate: $42.94 - $54.54/hr. Health benefits, holiday pay, and 401(k) program Employee referral bonus program Opportunity to contribute to high-impact projects with a leading biopharma company

Job Description SOKOL GxP Services is seeking a Quality Laboratory Technician to support QC laboratory operations in a GMP/FDA-regulated environment. This role is responsible for managing QC lab material needs, maintaining inventory accuracy, supporting material availability according to the QC schedule, and documenting material handling activities in compliance with GDP requirements. The ideal candidate will have hands-on experience with QC inventory management, SAP or LIMS, basic laboratory safety practices, and working knowledge of cGMP expectations. This position works within a team-based QC shift schedule and supports the timely availability, tracking, stocking, allocation, and condition management of laboratory materials. Responsibilities: • Manage material needs and requirements for QC laboratories;, • Maintain and manage QC laboratory inventory;, • Perform inventory control activities, including cycle counts, material stocking, scrapping, and related inventory tasks;, • Manage material expiry, allocation, and required material storage/condition requirements;, • Quantify and maintain materials used in the QC laboratory;, • Ensure materials are available on time according to the QC schedule;, • Record material handling data clearly, accurately, and in compliance with GDP requirements;, • Use ERP or laboratory systems such as SAP or LIMS to support inventory and material management activities;, • Work in a team-based, cross-functional environment to complete QC tasks according to assigned shift schedules;, • Follow basic laboratory safety practices and cGMP requirements; or High School diploma / GED with 5+ years of inventory management experience; • Hands-on experience maintaining and managing QC laboratory inventory is required;, • Experience with ERP or laboratory systems is required; SAP or LIMS preferred;, • Experience with inventory control activities such as cycle counts, stocking, scrapping, expiry management, material allocation, and material tracking;, • Knowledge of cGMP/FDA-regulated industry requirements;, • General understanding of cGMPs and GDP documentation expectations;, • Basic laboratory safety knowledge;, • Technical writing skills and experience;, • Proficiency with Microsoft Office applications;, • Ability to work within a team-based QC shift schedule;, • Strong attention to detail and ability to maintain accurate documentation; Competitive hourly rate: $28.32 - 35.97/hr (W-2 only, no C2C) Working Hours: Monday - Friday, regular business hours 12-month contract with possible extension Health insurance, holiday pay, 401(k) program, and other benefits

Job Description SOKOL GxP Services is a leading provider of GxP compliance, CQV/validation, and workforce solutions for life sciences manufacturing and quality operations. As a Cell Therapy Project Manager, you will play a pivotal role in driving continuous improvement initiatives within the Cell Therapy Global Quality team, ensuring projects are executed efficiently and in alignment with industry standards. Key responsibilities include: • Leading continuous improvement projects within the Cell Therapy Global Quality team;, • Scheduling and managing meetings, documenting minutes, and maintaining project dashboards and documentation (charter, milestones, risk log);, • Managing internal steering meetings and coordinating cross-functional activities with internal support teams;, • Engaging subject matter experts for change management and process impact discussions;, • Managing projects end-to-end, from initiation through closure, to meet contract obligations and charter deliverables;, • Running project governance processes including kickoff, status, and executive sponsor meetings, as well as reporting and risk/issue tracking;, • Managing resources to achieve deliverables and coordinating stakeholder communications;, • Planning, executing, controlling, and closing projects to meet scope, schedule, budget, and quality objectives using GPS standards and methodologies;, • Supporting the execution of change management strategies, defining change metrics, and measuring effectiveness;, • Identifying and analyzing stakeholders, delivering engagement activities, and ensuring leadership alignment;, • Bachelor’s degree in arts, sciences, or engineering;, • 8+ years of project management experience in a regulated or validated environment (life sciences manufacturing/quality context);, • Experience managing end-to-end projects, including scope, schedule, budget, and risk/issue tracking;, • Proficiency with formal project management tools/platforms for managing plans, milestones, and status reporting;, • Proficiency maintaining structured project documentation (project charter, milestones, risk log) using documentation and reporting tools;, • Experience coordinating cross-functional teams and subject matter experts to deliver project outcomes;, • Experience running project governance with senior leadership (steering committee and executive sponsor meetings).Preferred Qualifications:, • PMP certification;, • Experience with cell therapy or biopharmaceutical manufacturing projects;, • Strong organizational, critical thinking, and decision-making skills;, • Proven ability to proactively identify, document, resolve, or escalate risks and issues; Health insurance, holiday pay, 401(k) program, referral program, and other benefits Hourly rate, $: 80.7 - 85.7 12-month contract with possible extension Job Type: Hybrid (min 50% on-site required) Working hours: regular business hours. Rotating shift: 1 week - Tue/Thur onsite, 2 week - Tue/Wed/Thur onsite.

Job Description SOKOL GxP Services is seeking an Associate Scientist/Engineer to join our on-site team in Summit, NJ. This role is integral to supporting oral solid formulation studies, working hands-on in laboratory and pilot plant settings. You will collaborate with cross-functional teams and travel between Summit and New Brunswick sites as needed to access specialized equipment and facilities. Key responsibilities include: • Executing laboratory and pilot plant work to establish oral solid formulations;, • Designing and conducting experimental formulation studies;, • Performing material characterization and formulation testing;, • Developing and optimizing oral formulations using a design of experiments approach;, • Utilizing HPLC and dissolution testing techniques for oral formulations;, • Tracking and trending data for formulation development projects;, • Communicating effectively and transparently with peers and cross-functional partners;, • Bachelor’s degree in a science or engineering field;, • 0–3 years of relevant experience in pharmaceutical formulation, laboratory, or pilot-plant work (internship experience acceptable);, • Hands-on experience performing HPLC and dissolution testing for oral formulations;, • Experience working in cGMP/FDA-regulated pharmaceutical manufacturing environments (internship experience acceptable);, • Ability to travel between Summit, NJ and New Brunswick, NJ sites as needed.Preferred Qualifications:, • Advanced degree in a science or engineering field;, • Experience with oral solid formulation development;, • Experience with material characterization techniques such as DSC and/or TGA;, • Experience using Design of Experiments (DoE) to design and optimize formulation studies; Competitive hourly rate: $28 – $35.56/hr (W-2 only, no C2C) Working Hours: Monday - Friday, regular business hours 8-month contract with possible extension Health insurance, holiday pay, 401(k) program, and other benefits Employee referral bonus program

Job Description Job Title: Chemist I Location: Clark, NJ 07066 Duration: 12-Month Contract (Potential Extension Based on Performance & Budget) Pay Rate: $22.50/hr Shift: Standard Day Shift Job Overview: We are seeking a detail-oriented and motivated Chemist I to support product development and testing in the cosmetics/personal care space. The ideal candidate will have hands-on laboratory experience and a strong foundation in physical sciences, with exposure to stability testing and batching processes preferred. Key Responsibilities: • Perform physicochemical characterization and performance evaluation of cosmetic and hair care products, • Conduct laboratory testing including microscopy, rheology, and other internal methods, • Assist in designing experiments to evaluate stability, viscosity, and product performance, • Maintain accurate documentation and ensure full traceability from sample receipt to data reporting, • Support sample logistics and maintain stability records, • Explore and implement new methods for formula characterization Required Qualifications: • Bachelor’s degree in Chemistry, Physical Sciences, or related field, • 2+ years of laboratory or technical research experience (or relevant certification/diploma), • Strong organizational and documentation skills, • Proficiency in Microsoft Word, Excel, and PowerPoint, • Strong communication and teamwork skills, • Detail-oriented with critical thinking and analytical abilities Preferred Skills: • Experience in cosmetics, personal care, paint, or food industries, • Hands-on experience with pH testing, microscopy, viscometer/rheometer, or foam analyzer, • Familiarity with batching equipment (e.g., Olsa, Disconti, Silverson), • Experience with stability testing and formulation support Key Traits: • Highly organized and methodical, • Strong attention to detail and accuracy, • Ability to work independently and in a team, • Positive attitude with a continuous improvement mindset

Job Description SOKOL GxP Services is seeking a junior-level Associate Scientist to support deviation investigations and CAPA activities within a regulated biopharmaceutical environment. This role focuses on root cause analysis, investigation execution, and technical report writing, with cross-functional collaboration to ensure timely and compliant resolution of quality events. Responsibilities • Lead and support deviation investigations, including Environmental Monitoring (EM) events, • Perform root cause analysis using structured problem-solving tools (e.g., 5 Whys, Fishbone), • Author investigation reports, including hypothesis development, data analysis, and conclusions, • Develop, implement, and track CAPAs to ensure effective resolution, • Conduct GEMBA walks to support investigations and assess process conditions, • Collaborate with Quality, Manufacturing, and Subject Matter Experts (SMEs), • Support change control activities, including impact assessments, • Ensure investigations are completed within required timelines and communicate delays/escalations, • Participate in audit and inspection readiness activities, • 1+ year of experience in a GxP-regulated environment, • Experience with deviation investigations and/or CAPA processes, • Strong technical writing skills (investigations, reports), • Understanding of cGMP principles and regulatory expectations, • Ability to work cross-functionally in a fast-paced environment, • Experience with electronic Quality systems (eQMS) Preferred Qualifications • Experience in biopharmaceutical manufacturing, • Exposure to Environmental Monitoring or QC-related investigations, • Familiarity with data trending and basic statistical analysis, • Experience supporting regulatory inspections or audits Education • Associate’s degree required, • Bachelor’s degree preferred (Life Sciences, Engineering, or related field) Work Environment • Primarily office-based with some presence in manufacturing areas, • Potential travel between local sites as needed Competitive hourly rate: $37.44 - 47.55/hr (W-2 only, no C2C) Working Hours: Monday - Friday, regular business hours 6-month contract with possible extension Health insurance, holiday pay, 401(k) program, and other benefits

Job Description Job Title: MRI Technologist Location: New York, NY Job Type: Contract (9 Weeks, with high possibility of extension) Compensation: • Weekly Pay: $2,600 – $3,300 (based on experience)Schedule:, • Shift: Day Shift, • Hours: 9:00 AM – 5:00 PM, • Schedule: 5x7.5-hour shifts, • Operate MRI equipment to perform diagnostic imaging procedures, • Position patients and coils appropriately to obtain optimal image quality, • Educate patients on procedures and ensure comfort throughout the exam, • Review and verify MRI safety questionnaires prior to scanning, • Evaluate images for diagnostic quality and ensure timely transmission to PACS, • Maintain accurate documentation within the Radiology Information System, • Ensure MRI suite cleanliness and proper equipment maintenance, • Follow strict MRI safety protocols to prevent hazards, • Adhere to infection control and safety standards, • Collaborate with physicians and healthcare teams as neededRequirements:, • Strong knowledge of cross-sectional anatomy, MRI physics, and imaging techniques, • Excellent technical, analytical, and patient care skills, • Ability to work efficiently in a fast-paced clinical environmentEducation:, • Graduate of an AMA/J.C.E.R.T. approved Radiologic Technology programCertifications & Licensure:, • New York State License in Diagnostic Radiology (required), • ARRT (MRI) Certification required, • BLS (AHA) Certification required, • NYS DOH Radiography License requiredPreferred Experience: About Navitas Healthcare, LLC: It is a certified WBENC and one of the fastest-growing healthcare staffing firms in the US providing Medical, Clinical and Non-Clinical services to numerous hospitals. We offer the most competitive pay for every position we cater. We understand this is a partnership. You will not be blindsided and your salary will be discussed upfront.

Crew - - Responsibilities: Provide a seamless and authentic customer experience that is an extension of the brand; Drive sales while exceeding selling and service expectations for our customers; Assist in operational and product driven store tasks assigned by the management team; Share customer fee

Installation, troubleshooting, repair, and termination of Cat 5e, 6, coax, and fiber.Experience with video & security systems, including running video/audio cabling, DVR system setup & troubleshooting is a major plus.Experience with running phone lines, punch down blocks, & line/extension troublesho

Audio/Video Operations Engineer Remote but Need Candidates who are local to NJ 6+ months contract with high potential for extension. Are you a Audio/Video Operations Engineer with a passion for collaborating with multiple teams and an interest in working onsite? Don't wait.

Job Description Job Title: Certified Nursing Assistant Location: Edison, NJ Job Type: Contract (13 Weeks, Extension Possible) Shift: 11:00 PM – 7:00 AM (Weekend Required) Compensation: • Provide direct patient care including bathing, toileting, oral hygiene, and bed making, • Assist with patient comfort and daily living activities, • Measure and document vital signs, reporting any changes to the RN, • Perform glucose finger sticks and collect specimens (urine, stool, sputum), • Monitor and record patient intake/output and daily weights, • Maintain a safe patient environment by responding promptly to call lights, • Observe patient conditions and immediately report changes to the RN, • Act as a patient sitter when required, • Ensure cleanliness and safety of patient rooms and nursing units, • Deliver patient-centered care tailored to individual needs (age, culture, physical limitations, etc.), • Communicate effectively with patients, families, and healthcare team membersRequirements:, • Ability to work night shifts and weekends, • Strong patient care and communication skills, • Ability to work in a fast-paced healthcare environmentEducation:, • High School Diploma or GED (Required), • Completion of an approved CNA program (Required)Certifications & Licensure:, • Active New Jersey CNA License (Required) About Navitas Healthcare, LLC: It is a certified WBENC and one of the fastest-growing healthcare staffing firms in the US providing Medical, Clinical and Non-Clinical services to numerous hospitals. We offer the most competitive pay for every position we cater. We understand this is a partnership. You will not be blindsided and your salary will be discussed upfront.

Job Description Your Next Chapter Starts Now: Join Us! Join Our Team: HVAC Comfort Advisors Wanted! We are a trusted plumbing, electrical, heating, and air conditioning company with a legacy spanning over three generations. We take pride in being deeply rooted in the communities we serve, employing residents of the towns we call home. Join our dynamic team as an HVAC Comfort Advisor in a role that rewards your success with a 100% commission-based compensation structure. Unleash your potential and thrive in an exciting environment where your achievements directly impact your income. Elevate your career with us and redefine success in the HVAC industry. As a successful HVAC Comfort Advisor, you will be the guiding force for customers in selecting the ideal comfort systems tailored to their homes. What We Offer: • Earn unlimited commissions!, • 401-K with Match with company match., • Benefits Include major medical, prescription drug, optical, dental, orthodontia, long-term disability, and life insurance., • Participate in events like ball games, comedy clubs, dinners, awards, and more every quarter., • Company-provided uniforms., • Provide Stability - We have over 55 years in business., • Work with a fun, professional, and caring management team., • As we expand, so do the opportunities for career advancement., • Take pride in working for a company that makes a positive difference in the community. Responsibilities of our HVAC Comfort Advisor: • Offer comprehensive solutions to customers for their HVAC and home comfort requirements., • Consult with potential and existing customers to tailor HVAC system solutions to their specific needs., • Follow up on sales bids and leads, providing additional information as required., • Conduct post-sale follow-ups to ensure ongoing customer satisfaction., • Highlight and emphasize profitable features, quotes, prices, and credit terms during interactions., • Build and nurture lasting customer relationships for sustained business., • Communicates with our support staff, in a timely and efficient manner, with details of jobs, financing and job scheduling., • Communicates to Installers the job requirements and expectations of the customer through verbal communication, pictures, drawings and written forms., • Maintains contact with Installers and customers during installation to ensure a quality system is installed., • Demonstrate flexibility by being available to work evenings and weekends as needed. Who We're Looking For in the HVAC Comfort Advisor: • Prior Sales experience in HVAC preferred., • Sales Experience residential home services required., • Knowledge of standard installation processes for HVAC systems., • Customer Service skills., • Attention to detail., • Organizational skills., • Presentation skills., • Negotiation and Closing skills., • Ability to work evenings and weekends in a rotation to accommodate customer’s schedule., • Self-driven, highly detailed, and organized., • Comprehensive knowledge about the HVAC domain and its offerings., • Unwavering integrity with a fervent aspiration for both personal and collective professional enhancement. Our staff is regarded with a sense of pride and familial connection, reflecting our commitment to treating everyone as an extension of our family. With a dedicated focus on making homes and businesses safe, comfortable, and efficient, we uphold a strong commitment to quality service and community well-being. Powered by JazzHR XcNboyQMur

Job DescriptionSalary: Job Summary Under direction of the Vice President of Mfg Operations and Technical Services, the Plant Quality Manager coordinates and leads all aspects of the Quality Assurance and Food Safety/Defense programs at Walden Farms. Primary duties include managing the plants third-party audits, developing, revising, and implementing the HACCP plan, ensuring all employees are trained in and follow Good Manufacturing Practices, conducting internal audits, and ensuring regulatory compliance. Other duties include managing outside contractors as they relate to food safety (pest control, uniforms, sanitation, laboratory equipment), investigating/resolving customer complaints and ensuring compliance to all applicable food safety and regulatory requirements such as FDA, FSMA, CFIA, CODEX, etc. as required. Essential Functions (Other duties as assigned) • Instrumental in maintaining food safety procedures, policies and the assurance and verification of compliance., • Leads the development and implementation of the facility food safety, employee safety and quality training program., • Establishes Continuous Improvement initiatives and annual goals for the Quality Assurance program to assure excellent product quality, optimal efficiency, and customer satisfaction., • Develops tools to report on KPIs, analyze trends, and drive continuous process and quality improvements., • Acts as vital team member of Walden Farms plant leadership team with the Facilities leadership teams and other departments to support production, manage QA issues, daily dispositions, and resolutions as needed., • Coordinates company HACCP & HARPC program implementation, training, recordkeeping, and all related issues., • Responsible for reporting food safety, quality, and regulatory compliance concerns., • Oversees staff, organizes, and conducts internal audits; also oversees work with outside third-party auditing company., • Organizes and oversees all internal product testing, physical and sensory: raw ingredients, packaging components, mid-production, and finished product evaluation as needed., • Organizes, reviews, reports and manages all outside lab testing., • Responsible for keeping all product retains and records, in compliance with regulations., • Works with corporate technical teams to for fulfillment of customer requirements, including new product development., • Coordinate product line extension validation process and documentation with the manufacturing team., • Manage outside contractors such as Pest Control, Sanitation Chemicals and uniform vendors., • Manages EHS training and implementation of the safety program as directed., • Other duties as assigned. Required Qualifications • Bachelors Degree, preferably in Food Science, Biology, Chemistry, or a related field, • HACCP Certified, • 5+ years of experience in managing a team of food safety, QA professionals in a food/ personal care/ nutritional supplement/ pharmaceutical manufacturing environment, • Bilingual preferred (Spanish), • Proven record of success in managing 3rd party audit experience, • Experience coaching and mentoring department members, • FSMA Certified (PCQI) or experience with FSMA; able to test finished foods and record results to meet FSMA requirements, • Proven record of success in applying comprehensive, hands on knowledge of process controls, design of experiments, and root cause analysis, • Ability to conduct lab analyses, generate data, interpret results, and track trends, • Proven record of success in implementing process improvements, • Organized, process-driven, and detail oriented, • Must be able to perform mathematical calculation and analysis, • Strong written and verbal communication skills, • Must be proficient in Microsoft Excel, Word, and database programs Preferred Knowledge, Skills, Abilities & Other Characteristics • Strong leadership skills that inspire team confidence, collaboration and respect while motivating team members to contribute to continual improvement efforts, • Good written and oral communication skills, • Excellent critical thinking skills utilizing problem solving and root-cause analysis, • Excellent interpersonal skills necessary to build and maintain good working relationships with others within the organization, suppliers, and customers, • Proficient in MS Office applications (Word, Excel, Outlook, PowerPoint, Access, Visio), statistical analysis software (Minitab), and various business systems (e-Synergy, Macola, Crystal Reports, ADP), • Sense of urgency in completing tasks daily with accuracy

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing your opi

Abacus Corporation - - Responsibilities: Receive and process incoming stock and materials, ensuring accurate documentation and organization.Pick and fill orders from stock, adhering to customer specifications and company standards.Pack and ship orders efficiently, maintaining product integrity and

UNFI - - Responsibilities: Inspects assigned jack for safety issues; Identifies the correct pick location and pick sequence in accordance to the order; Picks the correct item and quantity, checking UPCs or item descriptions; Shrink wraps and labels with correct truck, stop and other required inform

Opportunities for Career Growth!.SSP America is a leader in the food travel industry, specializing in bringing a "Taste of Place" to airports across the Americas.With a commitment to creating an inclusive culture of care, we ensure that our team members thrive while delivering exceptional

We're currently looking for individuals across the country to take part in online paid research, including remote focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing your opi

Home Depot - - Responsibilities: Load and unload trucks within the facility; Move material within the facility using hand trucks, forklifts, or other equipment; Sort, staging, and transport products as required; Operate forklifts or other machinery to complete tasks; Assist with general warehouse d

Aerotek - - Responsibilities: Operate turret forklifts to pick, move, and store products in narrow aisle racking systems; Safely maneuver turret, stand-up, and sit-down forklifts in tight spaces while maintaining load stability; Retrieve and place pallets at varying heights, including high-level ra

ABF Freight - - Responsibilities: Load and unload trailers for the purpose of transporting a wide variety of cargo; Move cargo, drive a forklift or use a pallet jack or other freight handling equipment; Prepare wide varieties of freight for transit; Complete all required paperwork; Effectively oper

Responsibilities: Move, load, unload, and move furniture and inventory of various sizes safely; Use scanners and handheld devices to track inventory and locations; Perform quality control tasks including inspecting, repackaging, labeling, and sorting products; Operate material handling equipment whe

Abacus Corporation - - Responsibilities: Use Reach Truck, Cherry Picker or Electric Pallet Jack to load and unload designated trailers.Move product manually as required and verify/receive materials into inventory.Use MHE to pick, verify and pack orders according to operational standard practice.Con

Job Description Job Description Small Food Manufacturing company is looking to add a warehouse associate.The ideal candidates will perform the following tasks: -Receive Inbound shipment -Check the inbound shipment with any open Purchase Order to make sure that the product ordered, and quantity order

CMA CGM Group - 266 Old New Brunswick Road - Responsibilities: Develop and provide excellent customer service to internal and external customers at all times; Serve as a lead to staff and provide work direction; Perform the most complex operations and ensure employees are trained in all operational