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Formulation Scientist 1 year contract 5 days a week onsite in Summit, NJ Overview The Formulation Scientist will support the Skin Health R&D team, contributing to both innovation and base business (commercialized products) within the skincare portfolio. This role will focus on formulation development, lab execution, and scale-up activities for consumer skincare products, including anti-aging formulations. The ideal candidate will work under the guidance of senior scientists while also taking ownership of experiments, technical problem-solving, and project execution. Key Responsibilities • Support end-to-end product development for skincare formulations, including innovation and commercialization of existing products, • Execute laboratory experiments, including formulation development, testing, and analysis of skincare products, • Assist in product design, formulation optimization, and process development/scale-up activities, • Conduct Design of Experiments (DOE) to support investigations and product improvements, • Process formulated products at lab scale and support transition to manufacturing, • Collaborate cross-functionally with R&D, manufacturing, and external partners to support project execution, • Analyze consumer insights and contribute to innovation pipeline development, • Maintain accurate documentation, including technical reports and experimental data, • Ensure compliance with company procedures, cGMP standards, and regulatory requirements, • Support troubleshooting efforts related to formulation, supply disruptions, or product upgrades Required Qualifications • Bachelor’s degree in Chemistry, Chemical Engineering, Pharmacy, or related field, • 1–4 years of experience in formulation development (academic or industry), • Experience with personal care, cosmetic, OTC, or pharmaceutical products, • Strong foundation in formulated systems (emulsions, surfactants, suspensions, structured liquids), • Hands-on laboratory experience executing experiments and processing formulations, • Understanding of material chemistry and basic process equipment, • Experience supporting process development or scale-up activities, • Strong communication, documentation, and organizational skills, • Proficiency in MS Office (Excel, Word, PowerPoint) Preferred Qualifications • Experience formulating skincare or anti-aging products, • Familiarity with cGMP and regulatory standards, • Experience working with external manufacturing partners, • Exposure to technical project management or cross-functional collaboration, • Ability to work independently while contributing within a team environment

Our client, a well‑established distributor of specialty chemicals, is seeking an Outside Sales Representative to manage and grow a territory spanning Maine through Virginia. While the company serves multiple industries, this role will focus exclusively on the personal care market—selling ingredients used in soaps, lotions, creams, shampoos, cosmetics, and related formulations directly to end users. This is an excellent opportunity for a driven sales professional who understands chemical distribution and enjoys building deep, consultative relationships within R&D, formulation, and procurement teams. Qualified Candidates Will Have • Experience selling chemicals, • Experience selling into the personal care market is a strong plus, • A four‑year college degree is preferred, • A technical degree (Chemistry, Chemical Engineering, Biology, etc.) is a strong plus, • Ability to travel up to 50% throughout the territory Compensation & Benefits • Base salary: approximately $160K + Bonus: 20%, Car plan, Full benefits package To Apply Please send your resume in Word format, including sales accomplishments, along with a brief note about your current income. Gerri Lynn Zschetzsche Shelgin Partners Recruiting Agency / 636.625.2333

Immediate need for a talented Lab Facilities Specialist - III (Senior). This is a 06+months contract opportunity with long-term potential and is located in Rahway, NJ (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: 26-09532 Pay Range: $36/hr - $36.40/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: • Note: Shift: 7.30am-4pm EST., • 100% Onsite Role., • Associate Specialist, Laboratory Operations – Device Development & Technology, • The greatest inventions would not be brought to market without the right project management and operations/administrative support., • Woven into every part of CLIENT Research Laboratories (MRL), our operations/administrative team ensures that our R&D concepts become a reality for patients worldwide., • The MRL Device Development & Technology (DD&T) Organization within Pharmaceutical Sciences & Global Clinical Supply (PSCS) is seeking a highly motivated, Associate Specialist to support laboratory operations., • The position is an in-person position, operating from our Rahway, New Jersey site., • This position will receive day-to-day responsibilities from the Senior Specialist, Laboratory Operations Management – Device & Combination Product development., • Coordinate and perform general laboratory administrative duties including, but not limited to, maintaining testing, calibration and equipment maintenance scheduling, ordering routine & specialty supplies, and facilities management., • Maintain development and GXP laboratory equipment and instrumentation in accordance with internal and industry best-practices/standards., • Coordinate laboratory technical & safety training, including documentation lifecycle management., • Collaborate with key internal & external (outside DD&T) stakeholders to coordinate/arrange new vendor technology evaluations., • Support team with laboratory procurement needs including purchase orders, invoice payments and expense tracking., • Support team with domestic and international shipping of equipment (testing & manufacturing) and product samples (drug & combination product)., • Extraordinary attention to detail, independent judgement, and the ability to prioritize and execute work activities with minimal supervision., • Ability to interact professionally with internal and external colleagues both on-site and remotely to maintain laboratory workflows & operations. Key Requirements and Technology Experience: • Key skills; "calibration", "lab", “calibrate”, "troubleshoot", • Must be able to lift, box, and unbox up to 45 lbs unassisted, • Must be able to move pallets using a pallet jack., • Must be able to walk(5-10miles) everyday, sit and stand for longer duration., • Able to drive golf cart., • Have a valid driver's licence., • High School Diploma, • Minimum 2 years of relevant exeprience. Metrology exeprience preferred., • Advanced computer skills using MS Outlook, Teams, Project, SharePoint, Word, Excel, PowerPoint and Adobe., • Experience in device and combination product characterization & mechanical testing is highly preferred., • Experience in GXP-Analytical laboratory testing or management is highly preferred., • SAP/Concur or related system experience processing purchase orders (PO), expense reports, payment requests, vendor add forms, as well as stockroom inventory reports. Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy ___.

Pipeline Project Manager Summit, NJ ( Hybrid) Full Time What you will do This role is responsible for leading cross‑functional projects from development through launch, ensuring disciplined execution aligned with Client operating model, innovation playbooks, and project management standards. The individual will own the integrated project plan and partner closely with R&D, Marketing, Packaging, Operations, Finance, and other stakeholders to deliver business objectives on time and in a compliant, reliable manner. Success in this role requires strong business and technical acumen, the ability to proactively manage risk and resolve issues, and confidence presenting recommendations at governance forums. The position also plays a key role in advancing project management excellence through continuous improvement, knowledge sharing, and collaboration across the organization. Key Responsibilities • Lead projects from development through launch and execution in accordance with Client Operating Model, project management and innovation playbooks, standards, and tools., • Provide overall project management for regional or global, cross‑functional teams including R&D, Marketing, Packaging, Operations, Finance, and other stakeholders to deliver project objectives., • Proactively support teams by removing execution barriers, escalating issues as needed, and engaging key decision‑makers when projects deviate from plan., • Own the integrated project execution plan, including inputs to scope, business case, schedule, and launch timing., • Oversee and drive team activities to deliver project objectives in a compliant, reliable, and timely manner., • Plan and facilitate project activities including planning sessions, team meetings, decision forums, and documentation of actions and minutes., • Track critical milestones, establish contingency and acceleration plans, and lead issue resolution and risk management efforts., • Apply strong business acumen, technical expertise, and sound judgment to assess risk, develop mitigation strategies, and appropriately elevate issues., • Lead preparation and delivery of project updates, stage‑gate reviews, and recommendations for governance forums; serve as an independent advisor making Go/No‑Go recommendations and clearly communicating risks and trade‑offs., • Develop deep understanding of assigned Segment, Brand, or Need State strategies, business goals, technologies, and supply chain to enable sound decision‑making from charter through design, development, and launch., • Leverage project metrics and lessons learned to improve business outcomes, processes, and tools; contribute to building project management capability through coaching, supporting peers, and participation in Communities of Practice., • Maintain accurate project and portfolio data to support tracking, reporting, and visibility across all organizational levels. What We Are Looking For Required Qualifications: • A minimum of a Bachelor's Degree, • Minimum of 8 years of business/work experience., • Minimum of 5 years of project management experience, with at least 3 years of proven success in management of new product commercialization or renovation projects from ideation through to benefit realization., • Ability to influence and align cross‑functional teams at all levels of the organization without direct line authority., • Clear, concise communicator with strong verbal, written, and presentation skills; able to distill complex issues, risks, and trade‑offs for senior leaders, • Strong business and financial acumen, with working knowledge of financial principles and project evaluation methods to support sound recommendations, • Inclusive leader who delivers results through collaboration, trust, and constructive challenge, • Comfortable operating in ambiguous, fast‑changing environments and acting as a change agent to improve ways of working, • Proven track record of delivering projects in fast‑paced environments, balancing scope, quality, timeline, and cost, • Able to work independently, manage multiple priorities, and perform effectively under pressure, • Comfortable challenging the status quo and driving continuous process improvement. Desired Qualifications: • Master’s Degree or MBA or other advanced degree, • PMP certification and/or other industry and project management certification, • Experience working in Consumer Goods industry., • Experience in a GMP or regulated environment (Pharmaceutical, Medical Device, OTC), • Experience in Process Excellence / 6 Sigma methodologies

Global Environment Manager Summit, NJ ( Hybrid) Full Time What you will do Remote work options may be considered on a case-by-case basis and if approved by the Company The Global Environment Manager leads environmental compliance programs and advances corporate sustainability initiatives across operating sites. This role is accountable for regulatory compliance, data integrity, and continuous improvement in environmental performance. The role partners closely with cross‑functional teams—including Sustainability, Operations, Procurement, Corporate Real Estate, Legal, and Product R&D—as well as site, regional, and global EHS teams to reduce environmental risk, improve resource efficiency, and deliver on sustainability commitments. Key responsibilities include overseeing the development and implementation of EHS policies, ensuring regulatory compliance, and strengthening company‑wide sustainability programs. The manager provides subject‑matter expertise, leads teams, and drives initiatives that balance environmental risk reduction with business objectives. Key Responsibilities Environmental Compliance • Support compliance with environmental laws and regulations, including those governing air emissions, wastewater discharges, hazardous and non-hazardous waste, and chemical management (e.g., RCRA, CAA, CWA, TSCA, EPCRA, REACH)., • Provide support to site and regional EHS teams for permit applications, renewals, and regulatory reporting to federal, state, and local agencies., • Conduct environmental inspections and audits; track corrective actions to completion., • Maintain environmental management system (EMS) documentation, corporate level environmental standards, and training materials., • Partner with site operations and EHS teams to ensure regulatory requirements are integrated into daily activities and projects., • Connects externally to industry associations and thought leaders to benchmark our goals, programs and processes., • Respond to questions from and provide guidance to internal stakeholders regarding regulatory compliance and sustainable operations., • Support various global workstreams – e.g. PFAS, emerging regulations, CSRD – as needed. Sustainable Operations • In partnership with Global Sustainability and Operations, lead or support initiatives to drive sustainable operations. Key areas of focus:, • Reduce waste generation, increase reuse and recycling, and improve waste diversion performance., • Improve water efficiency and mitigation water/business interruption risk., • Other focus topics may include biodiversity and GHG/Net Zero, • Coordinate data collection, validation, and reporting of waste and water metrics to support regulatory reporting and sustainability goals., • Work to embed sustainability initiatives within functional team processes and procedures., • Evaluate suppliers and waste vendors to ensure alignment with company sustainability and compliance standards., • Develop and promote best practices for circular resource use and water stewardship across operations. Pharmaceuticals in the Environment (PiE) • Support initiatives to minimize release of active pharmaceutical ingredients (APIs) and other chemicals of concern to the environment., • Partner with R&D, Operations and EHS teams to assess and control PiE risks related to wastewater discharges and waste handling., • Maintain awareness of evolving regulations and industry best practices related to pharmaceuticals in the environment. Training and Communication • Develop and deliver environmental compliance and sustainability training for global, regional and site personnel., • Communicate updates on regulatory changes, corporate sustainability initiatives, and emerging environmental issues. What we are looking for Required Qualifications • Bachelor’s degree or equivalent in Environmental Science, Sustainability, Engineering, or a related field, • A minimum of 8 years of progressive experience in environmental compliance and sustainability management within complex organizational settings, • Strong understanding of environmental regulations (EPA, EU, local authorities) and sustainability reporting., • Experience managing waste, water, and chemical compliance programs., • Strong project management skills., • Demonstrated ability to lead, build, influence, and implement standard business processes and procedures., • Demonstrated critical thinking and analytical skills to evaluate data and challenge results., • Demonstrated experience with change management., • Outstanding leadership and collaboration with ability to gain trust and influence at all levels., • Demonstrated expertise in environmental data management, performance measurement, and regulatory compliance, • Proven ability to lead risk assessment and mitigation efforts, ensuring adherence to environmental health and safety regulations, • Proficiency in Microsoft Office applications, particularly Excel and PowerPoint, to support data analysis, reporting, and presentations Desired Qualifications • Six Sigma certification, • ISO14001 Lead Auditor or Auditor Training

Corporate Tax Manager - Methods, Credits & Incentives (R&D).Philadelphia, Pennsylvania, United States.Corporate Tax Manager - Methods, Credits & Incentives (R&D).Title: Corporate Tax Manager - Methods, Credits & Incentives (R&D) Status: Full-Time Location: Hybrid - Arlington, VA; Philadelphia, PA; P

Een toonaangevend onderzoeksinstituut zoekt een expert in computer vision en AI om complexe R&D- en klantprojecten te leiden.

Partner with Key Account Managers, Business Development, Sales, and R&D to deliver aligned commercial outcomes.

Collaborate with supply chain, manufacturing, R&D, commercial, and vendor management teams as needed. Ensure alignment of project goals with business objectives and compliance standards. Proficiency with project management tools such as MS Project, Smartsheet, or equivalent.

This role focuses on navigating the complexities of Research and Development (R&D) tax credits within the Methods, Credits & Incentives (MCI) practice. Research complex federal and state tax issues, specifically regarding R&D rules and relevant court cases. Economics, Statistics, Finance, Mathematic

A leading consumer goods company, located in Summit, New Jersey, is seeking an Executive Assistant to provide comprehensive support to the VP of R&D Integration Management.Responsibilities include managing calendars, coordinating meetings, and handling travel arrangements.The ideal candidate should

Job Description* Experience in data analyticsRequired Skills:Analytical Method Development, Antibody Drug Conjugates (ADC), Assay

Kenvue Is Currently Recruiting For a Executive Assistant Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. Role Role Reports To VP Global Regulatory Affairs/R&D Ops Location North America, United States,

POCS - Rahway: Associate Technician, Operations. Associate Technician, Operations. Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product deve

Experience in requirements management, business analysis, and product analytics within a technical or scientific environment. Skills: Business Analysis, Data Analytics, Pharma R&D domain experience specially focused in Omics Data products (Genomics, Metagenomics, Proteomics and Metabolomics). Functi

Analytical Method Development, Antibody Drug Conjugates (ADC), Assay Development, Biochemical Assays, Biological Assay Development, Capillary Electrophoresis (CE), Cell-Based Assays, Chromatographic Techniques, Clinical Trials, Cross-Functional Teamwork, External Collaboration, High Resolution Mass

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A leading pharmaceutical company is seeking an Associate Principal Scientist in Rahway, New Jersey.This role involves developing and qualifying analytical methods for Biologics drug products, requiring extensive experience in chromatography and molecular biology.The ideal candidate will excel in a c

This is an excellent opportunity for a driven sales professional who understands chemical distribution and enjoys building deep, consultative relationships within R&D, formulation, and procurement teams.