Trabajos nj en Plainfield, New Jersey - Page 9Crear alertas

Aduro Products was founded by three lifelong friends seeking to innovate and enhance everyday tech accessories. The company has since expanded to include divisions in electronics, sports & fitness, health & wellness, automotive, and beauty products. Known for its forward-thinking and innovative product solutions, Aduro Products has become a trusted household brand across the consumer goods industry. The company is dedicated to delivering high-quality products that improve everyday experiences. Role Description This is a full-time on-site role for a Sales Account Manager, based in Metuchen, NJ. The Sales Account Manager will manage accounts, build and maintain customer relationships, and ensure high levels of customer satisfaction. Responsibilities include working with all national retailers, identifying sales opportunities, and developing strategies to achieve sales targets. The role also involves effective communication with buyers and internal sales teams, and providing outstanding customer service to support business growth. Qualifications • Strong skills in Customer Service and Customer Satisfaction, • Proven experience in Account Management with all national retailers, • Proficiency in Lead Generation and developing sales opportunities, • Excellent Communication skills and the ability to collaborate with diverse teams, • Self-motivation, problem-solving abilities, and a results-driven mindset, • Experience in sales within the consumer goods industries, • Bachelor's degree in Business, Marketing, or a related field preferred

Job Description We are looking for a Sales Assistant / Administrator for an immediate hire opportunity in Avenel, NJ ! A well established construction, and fence company is looking for an experienced sales assistant within the construction industry. If you are looking to continue your career within a sales, administration, this is the ideal chance for you! Schedule: • 7:30am - 4:00pm Competitive Compensation Offered! • $60,000 - 65,000/yr (Based on experience) Responsibilities: • Provide administrative and operational support to the Commercial and Residential Sales Teams, • Enter new orders, update spreadsheets, and maintain accurate sales tracking and reporting, • Request and forward COIs for jobs, forward public certifications and documents for public jobs for bid, • Assist with preparing sales reports, job summaries, and performance data for management, • Answer and route customer calls, ensuring prompt and professional communication, • Coordinate with the Sales Team to ensure all quotes, follow-ups, and documentation are up to date, • Coordinate Marketing efforts and campaigns, track progress, • Support the General Manager with day-to-day administrative tasks, reporting, and special projects, • Communicate with customers, subcontractors, and internal departments to ensure smooth project flow, • Pre-qualifications, safety documents,, • Assign leads, • 6 salespeople, another department of 4 Qualifications: • Microsoft Office experience, • Previous experience in sales administration or other related fields, • Construction experience preferred, • Good customer service, and professional attitude, • Ability to prioritize and multitask, • Excellent written and verbal communication skills, • Strong attention to detail, • Strong organizational skills Immediate Benefits Upon Hire • Medical Plan, • Direct Deposit, • Dental Plan, • Vision/Eyewear Plan, • Life Insurance, • Referral Bonus Apply immediately on or call (908)-505-0415 today. Company DescriptionExpress Employment Professionals of Somerset, NJ is a leading staffing provider helping job seekers find work with a wide variety of local businesses. Because we're locally owned, we live in and work in this community and have a vested interest in its success. In addition to our staffing services, our team is actively involved with a wide variety of causes and organizations that help strengthen our beautiful city. Our Vision: To help as many people as possible find good jobs by helping as many clients as possible find good people.Express Employment Professionals of Somerset, NJ is a leading staffing provider helping job seekers find work with a wide variety of local businesses.\r\n\r\nBecause we're locally owned, we live in and work in this community and have a vested interest in its success. In addition to our staffing services, our team is actively involved with a wide variety of causes and organizations that help strengthen our beautiful city.\r\n\r\nOur Vision:\r\nTo help as many people as possible find good jobs by helping as many clients as possible find good people.

Job Description Job details and responsibilities : Title: CNA LTC-NJ Duration: 13 weeks with possible extension Shift: 11:00 PM – 7:00 AM. 5x8s Facility : JFK Hartwyck at Oak Tree, a rehabilitation and nursing cente Location: Edison, NJ Requirements: Required Skills & Experience: -Must be a Certified Nurse Assistant with a permanent NJ CNA license and a minimum 2 years prior experience working as a CNA in an LTC (subacute skilled nursing) setting. -Must be willing to manage care for patients with a variety of conditions, including COVID+ patients (NO EXCEPTIONS) Company DescriptionLanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

Our client, a children's apparel company, is seeking an Account Executive to join their team in Edison, NJ! This role is onsite 4 days per week. Responsibilities: • Manage the sales lifecycle and work to grow existing relationships, • Oversee sales goals and quotas, • Identify sales opportunities, • Work to gain new leads, • Maintain strong relationships with buyers Qualifications: • Prior wholesale experience is required, kid's apparel is a plus, • Experience working with retailers such as Walmart, Sams Club, Boscov, Macys, Nordstrom, or Von Maur, • Character licensing experience, • Strong written and verbal communication skills, • Must be proficient in MS Office, • ERP software experience is highly preferred, • Ability to work in a fast-paced environment, • Occasional travel Please submit your resume for consideration. You can use to collect and manage your references for free and share them with us or anyone else you choose. Candidates with references are always preferred by our clients. Now is the most important time to stand out from the crowd. We suggest that you ensure you have updated your LinkedIn profile and that you start collecting your references early.

Job Title: Regional Sales Representative Location: Edison, NJ Department: Sales Region: Tri-State/Northeast Reports To: National Sales Director / Head of Sales About Us: Since 2013, Vijay Home Foods has been crafting authentic dosa & idli batters and podis, helping today’s busy families enjoy the same wholesome flavors that generations have grown up with—without compromising on convenience. At the heart of what we do is a simple promise: to be a trusted kitchen partner by offering fresh, authentic, and naturally fermented foods—free from preservatives and baking soda. Our batters are created using traditional recipes, with clean ingredients, no additives, no preservatives, no baking soda. Vijay Home Foods also distributes one of India’s leading ice cream brand – Arun Ice Cream in the USA. About the Role: As Regional Sales Representative, you will be responsible for driving growth, building strong retail partnerships, and increasing brand pres ence across key markets in the region. You will act as a strategic thinker, managing retail accounts, working with distributors and food brokers, and overseeing sales execution with a focus on ethnic and mainstream grocery and wholesale channels. This role also involves maintaining accurate invoicing and accounts receivable (AR) tracking to support healthy business operations. Key Responsibilities: • Execute regional sales strategies to achieve volume, revenue, and profit targets for Vijay Home Foods batter, spiced powders, Arun Ice Cream and other products as and when launched., • Build long-term relationships with key retail accounts, distributors, independent stores, and ethnic grocery chains along with wholesale chains, • Manage customer invoicing, ensure timely submission of delivery slips, and maintain AR records in coordination with internal teams., • Monitor accounts receivable status for assigned accounts and assist in following up on outstanding payments., • Conduct regular market visits, store audits to ensure brand visibility and execution., • Confidently present and educate customers on Vijay Home Foods product portfolio, USPs, usage ideas, and promotional opportunities., • Collect product feedback, customer feedback and communicate the same to internal teams to foster sales., • Identify opportunities to expand product placement in ethnic and mainstream channels., • Drive execution of trade promotions, seasonal programs, and in-store activations in coordination with marketing and operations teams., • Analyze sales data and provide accurate forecasting, reporting, and insights to leadership., • Submit daily reports summarizing store visits, key discussions, observations, and action items. Qualifications: • High school diploma required; Bachelor's degree in Business, Marketing, Sales or related field preferred., • Minimum 2-3 years of experience in the food and beverage or consumer packaged goods (CPG) industry, preferably in retail grocery sales., • Experience working with Asian Indian products a plus., • At least 2–3 years of experience managing regional accounts or territory sales in the grocery/CPG space., • Prior experience with ethnic food products or specialty food categories is a strong advantage., • Experience working with food brokers, distributors, and independent retailers., • Proven success in sales negotiations, account management, and delivering revenue targets., • Experience in maintaining invoicing records and accounts receivable tracking., • Strong organizational and follow-up skills related to financial documentation and payment collections., • Proficient in Microsoft Office (Excel, PowerPoint, Word); CRM or ERP system familiarity is a plus., • Self-motivated, organized, and able to work independently in a remote, field-based role., • Valid driver’s license and reliable vehicle; willingness to travel regionally 80% or more, including overnight travel. Why Join Us: • Opportunity to be part of a fast-growing brand with a strong cultural identity and customer following., • Entrepreneurial, mission-driven team that values creativity, ownership, and performance., • Competitive compensation, travel reimbursement, and career growth potential. Salary: $52,000/yearly + Incentives

PRODUCTION ASSOCIATE (OVERNIGHT SHIFT) Join an Award-Winning Food Manufacturing team in Piscataway, NJ Are you ready to be part of a dynamic, fast-growing company in the refrigerated snack and dessert sector? Our team is recognized for innovation, quality, and a commitment to delivering delicious products that make people smile. Based in Piscataway, NJ, we pride ourselves on a positive, inclusive, and supportive work culture, where every team member’s contribution truly matters. We’re looking for enthusiastic Production Associates to join our overnight team. If you thrive in a collaborative environment, enjoy hands-on work, and want to be part of creating products people love, this is the perfect opportunity for you! Production Associate – Overnight Shift Shift: Monday, Wednesday, Friday nights | 8:30 PM – 9:00 AM Pay: From $15.50 to $18.00/hr + 4-hour incentive for completing full 36-hour week Bilingual Requirement: English/Spanish 📝 About the role As a Production Associate, you’ll play a key role in the creation of high-quality refrigerated snacks. You will assist with production activities while following Good Manufacturing Practices (GMP), ensuring compliance with safety, sanitation, and quality standards. Your work will help maintain efficient, safe, and high-quality operations, from handling raw materials to monitoring the production line. Key responsibilities: • Follow all safety and GMP guidelines, HACCP, and SQF standards, • Assemble, disassemble, and operate production equipment (extruders, enrobbers, flow pack machines), • Fill tanks with raw ingredients like chocolate or yogurt, • Monitor production, packaging, and labeling processes, • Perform basic quality checks and document results, • Maintain a clean, organized, and safe workstation, • Report any production, quality, or safety issues to supervisors What we’re looking for: • High school diploma or GED preferred, • 1 year of packing or food production experience preferred, • Ability to lift up to 50 lbs and frequently handle objects up to 25 lbs, • Comfortable working in refrigerated environments and occasionally in freezers, • Strong team player with good communication skills (bilingual English/Spanish a must), • Willingness to learn, adapt, and work overnight shifts, • Attention to detail and commitment to safety and quality Why you’ll appreciate working here We care about our people as much as our products.Benefits include: • Comprehensive healthcare (medical, dental, vision), • Supplemental coverage (accident, critical illness, hospital indemnity), • 401(k) retirement savings, • Life & disability insurance, • Employee assistance program and legal support, • Auto, home, and pet insurance options, • Exclusive employee discounts with preferred vendors Join a company where your work directly contributes to products enjoyed nationwide, your growth and development are supported, and your voice and contributions are valued. 🚀 Ready to apply? If you’re motivated, reliable, and excited to join a fun, fast-paced, and meaningful workplace, we want to hear from you! Apply today and start your journey with a team that’s passionate about quality, innovation, and people.

We are hiring a Millwright Planner for our Rahway, NJ site. This is an on-site role supporting sitewide millwright maintenance, installation, and alignment activities. This person will act as the technical planning lead for millwright work across the site. The role includes managing millwright work orders in SAP, developing detailed job plans, coordinating tools, rigging equipment, and materials, and serving as the SME for millwright-related technical questions. This is a strong fit for someone with deep hands-on mechanical knowledge and experience coordinating complex maintenance work. Key qualifications: • 10+ years of millwright or heavy mechanical maintenance/installation experience, • At least 2 years in planning, scheduling, or coordination preferred, • Experience using SAP or other CMMS systems, • Strong knowledge of machine alignment, couplings, bearings, gearboxes, conveyors, base grouting, structural repairs, and rigging/lifting practices, • Ability to develop job plans, rigging/lifting plans, manpower estimates, and material lists, • Pharmaceutical, laboratory, or highly regulated facility experience preferred, • Journeyman millwright certification, mechanical trade qualification, or equivalent hands-on experience strongly preferred Location: Rahway, NJ Work setting: On-site Compensation: $115,000–$130,000

About Kerry Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role We are hiring a Production Supervisor - 2nd shift (Monday-Friday) 2:00pm-10:30pm. This position will be in out Clark NJ Savory and Crystals plants. Key responsibilities • Responsible for leading production teams and other staff to achieve production targets in a safe and efficient manner. Overseeing roughly 15 hourly production personnel., • Coordinates production activities with procurement, maintenance, warehouse, and quality departments to achieve and sustain results., • Responsible for implementation of all manufacturing operations including the safety, production efficiencies, quality, customer service, and financial performance of the plant., • Leads team members by managing and executing plant processes through SAP enterprise software., • Leads team members in attaining plant production and quality targets., • Supports continuous improvement processes to ensure safety, quality, cost, and customer service goals are met., • Maintains an engaged and team-oriented workforce to meet business demands. Qualifications and skills • Bachelor’s degree preferred., • Minimum of 5 years of experience in similar roles., • Experience in manufacturing required; experience in food manufacturing highly preferred., • Authentic leadership with credibility among senior stakeholders and plant leadership., • Demonstrated ability to influence and coach leaders within the organization., • Strong interpersonal skills and ability to lead teams to success., • Excellent communication skills across all functions and levels of the business., • Proven ability to build and develop high-performing teams., • Project management experience with practical knowledge of tools and techniques. Compensation Data The pay range for this position is $63,600 - $106,000 in Annual Salary. Kerry typically does not hire an individual at the top or near the top of the range, as we are a pay-for-performance company, and this range is set to continue to reward performance annually while in role. Compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate within the above range may be influenced by a variety of factors including skills, qualifications, experience, and internal equity. In addition, this position is also eligible to earn a performance-based incentive compensation. Kerry offers a competitive benefits package, including medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, Employee Share Plan, Life, disability, and accident insurance, and tuition reimbursement. This job posting is anticipated to expire on April 30th, 2026. We may use artificial intelligence tools to support the review and assessment of applications and assist with scheduling interviews. We do not use AI to make decisions during the interview process. All candidate assessments and hiring decisions are made by our recruitment and leadership teams. Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at: ___. Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a “starter kit,” investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.

Company Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease. Why ImmunityBio? • ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases., • Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California., • Work with a collaborative team with the ability to work across different areas of the company., • Ability to join a growing company with professional development opportunities. Position Summary The Senior Scientist, Regulatory CMC will assist in the development of global Chemistry, Manufacturing and Control (CMC) regulatory strategy for investigational and marketed products and manage the preparation of dossiers in eCTD format. The Principal Scientist will interact with cross-functional teams on CMC regulatory strategy and regional regulatory requirements and interact with CMC subject matter experts (SMEs). This position will support the development of submission strategies for CMC modules and updates, including life cycle management; and generation of submission-ready content for the Quality/CMC sections of all clinical trial and marketing authorization applications for ImmunityBio, Inc. Essential Functions • Prepare and review Module 2 (QOS) and Module 3 documents in accordance with Common Technical Document (CTD) guidances and company standards., • Support the development of global CMC regulatory strategies., • Assist with the preparation or review of documents including pharmacy manuals, protocols, CMC reports, and other documentation., • Provide input and recommendations on CMC topics planned or performed., • Support the design of CMC protocols., • Interact with other groups when needed to address CMC related matters., • Assist with the preparation of responses to Health Authority comments and questions pertaining to CMC issues., • May train others on Regulatory Affairs SOPs, processes, and templates for review, preparation, QC, and finalization of documents and major sections of applications as appropriate., • Perform ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities. Education & Experience • Bachelor's Degree in life sciences or technical discipline with 6+ years' relevant progressive experience required; or, • Master's Degree in life sciences or technical discipline with 4+ years' relevant progressive experience required; or, • Doctorate degree in life sciences or technical discipline with 2+ years' relevant progressive experience required., • Experience in the preparation of the submission of CMC modules in eCTD format required, • Familiarity with organizing responses to Health Authority requests required, • Familiarity with regulatory submissions outside of the US a bonus Knowledge, Skills, & Abilities • Knowledge of Health Authority procedures and guidance regarding document management and electronic submission, • Knowledge of Health Authority CMC guidance documents and requirements, • Proficient in Electronic Document Management Systems, • Ability to work with firm deadlines and adapt quickly to changing requirements and priorities, • Strong organizational skills, written and oral communication skills, and attention to detail, • Knowledge of Biologic-based drugs including cell-based therapies, gene therapies, antibodies and recombinant proteins desired Working Environment / Physical Environment • This position works on site in Summit, NJ., • Regular work schedule is Monday - Friday, within standard business hours. Flexibility is available with manager approval., • This position may need to sit for long periods of time and use various computer programs., • This desk-based role involves the close study of scientific and regulatory documents., • This position will work closely with scientific colleagues throughout the day, often on a project team basis. This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location. $140,000 (entry-level qualifications) to $154,000 (highly experienced) annually The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed. ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options * Health and Financial Wellness Programs * Employer Assistance Program (EAP) * Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability * Healthcare and Dependent Care Flexible Spending Accounts * 401(k) Retirement Plan with Company Match * 529 Education Savings Program * Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks * Paid Time Off (PTO) includes: 11 Holidays * Exempt Employees are eligible for Unlimited PTO * Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day * We are committed to providing you with the tools and resources you need to optimize your Health and Wellness. At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

JOB DESCRIPTION: • Process & maintain customer orders in accordance with all sales policy & procedures. Including the acquisition, preparation and fulfillment of all approved needs of the deal., • Maintain & track inventory (machines & attachments) and process all necessary paperwork, including dealer transfers, demo/loans, locations, delivery dates, specifications and attached/unattached attachments. Communicate any inventory deviations to management., • Provide quotes and inventory availability in an accurate and timely manner following established guidelines and tools., • Maintain machine history folders on all new machinery ordered from machine release to completion., • Provide backup support for the other coordinators to ensure the successful execution of that job during absence of coordinator or in time of higher than usual business., • Provide management with attachment recommendations (both stock needs & stock excess) on as needed basis., • Establish & process all associated paperwork, vendor invoices, req debits/credits and other items need to complete machine/attachment accruals., • Organization & prioritizing of short term (daily) and long term (weekly-monthly) tasks along with the proper follow-up. RECOMMENDED QUALIFICATIONS: • High School Diploma or equivalent required., • Minimum 3 years' experience in industry and/or equivalent combination of training and experience which provides the required knowledge, skills and abilities., • Excellent communication and interpersonal skills; both verbal and written, • Strong organizational, project management and time management; ability to work independently and multitask effectively in a fast-paced environment., • Experience with Microsoft Office, Word, Excel, Power Point, Adobe Reader and other related software. Equal Opportunity Employer Foley, Incorporated does not discriminate against any person applying for employment based on race, color, sex, age, religion, national origin or citizenship status, physical or mental disability, marital status, sexual orientation, gender identity, status as a covered Veteran, or any other legally protected status. This contractor and subcontractor shall abide by the requirements of 41 CFR 60.300.5(a) and 41 CFR 60.741.5(a). These regulations prohibit discrimination against qualified individuals on the basis of disability and protected veteran status, and require affirmative action by covered prime contractors and subcontractors to employ and advance in employment qualified individuals with disabilities and protected veterans.

___ Job Type Full-time Description Company Description Citizant is a leading provider of professional IT services to the U.S. government. We seek to address some of our country's most pressing challenges in the areas of Agile application development, Enterprise Data Management, Enterprise Architecture, and Program Management support services - focusing on the U.S. Departments of Homeland Security and Treasury. We strive to hire only ethical, talented, passionate, and committed "A Players" who already align with the company's core values: Drive, Excellence, Reputation, Responsibility, and a Better Future. No matter how large we grow, Citizant will retain its collaborative, supportive, small-company culture, where successful team effort to address external and internal customer challenges is valued above all individual contributions. Duties and Responsibilities: Enrollment Process Management: • Schedule appointments and/or service walk-ins for Personal Identity Verification (PIV) Card Activations, Enrollments, Certificate Updates, and PIN Resets., • Answering phone calls/email inquiries related to PIV credentials and access control matters., • Coordinate and conduct the enrollment process for PIV cards, including verifying the identity of applicants and collecting required documentation., • Accurately collect and document personal information, biometric data (such as fingerprints), and other necessary details from applicants., • Verify the authenticity of provided documents and information to prevent fraudulent enrollment attempts., • Handle sensitive personal information carefully and adhere to data protection regulations and organizational security protocols., • Communicate clearly and professionally with applicants, explaining the enrollment process, required documents, and any additional steps they need to follow., • Provide excellent customer service to address questions and concerns related to the enrollment process., • Escalation management involves listening, understanding, and responding to customer needs and expectations., • Maintain accurate records of the enrollment process, including documentation of each applicant's information, enrollment date, and any issues encountered., • Stay up to date with relevant policies, regulations, and procedures related to PIV card enrollment., • Experience with Microsoft Excel for data management, coordination, and reporting., • Ability to adapt to changing security procedures and requirements., • Ability to adapt to changing security procedures and requirements., • Prior experience in a similar role, customer service, or administrative position may be advantageous., • Attention to detail and strong organizational skills., • Excellent interpersonal and communication skills., • Ability to handle confidential information with discretion., • Attend local hiring events 3 - 4 times a month (may vary, depending on the business need)., • The role primarily involves sedentary work., • There may be occasional instances of stair climbing., • Periodic standing and/or walking for extended durations may be required., • Occasional activities such as reaching, squatting, bending, pulling, grasping, holding, and lifting objects weighing 25 - 30 lbs., • Requires typing for most of the day., • US Citizenship is required., • Medical, dental, and vision insurance, • Life and Disability Insurance, • 401(k), • Generous Paid Time Off (PTO), • Flexible Spending Accounts (FSA), • Employee Assistance Program (EAP) Additional Information Citizant strives to be an employer of choice in the Washington metropolitan area. Citizant associates accept challenging and rewarding work and in return receive excellent compensation and benefits, as well as the opportunity for personal and professional development. Citizant is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. Salary Description $20.24

The ideal candidate is a board-certified OB/Gyn physician with current, active skills across the full spectrum of OB/Gyn care. TeamHealth is seeking a dedicated OB/Gyn physician to join our OB/Gyn hospitalist and outpatient clinic team at Hackensack Meridian Health JFK Medical Center in Edison, New

RWJBarnabas Health is seeking board-certified Child & Adolescent psychiatrists for outpatient positions with the Childrens Specialized Hospital. These positions are located in Central and Southern, NJ, extremely close to several community features and attractions. To learn more about this positi

Looking for a part-time position in a fast-paced environment? TeamHealth is seeking a part-time physician assistant (PA) or nurse practitioner (NP) to join our team in the emergency department (ED) at JFK Medical Center in Edison, New Jersey. As an emergency medicine (EM) advanced practice clinician

Job Title : Formulation Chemist Location: Clark, NJ (3 days onsite a week) Direct Client Job Summary: The Chemist – Hair Care, Scalp & Manageability Development is responsible for supporting the formulation and development of innovative consumer beauty products from concept through launch. This role coordinates development projects, refines formulations, ensures product stability and quality, and collaborates with cross-functional teams including marketing, regulatory, evaluation, and manufacturing. The position requires strong scientific knowledge, creativity, and project management skills to deliver products aligned with brand innovation strategies and global launch timelines. Key Responsibilities: • Independently execute product development projects from inception through officialization to meet launch timelines, • Develop, refine, and optimize product formulations, • Perform product stability testing and resolve formulation stability issues, • Monitor formula quality and conformity to specifications, • Manage multiple basic development projects simultaneously, • Identify appropriate raw materials and technologies for product development, • Proactively identify development challenges and propose effective solutions, • Collaborate with technical support groups including marketing, analytical, regulatory, evaluation, claims, and manufacturing teams, • Maintain awareness of scientific literature, patents, raw material technologies, and consumer trends, • Support transfer of formulations to manufacturing processes, • Maintain a safe, clean, and organized laboratory environment Required Skills: • Knowledge of cosmetic or personal care formulation principles, • Strong analytical and problem-solving abilities, • Effective communication and presentation skills, • Project coordination and time management skills, • Ability to work collaboratively in cross-functional teams, • Ability to work in a fast-paced environment and adapt to changing priorities Preferred Skills: • Experience in personal care or cosmetic product development, • Familiarity with hair care formulation and raw material technologies, • Understanding of the US hair care market and regulatory requirements

Job Description Walk-In Interview at MSN Pharmaceuticals Inc.! Join us at our facility on: Date: September 19th & 20th Time: 10:00 AM - 2:00 PM EST Where: #20, Duke Road Piscataway Edison, NJ 08854 Website: msnpi.com Linkedin : linkedin.com/company/msn-pi MSN Pharmaceuticals is looking for experienced professionals to join our Production Department at our facility in Piscataway, NJ for the following roles : • Granulation Operator : 3-5 years of Work Experience : A Shift, • Coating Operator : 3-5 years of Work Experience : A & B Shifts, • Packaging Operator : 3-5 years of Work Experience : A Shift Company DescriptionMSN PI is a fully owned subsidiary of the MSN group of companies .MSNPI develops and manufacture products for MSN group as well as specialized in contract development and manufacturing of high-quality generic pharmaceutical products. With more than 350 National & International patents filed, our portfolio offers over 300 APIs & 200 product formulations in multiple therapeutic categories.MSN PI is a fully owned subsidiary of the MSN group of companies .MSNPI develops and manufacture products for MSN group as well as specialized in contract development and manufacturing of high-quality generic pharmaceutical products. With more than 350 National & International patents filed, our portfolio offers over 300 APIs & 200 product formulations in multiple therapeutic categories.

Our client, a luxury fashion brand, is seeking a skilled Fashion Repair Artisan to support high-quality after-sales repairs for luxury fashion items on-site in Piscataway, NJ. This role plays a hands-on part in craftsmanship, quality assessment, and repair execution while partnering closely with operations and boutique teams to ensure a seamless client experience. Key Responsibilities • Perform high-quality repairs on handbags, accessories, and fashion items in accordance with established craftsmanship standards, • Assess incoming items to determine repair feasibility, required scope, prioritization, and timelines, • Inspect merchandise for quality issues and authenticity concerns, escalating when needed, • Collaborate with operations and retail partners to support repair requests and client needs, • Track repairs accurately within internal systems and adhere to workflow processes, • Participate in ongoing training to continuously refine technical skills and craftsmanship, • Additional duties as needed and assigned Role Qualifications • 2+ years of hands-on experience in fashion repair, craftsmanship, or a related technical specialty, • Strong attention to detail with a commitment to quality, service, and client experience, • Ability to manage and prioritize workload based on complexity and timelines, • Clear communicator with the ability to partner cross-functionally, • High school diploma required; technical, design, or trade education preferred, • Ability to work onsite full-time (5 days per week) Salary: $24 - $33/hr The description above is intended to describe the general nature and level of work being performed and is not an exhaustive list of all duties, responsibilities, and qualifications required. While PCG appreciates all applicants, only those qualified will be contacted. Thank you for your application. We look forward to hearing from you! If you believe you are a great candidate for this position, and the salary listed does not meet your expectations, we would still love to speak to you! PCG, in good faith, believes that this posted range of compensation is the accurate range for this role at this location at the time of this posting. PCG and our clients may ultimately pay more or less than the posted range depending on candidate qualifications. This range may be modified in the future. This role may also be eligible for additional compensation including incentive pay, discretionary bonuses, and a comprehensive benefits package, details of which will be provided during the hiring process. Pyramid Consulting Group, LLC is an Equal Opportunity Employer that takes pride in a diverse environment. We provide equal employment opportunities to all applicants and employees without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, marital or veteran status, disability, genetic information, or any other protected status under applicable law. We will provide reasonable accommodations to applicants and employees with disabilities. If you require a reasonable accommodation during the application or hiring process, please contact For positions subject to “Fair Chance” laws (including but not limited to California, Colorado, New York City, Los Angeles, and other jurisdictions), PCG will consider qualified applicants with arrest and conviction records in a manner consistent with applicable law. Please refer to our website: for access to our Right to Work and E-Verify.

Are you an experienced Scientist with a desire to excel? If so, then TALENT Software Services may have the job for you! Our client is seeking an experienced Scientist to work at their company in Rahway, NJ. Primary Responsibilities/Accountabilities: • Looking for a highly motivated individual who will support an experienced BioNMR team in fragment-based NMR screening, fragment-based lead discovery, and the detailed evaluation of ligand-protein interactions in state-of-the-art BioNMR laboratories., • This will involve the handling of chemical compound libraries and the preparation of small molecule-protein NMR screening samples and small molecule NMR QC samples using liquid handling robotics, the manipulation of chemical samples for NMR and other analytical methods, analysis of QC data, documenting and reporting analytical results in spreadsheets and chemical databases. Qualifications: • A BS or MS degree or equivalent in Analytical Chemistry or a related field is required., • Excellent laboratory skills in analytical chemistry or a related field are critical., • Experience in chemical compound handling, purification and characterization is a must. Background in analytical chemistry using NMR would be an advantage., • The ability to work on different projects in parallel is required., • The successful candidate should show a desire to learn and implement new methods and apply them to answer scientific questions., • The ability to work in a team and interact with colleagues in a multidisciplinary environment is important. Open communication, an independent and precise way of working, and excellent team work skills are critical. Good communication skills are required.

Job DescriptionJob Title: Dryer Operators Job Description We are seeking skilled Dryer Operators to set up, run, and monitor the process of drying chemical slurry. This role requires the ability to operate industrial dryers, troubleshoot, and perform minor repairs on process equipment. Operators will be responsible for drying wet products, packaging, and documenting the process. Responsibilities • Set up, operate, and monitor industrial dryers to dry chemical slurry., • Track and record production output using computers in the tracking system., • Troubleshoot and perform minor repairs on process equipment., • Understand the operation, start-up, shutdown, and potential hazards of each piece of equipment in the assigned work area., • Familiarize with the layout and purpose of equipment and its impact on the surrounding process and storage areas., • Maintain a full understanding of operating procedures, including process, safety, and maintenance protocols., • Comprehend the chemical and process hazards in the area.Essential Skills, • Experience in operating process equipment for 1-2 years., • Mechanical aptitude and ability to troubleshoot and perform minor repairs., • Proficiency in using computers for documentation and tracking production output.Additional Skills & Qualifications, • Familiarity with operating procedures and safety protocols., • Understanding of chemical processes and hazards., • Mechanical and technical aptitude in production environments.Why Work Here? Enjoy a generous benefits package including 2 weeks of vacation in the first year, increasing to 3 weeks after 3 years, with unused vacation reimbursement. Benefit from 5 PTO/sick days per year, 12 holidays, and a profit-sharing bonus of up to 15% of base salary. Additionally, take advantage of a 401k match up to 6% and tuition reimbursement. Join a team with low turnover and long-term stability, as the company invests in facility upgrades. Work Environment The role is based in an older manufacturing facility currently undergoing significant upgrades. Work within a small team, providing opportunities to learn various roles. The environment is conducive to developing diverse skills and gaining long-term stability. Job Type & Location This is a Contract to Hire position based out of AVENEL, NJ. Pay and Benefits The pay range for this position is $24.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program About Aerotek: We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Actively hiring "Capital Sourcing Specialist" at Edison, NJ for position at a hospital. pay rate is $30-$33/Hr. Please find below the Job Description: • Job Title : Capital Sourcing Specialist, • Duration : 3+ months (Possibility for extension), • Location : Edison NJ, • Pay Rate : $30-$33/Hr. Duties: • Negotiate and manage the purchase of capital equipment and services for the network., • Utilize PeopleSoft Financials and related automation tools., • Analyze spend data using Google tools across suppliers and categories., • Source and negotiate with manufacturers and suppliers for core products., • Meet with supplier reps to stay informed on products and services., • Communicate savings opportunities across Client and Value Analysis teams., • Review GPO contracts for savings on capital purchases., • Partner with departments to identify cost-saving initiatives and projects., • Present savings analyses and negotiate contracts through GPO or direct supplier deals., • Track and report cost-saving initiatives regularly., • Assist in equipment specification for construction and expansion projects., • Collaborate with planners, consultants, architects, and network staff on large projects., • Maintain project equipment tracking spreadsheets and order equipment on schedule., • Prepare RFPs, bid summaries, and vendor performance analyses as needed., • Source suppliers both domestically and internationally to support supply chain goals., • Support departments in supplier selection and contract negotiation through RFPs., • Collaborate with leaders and staff at all levels within HMH., • Work with Legal, Biomed, and Accounts Payable on contract matters., • Ensure procurement details are addressed in contract negotiations., • Ensure contracts are executed and maintained in the contract management system., • Identify substitute products during recalls, alerts, and shortages., • Support Healthy Hospitals Initiatives when applicable., • Manage liquidation of surplus/obsolete capital equipment using approved vendors or open market., • Other duties and projects as assigned., • Minimum of 5 years of relevant experience., • Ability to travel within the HMH network as needed., • Project management skills., • Highly organized with multitasking and time management abilities for aggressive deadlines., • Ability to adjust workload based on shifting priorities., • Excellent written and verbal communication skills. Bachelor’s degree (Business concentration preferred). Certified Materials & Resource Professional (CMRP) — at hire or obtained within 12 months. Benefits: Pride Health offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, , legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors.

Company Description Accu Reference Medical Lab is a state-of-the-art facility providing comprehensive diagnostic, screening, and evaluation testing for various diseases and health conditions. Certified under the federal government’s Clinical Laboratory Improvement Amendments (CLIA), the lab operates in compliance with all regulatory standards. Employing advanced diagnostic technology and highly skilled technicians, Accu Reference ensures precision and accuracy in its testing services. The laboratory is committed to continuous improvement through innovative techniques and technological advancements. Accu Reference Medical Lab is proud to be an equal opportunity employer. Role Description This is a full-time on-site role for a Cytotechnologist, located in Linden, NJ. The Cytotechnologist will examine cell samples to identify abnormalities, contribute to pathology diagnoses, and ensure quality control in laboratory procedures. The role involves preparing, analyzing, and interpreting cellular samples using advanced diagnostic equipment while maintaining adherence to clinical standards and laboratory protocols. Qualifications • Expertise in Laboratory Skills, Laboratory Medicine, and clinical procedures, • Knowledge and experience with Pathology and cellular analysis, • Proficiency in Quality Control to ensure accuracy and compliance in laboratory workflows, • ASCP certification or eligibility is highly preferred, • Attention to detail, strong analytical skills, and ability to work in a fast-paced environment, • Bachelor’s degree in Cytotechnology or related scientific discipline, • Familiarity with state and federal laboratory regulations is a plus

Job post summary Date posted: March 9, 2026 Pay: $41.00 - $48.00 per hour Job description: Licensed X Ray Technologist – Diagnostic Imaging Company: Madison Medical Location: Madison, NJ Job Type: Full-Time, In-Person About Madison Medical Madison Medical is a physician led, multidisciplinary practice delivering world class, out of network care. Our model integrates advanced sports medicine, medical wellness, rehabilitation, and concierge level service to produce exceptional clinical outcomes and an elevated patient experience. We operate at the intersection of clinical excellence, operational precision, and modern systems. Every patient interaction reflects professionalism, discretion, and thoughtful care coordination. We are building a forward thinking healthcare organization where technology, systems, and accountability support great clinicians and exceptional patient care. Position Overview We seek a licensed X Ray Technologist to support physicians with high quality diagnostic imaging across sports medicine, orthopedic, and rehabilitation care. This role plays a central part in the clinical workflow. Imaging accuracy, patient communication, and operational coordination drive the success of the position. The technologist works closely with physicians, rehabilitation teams, and clinical staff to support diagnosis, treatment planning, and coordinated patient care. This role is ideal for someone who: Work Schedule (Required) This role requires strict schedule reliability and rotating weekend availability. The schedule is fixed and non negotiable: Monday: 8:30 AM – 5:00 PM Tuesday: 7:00 AM – 3:30 PM Wednesday: 8:30 AM – 5:00 PM Thursday: 7:00 AM – 6:00 PM (split shifts) Friday: 7:30 AM – 1:30 PM Saturday: 8:30 AM – 1:00 PM (rotating) Consistent attendance and punctuality are critical to success in this role. How We Work at Madison Medical At Madison Medical: Systems matter more than opinions Clarity beats chaos Technology is a daily tool not a disruption Feedback is direct, professional, and timely Change is constant and supported You are expected to use our tools and workflows, not work around them. Core Responsibilities Perform diagnostic X ray imaging in support of physician evaluation and treatment planning Prepare patients for imaging procedures and explain the process clearly Position patients and equipment to produce accurate diagnostic images Follow all radiation safety and protection protocols for patients and staff Review imaging for quality and accuracy before physician review Document imaging procedures and results in CureMD Maintain imaging equipment and report technical issues Coordinate imaging workflow with physicians, rehabilitation teams, and clinical staff Assist in maintaining efficient patient flow across the practice Maintain professionalism and discretion when handling patient information Expectations for All Team Members All team members are expected to: Follow documented workflows and systems Use technology tools as designed Adapt as processes evolve Receive feedback professionally and apply it quickly Communicate clearly and without defensiveness Take ownership of outcomes not just tasks This Role Is a Strong Fit If You… Value precision, structure, and clinical accountability Work efficiently during high volume patient schedules Communicate clearly with patients and clinical teams Take pride in diagnostic accuracy and patient care Support collaborative multidisciplinary care This Role Is Not a Fit If You… Struggle with punctuality or schedule consistency Resist structured workflows or feedback Prefer informal or inconsistent clinical environments Avoid accountability when patient volume increases Expect roles to remain static Qualifications & Experience Active New Jersey license as an X Ray Technologist ARRT certification required Experience with digital radiography systems Knowledge of radiographic positioning and imaging protocols Strong attention to detail and image quality Professional communication with patients and clinical teams Compensation & Benefits 401(k) Medical, dental, and vision insurance Paid time off Professional development and tuition reimbursement Referral program Free parking Performance based growth opportunities Work Location: In person

Job Title: Analyst – Analytical Testing Location: Summit, NJ Duration: 6 Months No. of Positions: 1 Visa Status: US Citizen / Green Card JOB DESCRIPTION: The Analyst is responsible for supporting the method transfer and analytical testing with moderate supervision as part of Cell Therapy Technical Operations (CTTO) Team. • The analytical department is responsible for flow cytometry, cell-based potency, RT-qPCR/PCR and other analytical assays testing to support process characterization testing of the lentiviral vector and cell therapy drug product samples., • This includes the ability to interface with multiple groups, independently perform tasks, interpret results, and troubleshoot. REQUIRED COMPETENCIES (Knowledge, Skills, and Abilities):Advanced hands-on experience with various analytical techniques including flow-cytometry , molecular techniques • Scientific knowledge in the characterization and transfer of pharmaceutical products., • Experience with PCR and/or flow cytometry and/or mammalian cell culture is required., • Experience working in a regulated (GLP/GMP) environment in preferred., • Assay development, especially cell-based potency assays are preferred., • Assay qualification/validation experience is preferred., • Assay Technology Transfer (TT) experience is preferred., • Excellent organizational skills and ability to handle multiple tasks, • Highly motivated, willingness to acquire new skills, and ability to work with minimal supervision., • Excellent verbal and written communication skills., • Advanced problem- solving ability/mentality, technically adept and logical thinking., • Ability to represent the interests of the grou p on cross- functional teams., • Ability to work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects., • Ability to work with management locally and globally ., • Advanced a bili ty to communicate effectively with peers, department management and cross-functional peers. EDUCATION AND EXPERIENCE:B.S. with 4+ years’ work experience or M.S. with 2+ years’ experience in Molecular & Cellular Biology, Immunology, or related discipline. • DUTIES AND RESPONSIBILITIES:100% onsite required., • Perform experiments using the following methodologies: PCR, RT-qPCR, flow cytometry, mammalian cell culture, Luminex, MSD, and ELISA., • With moderate supervision design and execution analytical experiments of moderate complexity., • Perform data analysis, summarize and report experimental results., • Document/review laboratory work in notebooks that is detailed, accurate, timely, and in compliance with Good Lab Practices/Good Documentation Practices requirements., • Collaborate with the Quality Control and Analytical Development teams to advance analytical and development projects., • Ensure proper operation and perform routine maintenance of all laboratory equipment., • Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment., • Perform cell based in-vitro flow experiment, ELISA, qPCR to assess critical reagent concentration., • Capable of handling complex issues and solving problems with only general guidance., • Prepare and present continuous improvement projects to management., • Comprehensive understanding of regulatory guidelines and can independently develop, write and execute methods, protocols, reports and other related documents., • Complete all work in a timely manner. Perform peer review of testing data., • Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner., • Complete all reviews in accordance with required timelines., • Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required., • Participate in complex projects and continuous improvement efforts., • Communicate effectively with management regarding task completion, roadblocks, and resource needs., • Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles.

Patient Care Coordinator, Clinical Experience and Operations Company: Madison Medical Location: Madison, NJ Job Type: Full-Time, In Person Pay: $27.00 to $30.00 per hour About Madison Medical Madison Medical is a physician-led, multidisciplinary ambulatory care facility delivering out-of-network care across sports medicine, medical wellness, and rehabilitation. Based in Madison, New Jersey, we operate as a licensed multi-specialty musculoskeletal super group with a vertically integrated care model designed to deliver the full continuum of MSK and wellness services under one roof. Our clinical and operational structure reflects the infrastructure of a hospital-based outpatient center, with greater agility, stronger patient experience, and a sharper operational focus. We combine clinical excellence, structured systems, and modern technology to support high-level patient care across every stage of the patient journey. Our practice operates from multiple floors of dedicated clinical space at 345 Main Street, Madison, NJ, with active buildout underway to expand advanced recovery, regenerative medicine, and wellness services. We are also building Management Services Organization infrastructure to support future multi-site expansion. Our service lines span more than 15 specialties, including chiropractic medicine, interventional pain management, physical therapy and rehabilitation, primary care and sports medicine, podiatry, acupuncture, allergy testing and SLIT immunotherapy, hormone optimization, weight management, regenerative medicine, IV nutrient therapy, sleep medicine, athletic recovery, behavioral health integration, and telehealth. Our operational platform includes a multi-provider clinical team, C-suite leadership across operations and finance, full-cycle revenue cycle management, CureMD integrated with reporting and digital intake systems, and a dedicated patient acquisition and community outreach function. Position Overview Madison Medical seeks a Patient Care Coordinator to lead the patient journey from first contact through ongoing care. This person serves as the central point of communication between patients, providers, and internal teams, ensuring a smooth, professional, and well-coordinated experience at every touchpoint. This role begins with front-facing patient coordination and expands into cross-department operational support based on performance. Growth comes through accountability, precision, and follow-through. This role fits someone who thrives in a fast-paced, structured environment, takes ownership of outcomes, adapts quickly as workflows evolve, and communicates with professionalism and clarity. It is an operations-driven role centered on patient experience, accuracy, and execution. Work Schedule, Required This is a fixed schedule and requires consistent reliability, including rotating Saturdays. Monday, 8:30 AM to 5:00 PM Tuesday, 7:00 AM to 3:30 PM Wednesday, 8:30 AM to 5:00 PM Thursday, 7:00 AM to 6:00 PM, split shifts Friday, 7:30 AM to 1:30 PM Saturday, 8:30 AM to 1:00 PM, rotating Core Responsibilities The Patient Care Coordinator serves as the primary point of contact for new and returning patients and coordinates scheduling across providers with clinical awareness. This role manages check-in, check-out, and intake workflows, guides patients through onboarding and care plans, and helps patients understand insurance benefits and out-of-network coverage. This person also coordinates referrals, maintains accurate documentation, supports compliant recordkeeping in CureMD, and works across Outlook, Microsoft Teams, and RingCentral. The role includes tracking patient progress through internal systems and reporting tools, partnering with clinical and billing teams to improve patient flow, protecting patient confidentiality, and staying calm and solution-focused in high-volume settings. Expectations for All Team Members All team members are expected to follow documented workflows, use technology as designed, adapt as systems evolve, accept feedback and apply it quickly, communicate without defensiveness, and take ownership of results. Qualifications Candidates should have at least five years of experience in patient-facing roles within hospitals or private practice settings. Strong knowledge of insurance and out-of-network care models is required, along with experience coordinating multidisciplinary care. Proficiency with EMR systems and Microsoft platforms is essential, as are strong organizational and communication skills. Compensation and Benefits Madison Medical offers a competitive hourly rate of $27.00 to $30.00, along with a benefits package that includes 401(k), medical, dental, and vision insurance, paid time off, professional development and tuition reimbursement, a referral program, free parking, and performance-based advancement opportunities. Work Location Madison, NJ In Person Reliable commute required Additional Company Context Madison Medical Sports and Wellness is not a single-provider practice and not a traditional chiropractic office. We are a diversified healthcare enterprise built to reduce dependence on any one specialty, provider, or payer. Our model includes institutional-grade billing capability, recurring revenue through wellness and longitudinal care programs, real estate-backed expansion, and deep community integration through partnerships with schools, athletic programs, police departments, and municipal organizations. We are building the next generation of outpatient MSK care, combining hospital-level clinical breadth with the speed, structure, and patient experience of a modern growth-focused medical group. • Madison Medical is not where we started. It is what we have built, and we are still building.

Physician – Gastroenterology (Employed Partner Model) Madison Medical Sports & Rehabilitation Center Madison, NJ | Full-Time | In Person Compensation: Competitive base salary + collections-sharing model with significant performance-based upside About Madison Medical Madison Medical is a physician-led, multidisciplinary practice redefining modern healthcare through advanced diagnostics, regenerative therapies, and outcome-driven care. We integrate specialties under one roof to deliver a seamless, high-caliber patient experience — and we're expanding that model into gastroenterology. Position Overview We are seeking a BC/BE Gastroenterologist to join Madison Medical as an employed partner. This is not a traditional employment arrangement — you will share directly in collections, help spearhead and build our gastroenterology division from the ground up, and have the infrastructure, support, and clinical resources to practice at the highest level from day one. We are looking for someone hungry a physician who wants to own a modality, not just fill a schedule. You will have access to on-site fluoroscopy and a dedicated C-arm, an established referral network, and a leadership team fully invested in making this division a flagship service line. If you want to build something real and be rewarded for what you produce, this is the role. Clinical Focus Areas • Comprehensive GI evaluation and management (IBD, IBS, GERD, motility disorders, liver disease, colorectal screening, etc.), • Diagnostic and therapeutic endoscopy (EGD, colonoscopy), • Fluoroscopy-guided GI procedures utilizing on-site C-arm, • Coordination with our internal medicine, sports medicine, hormone/metabolic, and nutrition teams for integrative GI care, • Nutrition-related GI conditions, gut health optimization, and preventive gastroenterology, • Participation in colorectal cancer screening initiatives What We Offer • Employed partner model — direct participation in collections, not just a flat salary, • Malpractice insurance fully covered by Madison Medical, • 100% employer-paid health, dental, vision, and life insurance, • Profit-sharing retirement plan with employer contribution (401(k)), • Established patient referral pipeline across internal medicine, primary care, and specialty partners, • On-site fluoroscopy and C-arm — procedural capability without leaving the building, • Strong clinical and administrative support staff, • Credentialing and operational infrastructure already in place, • Modern facility with serious long-term growth trajectory, • Physician-led leadership that invests in your visibility and professional brand Qualifications • MD or DO from an accredited medical school, • Board Certified or Board Eligible in Gastroenterology (Required), • Active New Jersey medical license or eligibility to obtain, • Fellowship training in Gastroenterology (Required), • Proficiency in diagnostic and therapeutic endoscopy, • Experience with or interest in fluoroscopy-guided procedures a plus, • Strong communication skills and collaborative mindset, • Driven, growth-oriented physician ready to build and lead a division — not just see patients Benefits • 100% employer-paid health, dental, vision, and life insurance, • Malpractice insurance fully covered, • 401(k) profit-sharing plan with employer contribution, • Paid time off and paid holidays, • Full-time position — we are building something lasting and need someone committed to growing with us

Wakefern Food Corp. is the largest retailer-owned cooperative in the United States and supports its co-operative members' retail operations, trading under the ShopRite®, Price Rite®, The Fresh Grocer®, Dearborn Markets®, and Gourmet Garage® banners. Employing an innovative approach to wholesale business services, Wakefern focuses on helping the independent retailer compete in a big business world. Providing the tools entrepreneurs need to stay a step ahead of the competition, Wakefern’s co-operative members benefit from the company’s extensive portfolio of services, including innovative technology, private label development, and best-in-class procurement practices. Summary We are seeking a dynamic Organizational Change Management Lead to manage the people side of our Transformation projects and create a change management center of excellence as part of the Business Innovation and Transformation Services (BITS) team at Wakefern Tech. The Organizational Change Management Lead will be responsible for developing and implementing change management strategies, plans and deliverables that maximize employee adoption and usage while minimizing resistance. Additionally, they will be responsible for the creation of a common change management methodology, tools, templates and training. Key Responsibilities: • Partner with the Director, Business Innovation and Transformation Services to build out a Center of Excellence in Change Management including methodology, templates, tools and training., • Lead the change management workstream team for various transformational projects - Develop and implement change management strategies and plans that maximize employee adoption and usage while minimizing resistance. Manage OCM Action plans working across the Wakefern Food Corp. organization., • Supervise OCM Specialist and manage cross-functional teams to deliver OCM Workstream deliverables across Communication, Engagement and Training., • Create change strategies (stakeholder analysis and change impact analysis) as well as sponsor roadmap, communication, training, coaching and resistance management plans and their respective execution., • Partner closely with large transformational project teams (such as system implementations) to integrate change management activities into the overall project plans., • Assess the change impact by conducting impact analyses, assess change readiness, and identify key stakeholders. Ability to create process maps and documentation and analyze the people change impact., • Support the design, development, delivery, and management of communications regarding change initiatives., • Conduct change management training (e.g., Leading through change) and coaching to enhance management and employees’ understanding and skills necessary for change., • Build presentations and communications with experience working in various mediums (written, presentation, video, etc.), • Ability to work with a wide variety of people including executive leadership, management and front-line employees. Excellent communication, influencing and interpersonal skills., • Track and analyze risks and issues related to change initiatives, and development of corresponding risk mitigation plans., • Develop and use change metrics and measurements to assess the success of change initiatives., • Collaborate with various departments to drive the adoption of new strategies or processes. Qualifications: • Bachelor’s degree in business, HR, organizational development or related field., • Change management certification (e.g., Prosci) preferred., • 7-10 years of experience leading Organizational Change Management projects, specifically for large scale enterprise system implementations and building a center of excellence in Organizational Change Management., • Proven experience in managing organizational change initiatives at scale and building organizational change competencies throughout an organization., • Experience implementing change management as part of large enterprise systems projects a plus., • Strong leadership and project management skills., • Understanding of business process management. Training and experience in process improvement a plus., • Good business acumen with ability to understand how change management drives business results., • Excellent communication and interpersonal skills., • Ability to work effectively with a variety of stakeholders with a strong ability to assess personalities and team dynamics. Strong emotional quotient is required., • Strong influencing skills., • Strong analytical and problem-solving abilities., • Grocery, Retail, CPG or Wholesale experience a plus., • Consulting experience a plus. Working Conditions & Physical Demands • This position requires in person office presence 4 days a week in Edison, NJ, • This position may require travel Competencies • Communicate Effectively, • Drive for Results, • Embrace Change, • Develop You, • Build Relationships, • Stay Competitive

Company Description PLS Analytical provides comprehensive testing services for regulated product programs, specializing in nasal drug products, microbiological, analytical, and packaging component testing. The company offers innovative solutions for product characterization and risk assessment, including Particle Size Analysis and Nitrosamine Testing. Serving the pharmaceutical, nutraceutical, dietary supplement, cosmetic, and food industries, PLS Analytical operates as an FDA- and DEA-registered contract laboratory with CGMP and ISO 17025 certifications. Committed to quality, PLS Analytical also supports private label OTC manufacturing, packaging, and distribution through its partner network. Learn more at . Position Summary This is a full-time, on-site role for a Facility Engineer based in East Brunswick, NJ. The Facility Engineer will play a key role in managing facility operations in a cGMP-regulated pharmaceutical environment. This role is responsible for the maintenance, repair, and continuous improvement of HVAC systems, electrical and mechanical equipment, critical utilities and overall facility infrastructure. The Facility Engineer will oversee preventive maintenance planning, scheduling, contractor coordination and ensure all work is completed in compliance with cGMP, safety, and regulatory standards. Accurate cGMP documentation, system reliability, and operational efficiency are essential to success in this role. Key Responsibilities • Oversee the design, planning, construction, installation and maintenance of building systems, equipment and facility infrastructure., • Ensure all facility operations comply with FDA, cGMP, and safety regulations, including maintenance of required documentation., • Develop, execute and review IQ/OQ/PQ protocols for equipment, utilities, and in-process machinery., • Install, qualify and upgrade pharmaceutical manufacturing equipment as needed., • Troubleshoot electrical, mechanical, and integrated control systems for manufacturing machinery., • Lead and coordinate commissioning, installation, and validation activities with internal teams and external contractors., • Manage facility upgrades, electrical engineering projects and site expansion initiatives., • Evaluate project requirements , capacity constraints and cost estimates to support business needs., • Drive cost reduction, efficiency optimizations, safety improvements, and equipment reliability initiatives., • Supervise and support facility maintenance personnel, including mechanics and engineers., • Coordinate with warehouse , production and laboratory teams on facility support needs., • Implement and maintain preventive maintenance and calibration programs., • Lead EHS (Environment, Health, Safety) activities, including employee safety training and compliance., • Conduct risk assessments and support CAPA, FMEA and DFMEA activities., • Analyze facility performance data and maintenance reports to develop continuous implement plans. Qualifications • Strong expertise in Facilities Engineering and Facility Management (FM) to oversee and maintain building systems and equipment, at least 2 years of experience in the position offered., • Proficiency in Facilities Operations, including maintenance schedules and compliance with safety standards, • Ability to troubleshoot technical problems and resolve issues efficiently, • Experience with Preventive Maintenance programs to ensure equipment reliability, • Understanding of safety regulations and building codes, • Strong analytical and decision-making skills, • Bachelor’s degree in Engineering, Facilities Management, or a related field preferred, • Industry certification or licenses related to facility management is a plus

JOB TITLE: Associate Scientist Location: Summit, NJ (100% onsite) Duration: 6 months initial (possibility of extension for right candidate depending on performance) Work Schedule: first shift (9am to 5pm) Monday to Friday PURPOSE AND SCOPE OF POSITION: The Associate Scientist/Engineer is responsible for leading investigation reports in support of S12 CART operations. This includes execution of thorough root cause investigations, interviewing personnel, hypothesis testing and interpretation of results, authoring investigation reports, identifying corrective and preventive actions (CAPA), and troubleshooting complex problems. The successful incumbent must interface closely with different functional organizations, including Quality Assurance teams. REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: • Working experience of deviation investigations utilizing root cause analysis tools., • Working experience in the CAPA process and ability to identify and verify effectiveness., • Technical writing skills and ability to collaborate effectively in cross functional teams., • Proven ability to accurately and completely understand, follow, interpret, apply Global Regulatory and cGMP requirements., • Ability to support health authority inspections., • Knowledge of data trending and tracking, including use of statistical analysis software a plus., • Demonstrate advanced problem-solving ability / mentality, technical adeptness and logical thinking., • Ability to set priorities, manage timelines and effectively react/manage changing priorities., • Ability to work with management (global and site) and support corporate and departmental goals., • Ability to communicate honestly, transparently and effectively with peers, department management and cross functional peers., • Ability to utilize electronic Quality systems such as eQRMs (Enterprise Quality and Regulatory Management system) or Infinity., • Hands on experience preferred with CAR-T or biopharmaceutical manufacturing and Quality Control. Education and Experience • Minimum Associate degree required or preferred a Bachelor's Degree in science or engineering, preferably in Biochemistry, life sciences or related engineering discipline., • Minimum 1 year of relevant work experience, preferably in a health authority regulated environment., • Previous experience working in a biopharmaceutical manufacturing facility is preferred (CAR T a plus)., • An equivalent combination of education and experience may substitute. DUTIES AND RESPONSIBILITIES: • Conduct thorough investigations (Environmental Monitoring, deviations, etc.) utilizing root cause analysis tools., • Lead investigations and cross functional investigation teams, and close reports in a timely manner, • Perform GEMBA walks with stakeholders to better understand process steps and evaluate Root Cause Analysis., • Work with functional teams to propose effective CAPAs, develop CAPA plans and assure CAPA effectiveness., • Assess potential impact and risk to product or process associated changes may have upon change implementation and develop an appropriate mitigation strategy., • May Initiate change control documentation, • Identify functional area SMEs to perform impact assessments as part of the change management process., • Ensure all investigations are completed in a timely manner. Notify stakeholders of any delays in a timely manner., • Provide technical support for manufacturing investigations / CAPAs / change controls as needed., • Support deviation investigation defense during audits and site inspections related inquiries., • Handle complex issues and solve problems with minimal guidance., • Serve as author or technical reviewer of departmental procedures as appropriate., • Employ lean manufacturing / six sigma principles to continuously improve products, processes and systems., • Continuously support S12, living the "patients first” mission and fostering a "Right First Time” mindset. If hired, you will enjoy the following Eclaro Benefits: • 401k Retirement Savings Plan administered by Merrill Lynch, • Commuter Check Pretax Commuter Benefits, • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro If you feel you are qualified with the required skills and if you are interested, please free to send your word version most updated resume TAILORED to the job description above to or call (212)804-7476. Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Immediate need for a talented Business Solutions Manager 2. This is a 06+months contract opportunity with long-term potential and is located in Summit, NJ (Hybrid). Please review the job description below and contact me ASAP if you are interested. Job ID:26-07843 Pay Range: $45 - $47/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: • Lead insights to action initiatives through regular monitoring & analysis of global industry trends, category & competitor landscapes and business performance (sales, trends, market share, P&L) to derive actionable business recommendations and enhance strategy & innovation efforts, • Understand and advocate for consumer needs and preferences to support everyday decisions and business actions, • Partner with Market Insights & Research to mine consumer insights and category trends relevant to innovation development, • Partner with technical cross-functional partners to deliver competitive claims, packaging designs, and brand presence at shelf to drive business continuity & and new innovations, • Partner with R&D, Supply Chain and technical cross-functional partners to lead the end to end execution of key global body innovations on-time, and with excellence, • Work with key global agencies to support the creation of 360 communication toolkits to support body business continuity & innovation launches, including digital, social, e-commerce and influencer strategy and assets, • Collaborate with key global cluster and market stakeholders to ensure all innovation initiatives are globally relevant and designed to be consistently executed across all regions, • Support budget tracking & management, • Proactively look for opportunities to expand brand passion and improve consumer experiences with the brand to deliver brand growth goals. Key Requirements and Technology Experience: • Key Skills;A BA/BS in Marketing or a related business field, • A minimum of 5 years of marketing, innovation, and/or sales experience is required, • Previous brand management or sales experience at CPG is required., • Innovation experience in Beauty or Skin Care is strongly preferred, • Experience working with R&D, Market Research, Communications Agencies, Finance, Sales and Project Management is required., • Experience working with Legal, Regulatory, and global partners is preferred., • Proven ability to understand a consumer target and position a brand/project/innovation, • Works well independently while possessing strong leadership & communication skills and a demonstrated history of building collaborative, lasting relationships that deliver business results, • Ability to work well in a fast-paced environment and handle multiple priorities successfully, • Ability to work closely with cross functional and other internal teams, • High level of energy, drive, enthusiasm, and commitment with a strong bias for action and prioritization, • Outstanding verbal and written communication skills, as well as demonstrated ability to work confidently and respectfully at all levels of an organization, both internally and externally, • Someone who is highly creative with the ability to think out of the box, • Comfortable working with numbers, metrics & spreadsheets, • Able to influence key partners with ideas that build value. 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, colour, 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 ___.

Madison Medical | Madison, NJ Full-Time | In-Person | Rotating Saturdays Required Compensation: $85,000 – $100,000 per year ABOUT MADISON MEDICAL Madison Medical is a physician-led, multidisciplinary practice built for the future of healthcare. We operate with high clinical and operational standards. Our model relies on structured workflows, team collaboration, and technology-driven systems to deliver efficient, high-quality patient care. AI and automation support documentation, coordination, and communication. Clinicians use these tools daily and validate outputs for accuracy and compliance. POSITION SUMMARY This is a full-time Physical Therapist role focused on delivering high-quality outpatient care in a multidisciplinary setting. You will evaluate, treat, and guide patients through structured rehabilitation plans. You will work closely with physicians and other providers to support coordinated, outcome-driven care. KEY RESPONSIBILITIES Patient Evaluation & Treatment • Perform initial evaluations and reassessments, • Develop individualized treatment plans, • Deliver manual therapy and therapeutic exercise programs, • Provide functional movement training and mobility work, • Educate patients on injury prevention and home programs, • Complete accurate, timely EMR documentation, • Use AI-assisted documentation tools and validate for accuracy, • Coordinate care with physicians and providers, • Communicate patient progress clearly Required • Active New Jersey Physical Therapist license in good standing, • Current CPR/BLS certification, • 1–3 years of outpatient or orthopedic physical therapy experience, • Experience in a multidisciplinary medical setting, • Familiarity with EMR systems, • Comfort working within structured workflows COMPENSATION & BENEFITS Salary: $85,000 – $100,000 per year Benefits include: • 401(k), • Health, dental, and vision insurance, • Paid time off, • Tuition reimbursement, • Modern clinical environment WORK LOCATION Madison, NJ In person Full-time role with rotating Saturday coverage required Job Type: Full-time Benefits: • 401(k), • Dental insurance, • Health insurance, • Paid time off

Pride Health is hiring an EEG Technician (Electroencephalography) to support our client’s medical facility based in Edison, NJ 08818. This is a 41-week assignment with the possibility of a contract-to-hire opportunity and a great way to start working with a top-tier healthcare organization! Job Title: EEG Technician (Electroencephalography) Location: Edison, NJ 08818 W2 Pay (Local): $25/hr - $32/hr Schedule: 10:00 AM – 6:00 PM Start date: 03/30/2026 Role Overview: The EEG Technician performs electroencephalography monitoring for patients in neurology and epilepsy surgery programs. The role involves operating EEG equipment, collecting brain activity data, monitoring patients during procedures, and supporting neurologists in diagnosing neurological conditions. Key Responsibilities: Conduct EEG tests and monitor patients for seizure activity. Collect patient seizure history and explain procedures to patients and families. Record and analyze electrophysiology data and adjust equipment as needed. Assist neurologists and neurosurgeons during EEG monitoring in labs or operating rooms. Recognize artifacts in recordings and apply appropriate electrode placements and montages. Maintain and troubleshoot EEG equipment in the monitoring unit. Provide training to staff and ensure patient safety during procedures. Requirements: High school diploma or GED Completion of an accredited EEG training program OR 2 years of EEG experience At least 1 year of EEG experience with both inpatient and outpatient patients English proficiency Experience with Evoked Potentials and Nerve Conduction studies Familiarity with EEG systems such as Natus NeuroWorks and Nihon Kohden Working toward ABRET EEG Certification Patient Population: Adult and pediatric patients in ICU and the Epilepsy Monitoring Unit (EMU). Pride Global offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors.

Wakefern Food Corp. is the largest retailer-owned cooperative in the United States and supports its co-operative members' retail operations, trading under ShopRite, Price Rite Marketplace, The Fresh Grocer, Dearborn Market, Gourmet Garage, Fairway Market, and Di Bruno Bros. Wakefern provides independent retailers with the tools, innovation, and operational support needed to compete in a big-business world. Our teams leverage advanced technology, private label development, and best-in-class procurement practices to help member companies deliver exceptional value and service throughout the communities we serve. Summary This role supports both Oracle E‑Business Suite (EBS) development and SAP operational support. The Oracle portion focuses on development, enhancements, and troubleshooting within the Financials suite, while the SAP portion centers on supporting SAP processes—especially SAP BDC, data validation, and financial workflows. Additionally, this role contributes to cross‑platform AI initiatives and financial analytics, helping the organization leverage data insights, automation opportunities, and process optimization across ERP systems. Essential Functions Oracle EBS Development: • Develop, support, and enhance Oracle E‑Business Suite Financials modules (GL, AP, AR, Purchasing, iProcurement, Fixed Assets)., • Troubleshoot technical and data-related issues using PL/SQL and SQL tools., • Write functional and technical specifications based on business requirements., • Develop reports, forms, workflows, and integrations using Oracle tools (Reports, Forms, APEX, BI Publisher, ADF)., • Collaborate with finance and business teams to analyze requirements, design solutions, and support end users., • Prioritize tasks, manage project milestones, and drive development activities to completion. SAP Support & Enhancements • Provide day-to-day SAP support with emphasis on SAP BDC ., • Build, test, and maintain SAP BDC scripts to support batch-input processes., • Troubleshoot SAP issues, perform root-cause analysis, and assist with configuration or master data validation., • Support functional teams across finance-related SAP processes and data flows., • Document SAP processes, support knowledge transfer, and provide user assistance as needed., • Additional Functions, • Support development of AI-driven automation, machine learning insights, and predictive analytics for finance operations., • Develop dashboards, data models, and cross-system reporting integrating Oracle and SAP data., • Participate in continuous improvement initiatives, system upgrades, and cross-functional IT projects., • Assist in data governance, data quality review, and financial reporting accuracy initiatives. Qualifications • BS in Computer Science, Information Systems, or equivalent professional experience., • Strong analytical and problem-solving skills with the ability to work independently., • Excellent written and verbal communication skills, especially translating business needs into technical solutions., • Ability to organize workload, manage priorities, and meet deadlines in a hybrid-tech environment. Preferred • 5+ years of experience with Oracle EBS Financials (GL, AP, AR, Purchasing, iProcurement, Fixed Assets)., • Proficiency in PL/SQL, SQL Plus, and writing SQL queries for troubleshooting., • Experience with Oracle development tools: Reports, Forms, APEX, BI Publisher, ADF., • Experience using TOAD for Oracle., • SAP experience including SAP BDC development and SAP finance processes., • Experience with AI/ML tools or financial analytics platforms (Power BI, SAP Analytics Cloud, Python, etc.)., • Familiarity with retail financial systems and operational workflows., • Experience with Oracle WebCenter (WFR, SOA, Capture, IPM) is a plus. Working Conditions & Physical Demands This position requires in-person office presence at least 4x a week in Edison, NJ

Pay Rate: up to $85/hr on w2 (No C2C or 3rd parties) Location: Onsite in Summit, NJ General Summary: Provides technical expertise in the areas of design, development, testing and production scale-up of new packaging component and systems. • Has package development knowledge or background to execute packaging work processes for packaging projects., • Compiles and analyses data, identifies causes, draws conclusions and reports, • Manages processes and ensures that activities and project goals are achieved through engagement with the X-functional team, manufacturing sites and externally with packaging vendors., • Responsible for maintaining compliance, consistency of practices and work quality, • Ability to manage multiple projects simultaneously involving package development, materials selection, and manufacturing process/site changes., • Support manufacturing investigations, by collaborating with cross-functional teams from commercial & supply chain to execute optimization of processes, packaging materials, and constructions to enable the business innovation, GP and ESG targets. Key Responsibilities: • Partner with the cross-functional team to execute package development activities with minimal supervision., • Problem-solving and critical thinking skills., • Demonstrates specialized knowledge, experience and skill in scientific analysis, • Strong project management skills, able to manage multiple priorities., • Leverage digital tools such as CAD, and/or modelling & simulation in projects., • Demonstrates flexibility and agility to manage conflicting priorities., • Executes projects with technical rigor and translates output into specifications., • Develop and drive alignment for packaging development plans with the franchise squads KPIs: • Demonstrates understanding of packaging development work process and technical strengths to independently deliver package development activities and risk assessments., • Communicates (both written and verbal), to convey complex information clearly and logically., • Problem-solving skills, with the ability to execute tasks independently, seeking guidance as required., • Able to adapt and re-prioritize to changing priorities., • 5Good interpersonal skills and ability to build effective working relationships at all levels in the organization Education: • BS / MS in Packaging technology., • Mechanical / Polymer, Plastics or Chemical Engineering Work experience: • 5+ years of new package development/Technology transfer in CPG, food, or pharmaceutical companies., • Must be able to work independently Job Requirements Fundamentals: • Packaging domain expertise, • Package regulation knowledge, • Knowledge of the external ecosystem, • Knowledge of digital workflows (CAD, M&S), • Leading self, • Project Management, • Communication Capability

Job Description At Valcor Engineering Corporation, we design and manufacture advanced fluid control components and systems for the aerospace, nuclear, and scientific industries. Our team is dedicated to innovation, precision, and quality—values that have made us a trusted name for over 70 years. Join a company that’s shaping the future of aerospace technology, one part at a time. Position Summary: We are currently seeking an experienced Deburrer to join our manufacturing team. In this role, you’ll play a critical part in the final preparation of precision aerospace components by removing imperfections and ensuring all parts meet rigorous quality standards. Under general supervision working from blueprints, sketches, verbal and/or written specifications, operates and adjusts manual or numerically controlled machine tools to perform standard and repetitive sequence of operations. Additional job duties are as follows: • Sets up manual machines where speeds, feeds and sequences of tooling operations are ordinarily prescribed, • Operates numerically controlled machines where programs are approved and setups are made and maintained by others., • Removes burrs and rough edges from machine component parts using a variety of hand operations, such as; filing, deburring and performing polishing operations., • Removes scratches, burrs and tool marks from parts, using microscope or magnifier., • Uses standard shop measuring devices., • Sharpens drill tools on grinding wheel as necessary., • Operates automatic welding equipment., • Moves parts and materials to and from work area., • Maintains good housekeeping in work area., • Minimum 4 years of experience in a general machine shop environment, • Skilled in deburring and hand-finishing aerospace or high-precision components, • Familiarity with using microscopes or magnifying equipment for detailed work, • Able to read and interpret blueprints and technical drawings, • Experience operating manual shop tools and measuring devices, • Strong eye for detail and commitment to quality, • Dependable, safety-conscious, and team-oriented Salary Range:$29.56 To $33.62 Hourly Why Join Valcor? ✅ Competitive pay & benefits package ✅ Work with cutting-edge aerospace technology ✅ Collaborative, clean, and safety-first work environment ✅ Long-standing company with stability and growth opportunities ✅ Convenient location: 2 Lawrence Road, Springfield, NJ 07081 Job location is at 2 Lawrence Road, Springfield, NJ 07081 Please note: The salary range is based on our market pay structure. However, individual salaries are determined by a variety of factors including, but not limited to, business considerations, local market conditions, and internal equity, as well as candidate qualifications, such as skills, education, and experience. Employee Benefits: At Valcor Engineering, we support our employees in all aspects of their life, including their health and financial well-being. Regular employees scheduled to work 30+ hours per week are offered: health, dental, and vision insurance; health savings accounts; a 401(k) savings plan; long term disability coverage; and life and accident insurance. We also have an employee assistance program. Our leave programs include Vacation and PTO time off, paid holidays, as well as other types such as bereavement, and any applicable federal and state sick leave. Employees may participate in the company recognition program to receive monetary or non-monetary recognition awards. We are an equal opportunity employer and do not discriminate on the basis of race, color, religion, sex, national origin, age, disability, genetic information, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. All qualified applicants will be considered for employment without regard to these characteristics. We're an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Company DescriptionValcor Engineering is one of the largest and most recognized suppliers of fluid control products in the aircraft, aerospace and military fields. We specialize in the design and manufacture of Solenoid Valves and control components for liquids and gases in critical application in the aerospace, nuclear, light industrial and scientific industries.Valcor Engineering is one of the largest and most recognized suppliers of fluid control products in the aircraft, aerospace and military fields. We specialize in the design and manufacture of Solenoid Valves and control components for liquids and gases in critical application in the aerospace, nuclear, light industrial and scientific industries.

Senior Analyst, Sales Operations, Basking Ridge, NJ Who We Are Aucta Pharmaceuticals is an emerging product development pharmaceutical company.We are on our way to becoming a significant specialty pharmaceutical company in the U.S. marketplace integrating R&D, manufacturing, and commercialization. We focus on improved dosage forms for patients with a therapeutic focus in CNS and select orphan drug disease states. Aucta successfully launched its first branded product, Motpoly XR, in the epilepsy space with a targeted sales force in March 2024 and an expanded presence of 20 field sale territories and 3 inside sales positions in late 2024. Our objective is to enhance our marketing, managed care, and sales capabilities to support future pipeline products in neurology over the coming years. Position Description The Senior Analyst, Sales Operations, is a key member of Aucta’s Commercial Operations team and plays a critical role in enabling sales effectiveness, operational execution, and data-driven decision-making across the organization. This role serves as the primary point of contact and vendor manager for core Sales Operations platforms, including Veeva CRM, MMIT, and Power BI, and is responsible for managing core quarterly commercial processes such as Incentive Compensation updates, targeting changes, sales force size and structure adjustments, and system governance. In addition, this position leads the development and maintenance of training materials and delivers training for both field and inside sales and home office teams across Commercial Operations tools and platforms. This is a highly visible, hands-on role in a fast-growing environment that requires strong analytical skills, operational rigor, comfort working cross-functionally, and the ability to translate complex data and systems into clear, actionable guidance for the business. The role reports to the Director of Sales Operations. Primary Responsibilities: Sales Operations & Vendor Management • Serve as the primary point of contact and internal owner for Sales Operations tools and vendors, including Veeva CRM, MMIT, Power BI, and related commercial analytics platforms., • Manage vendor relationships, system enhancements, issue resolution, upgrades, and roadmap discussions to ensure tools meet evolving business needs., • Own and manage the quarterly change process for:, • Incentive compensation plan updates and calculations, • Targeting and call plan changes, • Sales force size, structure, and territory adjustments, • Ensure timely, accurate execution of all changes and clear communication with stakeholders., • Support forecasting, goal setting, and sales performance tracking activities. Analytics & Reporting • Utilize advanced Excel, SQL, and Power BI to analyze sales performance, trends, and operational KPIs., • Build, maintain, and enhance dashboards and reports to support Sales leadership, Commercial Operations, and Executive leadership., • Partner cross-functionally to translate business questions into data-driven insights. Training & Enablement • Develop, maintain, and continuously improve training materials (guides, SOPs, slide decks, job aids) for Sales Operations tools and processes., • Conduct training sessions for field and inside Sales and home office associates on:, • Veeva CRM functionality and best practices, • MMIT data usage and interpretation, • Power BI dashboards and reporting, • Other Commercial Operations platforms as needed, • Collaborate closely with Sales, Marketing, Managed Care, Finance, and leadership to support commercial execution., • Participate in sales meetings, planning sessions, and plan-of-action meetings as needed., • Bachelor’s degree in Business Administration, Finance, Analytics, Information Systems, or a related field., • 3-5+ years of experience in Sales Operations, Commercial Operations, or analytics roles, preferably within the pharmaceutical or healthcare industry., • Hands-on experience with Veeva CRM, MMIT, and Power BI strongly preferred., • Advanced proficiency in Microsoft Excel (including complex formulas and data modeling); SQL experience preferred., • Strong understanding of sales force structure, targeting, incentive compensation, and CRM processes., • Demonstrated ability to manage vendors and cross-functional stakeholders., • Strong communication and training skills, with the ability to explain technical concepts to non-technical audiences., • Highly organized, detail-oriented, and able to manage multiple priorities in a fast-paced environment. This position is based at our Basking Ridge, NJ site. It is an office-based role, requiring presence 5 days a week. The selected candidate must be able to commute to Basking Ridge, NJ Salary Range Aucta Pharmaceuticals considers a combination of education, experience, internal equity, and external market data when determining compensation. • Base Salary: $80,000 – $110,000 (commensurate with experience), • Bonus Incentive: 10% Benefits Aucta offers a competitive benefits package, including: • Medical, Dental, and Vision Insurance, • 401(k), • Life Insurance, • Short- and Long-Term Disability, • Paid Time Off (PTO) Aucta Pharmaceuticals is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. Please refrain from forwarding unsolicited resumes from agencies to Aucta Pharmaceuticals. Aucta is not liable for any fees incurred from the use of resumes from this source. We only compensate agencies with whom we have a formal agreement. For recruitment inquiries, please reach out directly through this post Applications will be accepted until the position is filled.

Title- Hospital Credentialing Specialist Pay range offered- $30-35/hr W2 37.5hrs/week Location- Summit, NJ 07901 Duration- 03+ months contract with strong possible extension Client- Direct Hospital Client 8a - 4p Focuses on verifying a healthcare provider’s qualifications (education, licenses, certifications, work history) to ensure they meet regulatory and organizational standards. NOT INSURANCE ROLE Duties: Essential Functions: Enforce regulatory compliance and quality assurance Prepare and maintain reports of credentialing activities such as accreditation, membership or facility privileges Ensure that all information meets legal, federal and state guidelines when processing applications Responsible for carrying out various credentialing processes in relation to physicians and allied health practitioners Process applications for initials applicants as well as reappointments (approximately 125-200 quarterly) Collect and process significant amounts of verification and accreditation information Maintain and update accurate information in the Echo database (includes education, training, experience, licensure) Prepare material for Credentials Committee meeting, MEC as well as Board of Trustees meeting Sets up and maintains provider information in Echo Maintains confidentiality of provider information Ensure compliance with the Bylaws at each location as it pertains to the credentialing process Schedule, and on occasion attend and take minutes for site based medical staff department meetings Process and collect dues for the site based medical staff Compiles and maintains current and accurate data for all providers Sets up and maintains provider information in online credentialing database Tracks license and certification expirations for all providers Maintains confidentiality of provider information All other duties as assigned Skills: Education: Qualifications: Knowledge of the credentialing process required Ability to organize and prioritize work and manage multiple priorities Excellent verbal and written communication skills Ability to research and analyze data Ability to work independently Ability to establish and maintain effective working relationships Excellent computer skills

Job Title : Tax Compliance Analyst Location: Berkeley Heights, NJ (3 days onsite a week) Direct Client The Tax Compliance Analyst III is responsible for preparing and filing accurate sales and use tax returns while ensuring compliance with state and local tax regulations. This role supports general ledger tax accounts, handles tax-related inquiries, conducts research on tax issues, and collaborates with internal teams to improve processes and maintain compliance. Key Responsibilities: • Prepare and file accurate and timely sales and use tax returns, • Prepare monthly sales/use tax journal entries, reconciliations, and supporting working papers, • Assist in determining nexus and identifying filing requirements across US state and local jurisdictions, • Register for tax compliance in applicable jurisdictions, • Respond to state and local tax notices and inquiries, • Conduct research on various tax issues, • Collaborate with corporate and divisional teams across departments, • Continuously improve processes and productivity, • Support special compliance and audit projects as assigned Required Qualifications: • Bachelor’s degree in Accounting or Finance, • Minimum 5 years of tax compliance experience, • Experience with SAP or equivalent financial software, • Experience with Taxware or other tax compliance software, • Strong proficiency in MS Office applications, • Strong analytical and communication skills, • Ability to work independently with a sense of urgency, • Strong organizational skills with attention to detail and ability to multitask, • Familiarity with general accounting concepts, practices, and procedures

Location: Madison, NJ Job Type : Full Time Compensation: $150,000 – $250,000 base salary + performance incentives Date Posted: February 20th , 2026 ABOUT MADISON MEDICAL Madison Medical is redefining modern healthcare through a physician-led, multidisciplinary model focused on outcomes, innovation, and a world-class patient experience. We deliver integrated care across primary care, sports medicine, pain and spine, rehabilitation, chiropractic, regenerative therapies, hormone optimization, metabolic medicine, allergy services, podiatry, and wellness-based medicine. Our model combines advanced diagnostics, high-level specialty collaboration, and proactive care strategies that prioritize performance, prevention, longevity, and long-term patient outcomes. We operate with high clinical and operational standards, and we believe that communication, patient education, and team alignment are essential parts of the medicine itself. POSITION OVERVIEW Madison Medical Sports & Rehabilitation Center is not a traditional primary care clinic, and this is not a conventional Internal Medicine role. We are seeking an Internal Medicine-trained physician (MD or DO) to serve as a Primary Care and Sports Medicine hybrid provider. This physician will manage an adult primary care panel while also integrating musculoskeletal and sports medicine care, regenerative medicine, hormone optimization, and metabolic performance care. This role is ideal for a physician who wants to practice full-scope adult internal medicine in a modern, outcomes-driven environment focused on function, vitality, and prevention, not symptom management alone. The physician will work in a collaborative care model alongside chiropractors, physical therapists, nurse practitioners, regenerative specialists, and pain/spine providers to ensure seamless, coordinated patient care. This position is intended for Internal Medicine-trained physicians and is not designed for PM&R/Physiatry specialists. CLINICAL FOCUS AREAS The ideal candidate will have experience or strong interest in: • Adult primary care (acute visits, chronic disease management, preventive medicine), • Sports medicine and musculoskeletal evaluation/treatment, • Cardiometabolic risk management (HTN, lipids, diabetes, insulin resistance), • Metabolic medicine and medical weight loss optimization, • Male and female hormone optimization (TRT, HRT, peptides), • Regenerative therapies (PRP, shockwave therapy, IV therapy/hydration), • Longevity, wellness, and performance-based medicine, • Allergy testing and immunotherapy protocols (training supported) KEY RESPONSIBILITIES The Primary Care and Sports Medicine Physician will: • Serve as a primary care provider for an adult patient panel, • Evaluate, diagnose, and treat acute and chronic medical conditions, • Develop individualized treatment plans focused on outcomes and long-term health, • Manage musculoskeletal complaints and sports-related injuries, • Order and interpret labs, imaging, and diagnostic testing, • Integrate hormone, metabolic, and performance medicine into care plans when appropriate, • Perform or train into fluoroscopy-guided spine/joint procedures, • Provide regenerative therapies and wellness-based treatment protocols as credentialed, • Participate in allergy testing and immunotherapy care protocols, • Educate patients on prevention, wellness, longevity, and performance optimization, • Coordinate care across Madison Medical’s multidisciplinary team, • Maintain accurate, timely, and compliant medical documentation, • Support quality improvement initiatives and clinical standards Clinic schedule aligns with Madison Medical’s existing physician/provider model. • Full-time position, • Patient volume expectations consistent with other physician roles, • Base Salary: $150,000 – $250,000 annually (based on experience and clinical fit), • Bonus Incentives: Generous performance-based compensation tied to productivity, quality metrics, and practice growth Madison Medical offers a competitive benefits package including: • Health insurance (employer-paid or high employer contribution depending on plan), • Dental insurance, • Vision insurance, • Life insurance, • 401(k) with employer contribution, • 10+ days paid time off starting year one, • Paid holidays Required: • MD or DO from an accredited medical school, • Board Certified or Board Eligible in Internal Medicine (required), • Active New Jersey medical license (or eligibility to obtain), • Strong ability to manage adult primary care patients longitudinally, • Excellent clinical judgment and patient communication skills, • Comfort practicing in both insured and cash-based models, • Sports medicine experience or fellowship training strongly preferred, • Experience in hormone optimization, metabolic medicine, or wellness optimization, • Experience with or willingness to train in fluoroscopy-guided procedures, • Familiarity with allergy testing and immunotherapy protocols This is a rare opportunity to practice Internal Medicine in a setting that blends: • True primary care continuity, • Sports and musculoskeletal medicine, • Advanced procedures and regenerative therapies, • Hormone and metabolic optimization, • Collaborative multidisciplinary infrastructure

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 ___.

Job Description CNC MILL MACHINIST / SET UP - All Shifts -- Manufacturing/Machine Shop N.J. Precision Technologies, Inc. – Mountainside, NJ Job Description PLEASE READ BEFORE APPLYING: • MINIMUM 5 YEARS SET-UP EXPERIENCE - CNC MILLING or TURNING SET-UP EXPERIENCE REQUIRED, • FULL TIME : FIRST SHIFT, SECOND SHIFT, THIRD SHIFT, WEEKEND SHIFTS AVAILABLE, • ALL HAAS CNC MACHINES and Kitamura, • STRONG WORKING KNOWLEDGE OF SET-UP TECHNIQUES FOR PRODUCTION AND PROTOTYPE., • STRONG WORKING KNOWLEDGE OF CNC PROGRAMMING AND EDITING WITH G & M CODES OR PROGRAMMING SOFTWARE., • ABILITY TO SET-UP & OPERATE USING VICES OR SIMILAR TOOLING HARDWARE AND FIXTURES., • MUST HAVE EXPERIENCE INSPECTING PARTS AND READING MICROMETER , CALIPER, HEIGHT GAGE AND DIAL INDICATOR, • BLUEPRINT READING A MUST. Responsibilities • Performs SET UP, PROGRAM TEST, FIRST PIECE "PROVE-OUT" RUN, in-process inspections, and CNC of precision-machined parts., • Works with production and engineering teams to address and resolve production issues in CNC Milling., • Responsible for selecting correct tooling hardware and measurement equipment., • Responsible for ensuring that the machines are well maintained ., • Working in accordance with ISO requirements., • Education: High school diploma or GED., • Experience: Minimum 5 years CNC Machining / Milling experience in a machine shop or manufacturing environment., • Measurement and inspection skills a must., • Strong knowledge of Blueprint reading with GD&T required., • Must have a strong aptitude in mechanical blueprints and drawings, • Must have a working knowledge of CAD systems., • Must be very detail oriented., • Strong math skills., • Ability to follow process plans, routers and inspection plans., • Has a strong background with workplace safety, OSHA regulations., • Must be able to effectively communicate with employees of varying education levels., • Comfortable working with very tight , "tenths" tolerances., • Must be experienced in measuring tools such as micrometers, calipers, height gage, dial indicators. 1.0 JOB DESCRIPTION SUMMARY 1.1 This position establishes the authority, reporting relationships, tasks and duties with performance standards for the CNC Specialist. 2.0 JOB TITLE 2.1 CNC Specialist 3.0 REPORTING RELATIONSHIPS 3.1 The CNC Specialist reports to the CNC Manager. 4.0 REQUIREMENTS 4.1 Education Required: High School diploma or GED. Preferred: Vocational School Certificate / Associates degree in Mechanical, MFG, IND Engineering technology. 4.2 Licensing, Registration, and certification Required: None. Preferred: None. 4.3 Experience Required: A minimum of one year experience in CNC or tooling production. 4.4 Skills, Knowledge, Abilities 4.4.1 Must have strong math skills. 4.4.2 Ability to read and understand engineering drawings. 4.4.3 Must be able to effectively communicate with other employees of varying education levels. 4.5 Physical Requirements 4.5 The physical requirements are stressful with the majority of time spent standing working with machinery. This position requires manual dexterity of the hands and the normal bending and twisting associated with plant operations. Walking, turning the head and torso, reaching, grasping, bending, stooping, kneeling and flexing the arms, legs, wrists, and fingers and the ability to lift at least forty (40) pounds. Must be able to work in areas with moderate to high noise levels. Must be able to constantly kneel, squat, climb and have full bending abilities at the waist (touch the toes). The body senses of sight (not color blind), hearing (safety) is required. Good vision to read diagrams and business documents. Must be able to wear safety glasses and hearing protection for prolong periods of time. 4.6 Mental: Basic math skills, mechanical engineering understanding, blueprint reading, as well as reading, writing and spelling and the ability to communicate clearly and effectively in English. 5.0 WORKING CONDITIONS 5.1 The majority of the time (95%) will be spent in a non-smoking plant environment. Temperatures will remain consistent throughout the year. Noise levels will be high in the plant area and moderate in the office area. Work hours will be dependant upon the weekly production and shipping schedules. Work hours may be long when specific projects are due, therefore, some extended schedules will be necessary. 6.0 TASKS AND DUTIES 6.1 Responsible for the proper operation of the machines. 6.2 Responsible for performing the daily machine set up process – clean the machine, complete the set up the machine for the first job. 6.3 Responsible for producing high quality finished products in accordance with the customer’s requirements. 6.4 Responsible for completing the job within the allotted job budget dollars. 6.5 Completes the bead blasting process when necessary. 6.6 Responsible for the proper operation and maintenance of the machines. Ensures the machine is maintained on a preventative basis. 6.7 Responsible for the machine programming functions. 6.8 Responsible for performing a quality control check on all jobs. 6.9 Responsible for setting up the machines for optimized speed and performance. 6.10 Responsible for completing the work in a safe manner. 6.11 Responsible for ensuring the shop area is clean and organized. 6.12 Responsible for accurately recording the time spent against the appropriate job. 6.13 Responsible for completing the work in accordance with ISO 9000 standards. 6.14 Responsible for working closely with the Manager with the development and implementation of the agreed upon training plan and schedule. 6.15 Ensures personal adherence to the company policies and practices. 6.16 Performs any other duties as may be assigned by the Manager. 7.0 MEASUREMENTS OF PERFORMANCE 7.1 Ability to produce each job in accordance with the customer’s requirements. 7.2 Ability to produce each job in accordance with the allotted number of production hours and optimize. 7.3 Ability to set-up as per the plot/print/router/set-up sheets in a timely manner. 7.4 Ability to edit programs (G & Mo codes and/or Mastercam) for efficient and practical parts production. 7.5 Ability to transmit program from database to local PC and to machines. 7.6 Ability to account and record the hours spent per job. 7.7 Consistently maintains the work area in a clean, organized and professional manner – ie: clean floors, machines, tools secured, etc. 7.8 Ability to work with minimal supervision. 7.9 Ability to service and maintain the machines to eliminate/minimize machine downtime 7.10 Ability to adhere to the company’s policies and procedures. 7.11 Has demonstrated a working knowledge level of the standard operating procedures as defined by ISO 9000. 7.12 Ability to work within the company’s safety practices and procedures. 7.13 Ability to complete the assigned training schedule. Company DescriptionNew Jersey Precision Technologies, Inc. is a high-tech Manufacturer located in Mountainside, New Jersey. We specialize in electrical discharge machining (EDM) and precision manufacturing of all mechanical components for the aerospace and medical device industries as well as tooling for the plastics industry and stamping industry. Our modern facility is fully climate controlled and utilizes more than 60 EDM and CNC machines. Our EDM & CNC departments are running 24 hours per day, 7 days per week. Our CNC Lathe, CNC Mill, Sinker EDM, Wire EDM & Small Hole Drilling EDM machines are state-of-the-art and the latest generation available. Our CNC Technicians and Electrical Discharge Machining technicians perform CNC Programming, CAD, Automated Set-ups and efficient production & prototype operations. NJPT believes in continual improvement programs including continual employee training programs. In addition to off sight custom training, in-house training and other learning methods, NJPT offers a complete tuition reimbursement program from those FULL-TIME individuals who may want to earn or complete a college degree. The NJPT FULL-TIME benefits package is outstanding with matching 401K retirment plan, profit sharing, Medical plan, Prescription plan, Dental & Optical plans, Credit Union, etc. NJPT is a US Department of Defense contractor and controlled by ITAR (International Traffic in Arms) government regulations to only hire citizens of the United States or those individuals with a US permanent resident green card. An equal opportunity employer, NJPT is committed to its employees and employee satisfaction. NJPT is a great place to work and a great place to grow. Please visit our Website: Jersey Precision Technologies, Inc. is a high-tech Manufacturer located in Mountainside, New Jersey. We specialize in electrical discharge machining (EDM) and precision manufacturing of all mechanical components for the aerospace and medical device industries as well as tooling for the plastics industry and stamping industry. Our modern facility is fully climate controlled and utilizes more than 60 EDM and CNC machines. Our EDM & CNC departments are running 24 hours per day, 7 days per week. Our CNC Lathe, CNC Mill, Sinker EDM, Wire EDM & Small Hole Drilling EDM machines are state-of-the-art and the latest generation available. Our CNC Technicians and Electrical Discharge Machining technicians perform CNC Programming, CAD, Automated Set-ups and efficient production & prototype operations. NJPT believes in continual improvement programs including continual employee training programs. In addition to off sight custom training, in-house training and other learning methods, NJPT offers a complete tuition reimbursement program from those FULL-TIME individuals who may want to earn or complete a college degree. The NJPT FULL-TIME benefits package is outstanding with matching 401K retirment plan, profit sharing, Medical plan, Prescription plan, Dental & Optical plans, Credit Union, etc. NJPT is a US Department of Defense contractor and controlled by ITAR (International Traffic in Arms) government regulations to only hire citizens of the United States or those individuals with a US permanent resident green card. An equal opportunity employer, NJPT is committed to its employees and employee satisfaction. NJPT is a great place to work and a great place to grow. \r\nPlease visit our Website:

Our client, a well-regarded regional defense litigation firm is seeking a Team Lead to join their Cherry Hill, NJ team. The ideal candidate will have 10+ years of general liability or insurance defense related experience as well as experience leading/training other attorneys. This position is hybrid remote, 2 days remote, 3 days in office per week. This is a partnership track position. Candidates should be admitted to practice in NJ. Competitive base salary 150k to 165k+, bonus and benefits.

Well-regarded regional defense litigation firm is seeking a general liability attorney to join their Cherry Hill, NJ team. The ideal candidate will have 1 to 30+ years of general liability or insurance defense experience. In this position, the attorney will manage their own case files. Trial experience is welcome but not required. This position is hybrid remote, 2 days remote, 3 days in office per week. This is a partnership track position. Competitive base salary 95k to 175k+, bonus and benefits.

About the Company What Makes Stephen Gould Exceptional Founded through a passion for entrepreneurship, our success is due to the ingenuity and tenacity of our extraordinary teams, bringing people and ideas together. With Stephen Gould, everything is within reach—including an exciting career opportunity. We want you to join our team and build on our incredible 80-plus years of excellence. Stephen Gould looks for people who want to design and develop exciting solutions for a variety of engaged and passionate clients across the globe. With headquarters in Madison, New Jersey, 40 locations throughout the U.S., and operations in six countries outside the U.S., we have grown tremendously while staying true to our 5 Principles: ___ About the Role What will I do? As a Legal Assistant, you will provide high-level administrative support to the Legal team in our corporate headquarters located in Madison, NJ. Stephen Gould offers a hybrid work environment, with this role requiring at least three (3) days per week in office. The office is a busy hub for Stephen Gould, and in this role, you must be comfortable communicating with all levels of employees, be highly organized and detailed oriented, and driven to adhere to deadlines in a fast-paced setting. Responsibilities • Provide high-level operational and administrative support to the Legal team., • Schedule meetings and manage calendars., • Draft and format routine correspondence, memos, and cover letters., • Assist with file and document management, including signature logistics., • Assist with contract operations, including routing contracts for signature, and tracking contract execution status., • Handle certificate of insurance requests and support customs inquiries., • Provide litigation support, such as litigation hold administration, docket calendar management, coordination with outside counsel and insurance carriers, and monitoring discovery compliance., • Perform other duties as assigned. Qualifications • 5+ years of administrative experience supporting a legal team or in a legal operations environment., • Associate degree in business or related discipline preferred., • Experience working in a corporate sales or a service operations related environment preferred. Required Skills • Basic understanding of legal procedures, requirements, and litigation processes., • Excellent proofreading and grammar skills., • Strong attention to detail and ability to multi-task effectively., • Excellent communication skills, including responsiveness to time-sensitive requests and the ability to route urgent matters appropriately., • High proficiency in Microsoft Word, Excel, Outlook and virtual communication and collaboration tools including Microsoft Teams, Webex and Zoom., • Familiarity with AI tools to support legal operations and document workflow. Pay Range and Compensation package Salary range: $60,000 - $82,000. This position is eligible for benefits, including paid time off, sick time, medical and dental benefits, and 401K contribution and company matching. Equal Opportunity Statement THIS POSITION DESCRIPTION IN NO WAY SATES OR IMPLIES THAT THESE ARE THE ONLY DUTIES TO BE PERFORMED BY THE EMPLOYEE(S) INCUMBENT IN THIS POSITION. EMPLOYEES WILL BE REQUIRED TO FOLLOW ANY JOB-RELATED INSTRUCTIONS AND TO PERFORM ANY OTHER JOB-RELATED DUTIES REQUESTED BY ANY PERSON AUTHORIZED TO GIVE INSTRUCTIONS OR ASSIGNMENTS. Stephen Gould is an equal opportunity employer. Applicants requiring a reasonable accommodation to participate in the hiring process should contact Human Resources.

Edison, NJ | Hybrid (1-3 days in office) About This Role We're looking for an experienced immigration attorney who's tired of the billable hour grind and wants to actually practice law (not just track time in six-minute increments). You'll handle a diverse caseload: adjustment of status, H-1Bs, E-2 investor visas, nonimmigrant visas, and removal defense. You'll have real autonomy to run your cases, a skilled team of paralegals and support staff to back you up, and a managing attorney. What Makes This Different • No billable hour pressure. We measure success by outcomes, not timesheets., • Actual work-life balance. Flexible schedule. Hybrid setup. We mean it., • A team that has your back. Experienced paralegals and support staff who know what they're doing., • A beautiful private office when you're in-person., • Women-owned, minority-led firm with a culture built on respect and integrity. What You'll Do • Conduct client consultations to assess case viability and develop legal strategy, • Manage a varied immigration caseload from intake through resolution, • Appear in immigration court for removal defense matters, • Prepare and file petitions, applications, and supporting documentation, • Provide legal counsel to clients navigating complex immigration issues, • Stay current on immigration law and policy changes, • Lead and mentor paralegals and support staff on your cases What We're Looking For • JD and license to practice in the U.S. (NJ Bar admission preferred), • 3-5+ years of immigration law experience, • Immigration court experience required, • Proficiency with case management software and immigration e-filing systems, • Growth mindset and leadership instincts Compensation & Benefits • Competitive salary: $100,000 – $130,000 (commensurate with experience), • Medical stipend, • PTO, • Flexible schedule About Us The Law Office of Abhisha Parikh is an immigration-focused practice in Edison, NJ. We handle everything from family-based petitions to complex employment visas to removal defense. We believe in responsiveness, accessibility, and treating clients with dignity—and we extend that same respect to our team.

Based in Woodbridge, NJ, we are a multidisciplinary law firm known for its client-focused approach collaborative culture and commitment to delivering practical results. The Woodbridge office is expanding and seeking an experienced Defense Paralegal to join a growing team handling sophisticated commercial motor vehicle defense UM/UIM premises liability construction accident and product liability matters. This role is ideal for a seasoned professional who values substantive legal work mentorship opportunities and long-term professional stability within a supportive firm environment. Responsibilities • Conduct independent subpoena review and summarization of discovery responses and medical records with complete accuracy and efficiency, • Schedule notice confirm and produce all records related to Independent Medical Examinations while calendaring relevant deadlines with strong follow-up, • Draft motions to compel sanctions motions for extraordinary relief and motions to enforce subpoenas with precision and attention to detail, • Perform verdict searches docket searches social media investigations and background searches while working collaboratively in a high-volume fast-paced environment Qualifications • Paralegal certificate or bachelor's degree required, • 5+ years of experience as a defense paralegal (commercial motor vehicle defense UM/UIM premises liability construction accident and product liability experience preferred), • Strong organizational communication and time management skills with the ability to thrive in a fast-paced high-volume environment, • Proficiency with Microsoft Office 365 ProLaw Excel and e-document management software preferred Join Us This is an excellent opportunity for an experienced paralegal seeking defense litigation exposure, mentorship and long-term stability. If this sounds like a fit, we encourage you to apply today

Our client, a well-regarded regional defense litigation firm, is seeking an attorney to join their Northern NJ team. The ideal candidate will have 3+ years of general liability or related experience. This position is hybrid remote and partnership track position. Candidates should be admitted to practice in NJ and NY. Competitive base salary 130k to 170k, bonus and benefits. Resumes may be sent to for review.

Job Description Class A CDL Tow Truck Driver or Vehicle Transport Driver Edison, NJ 08837 Class A CDL Truck Driver Summary: • Exciting opportunity for a growing forklift company for a Class A CDL Truck Driver for local heavy equipment deliveries. We are seeking someone who is mechanically inclined, has great people skills, and a desire for something more! If you can work with your hands, like to deal directly with the customer, and take pride in your work. This job will allow you to grow with our business and work directly with ownership in a fast-paced environment. We are seeking Truck Driver who can problem solve and think independently while completing tasks accurately and efficiently RESPONSIBILITIES: • Work independently to transport needed forklifts to and from customer locations with a commercial truck, • Drive vehicles to deliver and pick up forklifts/aerial lifts as needed, • Stock and assist with moving of forklifts and equipment, • Maintain tools, equipment, and delivery truck in efficient operating condition, keep clean (inside & out), • Unload and load forklifts, tie down and related items from the truck as required, • Lift a minimum of fifty-five (55) pounds, • Ability to maintain and follow written documents as instructed, • Ability to location customer's location and use GPS to follow, • Ability to operate forklifts, • Follow all safety and OSHA requirements while at a customer facility or at the company's location SKILLS REQUIRED: • Safely operate a heavy or tractor-trailer truck, • Load and unload cargo/forklifts along with tying down the equipment, • Properly track and document activity log, • Report any issues or incidents to dispatch, • Inspect truck before and after a trip, • Perform a repeated and repetitive movement QUALIFICATIONS: • Previous experience in truck driving or other related fields, • Able to drive a manual shift, • High School diploma or general education degree (GED), • Must meet and maintain qualifications for Commercial Drivers, • Commercial driver's license, • OSHA certified in forklift safety is a plus, • Self-starter and can work independently, • Great organizational and multi-tasking skills, • Ability to handle physical workload, • Strong work ethic, • Exceptional Driving record BENEFITS: • Union Pension Plan, • Medical, Dental, Vision benefits available, • Vacation Time, • Retirement Plan Opportunities, • Overtime Opportunities, • Competitive wages, • Supplemental Pay (bonus pay, commission pay, signing bonus) Starting Salary Range: $22-30 an hour All candidates will be required to submit to drug screening and motor vehicle background checks. We are an equal opportunity employer, and we are an organization that values diversity. We welcome applications from all qualified candidates, including minorities and persons with disabilities. req22-01200

Company Description Busy solo practitioner in Clark, NJ, focusing on Personal Injury Litigation, Workers Compensation, Municipal Court and Real Estate. This position for Personal Injury Litigation. Role Description This is a full-time, on-site role for a Litigation Paralegal based in Clark, NJ. The Litigation Paralegal will be responsible for legal document preparation, reviewing documents, conducting legal research, drafting pleadings, and preparing motions. Additional tasks may include organizing case files, coordinating with attorneys and clients, and ensuring case deadlines are met. Seeking a motivated, hard working individual who is able to manage a heavy caseload, all while maintaining their humanity and sense of humor.....because if you can't find a reason to laugh, you're doing something wrong! In need of a knowledgeable, reliable and competent "right-hand" man/woman who is able to work independently and understands the importance of generating solid work with attention to detail . Candidate will work along side a junior paralegal who assists on the pre-litigation matters. Salary is commensurate with experience. Qualifications • Personal Injury Law: 3 years experience., • Proficiency in Legal Document Preparation and Document Review, • Strong skills in Legal Research and understanding legal procedures, • Experience with drafting Pleadings and preparing Motions, • Excellent organizational and time management skills, • Strong attention to detail and ability to work in a fast-paced legal environment, • Knowledge of New Jersey legal system and procedures is a plus, • Bachelor's degree in Legal Studies, Paralegal Studies, or related field preferred, • Paralegal certification is highly desirable, • Bilingual is preferred, but not required