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Job Description🚨 Industry-Leading Manufacturing Company in Orangeburg, NY is URGENTLY Hiring Cleanroom Production Compounders! 🚨 💼 Position: Cleanroom Production Compounder 📍 Location: Orangeburg, NY 💰 Pay: $17–$18/hour + Shift Differential 🕒 Shifts Available: • 2nd Shift: 3PM–11PM ($0.50/hr differential), • 3rd Shift: 11PM–7AM, Sunday–Thursday ($1.00/hr differential), • Compound liquids following GMP and daily production schedules, • Stock production floor with required materials, • Remove empty barrels and manage warehouse logistics, • Maintain cleanliness and organization of the work areaMust-Have Qualifications:, • High School Diploma or GED, • 0–2 years of chemical handling/mixing experience preferred, • If no compounding experience, warehouse/manufacturing experience is a plus, • Strong math and communication skills, • Team-oriented, go-getter mentalityNice-to-Have Skills:, • Blending, • Batch making ✅ Tons of room for upward mobility ✅ Union eligibility upon permanent hire ✅ Basic maintenance mechanic training ✅ Opportunity for overtime Pay and Benefits The pay range for this position is $17.00 - $18.00/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, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Orangeburg,NY. Application Deadline This position is anticipated to close on Sep 26, 2025. 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.

One of our clients is currently seeking a plant manager. They are a leading provider in the meat processing industry, known for our commitment to quality, safety, and operational excellence. As we continue to expand, we are seeking a seasoned Plant Manager to lead our facility and ensure smooth, efficient, and compliant operations. Position Overview The Plant Manager will be responsible for overseeing all aspects of daily operations within the meat processing facility. This includes managing production, ensuring regulatory compliance, optimizing performance, and leading a team of supervisors and staff. The ideal candidate will bring strong leadership, industry expertise, and a passion for continuous improvement. Key Responsibilities • Direct and manage plant operations including production, maintenance, quality assurance, and logistics, • Ensure compliance with USDA, FDA, OSHA, and other applicable regulations, • Monitor and improve key performance indicators (KPIs) across departments, • Develop and implement strategies to enhance productivity and reduce operational costs, • Lead and mentor plant personnel, fostering a culture of safety and accountability, • Collaborate with senior leadership on budgeting, forecasting, and strategic planning, • Bachelor’s degree in Food Science, Engineering, Business, or a related field (preferred), • Minimum of 5 years’ experience in meat processing or food manufacturing, with at least 3 years in a leadership role, • Strong knowledge of HACCP, GMP, and food safety protocols, • Proven leadership and team management skills, • Excellent communication, problem-solving, and organizational abilities, • Bilingual (English/Spanish) is a plus

Links Technology is currently seeking a motivated and skilled Project Manager (Pre-Clinical Development) to join our client's team in Tarrytown, NY. Our client is a leading Pharma/Biotech firm. This is a long-term contract role offering a hybrid work schedule of 4 days onsite. Responsibilities of the Project Manager Project Manager (Pre-Clinical Development): • Act independently to execute highly complex or specialized IT projects, ensuring they deliver on scope, schedule, cost, and quality., • Drive the discovery phase to gather initial requirements and business goals, establishing a validated business case with stakeholders., • Implement and maintain project plans, budgets, and staffing requirements, providing overall direction to the project team., • Manage and control changes throughout the project lifecycle, while proactively mitigating risks and resolving issues to keep the project on track., • Oversee third-party vendor resources to ensure day-to-day execution aligns with project goals and contractual obligations., • Provide clear and effective project status updates to all stakeholders, anticipating challenges and communicating dependencies, issues, and risks., • Collaborate with cross-functional teams to ensure consistent and collaborative project delivery., • Lead the customization and integration of Commercial Off-The-Shelf (COTS) applications, ensuring tailored solutions meet specific business requirements., • Train individuals and teams on industry-recognized project management standards and methodologies., • Bachelor's (BA/BS) Degree in a related field such as Computer Science., • Experience working with LIMS, ELN, or AWS, • Familiar with Bioanalytical Sciences including Assay Development, Bioanalysis, Quality Control and Scientific Writing., • Understanding of Pharma-FDA reporting processes and regulatory submission standards (ICH, DIA CTD), • PMP certification or equivalent., • Experience with agile and/or waterfall-based delivery approaches., • Proficiency in project management tools like Microsoft Project and experience with Jira and Atlassian tools., • A demonstrated track record of delivering high-quality, successful, and on-budget projects. Benefits of the IT Project Manager: • MUST be able to work onsite 4 days per week in Tarrytown, NY, • 10 Days PTO, • Health, Dental, and Vision Insurance, • Matching 401k, • Pay Range: $95/hr - $110/hr

Job Description JOB TITLE: Manufacturing Technician LOCATION: Hawthorne, NY (on-site) TYPE: Full time, regular COMPENSATION: $25.00/hr - $30.00/hr Clarapath is a medical robotics company based in Westchester County, NY. Our mission is to transform and modernize laboratory workflows with the goal of improving patient care, decreasing costs, and enhancing the quality and consistency of laboratory processes. SectionStar™ by Clarapath is a ground-breaking electro-mechanical system designed to elevate and automate the workflow in histology laboratories and provide pathologists with the tissue samples they need to make the most accurate diagnoses. Through the use of innovative technology, data, and precision analytics, Clarapath is paving the way for a new era of laboratory medicine. Role Summary: The Manufacturing Technician will play a key role in supporting the production and assembly of our advanced electro-mechanical device, SectionStar™, as part of a close-knit manufacturing team. This hands-on role includes mechanical and electrical assembly, wiring, inspection, testing, and system calibration. The ideal candidate will have experience working in a fast-paced, quality-driven production environment—preferably within the medical, optical, or automotive industries—and possess a strong understanding of both manufacturing and electrical processes. We are looking for a detail-oriented, team-focused individual who values precision and views medical device development as a competitive advantage. Responsibilities: • Assemble, install, and calibrate electro-mechanical and electrical subsystems, wiring harnesses, and components per technical documentation and specifications, • Interpret and work from wiring diagrams, blueprints, work instructions, and engineering drawings, • Troubleshoot and repair mechanical, electrical, and electronic components, • Conduct quality checks and functional tests on components and systems to ensure regulatory and performance compliance, • Identify, analyze, and resolve wiring discrepancies and assembly issues, • Maintain accurate records of testing procedures, wiring configurations, and any modifications, • Support ongoing process improvements and documentation updates, • Ensure safety standards and regulatory requirements (e.g., ISO 13485, FDA) are consistently followed, • Collaborate cross-functionally with engineering, quality, and design teams to drive successful builds and efficient production workflows, • Maintain and troubleshoot manufacturing equipment and support preventive maintenance activities, • High school diploma or GED required; technical certification or associate degree in a related field preferred, • 1–3 years of experience in manufacturing and/or electrical assembly, ideally in medical devices or similar industries, • Proficient in electrical wiring techniques, soldering, and crimping, • Strong understanding of electro-mechanical systems, schematics, and diagnostic tools, • Familiarity with electrical safety codes, ISO 13485, and GMP standards a plus, • Ability to use hand tools, power tools, and testing instruments effectively and safely, • Strong attention to detail, problem-solving skills, and organizational discipline, • Ability to work independently and collaboratively in a fast-paced, team-oriented environment This role requires standing for extended periods, working with small components, and operating machinery in a fast-paced production environment. Flexibility to work occasional overtime may be required to meet production demands. Company Offers: • Competitive salary, commensurate with experience and education, • Comprehensive benefits package available: (healthcare, vision, dental and life insurances; 401k; PTO and holidays), • Overtime opportunities available for those interested in additional hours, • A collaborative and diverse work environment where our teams thrive on solving complex challenges

Job Description JOB TITLE: Senior Full Stack Developer LOCATION: Hawthorne, NY (on-site) TYPE: Full time, regular COMPENSATION: $120,000 - $160,000/yr Clarapath is a medical robotics company based in Westchester County, NY. Our mission is to transform and modernize laboratory workflows with the goal of improving patient care, decreasing costs, and enhancing the quality and consistency of laboratory processes. SectionStar™ by Clarapath is a ground-breaking electro-mechanical system designed to elevate and automate the workflow in histology laboratories and provide pathologists with the tissue samples they need to make the most accurate diagnoses. Through the use of innovative technology, data, and precision analytics, Clarapath is paving the way for a new era of laboratory medicine. Role Summary: The Senior Full Stack Developer will play a key role in designing, developing, and maintaining software solutions for SectionStar, a mechatronic device. This role is multi-disciplinary with responsibility for ensuring all front-end and back-end components of our applications are scalable, robust, and user-friendly. The ideal candidate will have extensive experience optimizing web development frameworks, databases and cloud services. We are looking for a team player who views medical device development as a competitive advantage. Responsibilities: • Architect and build the user interface to the device, • Implement modern web UI using latest technology and best practices, • Create formal documentation for a FDA process, • Develop and execute unit and system tests of prototype designs, • Mentor junior developers, provide guidance, and help resolve technical challenges, • Bachelor’s degree in Computer Science, Engineering, or related field. Master’s degree a plus, • 6+ years of professional experience in full stack development, • Proficient in front-end technologies: HTML, CSS, JavaScript, and modern frameworks (React, Angular, Vue.js), • Strong back-end development skills with experience in Node.js, Python, Ruby, Java, or similar languages, • Experience with databases: MySQL, PostgreSQL, MongoDB, or similar, • Familiarity with Graph QL and RESTful API design and implementation, • Knowledge of version control systems (ex: Git), • Experience with cloud platforms (AWS, Azure, Google Cloud) and containerization (Docker, Kubernetes), • Strong problem-solving skills and the ability to think critically and creatively, • Excellent communication skills, both written and verbal, • Ability to work independently and as part of a team, • Strong organizational skills and attention to detail, • Experience with microservices architecture, a plus, • Familiarity with agile methodologies and project management tools (JIRA, Trello), a plus, • Contributions to open-source projects or a portfolio of personal projects, a plus, • Experience with test-driven development (TDD) and automated testing frameworks, a plus, • Prior experience integrating and interfacing with Clinical Laboratory Information Systems (LIS) or similar healthcare information systems, a plus, • Prior experience developing vision systems for process and quality control applications, a plus, • Competitive salary, commensurate with experience and education, • Comprehensive benefits package available: (healthcare, vision, dental and life insurances; 401k; PTO and holidays), • A collaborative and diverse work environment where our teams thrive on solving complex challenges, • Ability to file IP with the company, • Connections with world class researchers and their laboratories, • Collaboration with strategic leaders in healthcare and pharmaceutical world

Job DescriptionJob Title: Quality Assurance ManagerJob Description The Quality Assurance Manager will play a pivotal role in ensuring that all products meet the highest standards of quality and compliance within the wholesale trade industry. This position involves developing and implementing quality assurance policies and procedures that align with the company's commitment to providing a safe work environment with regulatory requirements and industry best practices. The manager will lead a team of quality professionals, providing guidance and support to ensure effective testing and evaluation of products. Additionally, the role requires close collaboration with suppliers and manufacturing teams to address safety and product quality issues and drive continuous improvement initiatives. Ultimately, the Quality Assurance Manager will be responsible for safeguarding the integrity of our products and maintaining customer trust through rigorous quality assurance processes. Responsibilities • Mentor and lead all employees within the Quality Assurance department to achieve goals related to employee safety, quality control, customer demands, and environmental sustainability., • Collaborate with Engineering and Production Managers to lead continuous improvement activities and procedures to ensure efficient and compliant processes., • Implement new procedures and policies to improve quality., • Assess training needs and ensure employees receive proper and timely training., • Oversee the training of all quality assurance personnel and other affected personnel., • Administer Employee Performance Reviews and Disciplinary Actions for all quality assurance and quality control staff., • Create and implement KPIs for quality assurance and quality control., • Ensure compliance with all company control documents, including SOPs, Guidelines, Process Descriptions, and Forms and Checklists., • Ensure all employees adhere to the company’s cGMP and ISO standards., • Develop and communicate monthly business reviews with performance and trending information., • Create and maintain performance indicators, quality benchmarks, and measures for the quality assurance department., • Oversee all QA testing, performance indicators, and benchmarks for all projects., • Drive quality certifications and lead all audits, including ISO, Customer, and Internal., • Renew and maintain all documentation regarding certifications and other company licenses related to quality control and assurance., • Conduct quality audits of vendors and suppliers to ensure conformity., • Develop complaint investigation procedures, document recommendations for corrective actions, and ensure proper follow-up., • Investigate and provide support for recall and return of non-conforming raw materials., • Track, review, and approve payroll for all quality assurance personnel, managing overtime as necessary., • Develop an annual budget and forecasts, explaining any significant variance between actual and budgeted/forecasted figures., • Oversee the daily functions of all quality assurance and quality control personnel, ensuring effective and efficient resource allocation., • Ensure proper flow of information to all quality assurance and quality control staff., • Act as a liaison between different departments to provide status updates on projects., • Ensure adherence to company and quality standards in job duties., • Proven experience in quality assurance and quality management., • Strong knowledge of ISO standards and cGMP/QSR in a highly regulated field such as pharmaceuticals, food, or automotive., • Experience in audit and investigations, including CAPA., • Understanding of Lean Manufacturing principles, 5S, Six Sigma, and other quality improvement methods., • Familiarity with OSHA and EHS regulations., • Proficiency in ERP/MRP systems, preferably SAP., • Intermediate to advanced computer knowledge, particularly in Microsoft Office Suite/MS 365., • Ability to read, analyze, and interpret technical procedures and documents., • Bachelor’s degree in Science, Engineering, or a related field., • Experience with FDA regulations., • Experience in a feedback-driven organization., • Excellent communication skills. This position requires the individual to be onsite 5 days per week, reporting directly to the President of the company and working alongside engineering and operations management. The team comprises nine quality professionals. The company's US operations are headquartered in Blauvelt, NY, with plans to relocate to a new facility in Chestnut Ridge, NY within two years, offering increased production capacity and a training center. The organization values feedback and encourages participation in committees and community initiatives. The company is experiencing growth, with plans to double in size over the next five years, providing opportunities for career advancement. The new leadership team is enhancing benefits and perks, promoting a positive and inclusive work culture. Job Type & Location This is a Permanent position based out of Blauvelt, New York. Pay and Benefits The pay range for this position is $135000.00 - $150000.00/yr. PTO Vacation, Sick Time (NYS), benefits medical, health, dental, 401K Workplace Type This is a fully onsite position in Blauvelt,NY. Application Deadline This position is anticipated to close on Sep 20, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionPrestige Consumer Healthcare is a company that focuses on product innovation and quality in the over-the-counter healthcare and women’s health categories to better improve the lives of our customers and their world. For generations, our trusted brands have helped consumers care for themselves and their loved ones. We are one of the largest independent providers of over-the-counter products in North America, and we are constantly improving and creating products that match the ever-changing lifestyles and needs of people and families everywhere. JOB SUMMARY: The Senior Director of Information Technology is responsible for the planning, organizing, and execution of all IT Software business applications and related projects to ensure optimal functioning of IT/business systems. This role involves working with new solutions, procurement, and maintenance of software programs. MAJOR RESPONSIBILITES/ACTIVIES: • Analyzes complex business needs presented by the user community and/or clients and recommends technical solutions., • Leads and manages IT teams, providing guidance, mentoring, and performance management., • Champion innovation and process improvement across support functions, • Leverage automation, self-service, and AI/ML insights to optimize efficiency, • Ensures the consistency and maintainability of existing applications by creating, maintaining, and enforcing standards/procedures for implementing technical solutions., • Assists the VP of IT and CISO with long and short run IT planning., • Manages the ongoing support for Corporate critical systems, SAP and EDI IBM Sterling., • Leads evaluation selection and implementation of all IT software systems., • Executes established goals and ensures that corporate-wide goals are complimented and supported., • Continually evaluates established policies and procedures and updates or modifies them as necessary., • Periodically reviews the Company’s information needs and modifies the systems as required., • Ensures the implementation of cost effective and efficient systems and computer operations designed to meet current and future information needs., • Ensures that users’ and clients’ needs are met and that they are fully capable of utilizing established systems., • Ensures that equipment, peripheral devices, and software are set up and operated in accordance with prescribed instructions., • Ensures that IT systems are secure, properly backed up, and appropriately documented., • Manages and oversees department expenses. Pursues cost-saving measures., • Provides leadership to personnel through effective objective setting, delegation, and communication. Conducts staff meetings as required. Directs, schedules, and coordinates Department functions., • Produces detailed timeline for each application release and implements effective project control by monitoring the progress of the software release and reporting the status., • Directs and prioritizes the workload of personnel., • Reviews all designs, code and unit test plans where applicable., • Approves all business requirements prior to the technical solution., • Participates on all hardware and software evaluations and maintains vendor contracts., • Represents the IT function at customer review meetings when appropriate., • Performs liaison duties between users, operations, and programming personnel in the areas of systems design, modifications or trouble shooting., • Bachelor’s degree in Computer Science, Information Systems, or related field; Master's degree preferred., • Strong SAP background with respect to MM, QM, PP, SD, FI modules is a must, • Experience with Manufacturing and FDA regulations are a must, • Minimum of eight (8) years of experience within information technology, • Experience in the most current technologies and products used in the industry., • Technical capability, business acumen, strategic thinking, customer/client focus, • Leadership, • Excellent communication (verbal and written), interpersonal, and collaboration skills are a must and the ability to communicate with all levels of Management including Senior Leadership and the Board of Directors, • Experience working with finance teams is a plus, • Sarbanes Oxley experience is a plus, • Ability to organize and work effectively with project teams made up of internal staff and/or external parties (agents, vendors, etc.), • Demonstrated experience and relevant expertise in the configuration and deployment of IS business solutions LANGUAGE SKILLS: Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. MATHEMATICAL SKILLS: Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. REASONING ABILITY: Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit. The employee frequently is required to talk or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually moderate. No Sponsorship: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. #HybridWork: We follow a Hybrid work schedule. All applicants must be able to work in our Tarrytown office Tues/Wed/Thurs (remote on Mon/Fri). Work Hours: 40 hours per week. Salary Range: $200,000 - $250,000 Powered by JazzHR eovxVvRwX2

Job DescriptionPrestige Consumer Healthcare is a company that focuses on product innovation and quality in the over-the-counter healthcare and women’s health categories to better improve the lives of our customers and their world. For generations, our trusted brands have helped consumers care for themselves and their loved ones. We are the largest independent provider of over-the-counter products in North America, and we are constantly improving and creating products that match the ever-changing lifestyles and needs of people and families everywhere. JOB SUMMARY: The Vice President (VP), Quality Assurance and Regulatory Affairs will report to the Chief Executive Officer and will ensure the regulatory and quality compliance of Prestige products throughout their lifecycles and will monitor regulatory and quality developments potentially affecting the business. The VP will also lead Medical Affairs activities including clinical studies, Customer Contact Center, and pharmacovigilance. Product categories include OTC monograph drugs, OTC NDAs, Medical Devices, Cosmetics, Dietary Supplements, and EPA-registered products. The VP, Quality Assurance and Regulatory Affairs will design, implement, and monitor effective compliance strategies that align with the Company's business goals. The VP has a solid over the counter (OTC) healthcare Quality and Regulatory Affairs background and will assure that all products and contractors meet the applicable quality and regulatory requirements. The VP will develop strategy that supports all brands and new products as well as operational initiatives. MAJOR RESPONSIBILITES/ACTIVIES: • The VP, Quality Assurance and Regulatory Affairs serves as a management representative., • The VP, Quality Assurance and Regulatory Affairs will direct and oversee the Company's Quality Assurance, Regulatory Affairs, and Medical Affairs organization to lead the development and implementation of the Company's compliance strategies for its complete portfolio of products., • The VP, Quality Assurance and Regulatory Affairs serves as the Quality Representative (QR) and Management Representative (MR) including:, • ensuring that quality management system requirements are effectively established, documented, implemented, and maintained and meet customer requirements;, • reporting to top management on the performance and effectiveness of the quality management system and any need for improvement;, • ensuring the promotion of awareness of applicable quality system and regulatory requirements throughout the organization; and, • acting as liaison with external parties on matters relating to the Quality Management System., • The VP, Quality Assurance and Regulatory Affairs will foster close cooperative relationships with all functions in the company relative to compliance, working with Marketing, Product Development, Package Development, Legal, and Operations to execute all product and labeling claims and strategies for the company’s brands., • The VP will lead and apply Quality Assurance and cGMP expertise for OTC drug products (monographed and NDA/ANDA), medical devices, dietary supplements, and cosmetics., • The VP will confirm the cGMP compliance of third-party contract manufacturers (Contractors) by developing and executing Prestige Consumer Healthcare' Quality Assurance programs to ensure the marketing of safe, stable, and legal product., • The VP will maintain New Drug Applications, 510Ks, and other regulatory documentation for all products., • The VP will monitor global Regulatory and Quality developments affecting Prestige products through participation in industry associations, monitoring of newsletters and government websites and other methods, and communicate significant issues within the organization., • Bachelor's Degree in Scientific or health related field; master’s degree preferred REQUIRED KNOWLEDGE:, • Strong knowledge of US OTC NDA, monograph drug, and medical device regulatory requirements and submissions, • Strong knowledge of FDA and FTC claims support requirements, • Strong Knowledge of cGMP regulations and requirements in all aspects of manufacturing and distributing OTC drugs and medical devices, • Strong Knowledge of ISO 13485:2016, • Working knowledge of Canadian, EU, and Latin American regulations, • Working knowledge of US clinical research methods, • Excellent written and verbal communication skills, • Demonstrated ability to work with people in an effective and positive mannerEXPERIENCE REQUIRED:, • 20+ years of experience in US and Canada Quality Assurance and/or Regulatory Affairs in CPG industry; global experience a plus, • NDA or 510(k) submission and/or maintenance experience LANGUAGE SKILLS: Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. MATHEMATICAL SKILLS: Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. REASONING ABILITY: Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit. The employee frequently is required to talk or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually moderate. Salary Range: $250,000 - $300,000; this range reflects a variety of factors including, but not limited to, candidate experience, qualifications, geographic location, and prevailing market conditions. Compensation also includes a discretionary annual bonus, long-term incentives, and a solid, well-rounded benefits package. No Sponsorship: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. #HybridWork: We follow a Hybrid work schedule. All applicants must be able to work in our Tarrytown office Tues/Wed/Thurs (remote on Mon/Fri). Work Hours: 40 hours per week. Powered by JazzHR hRt7AzjqnA

Job Description JOB TITLE: Systems Engineer LOCATION: Hawthorne, NY (on-site) TYPE: Full time, regular COMPENSATION: $140,000 - $165,000/yr Clarapath is a medical robotics company based in Westchester County, NY. Our mission is to transform and modernize laboratory workflows with the goal of improving patient care, decreasing costs, and enhancing the quality and consistency of laboratory processes. SectionStar™ by Clarapath is a ground-breaking electro-mechanical system designed to elevate and automate the workflow in histology laboratories and provide pathologists with the tissue samples they need to make the most accurate diagnoses. Through the use of innovative technology, data, and precision analytics, Clarapath is paving the way for a new era of laboratory medicine. Role Summary: The Systems Engineer will play a key role in the design, integration, and optimization of Clarapath’s advanced electro-mechanical medical device, SectionStar™. This position is essential for driving cross-functional alignment, troubleshooting complex system-level issues, and ensuring seamless integration between hardware, software, and production workflows. The ideal candidate will have a deep understanding of systems engineering principles, a strong analytical mindset, and experience working within regulated environments. We’re looking for a collaborative team player who sees system-level design and development as a key competitive advantage in advancing medical device innovation. Responsibilities: • Develop and maintain system-level architecture and requirements for SectionStar™, • Lead integration of electrical, mechanical, software, and firmware subsystems, • Translate customer and clinical requirements into clear, testable system specifications, • Collaborate with R&D, manufacturing, and quality teams to ensure smooth design transfer and system verification, • Identify and resolve system-level issues through root cause analysis and structured troubleshooting, • Manage interface definitions, risk analyses (ex: FMEA), and design documentation, • Support regulatory submissions by generating system-level documentation and participating in design reviews, • Bachelor’s degree in Systems Engineering, Mechanical Engineering, Electrical Engineering, or related field; Master’s degree preferred, • 8+ years of experience in systems engineering or cross-disciplinary product development, • Strong understanding of product lifecycle management, risk analysis, and V&V processes, • Hands-on approach to integration and problem solving; experience working closely with manufacturing and testing environments, • Excellent analytical and communication skills, • Experience in medical devices or regulated industries, a plus (FDA, ISO 13485, etc.), • Competitive salary will be commensurate with experience and education, • Comprehensive benefits package available: (healthcare, vision, dental and life insurances; 401k; PTO and holidays)., • A collaborative and diverse work environment where our teams thrive on solving complex challenges, • Ability to file IP with the company, • Connections with world class researchers and their laboratories, • Collaboration with strategic leaders in healthcare and pharmaceutical world

Job DescriptionProduct Testing & Compliance Coordinator Who you must be We are looking for a highly organized, detail-oriented individual that ensures Two’s Company products are compliant with all applicable consumer product safety regulations and industry standards. The Product Compliance Coordinator partners with our internal and external teams to ensure our products meet consumer product safety regulations and industry standards. This position will report to the Product Testing & Compliance Manager This is a hybrid position, candidate must be able to commute to Elmsford, NY. What we need you to do As the Product Compliance Coordinator, you will play a key role in ensuring that our products meet all Federal and State safety requirements. Partner with cross-functional teams, including product development, inventory management, and quality assurance, to ensure compliance standards are met throughout the product lifecycle. Communicate with external third-party testing labs to conduct product testing ensuring all products meet Federal and State regulations. Perform XRF Analyzer scans of pre-production samples and communicate results. Manage and update compliance database in Netsuite and report on product testing status, timeline and results to internal teams. Maintain regulatory compliance records and ensure that records are properly kept, traceable and meet appropriate testing and submission processes. Participate in cross-functional meetings and provide compliance updates. Handle compliance documentation requests. Participate in tasks and assignments related to product compliance as needed. What you must have Bachelor's Degree in Business Administration, Supply Chain Management, or a Related Field 1-2 years of experience in product compliance within the home goods, textiles, cosmetics, and toys/baby industries preferably in wholesale or retail Entry level understanding of Federal and State product compliance standards, including CPSC, CPSIA, FDA, ASTM, and Prop 65 Experience working with domestic and international third-party testing labs Analytical, detail oriented, self-starter with excellent project management and follow-up skills Ability to work collaboratively with cross-functional teams Strong verbal and written communication skills, with the ability to clearly convey information in a concise manner Embraces a fast-paced working environment with a high sense of urgency Demonstrated ability to make good decisions and exercises sound judgement Proficient in Microsoft Office – Outlook, Word, Excel Experience working with Netsuite and File Maker a plus Benefits of working here We offer a competitive compensation package, robust benefits and our atmosphere is vibrant, engaging, productive and fun! Two’s Company is dedicated to innovation and trendsetting in the giftware industry and prides itself in providing the Global Market with high style fashion, gift and home products at moderate prices. Two’s has evolved over the years into a powerhouse brand in multiple categories and a dynamic sales organization that serves as advocates for our retail partners. Today, Two’s Company has four divisions: the signature Two’s Company Gift and Home décor line, the couture Tozai Home collection of decorative accessories, the whimsical Cupcakes & Cartwheels, 2 Chic a fashion accessories line and 2 Chic Luxe a ready-to-wear fashion and accessories line. Pay Range Elmsford, New York: $55,000 - $65,000 USD Powered by JazzHR 60E3P3NKP4

Job Description Position Summary: We are seeking a highly motivated Automation/Validation Engineer with expertise in Computer System Validation (CSV), equipment validation, and automation systems. The role involves supporting commissioning, qualification, and validation (CQV) activities across equipment, facilities, and utilities, ensuring compliance with GMP regulations. Hands-on experience with Kneat (e-validation platform), DeltaV DCS, and preparation/execution of validation deliverables (URS, FAT, SAT, IQ/OQ/PQ) is required. Key Responsibilities: Validation & Documentation Author, review, and execute validation documentation including User Requirement Specifications (URS), Functional Specifications, Design Qualification (DQ), FAT, SAT, IQ, OQ, and PQ. Manage validation lifecycle documentation using Kneat. Perform risk assessments (FMEA, GxP impact assessments, traceability matrices). Automation Systems (DeltaV & others) Support automation projects involving DeltaV Distributed Control Systems (DCS), PLCs, and SCADA systems. Collaborate with automation and process engineering teams to ensure system integration, configuration, and qualification. Troubleshoot and support control system operations during commissioning and validation. Equipment & Utility Validation Execute validation protocols for GMP manufacturing equipment, laboratory instruments, facilities, and utilities (e.g., purified water, clean steam, HVAC, compressed gases). Support equipment qualification from FAT/SAT through operational readiness. Ensure systems meet regulatory requirements (FDA, EMA, ICH, Annex 11, 21 CFR Part 11). Compliance & Quality Ensure adherence to company quality standards and global regulatory requirements. Support audits and inspections by providing validation and automation documentation. Drive continuous improvements in validation strategies and procedures. Qualifications & Skills: Bachelor’s degree in Engineering (Automation, Electrical, Mechanical, Chemical, or related field). 3–7+ years of experience in automation engineering, CSV, or equipment validation within a GMP-regulated environment (biotech/pharma/medical device). Proficiency with Kneat Gx for electronic validation document management. Hands-on experience with DeltaV DCS and automation systems. Strong knowledge of validation lifecycle (URS, DQ, FAT, SAT, IQ/OQ/PQ). Familiarity with facilities & utilities systems (water systems, clean utilities, HVAC). Strong understanding of GAMP 5, 21 CFR Part 11, Annex 11, and FDA/EMA guidelines. Excellent technical writing, problem-solving, and communication skills. Preferred Experience: Experience in biologics, sterile manufacturing, or API facilities. Knowledge of MES, LIMS, and other GMP computerized systems. Prior involvement in CQV projects and capital projects.

Responsibilities: US Agent for all products, responsible for communication between the FDA and manufacturing sites.Communicate and follow-up status with FDA for any Chemistry, Bioequivalence and Patents issues and correspondences on both pending and approved applications.Lead, guide, and train the C

Job Description JOB TITLE: Electrical Engineer LOCATION: Hawthorne, NY (on-site) TYPE: Full time, regular COMPENSATION: $110,000 - $140,000/yr Clarapath is a medical robotics company based in Westchester County, NY. Our mission is to transform and modernize laboratory workflows with the goal of improving patient care, decreasing costs, and enhancing the quality and consistency of laboratory processes. SectionStar™ by Clarapath is a ground-breaking electro-mechanical system designed to elevate and automate the workflow in histology laboratories and provide pathologists with the tissue samples they need to make the most accurate diagnoses. Through the use of innovative technology, data, and precision analytics, Clarapath is paving the way for a new era of laboratory medicine. Role Summary: The Electrical Engineer will play a key role in the design, development, and integration of electrical systems for Clarapath’s advanced electro-mechanical medical device, SectionStar™. This position is essential for supporting PCB design, wiring schematics, power systems, and embedded hardware components, while ensuring seamless integration with mechanical and software subsystems. The ideal candidate will have a strong foundation in hardware electrical design and a working knowledge of software development for embedded systems. We’re looking for a hands-on, detail-oriented team player who thrives in a fast-paced environment and views electrical engineering as a critical driver of innovation in medical device development. Responsibilities: • Design and develop system-level electrical schematics, including electrical isolation strategies, detailed PCB layouts, wiring harnesses, and power distribution networks for SectionStar™, • Design precision electromechanical components and assemblies using CAD tools to support integration with hardware systems, • Build and assemble cable harnesses and prototype analog and digital circuits, primarily for sensor integration and device control, • Develop low-level device control software, including experience programming in C++ and working with FPGA-based systems for embedded control and signal processing, • Model and develop complex electrical systems throughout the device, such as stepper and DC motor control, AC power systems, low-voltage data lines, and high-sensitivity analog and digital circuits, • Support prototyping, unit, and system-level testing of electrical hardware, including building test fixtures instrumented with data acquisition system, • Troubleshoot and resolve hardware issues throughout development and manufacturing phases to ensure device reliability and manufacturability, • Participate in design reviews, risk assessments (ex: FMEA), and create documentation such as schematics, wire harness drawings, PCB files, and component specifications to support FDA regulatory processes, • Assist in the development and maintenance of test procedures, validation protocols, and compliance documentation, • Contribute to continuous improvement initiatives by identifying opportunities to enhance system performance and streamline manufacturing, • Bachelor’s degree in Electrical Engineering or a related field; Master’s degree preferred, • 5+ years of experience in electrical design, preferably within medical device development or regulated industries, • Proven design record with competency in designing large electromechanical system components, including high-sensitivity analog and data systems, power conditioning for motors and high inrush current components, • Experience designing embedded hardware such as microcontrollers and FPGAs, with exposure to software/firmware programming in C++, • Proficiency with PCB design tools and electrical CAD software (Altium Designer preferred, Eagle acceptable), • Strong analytical and problem-solving skills, including modeling, simulation, and hands-on lab bench experience (soldering, wiring, troubleshooting, and use of test equipment), • Familiarity with Linux systems and microprocessors, • Proficiency in Microsoft Office applications including Excel, PowerPoint, and Word, • Excellent interpersonal, verbal, and written communication skills, • Effective time management skills with the ability to prioritize and meet deadlines in a fast-paced, multidisciplinary environment, • Ability to work independently and collaboratively within a team, • Flexibility to adapt to changing priorities and drive to meet aggressive milestones and deadlines, • Competitive salary will be commensurate with experience and education, • Comprehensive benefits package available: (healthcare, vision, dental and life insurances; 401k; PTO and holidays)., • A collaborative and diverse work environment where our teams thrive on solving complex challenges, • Ability to file IP with the company, • Connections with world class researchers and their laboratories, • Collaboration with strategic leaders in healthcare and pharmaceutical world

Job DescriptionOur client is an emerging, early commercial-stage, expanding NASDAQ-listed medical innovator introducing disruptive tissue reconstructive therapies to the healthcare delivery marketplace. The company's senior leadership is comprised of medical device veterans from top "Blue Chip" organizations. Position Overview This position is responsible for generating sales of the Company’s product portfolio in their assigned geographic territory. As such, the Account Manager will develop and maintain strong working relationships with surgeons, hospital administrators and nursing staff to ensure appropriate use of the Company’s FDA cleared products. The successful candidate must be able to communicate complex clinical data with the goal of assisting surgeon in appropriate product selection based on patient co-morbidities and wound classifications. Essential Duties & Responsibilities • Responsible for educating physicians on the benefits to patients of Company Products, benefits to hospitals of Company Products, ease of use, and appropriate technique and placement of the Company Product portfolio, • Communicate complex clinical data with the goal of assisting surgeon in appropriate product selection based on patient co-morbidities and wound classifications, • Work closely with the Company’s commercial team (marketing, customer service, commercial development) to achieve successful outcomes for hospitals, surgeons and patients, • Develop business plans to ensure that short-term revenue objectives are met while longer-term opportunities are optimized in their geographic area, • Maintain and update the Company’s CRM database as appropriate with current hospital, surgeon information in their geographic area, • 7+ years of experience in the life science industry, preferably in the biologics space; experience in hernia repair, abdominal wall reconstruction, breast reconstruction preferred, • Experience handling biologic tissue-based materials, • Extensive knowledge of both clinical needs of physicians and mechanisms of action of host response to biologic implants, • Ability to identify new market opportunities for biologic constructs based on unmet needs of general and reconstructive surgeons, • Ability to juggle multiple tasks and prioritize work appropriately with a focus on timelines and deliverables, • Strong communication (written, oral and interpersonal) and presentation skills; demonstrated experience presenting to diverse audiences including, but not limited to, employees, physicians and key opinion leaders, • Excellent judgment and decision-making capabilities; ability to formulate business solutions for a myriad of challenges, • Ability to work collaboratively with various internal departments and leaders; ability to drive results through partnership, mutual respect and trustOTHER: This position is field-based and requires frequent travel. Successful candidate must have a valid driver’s license and will be subject to DMV and other required background and reference checks.

Job Description Production Associate As a Medical Device Kitting/Production Associate at Polymedco, you will play a crucial role in assembling and packaging life-saving colorectal cancer (CRC) FIT kits. These kits are essential for early cancer detection, making a real difference in patients' lives. You'll be part of a dedicated team ensuring that every kit meets our high-quality standards and is ready for use in medical practices nationwide. This role is perfect for individuals who enjoy working with their hands, take pride in attention to detail, and thrive in a team environment. Key Responsibilities: • Kit Assembly & Packaging:, • Assemble and kit medical devices with care, following clear work instructions., • Ensure all components are included in the correct quantities., • Operate packaging equipment and finalize kit packaging with precision., • Label, seal, and ensure kits are ready for shipment., • Document any quality issues and participate in continuous improvement processes., • Inventory & Materials Handling:, • Manage the inventory of raw materials and finished products, ensuring smooth production., • Pick and pull inventory items, using tools such as pallet jacks and rolling staircases., • Quality & Compliance:, • Follow Good Manufacturing Practices (GMP), FDA, and ISO regulations to ensure product safety., • A commitment to quality and the satisfaction of knowing your work helps save lives., • Ability to follow detailed instructions and work efficiently in a fast-paced environment., • High school diploma or equivalent (previous manufacturing or kitting experience is a plus)., • Excellent attention to detail and manual dexterity for working with small components., • Ability to stand or sit for long periods while performing repetitive tasks., • Full-time, day shift. Overtime and weekend shifts may be required during peak production., • Be a part of a mission-driven company that improves patients' health and well-being., • Stability and opportunities for growth and advancement in medical device manufacturing., • Monday-Friday, 9:00 AM - 5:00 PM, • $18.00 - $19.00 per hour

Job Description🚨 Industry-Leading Manufacturing Company in Orangeburg, NY is URGENTLY Hiring Cleanroom Production Compounders! 🚨 💼 Position: Cleanroom Production Compounder 📍 Location: Orangeburg, NY 💰 Pay: $17–$18/hour + Shift Differential 🕒 Shifts Available: • 2nd Shift: 3PM–11PM ($0.50/hr differential), • 3rd Shift: 11PM–7AM, Sunday–Thursday ($1.00/hr differential), • Compound liquids following GMP and daily production schedules, • Stock production floor with required materials, • Remove empty barrels and manage warehouse logistics, • Maintain cleanliness and organization of the work areaMust-Have Qualifications:, • High School Diploma or GED, • 0–2 years of chemical handling/mixing experience preferred, • If no compounding experience, warehouse/manufacturing experience is a plus, • Strong math and communication skills, • Team-oriented, go-getter mentalityNice-to-Have Skills:, • Blending, • Batch making ✅ Tons of room for upward mobility ✅ Union eligibility upon permanent hire ✅ Basic maintenance mechanic training ✅ Opportunity for overtime Pay and Benefits The pay range for this position is $17.00 - $18.00/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, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Orangeburg,NY. Application Deadline This position is anticipated to close on Sep 24, 2025. 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.

Job Description We seek to provide comfort and joy, to care for, and nurture life by sharing our unique pastries, cake, pies, breads and treats. We bake everything from scratch using high-quality ingredients. As a Overnight Bakery Production Team Member you will identify and select ingredients, prepare, form and bake items in our pastry, bread or Viennoiserie departments. At Tatte Bakery we bake everything from scratch and use high quality ingredients. Our overnight bakery production team members must thrive in a fast-paced work environment while adhering to cleanliness and sanitation standards for the entire kitchen and dish area. Most importantly, they must take pride in what they do and be team player. Our talented Overnight bakery team members help in all aspects of our product creation process. Responsibilities include: • Identify and select ingredients to follow recipes, • Scale given recipes to match production needs, • Sheeting, shaping, and preparing doughs in a modern-manufacturing environment, • Building composed desserts, • Making housemade jams, fillings, mousses, etc., • Topping, finishing, and decorating desserts, • Adhere to cleanliness and sanitation standards (FDA Guidelines), • Prior experience working in a high-volume bakery production, banquet production kitchen, restaurant kitchen, or similar environment is helpful, but we are open to training ambitious candidates who have a demonstrated interest in working as a bakery production team member. Prior experience is not a requirement., • Desire to help where needed and work as part of a team., • Passion for cooking with a keen eye for freshness, quality and cleanliness., • An appetite for learning (and delicious pastries, cakes, and confections), • Thrive in face-paced, team-oriented environment, • Take pride in what they do, • Spanish &/or Portuguese language skills a plus, • Ability to safely and successfully perform the essential job functions consistent with federal, state, and local standards, including meeting qualitative and/or quantitative productivity standards, • Able to grasp, reach overhead, push, lift, manipulate and carry up to 50 pounds, • Competitive pay (ranging from $20.50-$25/hour, commensurate with experience and skills), • Free Employee Assistance Program services, • A generous team member discount, • Health + dental benefits for full-time team members, • 401k benefits (with a vesting match), • Opportunities to learn, develop, and grow with us, including training in various pastry and confection processes

A National General Contractor specializing in commercial projects, from full build outs and renovations to large scale projects is seeking a talented Assistant Project Manager to help assist with new and existing construction.This position is based out of their office in Union County, NJ.Benefits +

Assistant Project Manager (White plains, NY): Support implementation of construction project management/project controls/scheduling/cost estimation.Compliance with NYC Building Codes/Practices, QA/QC policies.Requires bachelor's degree in civil engineering/closely related 2 years of relevant experi

For over 40 years, Health Monitor has been a nationally recognized, targeted healthcare marketing platform for the Pharma/OTC industry.Our in-house, award-winning content studio creates bespoke healthcare education that fosters more productive patient-physician dialogues at every point of care—we

Johnson Service Group (JSG) is currently looking for a Project Safety Manager.This is a direct hire opportunity with an integrated Construction, Design and Technology solutions firm located in Pearl River NY.Pay $110K Responsibilities Ensure job sites are complying with OSHA and NYS safety standards

A National General Contractor specializing in commercial projects, from full build outs and renovations to large scale projects is seeking a talented Assistant Project Manager to help assist with new and existing construction.This position is based out of their office in Union County, NJ.Benefits +

For over 40 years, Health Monitor has been a nationally recognized, targeted healthcare marketing platform for the Pharma/OTC industry.Our in-house, award-winning content studio creates bespoke healthcare education that fosters more productive patient-physician dialogues at every point of carewe cal

A growing civil construction and site development firm is seeking a hands-on Senior Project Manager to lead complex land development and municipal infrastructure projects.The ideal candidate has 10+ years of field-driven experience, with a background in sitework and utility-heavy scopes.This is a fu

We are seeking an experienced Project Manager to support our client's team.The ideal candidate will bring a strong background in project management, agile methodologies, and project development while demonstrating exceptional interpersonal skills and the ability to thrive in a collaborative, large-t

At SERVPRO of Elmsford, we're seeking a Construction Project Manager who wants to make a meaningful impact in our community.You'll have the chance to oversee and execute projects that directly contribute to rebuilding lives by restoring homes and businesses.As a Construction Project Manager at SERVP

Construction Project Manager, Geothermal Construction.Brightcore Energy provides end-to-end energy efficiency and clean energy measures to commercial, industrial, and institutional clients.We have the intellectual and financial capital to develop, implement, fund, and maintain clean energy solutions

At Renovo Construction, we have an immediate need for Construction Project Managers.Tired of not knowing where your next job will be? Looking for stability and a steady stream of projects? Are you interested in retail and working with some of the most recognized brands in the country? If you answere

Morgan Stanley is a leading global financial services firm providing a wide range of investment banking, securities, investment management and wealth management services.The Firm's employees serve clients worldwide including corporations, governments and individuals from more than 1,200 offices in 4

Construction Project Manager Public Projects.Opportunity to work on impactful public sector projects in your local community.Join a reputable Project Management firm with over 100 years of success.A longstanding construction management firm established over 100 years ago, specializing in public sect

Position Summary: At Ivy Rehab, we're "All About the People"! As a Project Portfolio Manager, you will play a crucial role in our mission to help enable people to live their lives to the fullest.Job Description: The Project Portfolio Manager will report to the Senior Manager of Finance and be an int

Johnson Service Group (JSG) is currently looking for a Project Safety Manager.This is a direct hire opportunity with an integrated Construction, Design and Technology solutions firm located in Pearl River NY.Pay $110K Responsibilities Ensure job sites are complying with OSHA and NYS safety standards

Frontier-Kemper, a Tutor Perini Company, is seeking a Change Control Manager to join our Kensico-Eastview Connection Tunnel Project in White Plains, New York.Excellence in Underground and Heavy Civil Construction.At Frontier-Kemper, we specialize in heavy civil construction and underground mine deve

Commercial Drywall Project Manager/Estimator.GPAC: #1 Commercial Drywall Recruiting Firm in North America: WORK FOR A LEADING CONTRACTOR.I am working with multiple well-respected, firmly established Commercial Drywall Contractors seeking experienced Project Managers and Estimators.This is an excitin

Engineering Project Manager Or Project Engineer.Brief Overview Of Role: The Engineering Project Manager or Project Engineer is responsible for coordination and management of the engineering design process and execution on a project basis for multi-disciplined engineering design projects.The Project

The NYC Department of Environmental Protection (DEP) enriches the environment and protects public health for all New Yorkers by providing 1.DEP is the largest combined municipal water and wastewater utility in the country, with nearly 6,000 employees.DEP's water supply system is comprised of 19 rese

Lightpath is seeking a highly organized and detail-oriented Senior Project Manager to join our team.The ideal candidate will bring a strong understanding of telecommunications industry practices and procedures, along with the analytical skills to evaluate data, explore multiple solution paths, and a

Opportunities with Optum in the Tri-State region (formerly CareMount Medical, ProHEALTH New York and Riverside Medical Group).Come make a difference in the lives of people who turn to us for care at one of our hundreds of locations across New York, New Jersey and Connecticut.Work with state-of-the-a

The New York City Department of Environmental Protection (DEP) protects public health and the environment by supplying clean drinking water, collecting, and treating wastewater, and reducing air, noise, and hazardous materials pollution.DEP is the largest combined municipal water and wastewater util

Location: White Plains, NY, 10601 - Hybrid schedules are permissible with a minimum of 3 days on-site, depending on assignment.Duration: 12+ months Pay Range: $55.W2) Schedule: Monday through Friday 7.

Morgan Stanley is a leading global financial services firm providing a wide range of investment banking, securities, investment management and wealth management services.The Firm's employees serve clients worldwide including corporations, governments and individuals from more than 1,200 offices in 4

A reputable and steadily growing general contractor with deep roots in the Westchester and Lower Hudson Valley region, known for delivering high-quality ground-up construction in commercial, mixed-use, healthcare, and municipal sectors.The firm values long-term partnerships, career development, and

Location: White Plains, NY (3 days Onsite) Duration: 12 months contract.At Cogent Infotech, we believe in creating opportunities that empower individuals and transform organizations.With over 21 years of excellence in consulting and talent solutions, we pride ourselves on building inclusive workplac

Opportunities with Optum in the Tri-State region (formerly CareMount Medical, ProHEALTH New York and Riverside Medical Group).Come make a difference in the lives of people who turn to us for care at one of our hundreds of locations across New York, New Jersey and Connecticut.Work with state-of-the-a

Creighton Manning Engineering and Surveying, a GAI Company is seeking a Project Manager with 10+ years of experience in water/wastewater engineering to join our talented and energetic team in Upstate New York with the flexibility to work out of our Albany, Poughkeepsie, Syracuse or White Plains offi

Understanding of Pharma-FDA reporting processes and regulatory submission standards (ICH, DIA CTD).

Join our growing team as a Amazon Picker/Packer to support the preparation and delivery of goods or services, follow safety procedures and company policies, and respond promptly to inquiries and resolve basic issues.Other duties include coordinate tasks to ensure deadlines are met, gain knowledge of

Project Manager - Small On-Site.Linde Engineering North America LLC.Tonawanda, NY, United States | req24831.Independently manages multiple small to mid-size EPC projects simultaneously.Supports new plant proposals as required.Recognizes problems or situations that are new or without clear precedent.