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MedCadre is seeking a travel nurse RN Care Manager for a travel nursing job in Nyack, New York. Job Description & Requirements • Specialty: Care Manager, • Discipline: RN, • Start Date: 06/01/2026, • Duration: 13 weeks, • 40 hours per week, • Shift: 8 hours, days, • Employment Type: Travel Registered Nurse (RN) – Case Manager Location:Nyack, NY 10960 Schedule: Monday to Friday | 8-hour shifts Shift timing: 8:00 AM – 4:30 PM or 8:30 AM – 5:00 PM Hours/week: 40 hours per week | No weekends Start Date: 06/01/2026 Company Overview: At MedCadre, we connect exceptional healthcare professionals with world-class career opportunities while upholding the highest standards of ethics, fairness, and integrity. As a Joint Commission–accredited leader in healthcare staffing, we ensure trust and peace of mind for both our clinicians and partner facilities. Position Overview: We are seeking an experienced Registered Nurse (RN) Case Manager to join an acute care setting. The ideal candidate will coordinate patient care, ensure appropriate utilization of resources, and support patients through their healthcare journey. Key Responsibilities: • Coordinate and manage patient care plans in an acute care environment, • Perform utilization review and discharge planning, • Collaborate with physicians, nurses, and interdisciplinary teams, • Ensure compliance with healthcare regulations and standards, • Monitor patient progress and adjust care plans as needed, • Maintain accurate documentation using EPIC charting system, • Active RN license (required), • Minimum 2 years of Case Management experience, • AHA - BLS, • Experience in acute care setting, • Familiarity with EPIC charting system Please submit your resume to manas(at)medcadre.com. Qualified candidates will be contacted promptly for next steps. About MedCadre At MedCadre, headquartered in Irvine, California and serving healthcare organizations nationwide, we connect exceptional clinicians with world-class career opportunities while upholding the highest standards of ethics, fairness, and integrity. As a Joint Commission–accredited and ISO 9001–certified leader in medical staffing, we strictly adhere to healthcare regulations, ensuring trust and peace of mind for both our clinicians and partner facilities. Guided by our core values; Results, Approachability, Care, and Emergency (RACE), we foster an environment where you can grow professionally, build meaningful relationships, and deliver outstanding patient care. When you join MedCadre, you become part of a broad network dedicated to advancing healthcare, improving lives, and shaping the future of patient outcomes together. We are an Equal Opportunity Employer and embrace diversity at every level of our organization Learn more about us Benefits • 401k retirement plan, • Health Care FSA, • Vision benefits, • Dental benefits, • Retention bonus, • Medical benefits, • Referral bonus, • Sick pay, • Weekly pay

Job Description Note: Territory for this role will include North Carolina, California (LA), and Texas. Candidates must be willing to travel frequently and be located near an airport hub. The Account Manager is the face of Dempsey Corporation to Customers and Prospects in their assigned territory. They are responsible for growing their assigned territory and developing strong business relationships. They are considered a valuable resource that is relied on by food processors to provide timely ingredient information on the products that we represent. The Account Manager will initiate, manage, and bring to a successful conclusion new projects while managing and servicing their existing book of business with their customers. Duties and responsibilities • Generates new ideas for increasing sales revenue to ensure sales targets are met, and revenue increases year over year., • Manages accounts for existing clients by gathering, tracking, and analyzing all pertinent information, such as, but not limited to, historical data and pricing strategies; maintains ongoing relationships with the clients through telecommunications and face-to-face contact, to secure repeat business and generate additional revenues., • Creates new business opportunities by pursuing and developing relationships with new accounts; researches new leads and gathers information on their business and past events through an internet search, and discussions with network contacts; makes contact with appropriate personnel and arranges to meet to familiarize potential customers with Dempsey offerings; follows-up with potential new client regularly to secure new business and increase sales revenues., • Develops clear and specific written proposals/quotations for potential new clients; presents proposals to clients; overcomes client objections to secure the account., • Networks on an on-going basis, in a professional manner, with industry counterparts to maintain good business relationships and remain apprised of industry trends to maintain a competitive status for the business; utilizes this research in the development of new, improved selling tools; attends industry-related functions including, conferences, seminars, trade shows and social events; reports back to management on market trends and competitive activities., • Attend tradeshows as required, to remain current with upcoming industry trends., • Coordinate suppliers’ visits and joint calls, including but not limited to travel and hotel reservations., • Liaises regularly with internal sales/ marketing/customer service and production and purchasing staff to ensure orders are delivered on time and according to customer specifications., • Updates and distributes sales pipeline documents as required., • Adhere to all company policies. Complete all training assigned and update the company's HRIS as required., • Required to participate in all training and development opportunities provided by the company, and will update their training records in the company’s HRIS (ISO audit requirement), • Must have a Science degree, preferably Food Science, or several years of proven experience working in a similar role, • A minimum of 5 (five) years of experience in an account management role is preferred. Equivalent experience in food product development or R&D will be considered., • Experience in the health, flavours, or nutrition industry would be considered an asset., • Excellent knowledge of Account Management, Sales and Marketing Principles, and Customer Service, • Proven record for cultivating new business and building relationships, • Fully proficient in Microsoft Word, Excel, and Internet search engines, • Familiarity with eChempax is an asset, • Excellent written and verbal communication skills, • Excellent organizational and prioritization skills, • Flexible and adaptable, • Ability to attend and conduct presentations., • Valid Ontario Driver's License essential, • Valid passport essential PI58040531e2ca-25405-40273602

Join our team and Be You Be Aptar Aptar is seeking a Molding Process Technician based in Congers, NY. The primary function of the Molding Process Technician is to operate injection molding equipment in order to successfully meet production demands and quality standards. As a Molding Process Technician, you will: • Perform set-up of molds for all mold changes, set up robots and other equipment performing necessary, • Assist in preventative maintenance and repair of molding machines, peripherals (robots, grinder, mixer, loaders), • Perform cleaning of the machines and of the production area, • Maintain a safe work environment following Company’s safety, ISO standards, • Ensure molded components meet all product quality criteria including dimensional criteria, • Communicate to supervisor and other technicians and document all technical information and issues, • Maintain records, files and other documentation pertinent for a cGMP environment. Who we are looking for: Required Skills: • 2 or more years of experience working with Plastic injection molding equipment including machine adjustment, mold installation, and removal, • Detail oriented, • Strong mechanical aptitude and mechanical skills., • Preferred: Familiarity with automation 6/3 robotics, • General knowledge of plastic materials and processes, • Preferred: Ability to work different work shifts, • Ability to work and operate machinery in a Clean Room Environment., • Physically capable of the required work including but not limited to: Extensive use of manual dexterity, ability to grip, firmly hold, turn and practice strong hand coordination in order to troubleshoot, service and repair industrial equipment and use hand tools to perform the same., • Ability to regularly stand, walk, and bend during performance of essential job duties. Ability to lift up to 50 pounds., • Understands and practices safe working procedures. Observes safety rules and policies; brings to managements’ attention any unsafe acts or conditions Who We are At Aptar, we leverage insights, design, engineering and science to develop drug and consumer product dosing, dispensing and protection technologies for many of the world’s leading brands. Aptar in turn makes a meaningful difference in the lives, looks, health and homes of millions of patients and consumers around the world. Our innovations nasal drug delivery for emergency medicines, precise fragrance applications, mess-free ketchup dispensing for kids, connected technologies that support patients in adhering to their treatments and much more With manufacturing facilities across North America, Europe, Asia and South America, and a dedicated team of over 13,000 employees in about 20 countries, Aptar is committed to creating impactful innovations for our customers and their consumers. Our Culture At Aptar, our success is driven by the individuals who contribute their unique talents and perspectives every day. We believe that when you bring your authentic self to work, we all thrive. How We Support Our Employees • An exciting, inclusive and value based working environment, • Award-winning corporate university offering personal development and training opportunities., • Competitive base salary and performance-based bonus plan., • Contribute to the communities where we reside., • Innovative benefits plan which includes: 401k & Retirement Savings plan, vacation, medical, dental, vision, life, disability, pet insurance, wellness plan, and generous paid maternity/paternity leave. Compensation and Base Annual Pay In compliance with pay transparency requirements, the salary range for this role is USD $36.00 to USD $45.00 per hour. This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. Aptar also offers a variety of benefits, including health, life, and disability insurance, 401(k) match and employer retirement savings contribution, flexible spending accounts, EAP, education assistance, parental leave, paid time off, company-paid holidays, and more. The specific programs and options available to an employee may vary depending on location, pay class, or other factors. Aptar is an equal opportunities employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief. Stay updated on career opportunities by following us on LinkedIn!

Join our team and Be You, Be Aptar Aptar Pharma is seeking a Director of Quality based onsite in Congers, NY. Primary Purpose Summary The Director of Quality is accountable for driving total quality and all quality functions of Aptar Pharma North America's full and complete product line and development lifecycle. This role will lead the Congers Quality department and its related activities covering the three Pharma divisions Prescription (Rx), Consumer Health Care (CHC), and Injectables (INJ). Accountable for the direction of North America Quality function and team who are leading all through daily operations and systems; as well as overall acceptance or rejection of product. Responsible to keep abreast of industry trends, as well as corporate initiatives that drive continuous quality improvement in a lean operating model. Ensures compliance with applicable cGMPs, FDA requirements, product and market related requirements and internal procedures. Approves Annual Product Reviews, is a member of the Change Control Committee, and oversees all Quality Key Performance Indicators (KPI's) to ensure objectives and customer satisfaction are met. This is an onsite position based in our Congers, NY facility and is also a member of Aptar Congers management committee. Detailed Description Primary Duties and Responsibilities *Lead QC, QA, QS and QE functional areas developing and following strategies and oversight ensuring compliance, quality standards and manufacturing output are met Accountable for maintaining the respective ISO certifications( ISO 15378) • Oversee prioritization of Quality activities to ensure KPI's & customer satisfaction are met., • Enable and enhance cross-functional collaboration, participate in company meetings to coordinate functions and operations between departments, including alignment of cross functional objectives, • Lead customer audits, regulatory inspections and administer a robust internal auditing system to ensure compliance with applicable cGMP and FDA requirements,, • Lead and develop a large and diverse quality organization with a strong emphasis on digital transformation within quality processes,, • Drive compliance via management and maintenance of plans and training;, • Employ smart, actionable metrics to track; Ensure Company processes are in compliance with cGMP and FDA guidelines., • Partner with the divisional global quality leaders to optimize the quality practices and product specific requirements and to leverage best practices employed within the Congers site or other Aptar Pharma sites, • Achieve financial objectives by preparing budgets, scheduling expenditures, analyzing variances, compiling and studying costs and initiating corrective actions., • Responsible for timely hiring, training, development and support of qualified staff to ensure effective execution of roles and responsibilities., • Responsible for timely updates of departmental achievements and challenges to management with a focus on operations performance and productivity, staff development, continuous improvement, ensure corrective and preventative actions are in place, key projects support and identification and resolution of obstacles to maintain a highly productive functional group., • Ensure compliance of product transfers. Required Qualifications • Education: BS in Biology, Chemistry, Pharmacy or engineering disciplines; Graduate degree preferred, • Experience: minimum of 15 years in Quality, Operations, R&D. Medical device or pharmaceutical industry with strong working knowledge of quality assurance., • Skills: Multi-discipline expertise and experience in Quality roles and strong leadership skills. Excellent working knowledge, understanding and experience with the practical implementation of FDA and EMA regulations and guidelines in other regulatory standards. Who We are At Aptar, we leverage insights, design, engineering and science to develop drug and consumer product dosing, dispensing and protection technologies for many of the world's leading brands. Aptar in turn makes a meaningful difference in the lives, looks, health and homes of millions of patients and consumers around the world. Our innovations nasal drug delivery for emergency medicines, precise fragrance applications, mess-free ketchup dispensing for kids, connected technologies that support patients in adhering to their treatments and much more With manufacturing facilities across North America, Europe, Asia, and South America, and a dedicated team of over 13,000 employees in about 20 countries, Aptar is committed to creating impactful innovations for our customers and their consumers. Our Culture At Aptar, our success is driven by the individuals who contribute their unique talents and perspectives every day. We believe that when you bring your authentic self to work, we all thrive. How We Support Our Employees • An exciting, inclusive and value based working environment, • Award-winning corporate university offering personal development and training opportunities., • Competitive base salary and performance-based bonus plan. Aptar Pharma offers a competitive total rewards package including base salary or base hourly rate determined by many factors including the role, experience, knowledge, skill set and location. For those in eligible roles, discretionary incentive compensation which may be awarded in recognition of individual achievements and contributions. The typical base annual salary range for the position of Director of Quality to the specific work location of: Congers, NY region is USD $206,000 to $279,000 per year. Additional details about total compensation and benefits are provided during the hiring process. Aptar is an equal opportunities employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief. Stay updated on career opportunities by following us on LinkedIn!

Mold Maker Work Location: Congers NY Who We Are Improving Health through Science and Technology!AtAptar Pharma, we specialize in Drug Delivery offering Innovative Devices, Services and Solutions focused on the Patient Experience.Aptar Pharmais part of Aptar Group, a global leader of dispensing systems for the packaging industry. Aptar Pharma has been setting the standard in drug delivery for decades providing health technology solutions and services enabling effective patient treatment.Be You, Be Aptar! What You Will Do at Aptar Pharma: The primary mission of theMold Makerunder limited supervision, performs a variety of operations to construct, repair or maintain in-house molds/tooling. Assignments may require the use of ordinary tool room equipment and/or outside tooling suppliers and sub-contractors. This position requires working with very tight part/steel drawing specifications/tolerances, which translates to high quality standards What Aptar Pharma Is Looking For: Primary Duties and Responsibilities: • Comply with cGMP ensuring such practices are followed by staff., • Maintain a safe work environment., • Maintain detail log history of tasks performed., • Maintain work area in a neat and orderly condition., • Participate in the analysis of defects., • Analyze blueprints for mold requirements., • Examine mold, spare parts for accuracy and conformity., • Communicate to supervisor any issues or problems., • Insure all molds are prepared for daily production., • Ensure molded components meet all product quality criteria including dimensional and visual., • Maintain, repair, clean and alter molds, components/tools and document all work., • Fit spare parts for existing tools, enhance components., • Assemble repair, inspect, clean and polish molds using skill and care while handling and polishing, • critical surfaces., • Lay out, fabricate and assemble metalworking dies, molds, and machine tool fixtures by analyzing, • blueprints, sketches, models and engineering or shop specifications., • Use a variety of machinist's hand tools and precision measuring instruments., • Set up and operate CNC lathes, milling machines and surface grinders., • Compute dimensions; determine machining and material or parts requirements., • Solve problems relating to unusual material, work-holding arrangements, machine settings,, • fabrication methods, and production processes., • Modify and/or construct tools, jigs, fixtures, robot arms, molds and mold components., • Understand form fit and functions in mold construction., • Perform close-tolerance machining using detailed blueprints, drawings, and sketches., • Uses precision measuring instruments in the fabrication of various mold components and plastic, • tools and parts., • Perform accurate layout of tolerance and angles required to complete assignments., • Recommend design improvements and/or substitutions of material as required., • Interface with other functional departments., • Other assigned duties. What you will bring on the journey: Education: • 5 years' experience working as a mold/tool maker., • Knowledge of molding process and ability to troubleshoot problems., • Good mathematical and mechanical aptitude. Skills/Abilitie • Pharmaceutical knowledge., • ISO knowledge., • Injection molding experience. What We Offer • An exciting, diverse and value based working environment., • Award-winning corporate university offering personal development and training opportunities., • Competitive base salary, • Contribute to the communities where we reside. BE YOU, BE APTAR! Aptar is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information Aptar Pharma, NA 250 Route 303 North Congers, NY 10920 Improving Health through Science and Technology! Nearest Major Market:New York City

Co-Op Student / Intern Improving Health through Science and Technology! At Aptar Pharma, we specialize in Drug Delivery offering Innovative Devices, Services and Solutions focused on the Patient Experience. Aptar Pharma is part of Aptar Group, a global leader of dispensing systems for the packaging industry. Aptar Pharma has been setting the standard in drug delivery for decades providing health technology solutions and services enabling effective patient treatment. Be You, Be Aptar! What You Will Do at Aptar Pharma: Aptar Pharma NA is seeking Co-Op students and Interns within several technical areas of our business. As a Co-Op Student or Intern, you gain valuable work experience, enhance your knowledge in engineering and science and satisfy your curiosity for industrial technology! What Aptar Pharma Is Looking For: • Utilize mechanical skills to install, remove and adjust Injection Molding machinery and equipment., • Troubleshoot Injection Molding machines, follow process to resolve failures and other problems., • Perform set-up of molds for all mold changes., • Assist in preventative maintenance and repair of molding machines, molds, peripherals and (robots)., • Coordinate and set-up machines, robots and other equipment performing necessary tests to ensure company compliance., • Perform cleaning and general maintenance tasks., • Maintain a safe work environment following Company's safety, and ISO standards., • Achieve adequate production levels while maintaining the expected product quality., • Ensure molded components meet all product quality criteria., • Communicate to supervisor and other technicians; document all technical information/issues., • Participate in reducing the rate of scrap., • Assist in training of employees in proper work methods for safe and efficient performance of job duties., • Maintain records, files and other documentation pertinent to assignments., • Assume additional responsibilities as required. What you will bring on the journey • High School Diploma or equivalent., • Basic mechanical aptitude and mechanical skills including troubleshooting., • 1-3 years of experience working with injection molding equipment including machine adjustment, troubleshooting and mold installation and removal., • General knowledge of plastic materials and processes., • Detail oriented., • Ability to implement and tune all peripherals (6 axis robot, grinder)., • Strong verbal and written communication skills., • Good mathematical aptitude., • Effective computer skills. Manufacturing knowledge., • ISO knowledge., • Quality Control experience. What We Offer • An exciting, diverse and value based working environment., • Award-winning corporate university offering personal development and training opportunities., • Competitive base salary, • Contribute to the communities where we reside., • Innovative benefits plan which includes: 401k plan with Company matching benefit, paid time off, medical, dental, vision, life, disability and more Compensation and Base Annual Pay In compliance with pay transparency requirements, the hourly rate range for this role isUSD $23 to USD $25 per hour.This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. Aptaralso offers a variety of benefits, including health, life, and disability insurance, 401(k) match and employer retirement savings contribution, flexible spending accounts, EAP, education assistance, parental leave, paid time off, company-paid holidays, and more. The specific programs and options available to an employee may vary depending on location, pay class, or other factors. BE YOU, BE APTAR! Aptar is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information Aptar Pharma, NA 250 Route 303 North Congers, NY 10920 Improving Health through Science and Technology!

Molding Process Technician (Weekends) Improving Health through Science and Technology! At Aptar Pharma, we specialize in Drug Delivery offering Innovative Devices, Services and Solutions focused on the Patient Experience. Aptar Pharma is part of Aptar Group, a global leader of dispensing systems for the packaging industry. Aptar Pharma has been setting the standard in drug delivery for decades providing health technology solutions and services enabling effective patient treatment. Be Aptar! What You Will Do at Aptar Pharma: Our Technicians operate injection molding equipment in order to successfully meet production demands and quality standards. Duties include but are not limited to: • Utilize your mechanical skills to install, remove and adjust Injection Molding machinery and equipment, • Troubleshoot Injection Molding machines, follow process to resolve failures, other problems, • Perform set-up of molds for all mold changes, • Assist in preventative maintenance and repair of molding machines, molds and peripherals (robots), • Coordinates and sets up machines, robots and other equipment performing necessary tests to ensure company compliance. Trains employees in the correct procedures for operation as needed., • Perform cleaning and general maintenance tasks, • Maintain a safe work environment following Company's safety, ISO standards, • Achieve adequate production levels while maintaining the expected product quality, • Ensure molded components meet all product quality criteria including dimensional criteria, • Communicate to supervisor and other technicians and document all technical information and issues, • Participate in reducing the rate of scrap, • Assists in training of employees in proper work methods for safe and efficient performance of job duties., • Maintains records, files and other documentation pertinent to assignments., • Strong mechanical aptitude and mechanical skills., • 1-3 years of experience working with injection molding equipment including machine adjustment, troubleshooting and mold installation and removal, • Familiarity with automation 6/3 robotics, • General knowledge of plastic materials and processes, • Detail oriented, • Ability to implement and tune all peripherals (6 axis robot, grinder), • Strong verbal and written communication skills, • Strong Mathematical aptitude, • Ability to read blueprints, use precision measuring/inspection tools, • Effective computer skills, documentation, reporting, file management and web skills, • Ability to work different work shifts, • Continual improvement mindset. Self-Learner, trend of continuous learning, • Ability to work and operate machinery in a Clean Room Environment., • Physically capable of the required work including but not limited to: Extensive use of manual dexterity, ability to grip, firmly hold, turn and practice strong hand coordination in order to troubleshoot, service and repair industrial equipment and use hand tools to perform the same. Ability to regularly stand, walk, and bend during performance of essential job duties. Ability to lift up to 50 pounds. What We Offer • An exciting, diverse and value based working environment, • Award-winning corporate university offering personal development and training opportunities., • Competitive base salary, • Contribute to the communities where we reside., • Innovative benefits plan which includes: 401k plan with Company matching benefit, paid time off, medical, dental, vision, life, disability and more Compensation and Base Annual Pay In compliance with pay transparency requirements, the salary range for this role isUSD $36.00 to $45.00 per hour.This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. Aptaralso offers a variety of benefits, including health, life, and disability insurance, 401(k) match and employer retirement savings contribution, flexible spending accounts, EAP, education assistance, parental leave, paid time off, company-paid holidays, and more. The specific programs and options available to an employee may vary depending on location, pay class, or other factors. BE YOU, BE APTAR! Aptar is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information Aptar Pharma, NA 250 Route 303 North Congers, NY 10920 Improving Health through Science and Technology!

Active Listening, Asset Care Management, Attention to Detail, Batch Records, Basic Troubleshooting, CMMS, Documentation & Record Keeping, Environmental & Safety Testing, Equipment Operation, FDA Regulations, GMP Compliance, Instruction Following, ISO Standards, Manufacturing, Preventive Maintenance,

Active Listening, Asset Care Management, Attention to Detail, Batch Records, Basic Troubleshooting, CMMS, Documentation & Record Keeping, Environmental & Safety Testing, Equipment Operation, FDA Regulations, GMP Compliance, Instruction Following, ISO Standards, Manufacturing, Preventive Maintenance,

Mold Maker Work Location: Congers NY Who We Are Improving Health through Science and Technology!AtAptar Pharma, we specialize in Drug Delivery offering Innovative Devices, Services and Solutions focused on the Patient Experience.Aptar Pharmais part of Aptar Group, a global leader of dispensing systems for the packaging industry. Aptar Pharma has been setting the standard in drug delivery for decades providing health technology solutions and services enabling effective patient treatment.Be You, Be Aptar! What You Will Do at Aptar Pharma: The primary mission of theMold Maker under limited supervision, performs a variety of operations to construct, repair or maintain in-house molds/tooling. Assignments may require the use of ordinary tool room equipment and/or outside tooling suppliers and sub-contractors. This position requires working with very tight part/steel drawing specifications/tolerances, which translates to high quality standards What Aptar Pharma Is Looking For: Primary Duties and Responsibilities: • Comply with cGMP ensuring such practices are followed by staff., • Maintain a safe work environment., • Maintain detail log history of tasks performed., • Maintain work area in a neat and orderly condition., • Participate in the analysis of defects., • Analyze blueprints for mold requirements., • Examine mold, spare parts for accuracy and conformity., • Communicate to supervisor any issues or problems., • Insure all molds are prepared for daily production., • Ensure molded components meet all product quality criteria including dimensional and visual., • Maintain, repair, clean and alter molds, components/tools and document all work., • Fit spare parts for existing tools, enhance components., • Assemble repair, inspect, clean and polish molds using skill and care while handling and polishing, • critical surfaces., • Lay out, fabricate and assemble metalworking dies, molds, and machine tool fixtures by analyzing, • blueprints, sketches, models and engineering or shop specifications., • Use a variety of machinist's hand tools and precision measuring instruments., • Set up and operate CNC lathes, milling machines and surface grinders., • Compute dimensions; determine machining and material or parts requirements., • Solve problems relating to unusual material, work-holding arrangements, machine settings,, • fabrication methods, and production processes., • Modify and/or construct tools, jigs, fixtures, robot arms, molds and mold components., • Understand form fit and functions in mold construction., • Perform close-tolerance machining using detailed blueprints, drawings, and sketches., • Uses precision measuring instruments in the fabrication of various mold components and plastic, • tools and parts., • Perform accurate layout of tolerance and angles required to complete assignments., • Recommend design improvements and/or substitutions of material as required., • Interface with other functional departments., • Other assigned duties. What you will bring on the journey: Education: • 5 years' experience working as a mold/tool maker., • Knowledge of molding process and ability to troubleshoot problems., • Good mathematical and mechanical aptitude. Skills/Abilities: • Pharmaceutical knowledge., • ISO knowledge., • Injection molding experience. What We Offer • An exciting, diverse and value based working environment., • Award-winning corporate university offering personal development and training opportunities., • Competitive base salary, • Contribute to the communities where we reside. BE YOU, BE APTAR! Aptar is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information Aptar Pharma, NA 250 Route 303 North Congers, NY 10920 Improving Health through Science and Technology! Nearest Major Market:New York City Find similar jobs:

Job Title: Mold Maker (Tool & Die) Location: Rockland, Westchester County, & Hudson Valley Area Schedule: On-site, Monday–Friday (5 days/week) Pay Rate: $40–$50/hour (based on experience) Overview: A well-established manufacturing organization is seeking a skilled Mold Maker (Tool & Die) to join its team. This role is responsible for constructing, repairing, and maintaining in-house molds and tooling with minimal supervision. The position requires working with tight tolerances and high-quality standards, utilizing a variety of tool room equipment and collaborating with external tooling vendors when needed. Key Responsibilities: • Follow cGMP guidelines and ensure compliance across all activities, • Maintain a safe, clean, and organized work environment, • Keep detailed logs of all work performed, • Analyze blueprints and engineering drawings to determine mold requirements, • Inspect molds and components for accuracy and quality compliance, • Troubleshoot and resolve mold-related issues (e.g., flashing, galling, venting, cooling), • Disassemble, assemble, repair, clean, and polish molds with precision, • Perform close-tolerance machining using CNC lathes, milling machines, and grinders, • Fabricate and assemble dies, molds, fixtures, and tooling components, • Use precision measuring instruments to ensure accuracy, • Modify and enhance existing molds, tools, and components, • Collaborate with cross-functional teams and communicate issues to supervisors, • Ensure molds are production-ready and meet all dimensional and visual quality standards, • Recommend design improvements and material substitutions when applicable Education: • High school diploma or equivalent required, • Minimum 3 years of experience as a mold/tool maker, • At least 1 year of experience working with injection molds, • Strong understanding of molding processes and troubleshooting techniques, • Injection molding experience required, • Familiarity with ISO standards preferred, • Pharmaceutical industry experience is a strong plus (not required), • Strong mathematical and mechanical aptitude, • Ability to interpret complex blueprints and specifications, • Excellent problem-solving skills and attention to detailTravel:, • Occasional travel may be required, though it is not expected to be frequentPay Details: $40.00 to $50.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: • The California Fair Chance Act, • Los Angeles City Fair Chance Ordinance, • Los Angeles County Fair Chance Ordinance for Employers

Job DescriptionJob Title: Mold Maker (Tool & Die) Location: Rockland, Westchester County, & Hudson Valley Area Schedule: On-site, Monday–Friday (5 days/week) Pay Rate: $40–$50/hour (based on experience) Overview: A well-established manufacturing organization is seeking a skilled Mold Maker (Tool & Die) to join its team. This role is responsible for constructing, repairing, and maintaining in-house molds and tooling with minimal supervision. The position requires working with tight tolerances and high-quality standards, utilizing a variety of tool room equipment and collaborating with external tooling vendors when needed. Key Responsibilities: • Follow cGMP guidelines and ensure compliance across all activities, • Maintain a safe, clean, and organized work environment, • Keep detailed logs of all work performed, • Analyze blueprints and engineering drawings to determine mold requirements, • Inspect molds and components for accuracy and quality compliance, • Troubleshoot and resolve mold-related issues (e.g., flashing, galling, venting, cooling), • Disassemble, assemble, repair, clean, and polish molds with precision, • Perform close-tolerance machining using CNC lathes, milling machines, and grinders, • Fabricate and assemble dies, molds, fixtures, and tooling components, • Use precision measuring instruments to ensure accuracy, • Modify and enhance existing molds, tools, and components, • Collaborate with cross-functional teams and communicate issues to supervisors, • Ensure molds are production-ready and meet all dimensional and visual quality standards, • Recommend design improvements and material substitutions when applicable, • High school diploma or equivalent required, • Technical training or related experience preferredExperience:, • Minimum 3 years of experience as a mold/tool maker, • At least 1 year of experience working with injection molds, • Strong understanding of molding processes and troubleshooting techniques, • Proficiency with tool room equipment and machine practicesSkills & Abilities:, • Injection molding experience required, • Familiarity with ISO standards preferred, • Pharmaceutical industry experience is a strong plus (not required), • Strong mathematical and mechanical aptitude, • Ability to interpret complex blueprints and specifications, • Excellent problem-solving skills and attention to detailTravel:, • Occasional travel may be required, though it is not expected to be frequent Pay Details: $40.00 to $50.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: • The California Fair Chance Act, • Los Angeles City Fair Chance Ordinance, • Los Angeles County Fair Chance Ordinance for Employers, • San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Job Description Summary: We are seeking a detail-oriented Quality Inspector to join our team. This role is responsible for inspecting raw materials, in-process components, and finished products to ensure they meet company and customer specifications. The ideal candidate has strong attention to detail and experience working in a manufacturing or quality environment. Responsibilities: • Perform incoming, in-process, and final inspections of parts and materials, • Read and interpret blueprints, engineering drawings, and specifications, • Use precision measuring instruments (calipers, micrometers, gauges, height gauges, etc.), • Document inspection results and maintain accurate records, • Identify and report non-conforming products and assist with corrective actions, • Ensure compliance with company quality standards and procedures (ISO/AS standards as applicable), • Perform first article inspections (FAI) as required, • Work closely with production and engineering teams to resolve quality issues, • Maintain a clean and organized inspection area, • Follow all safety procedures and company policies Qualifications: • 2+ years of quality inspection experience preferred, • Experience in a manufacturing environment required, • Ability to read and interpret blueprints and technical drawings, • Proficiency with measuring tools and inspection equipment, • Strong attention to detail and documentation skills, • Basic computer skills for data entry and reporting, • Knowledge of ISO 9001 and/or AS9100 standards is a plus, • Ability to work independently and as part of a team, • Willingness to work overtime as needed Schedule & Compensation: • Full-time position (40 hours per week), • Overtime required based on production needs, • We offer a generous compensation package, which includes competitive hourly up to $20.00 p/h D.O.E, Health Insurance, Vision, Dental, 401K, Vacation & sick/personal days and Life insurance. $250.00 SIGN-ON BONUS EDUCATION and/or EXPERIENCE: High School Diploma or GED; College degree a plus. Equivalent combination of education and experience. WORK ENVIRONMENT: Manufacturing. Fast paced. Must be able to lift and or move up to 50 lbs. AAP/EEO Statement Metallized Carbon Corporation has been and will continue to be an equal opportunity employer. Applicants are recruited, hired, assigned and promoted without regard to race, religion, color, national origin, citizenship, sex, veteran's status, age or disability. ITAR Statement: This position requires compliance with ITAR requirements. Must be a "U.S. Person" (per ITAR 120.15) and are required to show proof substantiating this upon being hired. Company DescriptionFor over 75 years now Metallized Carbon Corporation has been the leader in manufactured engineered carbon graphite solutions for severe service lubrication. Throughout the world, we provide products and services to various industries that deal with sophisticated equipment. Whether aerospace, food service, automotive or petrochemical, you are sure to find carbon graphite bearings, seals or other items produced by METCAR. If you are looking for a highly technical career in a challenging environment, please contact us today.For over 75 years now Metallized Carbon Corporation has been the leader in manufactured engineered carbon graphite solutions for severe service lubrication. Throughout the world, we provide products and services to various industries that deal with sophisticated equipment. Whether aerospace, food service, automotive or petrochemical, you are sure to find carbon graphite bearings, seals or other items produced by METCAR. If you are looking for a highly technical career in a challenging environment, please contact us today.

Job Description About Us: Metallized Carbon Corporation (Metcar) is a leading manufacturer of carbon and graphite components, committed to precision, quality, and continuous improvement in a fast-paced manufacturing environment. For over 75 years Metallized Carbon Corporation has been the leader in highly engineered carbon graphite solutions for severe service lubrication. Throughout the world, we provide products and services to various industries that deal with sophisticated equipment. Whether aerospace, food service, petrochemical or power, you are sure to find bearings, seals and other self-lubricating mechanical components produced by METCAR. If you are looking for a highly technical career in a challenging environment, please contact us today. Position Summary: We are seeking a detail-oriented Quality Inspector to join our team. This role is responsible for inspecting raw materials, in-process components, and finished products to ensure they meet company and customer specifications. The ideal candidate has strong attention to detail and experience working in a manufacturing or quality environment. Responsibilities: • Perform incoming, in-process, and final inspections of parts and materials, • Read and interpret blueprints, engineering drawings, and specifications, • Use precision measuring instruments (calipers, micrometers, gauges, height gauges, etc.), • Document inspection results and maintain accurate records, • Identify and report non-conforming products and assist with corrective actions, • Ensure compliance with company quality standards and procedures (ISO/AS standards as applicable), • Perform first article inspections (FAI) as required, • Work closely with production and engineering teams to resolve quality issues, • Maintain a clean and organized inspection area, • 2+ years of quality inspection experience preferred, • Experience in a manufacturing environment required, • Ability to read and interpret blueprints and technical drawings, • Proficiency with measuring tools and inspection equipment, • Strong attention to detail and documentation skills, • Basic computer skills for data entry and reporting, • Knowledge of ISO 9001 and/or AS9100 standards is a plus, • Ability to work independently and as part of a team, • Full-time position (40 hours per week), • Overtime required based on production needs WORK ENVIRONMENT: Manufacturing. Fast paced. Must be able to lift and or move up to 50 lbs. Apply online: - Walk-ins welcome. Se habla Espanol. Tel. (914)-941-8554. We are located at: 19 S. Water St., Ossining, NY. Next to Ossining, NY railroad station. AAP/EEO Statement Metallized Carbon Corporation has been and will continue to be an equal opportunity employer. Applicants are recruited, hired, assigned and promoted without regard to race, religion, color, national origin, citizenship, sex, veteran's status, age or disability. ITAR Statement: This position requires compliance with ITAR requirements. Must be a "U.S. Person" (per ITAR 120.15) and are required to show proof substantiating this upon being hired.

Job Description About Us: Metallized Carbon Corporation For over 75 years now Metallized Carbon Corporation has been the leader in manufactured engineered carbon graphite solutions for severe service lubrication. Throughout the world, we provide products and services to various industries that deal with sophisticated equipment. Whether aerospace, food service, automotive or petrochemical, you are sure to find carbon graphite bearings, seals or other items produced by METCAR. If you are looking for a highly technical career in a challenging environment, please contact us today. Job Summary: We have an exciting and rewarding opportunity for a Manufacturing Engineer. Excellent opportunity for a highly motivated and self-directed individual to join a stable and reputable manufacturing company of engineered mechanical components. The Manufacturing Engineer is responsible for developing, standardizing, and improving manufacturing processes to ensure product quality, cost efficiency, and production reliability. This role will work closely with production, quality, and maintenance teams to optimize workflows, resolve shop-floor issues, and support continuous improvement initiatives across CNC machining, programming, set up, fabrication, and assembly operations. Responsibilities: • Develop, document, and standardize manufacturing processes, methods, and work instructions to improve productivity, consistency, and safety., • Analyze production data to identify and resolve process inefficiencies, bottlenecks, and quality issues., • Provide hands-on engineering support on the shop floor, assisting operators and supervisors in problem-solving and technical troubleshooting., • Design and implement tooling, jigs, and fixtures to improve manufacturing accuracy, setup efficiency, and repeatability., • Collaborate with Quality, Maintenance, and CNC Programming teams to verify accuracy and conformity of parts and processes to specifications., • Evaluate and recommend manufacturing methods, equipment, and technology upgrades to support cost reduction and continuous improvement initiatives., • Support new product introduction (NPI) by developing process flows, work instructions, and required tooling., • Ensure alignment with ISO/Quality Management Systems and other applicable standards and regulations., • Bachelor’s Degree in Mechanical Engineering or related technical discipline required., • 5–7 years of experience in a manufacturing engineering role within an industrial, machining, or fabrication environment., • Proven experience with CNC machining processes, programming, set up, tooling design, and fixture development., • Strong understanding of manufacturing methods, process optimization, and lean manufacturing principles., • Exposure to quality systems (ISO 9001, AS9100, or equivalent) and experience working cross-functionally with quality teams., • Proficient in CAD software (SolidWorks, AutoCAD, or similar) and ability to create or interpret engineering drawings and models., • Excellent analytical, problem-solving, and communication skills. Benefits Package Includes: Salary commensurate with experience ($75K - $90K). Comprehensive health insurance plan, 401k retirement plan, Sick/personal days, Vacation, paid holidays, Life insurance, STD, LTD, AD&D insurance coverage. ITAR Statement This position requires compliance with ITAR requirements. Must be a “U.S. Person” (per ITAR 120.15) and are required to show proof substantiating this upon being hired. AAP/EEO Statement Metallized Carbon Corporation has been and will continue to be an equal opportunity employer. Applicants are recruited, hired, assigned and promoted without regard to race, religion, color, national origin, citizenship, sex, veteran's status, age or disability.

Job Description JOB TITLE: Embedded Software Engineer LOCATION: Hawthorne, NY (on-site) TYPE: Full time, regular COMPENSATION: $115,000 – $155,000/yr Clarapath is a medical robotics company based in Westchester County, NY, dedicated to transforming and modernizing laboratory workflows. Our mission is to improve patient care by increasing efficiency, reducing costs, and enhancing the quality and consistency of laboratory processes. Our portfolio includes SectionStar™ and TrimStar Pro™, innovative electro-mechanical systems designed to automate and elevate critical steps in the histology workflow. SectionStar™ delivers high-quality, consistent tissue sections, while TrimStar Pro™ streamlines and standardizes the trimming process - together enabling laboratories to operate with greater precision, throughput, and reliability. At Clarapath, we bring together experts across engineering, data science, robotics, healthcare innovation, and laboratory operations. Our R&D team drives innovation, product enhancements, and a strong pipeline of new solutions, while our manufacturing team oversees production and quality control at our ISO-certified facility. Also based in our New York headquarters are our sales, marketing, administrative, and service teams, who work closely together to ensure every customer receives a seamless, personalized experience at every touchpoint. Role Summary: The Embedded Software Engineer will be working alongside our existing software engineers, electrical engineers on medical device development. This role is multi-disciplinary with technical responsibility for designing, developing, and testing device control software, both at the driver and at the application level. We are looking for a team player who views medical device development as a competitive advantage. Responsibilities: • Design, develop and maintain embedded software applications for various platforms, including microcontrollers and microprocessors, • Develop drivers for interfacing with motor controllers, cameras, scanners, and PLC systems, • Collaborate with hardware engineers to define system requirements and develop software architecture designs, • Implement real-time operating systems (RTOS) and device drivers to support hardware functionality, • Write efficient and reliable code in C/C++ for embedded systems, ensuring optimal performance and resource utilization, • Conduct unit testing and debugging of software modules to identify and resolve defects, • Participate in code reviews and provide constructive feedback to ensure code quality and maintainability, • Work closely with cross-functional teams, including firmware engineers, hardware engineers, and QA testers, to integrate software components and validate system functionality, • Stay updated on emerging technologies and industry trends related to embedded software development, and incorporate best practices into our development processes, • Document software designs, specifications, and test procedures to support product development and regulatory compliance efforts, • Bachelor’s degree in Computer Science, Electrical Engineering, or related field. Master’s degree preferred, • 5+ years of experience in embedded software development, with a strong proficiency in C/C++ and Python programing languages, • Prior experience working in a LINUX environment, • Prior experience working with GIT or other code repository systems, • Solid understanding of the TCP/IP protocol stack, • Solid understanding of multithreading and real-time embedded systems, including RTOS, device drivers, and hardware-software interfaces, • Prior experience utilizing PID-based control for motion and temperature regulation, • Experience with embedded development tools and environments, such as IDEs, debuggers, and version control systems, • Familiarity with microcontroller architectures and peripheral interfaces (ex: Ethernet, Serial, UART, SPI, I2C, GPIO), • Familiarity with industrial communication protocols such as MODBUS, • Knowledge of software development lifecycle (SDLC) processes and quality assurance principles, • Strong analytical and problem-solving skills, with the ability to troubleshoot complex software issues, • Excellent communication and teamwork abilities, with a collaborative approach to problem-solving, • Demonstrated ability to work effectively in a fast-paced, deadline-driven environment, • Prior experience in Agile development methodologies and continuous integration practices, a plus, • Experience with robotics platforms like ROS or YARP, a plus, • Experience interfacing with Clinical Lab Information Systems, a plus, • Experience in addressing data security and compliance with HIPPA regulations, a plus, • Histology laboratory workflow experience, 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 Description Overview 170+ Years Strong. Industry Leader. Global Impact. At Pinkerton, the mission is to protect our clients. To do this, we provide enterprise risk management services and programs specifically designed for each client. Pinkerton employees are one of our most important assets and critical to the delivery of world-class solutions. Bonded together, we share a commitment to integrity, vigilance, and excellence. Pinkerton is an inclusive employer who seeks candidates with diverse backgrounds, experiences, and perspectives to join our family of industry subject matter experts. The Supply Chain Security Operations Manager, assigned to a specific client, will identify security risks and vulnerabilities across the client's supply chain partners while interpreting and communicating corporate security policies. This role involves collaborating closely with partners to ensure corrective actions align with Global Security management, tracking their implementation, and performing validations. This position can be located in Boston, MA or New York City, NY. Responsibilities • Represent Pinkerton’s core values of integrity, vigilance, and excellence., • Identify security risk and vulnerabilities across client’s supply chain partners., • Interpret and communicate the client’s corporate security and investigative policies., • Work closely with client’s supply chain partners to ensure corrective action plans are drafted and align them with the Global Security management., • Track implementation of corrective action plans by supply chain partners and perform field validations to ensure the proper implementation of such plans, • Support and/or conduct global security assessments and audits of supply chain partners and prospective suppliers., • Engage with third-parties to assign security services to mitigate elevated risks within the global supply chain environment, where directed., • Direct the activities of field operations personnel engaged in providing security services to ensure they are following all policies, procedures, and best practices., • Monitor in-transit shipments, apply risk mitigation measures, and provide assurance that shipments have arrived intact at their intended destination., • Identify trends and report them to global security management., • Support supply chain incident investigations and tracking through field investigations., • Interface other client corporate and local staff functions relative to security and investigations., • Conduct, coordinate and/or perform investigations as required., • Establish and maintain liaison with governmental law enforcement and security agencies., • Participate in local/regional security mutual aid organizations dealing with regional security issues related to TAPA, CTPAT, and others., • Provide leadership in the continued implementation of the common security process and review the results with the client and the security service providers., • Facilitate the common implementation of best business practices in combination with continuous improvement programs., • Promote consistent and enthusiastic focus on client service., • All other duties, as assigned. Qualifications Bachelor's degree with at least eight years in supply chain management or an equivalent combination of education and experience, sufficient to perform the essential functions of the job as determined by the company. • CPP, PSP, and/or TAPA certifications, preferred., • Knowledge of security operations, loss prevention, asset protection and/or IP protection, preferred., • Knowledge of loss prevention, asset protection, and/or IP protection, preferred., • Understanding of environment, health, and safety (EHS) as it relates to supply chains., • Knowledge of ISO 28000, ISO 31000, ISO 17712, and ISO 27002., • Understanding of governmental supply chain security programs, AEO, NEEC, PIP, WCO, and TAPA., • Understanding of inventory management and reconciliation principles., • Effective management and influencing without authority skills., • Serve as a positive and effective team member., • Able to manage multiple projects simultaneously., • Able to formulate action plans for process improvement initiatives including complex data analysis., • Customer orientated and results driven., • Able to make sound decisions, with the client’s best interest in mind, while under severe time constraints/pressures. With or without reasonable accommodation, requires the physical and mental capacity to effectively perform all essential functions; • Regular computer usage., • Occasional reaching and lifting of small objects and operating office equipment., • Frequent climbing, walking while performing investigations within an industrial environment where there may be exposure to dust and common warehouse industrial hazards while wearing personal protective equipment.

Job Description About Schreiner The Schreiner Group is a privately held, family-owned organization, operating with over 1,500 employees across three locations (Germany, China, US). As an internationally active, high-tech label manufacturer, we are mostly a strategic partner for our customers in the healthcare & automotive industries markets. Our core business is innovative high-tech labels and functional parts. We increase the added value for our customers through suitable system solutions and services. The North American operations are currently headquartered in Blauvelt, NY with plans to relocate to Chestnut Ridge, NY within the next two years. The brand-new location will offer the increased production, warehousing, and shipping capacity needed to support our continued growth in the market. In addition, the new facility will include a training center for our employees to enhance their skills, and to test new innovations. By focusing on our customers' needs, we can deliver excellent service in support of their goals. About the Role: The Maintenance & Facilities Manager is a vital role among the Operations team, reporting directly to the Director of Operations for North America. This role will be responsible for building and managing a team of facilities and maintenance technicians in direct support of our production processes. The primary focus is on developing a team that can perform scheduled, preventative maintenance, troubleshoot concerns as they arise. This individual will be responsible for the M&F budget creation and adherence, process ownership of ERP systems, and aligning schedules to best support the needs of production and sales. Summary Responsible for the building and managing a team focused on reliable operation, regulatory compliance, and continuous improvement of all facilities, utilities, and production equipment. • Hires, develops and manages technicians and other personnel within scope, • Manages contractors, spare parts, and capital projects to support manufacturing, laboratories, and warehousing operations., • Leads preventive and predictive maintenance programs to ensure high equipment availability, safety, and regulatory compliance., • Acts as Process Owner for all systems and ERP configuration or projects Lead, train, develop, schedule, and supervise maintenance technicians • Delegate tasks and responsibilities to direct and indirect reports as appropriate, • Develop and manage departmental budgets, labor planning, and overtime control., • Establish KPIs for uptime, PM compliance, response time, and cost control., • Ensure compliance with agencies such as EHS, OSHA, EPA, and internal quality systems., • Review and approve work orders, change controls, deviations, and CAPAs., • Manage vendor performance, service contracts, and qualification of external service providers. Oversee execution of preventive, predictive, and corrective maintenance activities. • Ensure calibration, validation, and requalification of critical equipment and utilities., • Coordinate emergency repairs to minimize production downtime., • Manage CMMS systems (e.g., SAP, or equivalent) for work orders, PMs, and asset history., • Monitor equipment performance, breakdown trends, and spare parts usage. Develop and implement long-term maintenance and asset reliability strategies. • Drive continuous improvement in reliability, cost, and energy efficiency., • Support capacity expansion, facility upgrades, and capital investment planning., • Lead root cause analysis and reliability-centered maintenance (RCM) initiatives., • Align maintenance strategy with production, quality, and business objectives., • Identify and implement new technologies for predictive maintenance and automation. Ensure all facilities meet safety, environmental, and building code requirements. • Support sustainability and energy reduction initiatives., • Participate in cross-functional teams for production planning, validation, and quality improvement., • Lead emergency preparedness, fire protection, and business continuity planning. Authority to assign, prioritize, and approve maintenance work. • Authority to stop equipment or operations that pose safety or quality risks., • Responsible for compliance with GMP, EHS, and regulatory standards., • Responsible for maintaining facility and equipment readiness for audits and inspections., • Authority to select, approve, and manage service providers and spare parts suppliers. Education • Bachelor’s degree or higher in Engineering (Mechanical, Electrical, Industrial), Facilities Management, Industrial Technology, or related discipline., • 5-10 years’ experience in facilities, utilities, or equipment maintenance in manufacturing, pharma, medical devices, or regulated industries., • 3+ years in a supervisory or management role preferred., • 3+ years of experience managing workflows via ERP system, preferably SAP, • Experience with GMP, validation, CMMS, and regulatory inspections., • Ability to lift up to 30 pounds., • Ability to walk, stand, climb ladders, & work in mechanical rooms & production areas., • Ability to sit or stand for extended periods., • Ability to respond to emergency maintenance situations, including after-hours support.

Job Description Position Overview: The Director of Technical Services is responsible for leading the strategic, operational, and regulatory functions of the technical support department to ensure alignment with organizational goals. This role provides direct leadership to all Technical Support, Biomedical Engineering, and Installation staff, driving performance, accountability, and professional development across teams. The position oversees budget planning and cost center management, provides advanced technical expertise for instrumentation and test systems, and leads troubleshooting and resolution of complex hardware, software, and customer-related issues. Working cross-functionally with Marketing, Product Management, QA/Regulatory, and commercial teams, the Technical Operations Manager supports new product validations, training initiatives, and quality compliance. The role ensures adherence to FDA, ISO 13485, Canadian Medical Device regulations, Joint Commission standards, and other applicable laboratory and regulatory requirements while developing and maintaining SOPs, audit processes, and quality systems. Additionally, this position manages contracted service providers, oversees documentation within technical support systems, evaluates QC and calibration data, and drives continuous improvement initiatives to enhance operational efficiency, regulatory compliance, and customer satisfaction. Key Responsibilities: • Strategic Planning: Develop and implement strategic plans for the department in conjunction with VP, ensuring alignment with organizational goals and objectives., • Budget Management: Develop and manage budgets for technical operations cost center, including forecasting, expense tracking and capital assess planning and ensure budget adherence., • Leads all technical support, biomedical engineering and installation staff and support all functions of technical operations, installation, troubleshooting and service., • Provide technical support for the performance of routine and special tests of Polymedco instrumentation and equipment according to established protocol., • Assist in evaluation, diagnosing, and resolution of higher level customer complaints., • Troubleshoot both hardware and software related problems on equipment and analyzers., • Lead technical training for commercial team and new employees. Develop training material and serve as a resource in instrument operation and maintenance., • Collaborate with Marketing/Product management and QA/regulatory departments on validations and support of new products., • Evaluate Quality Control/Calibration data. Provide troubleshooting recommendations., • Work on new test systems and make recommendations regarding technical procedures. Perform evaluation of new equipment. Assist in developing and writing test procedures and Standard Operations Protocol., • Manage and oversee the contracted service providers ensuring they are meeting their commitments., • Collaborate with Quality team to ensure metrics are aligned with leadership drive KPIs., • Initiate, maintain and complete all necessary documentation in the Technical Support Software System (CQ). Develop, evaluate and assist with interpretation of data for the purpose of account correlation and troubleshooting., • Ensure compliance with internal policies listed in Employee Handbook, internal department processes and all SOP’s, • Perform internal quality auditing as needed., • Develop procedures and SOPs for parts management, complaint handling, equipment maintenance, staff and customer training, communication with partners, as well as other activities., • Demonstrate knowledge of Laboratory Regulatory Agencies and policies, applicable FDA regulations, ISO 13485:2003 standards and Canadian Medical Device regulations., • Travel up to 25%, • Occasional off hours work, • Ability to train and guide others., • Previous experience in the diagnostics or medical devices industry., • Experience working in a fast-growing company and driving transformation, • Minimum of bachelor’s degree or a combination of education, training and/or 10 years experience in a related field, • Minimum 10 years experience on laboratory equipment and instruments or other related equipment.

Job Description Manufacturing Engineer Location: Croton-on-Hudson, NY Client does not offer Relocation. Must live commutable distance. Compensation: $75,000 – $90,000 (depending on experience) MUST HAVE CNC OPERATIONS EXPERIENCE. A stable and reputable manufacturing company is seeking a Manufacturing Engineer to support and improve production operations. This is an excellent opportunity for a hands-on, self-directed individual to play a key role in optimizing manufacturing processes, improving efficiency, and supporting continuous improvement initiatives across machining and production environments. Qualifications: • Bachelor’s Degree in Mechanical Engineering or related technical discipline required, • 5–7 years of experience in a manufacturing engineering role within a machining or fabrication environment, • Strong experience with CNC machining processes, programming, setup, tooling, and fixture design, • Solid understanding of process optimization and lean manufacturing principles, • Experience working with quality systems such as ISO 9001, AS9100, or similar, • Proficiency in CAD software (SolidWorks, AutoCAD, or similar), • Strong analytical, problem-solving, and communication skills, • Ability to work both independently and collaboratively in a fast-paced environment Key Responsibilities: • Develop, document, and standardize manufacturing processes and work instructions to improve efficiency and consistency, • Analyze production data to identify and resolve process inefficiencies, bottlenecks, and quality issues, • Provide hands-on support on the shop floor, assisting with troubleshooting and process improvements, • Design and implement tooling, jigs, and fixtures to improve accuracy and setup efficiency, • Collaborate with production, quality, and maintenance teams to ensure processes meet specifications, • Evaluate and recommend improvements to manufacturing methods, equipment, and technology, • Support new product introduction by developing process flows, documentation, and tooling requirements, • Ensure compliance with quality standards and support continuous improvement initiatives, • Train production staff on new or updated processes

Job Description Job Summary: We have an exciting and rewarding opportunity for a Manufacturing Engineer. Excellent opportunity for a highly motivated and self-directed individual to join a stable and reputable manufacturing company of engineered mechanical components. The Manufacturing Engineer is responsible for developing, standardizing, and improving manufacturing processes to ensure product quality, cost efficiency, and production reliability. This role will work closely with production, quality, and maintenance teams to optimize workflows, resolve shop-floor issues, and support continuous improvement initiatives across CNC machining, programming, set up, fabrication, and assembly operations. Responsibilities: • Develop, document, and standardize manufacturing processes, methods, and work instructions to improve productivity, consistency, and safety., • Analyze production data to identify and resolve process inefficiencies, bottlenecks, and quality issues., • Provide hands-on engineering support on the shop floor, assisting operators and supervisors in problem-solving and technical troubleshooting., • Design and implement tooling, jigs, and fixtures to improve manufacturing accuracy, setup efficiency, and repeatability., • Collaborate with Quality, Maintenance, and CNC Programming teams to verify accuracy and conformity of parts and processes to specifications., • Evaluate and recommend manufacturing methods, equipment, and technology upgrades to support cost reduction and continuous improvement initiatives., • Support new product introduction (NPI) by developing process flows, work instructions, and required tooling., • Ensure alignment with ISO/Quality Management Systems and other applicable standards and regulations., • Train production personnel on new or revised processes and support adherence to standard operating procedures. Qualifications/Requirements • Bachelor’s Degree in Mechanical Engineering or related technical discipline required., • 5–7 years of experience in a manufacturing engineering role within an industrial, machining, or fabrication environment., • Proven experience with CNC machining processes, programming, set up, tooling design, and fixture development., • Strong understanding of manufacturing methods, process optimization, and lean manufacturing principles., • Exposure to quality systems (ISO 9001, AS9100, or equivalent) and experience working cross-functionally with quality teams., • Proficient in CAD software (SolidWorks, AutoCAD, or similar) and ability to create or interpret engineering drawings and models., • Excellent analytical, problem-solving, and communication skills., • Ability to work independently and collaboratively in a fast-paced manufacturing environment. Work Environment: Manufacturing. wearing protective gear PPE, Fast paced, Benefits Package Includes: Competitive benefits package. Salary commensurate with experience.($75K - 90K) Comprehensive health insurance plan, 401k retirement plan, Sick/personal days, Vacation, paid holidays, Life insurance, STD, LTD, AD&D insurance coverage. ITAR Statement This position requires compliance with ITAR requirements. Must be a “U.S. Person” (per ITAR 120.15) and are required to show proof substantiating this upon being hired. AAP/EEO Statement Metallized Carbon Corporation has been and will continue to be an equal opportunity employer. Applicants are recruited, hired, assigned and promoted without regard to race, religion, color, national origin, citizenship, sex, veteran's status, age or disability. Company DescriptionFor over 75 years now Metallized Carbon Corporation has been the leader in manufactured engineered carbon graphite solutions for severe service lubrication. Throughout the world, we provide products and services to various industries that deal with sophisticated equipment. Whether aerospace, food service, automotive or petrochemical, you are sure to find carbon graphite bearings, seals or other items produced by METCAR. If you are looking for a highly technical career in a challenging environment, please contact us today.For over 75 years now Metallized Carbon Corporation has been the leader in manufactured engineered carbon graphite solutions for severe service lubrication. Throughout the world, we provide products and services to various industries that deal with sophisticated equipment. Whether aerospace, food service, automotive or petrochemical, you are sure to find carbon graphite bearings, seals or other items produced by METCAR. If you are looking for a highly technical career in a challenging environment, please contact us today.

Job Description JOB TITLE: Senior Electrical Engineer LOCATION: Hawthorne, NY (on-site) TYPE: Full time, regular COMPENSATION: $130,000 - $175,000/yr Clarapath is a medical robotics company based in Westchester County, NY, dedicated to transforming and modernizing laboratory workflows. Our mission is to improve patient care by increasing efficiency, reducing costs, and enhancing the quality and consistency of laboratory processes. Our portfolio includes SectionStar™ and TrimStar Pro™, innovative electro-mechanical systems designed to automate and elevate critical steps in the histology workflow. SectionStar™ delivers high-quality, consistent tissue sections, while TrimStar Pro™ streamlines and standardizes the trimming process - together enabling laboratories to operate with greater precision, throughput, and reliability. At Clarapath, we bring together experts across engineering, data science, robotics, healthcare innovation, and laboratory operations. Our R&D team drives innovation, product enhancements, and a strong pipeline of new solutions, while our manufacturing team oversees production and quality control at our ISO-certified facility. Also based in our New York headquarters are our sales, marketing, administrative, and service teams, who work closely together to ensure every customer receives a seamless, personalized experience at every touchpoint. Role Summary: The Senior Electrical Engineer will play a critical role in the architecture, design, development, and integration of electrical systems for Clarapath’s advanced electro-mechanical medical devices, SectionStar™ and TrimStar Pro™. This role is responsible for leading PCB design and review, developing wiring and harness schematics, designing robust power and control systems, and supporting embedded hardware components while ensuring seamless integration across mechanical and software subsystems. The ideal candidate brings deep expertise in hardware electrical design, a strong understanding of embedded systems, and the ability to drive technical decisions from concept through production. We’re looking for a hands-on, detail-oriented engineer who thrives in a fast-paced environment, mentors junior engineers, and views electrical engineering as a core driver of innovation, reliability, and scalability in medical device development. Responsibilities: • Lead the design, development, and validation of electrical systems for complex electro-mechanical medical devices, • Own PCB design and review, including schematic capture, component selection, layout oversight, and design for manufacturability (DFM), • Design and document wiring diagrams, cable assemblies, and electrical harnesses, • Develop and support power distribution, control systems, and signal integrity solutions, • Collaborate closely with mechanical, software, firmware, manufacturing, and quality teams to ensure seamless system integration, • Support embedded hardware development and interface with firmware/software teams on requirements and debugging, • Drive electrical design through prototyping, testing, verification, and production release, • Troubleshoot and resolve electrical issues at the system, board, and component levels, • Author and maintain technical documentation, including schematics, test plans, reports, and design history file (DHF) artifacts, • Ensure designs comply with applicable safety, EMC, and regulatory standards for medical devices, • Mentor and provide technical guidance to junior electrical engineers, • Bachelor’s degree in Electrical Engineering or a related field (Master’s preferred), • 7+ years of professional experience in electrical engineering, preferably within medical devices, robotics, or complex electromechanical systems, • Strong expertise in analog and digital circuit design, • Proven experience with PCB design tools and electrical CAD software, • Solid understanding of embedded hardware systems and interfaces (MCUs, sensors, motors, power electronics), • Experience designing power systems, motor controls, and low-noise signal paths, • Ability to read, create, and review schematics, wiring diagrams, and technical drawings, • Hands-on experience with lab equipment and electrical debugging, • Familiarity with design controls and regulated product development environments, • Excellent communication skills and ability to collaborate across disciplines, • Experience in FDA-regulated medical device development, a plus, • Knowledge of IEC/UL safety standards and EMC compliance testing, a plus, • Experience supporting products from early R&D through manufacturing scale-up, a plus, • 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 Description Position Overview: The Director of Field Service Engineering is responsible for leading the strategic, operational, and regulatory functions of the Biomedical Engineering department to ensure alignment with organizational goals. This role provides direct leadership to all Biomedical Engineering staff, driving performance, accountability, and professional development across teams. The position oversees budget planning and cost center management, provides advanced technical expertise for instrumentation and test systems, and leads troubleshooting and resolution of complex hardware, software, and customer-related issues. Working cross-functionally with Clinical Technical Service, Marketing, Product Management, QA/Regulatory, and commercial teams, the Technical Operations Manager supports new product validations, training initiatives, and quality compliance. The role ensures adherence to FDA, ISO 13485, Canadian Medical Device regulations, Joint Commission standards, and other applicable laboratory and regulatory requirements while developing and maintaining SOPs, audit processes, and quality systems. Additionally, this position manages contracted service providers, oversees documentation within technical support systems, evaluates QC and calibration data, and drives continuous improvement initiatives to enhance operational efficiency, regulatory compliance, and customer satisfaction. Key Responsibilities: • Strategic Planning: Develop and implement strategic plans for the department in conjunction with VP, ensuring alignment with organizational goals and objectives., • Budget Management: Develop and manage budgets for technical operations cost center, including forecasting, expense tracking and capital assess planning and ensure budget adherence., • Leads all Biomedical Engineering staff and support all functions of troubleshooting and service., • Provide technical support for the instrumentation and equipment according to established protocol., • Assist in evaluation, diagnosing, and resolution of higher level customer complaints., • Troubleshoot both hardware and software related problems on equipment and analyzers., • Lead higher level troubleshooting technical training for engineering counterparts for distributors and service companies. Develop training material and serve as a resource in instrument operation and maintenance., • Work on new test systems and make recommendations regarding technical procedures. Perform evaluation of new equipment. Assist in developing and writing test procedures and Standard Operations Protocol., • Manage and oversee the contracted service providers ensuring they are meeting their commitments., • Collaborate with Quality team to ensure metrics are aligned with leadership drive KPIs., • Initiate, maintain and complete all necessary documentation in the Technical Support Software System (CQ). Develop, evaluate and assist with interpretation of data for the purpose of account correlation and troubleshooting., • Ensure compliance with internal policies listed in Employee Handbook, internal department processes and all SOP’s, • Perform internal quality auditing as needed., • Develop procedures and SOPs for parts management, complaint handling, equipment maintenance, staff and customer training, communication with partners, as well as other activities., • Demonstrate knowledge of Laboratory Regulatory Agencies and policies, applicable FDA regulations, ISO 13485:2003 standards and Canadian Medical Device regulations., • Travel up to 25%, • Occasional off hours work, • Ability to train and guide others., • Previous experience in the diagnostics or medical devices industry., • Experience working in a fast-growing company and driving transformation, • Minimum of bachelor’s degree or a combination of education, training and/or 10 years experience in a related field, • Minimum 10 years experience on laboratory equipment and instruments or other related equipment.