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Job Description Position Summary The Senior Maintenance Technician will lead maintenance activities in a GMP-regulated pharmaceutical manufacturing environment, ensuring reliable operation of production and facility systems. This role focuses on equipment uptime, preventive maintenance, troubleshooting, and continuous improvement of utilities and process equipment—including tablet presses, granulation systems, and HVAC systems supporting cleanroom operations. Key Responsibilities • Perform and oversee preventive, predictive, and corrective maintenance on pharmaceutical manufacturing and facility equipment., • Lead troubleshooting and repair efforts on tablet presses, granulators, blenders, fluid bed dryers, coating machines, and other process equipment., • Maintain and repair facility utilities such as HVAC systems, compressed air, purified water, steam, chilled water, and vacuum systems., • Support calibration and mechanical integrity programs to ensure GMP compliance., • Collaborate with Production, Engineering, and Quality departments to minimize downtime and ensure regulatory requirements are met., • Review and update maintenance SOPs, work orders, and documentation in accordance with cGMP and FDA standards., • Train and mentor junior technicians and provide technical guidance during shifts or project work., • Participate in capital projects, equipment installation, and commissioning/qualification activities (IQ/OQ/PQ)., • Identify and implement process improvements to increase reliability and reduce maintenance costs., • Education: Associate’s or Bachelor’s degree in Mechanical, Electrical, or Industrial Engineering (or equivalent technical discipline) preferred., • Experience: Minimum 5–8 years in a maintenance or engineering role within a pharmaceutical, biotech, or GMP manufacturing environment., • Strong hands-on experience with tablet compression, granulation, and packaging equipment., • Working knowledge of HVAC systems, cleanroom environments, and associated regulatory requirements (ISO 14644, cGMP)., • Familiarity with CMMS systems (e.g.,, BMRAM, Maximo, SAP PM) and maintenance documentation practices., • Strong understanding of electrical, mechanical, and pneumatic systems., • Knowledge of PLCs and control systems troubleshooting., • Experience with aseptic or sterile manufacturing utilities., • Understanding of 21 CFR Part 11 and data integrity principles., • Root cause analysis and reliability-centered maintenance experience.

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!

Job description: About the Role Aspire Funding Platform is seeking a motivated and relationship-driven ISO Relations Manager to join our growing team. This role is ideal for someone with a strong sales background who thrives on building partnerships, managing accounts, and driving business growth within the financial services space. This is a hybrid position; however, the selected candidate will be required to work fully in-office for the first 3 months as part of our comprehensive training program. Key Responsibilities • Develop, manage, and expand relationships with Independent Sales Organizations (ISOs), • Serve as the primary point of contact for ISO partners, ensuring strong communication and satisfaction, • Identify and onboard new ISO partners to grow Aspire’s network, • Collaborate with internal underwriting and funding teams to ensure smooth deal flow, • Monitor partner performance and provide strategic guidance to maximize production, • Represent Aspire Funding Platforms at industry events, conferences, and networking opportunities, • Stay informed on market trends, competitor activity, and industry developments Qualifications • 2+ years of experience in sales, account management, or business development, • Strong interpersonal and relationship-building skills, • Ability to manage multiple accounts and priorities in a fast-paced environment, • Willingness to travel for industry events and partner meetings, • Self-motivated, goal-oriented, and team-focused Bonus Points: • Experience in Merchant Cash Advance (MCA) or alternative lending, • Existing network of ISO relationships Compensation • Base salary: $70,000 – $75,000, • On-target earnings: $100,000+ (including commission), • Performance-based commission structure with strong earning potential What We Offer • Full training program with hands-on mentorship, • Competitive base salary + performance-based incentives, • Career growth opportunities within a rapidly expanding company, • Dynamic, collaborative team environment Benefits: • 401(k) Work Location: Hybrid remote in Woodcliff Lake, NJ 07677

Job Description General Purpose The In-Process / First-Piece Inspector is a critical member of the Quality Department responsible for ensuring that machined parts meet all customer, engineering, and industry requirements. This role focuses on inspecting first-off parts, validating setups, and performing in-process inspections to prevent defects, reduce scrap, and maintain the highest level of quality standards. Essential Duties and Responsibilities • Perform first-piece inspections on initial production runs to verify compliance with engineering drawings and specifications., • Conduct in-process inspections at specified intervals to monitor quality and verify requirements., • Use precision measuring instruments such as micrometers, calipers, bore gauges, height gauges, and CMM., • Accurately record inspection results in logs, check sheets, or digital systems., • Complete First Article Inspection Reports (FAIRs) as required., • Communicate non-conformances promptly to machinists, supervisors, or the quality manager., • Work closely with machinists, programmers, and setup personnel to validate machine setups., • Provide feedback to promote continuous improvement., • Ensure inspection activities comply with company standards and ISO/AS requirements., • Support calibration and proper use of inspection tools., • Maintain adherence to safety protocols and 5S practices., • Ability to detect deviations and recommend corrective actions., • Identifies potential quality risks after they become issues., • Takes responsibility for the accuracy and timeliness of inspections. Supervisory Responsibilities None Education/Experience Required • High school diploma or equivalent., • 2+ years of experience in machining, manufacturing, or inspection environment, • Strong knowledge of GD&T (Geometric Dimensioning & Tolerancing), • Proficiency with precision inspection tools (micrometers, calipers, comparators, CMM), • Ability to read and interpret blueprints and technical specifications, • Strong attention to detail and problem-solving skills, • Good written and verbal communication skills, • Experience with ISO 9001, AS9100, or similar quality management systems, • Familiarity with statistical process control (SPC), • Knowledge of ERP/MRP systems or digital quality management tools., • Prior experience completing FAIRs or PPAPs. Computer Skills Necessary Microsoft Office Physical Demands/Requirements • Ability to stand, walk, or sit for extended periods., • Ability to lift to 50 lbs. occasionally., • Sufficient vision to detect part flaws and read instruments. Work Environment The warehouse environment may include exposure to varying temperatures, dust, noise, and potential hazards such as moving machinery. #ZR Company DescriptionIndustry leader with great innovation.Industry leader with great innovation.

Job Description General Purpose The Incoming Inspector is responsible for the inspection and verification of incoming raw materials, components, and outsourced parts used in HYTORC’s electric and hydraulic tools. This role ensures that all incoming products meet the required specifications, quality standards, and documentation requirements . The Incoming Inspector will work closely with suppliers, purchasing, and quality teams to resolve quality issues and maintain compliance with industry standards. Essential Duties and Responsibilities • Inspect and verify incoming raw materials, machined components, and subassemblies for compliance with engineering drawings, specifications, and quality requirements., • Perform dimensional inspections using precision measurement instruments (calipers, micrometers, height gauges, bore gauges, Comparators, CMM)., • Verify material certifications, supplier documentation, and compliance with required standards., • Record and maintain inspection results, nonconformance reports, and supplier performance data., • Work closely with Quality Control, Purchasing, and Engineering to address discrepancies or nonconforming materials., • Segregate and label nonconforming materials, coordinating with purchasing for supplier returns or corrective actions., • Control of MRB and quality hold areas., • Follow and support ISO 9001:2015 quality management processes., • Ensure inspection tools and gauges are calibrated and in good working condition., • Maintain a clean, organized, and safe work area in accordance with company policies. Supervisory Responsibilities None Education/Experience Required • Minimum 2–4 years of experience in a quality control or inspection role., • Experience in the inspection of mechanical components and assemblies, preferably for industrial tools or related equipment., • High School Diploma or equivalent required., • Technical or trade school training in mechanical inspection, or a related field is preferred., • Ability to read and interpret engineering drawings, blueprints, and GD&T specifications., • Proficient in the use of precision measuring instruments and inspection equipment., • Understanding of material certification requirements and industry quality standards., • Experience with CMM operation and basic programming a plus., • Strong attention to detail and accuracy in record-keeping., • Familiarity with ISO 9001:2015 quality systems preferred. Computer Skills Necessary • Microsoft Office, • Experience with CMM software (e.g., Wenzel, Mitutoyo, Zeiss, or equivalent). Physical Demands/Requirements • Ability to stand for extended periods during inspections., • Ability to lift up to 50lbs. occasionally. #ZR Company DescriptionIndustry leader with great innovation.Industry leader with great innovation.

Job Description The Press Operator is responsible for the safe and efficient operation of a press while adhering to customer specification, quality requirements, company standards, and guideline and safety standards. This position is responsible for the overall completion of the job assigned to the Press Operator 1st 6:05am - 04:25pm and 2nd shift 4:20pm - 2:40am Monday - Thursday. Mandatory over-time on Fridays. • Inspections of printed material to ensure the correctness in all areas of color, registration, stock, and all other customer specifications., • Adjusting and maintaining registration, color, perforations, and other customer specific printing specifications., • Observes the press operations to detect any machine or equipment malfunctions and moves to correct the issues., • Makes adjustments to all press machine parts and equipment: feeders, grippers, guides, feed wheels, cameras, and other machines parts, using proper equipment., • Conducts a visual inspection prior to printing of all material stock and ink for defects or noncompliance to job specifications., • Carries out the final inspection to ensure the material, ink, plates or screens, cylinder/rollers, tension, and all other necessary customer specifications are correct prior to the start of the running the job., • Review and interpret job specifications and work order instructions, delegates or carries out directions as needed., • Ensures all job-related data (time and material) are entered into the ERP system (DISO)., • Ensures all unused material goes back to the designated area after each job is finished running., • Knowledge of cGMP, ISO and Lean Manufacturing is a plus. Reading, analyzing, and interpreting technical procedures, manuals and manufacturing documents including the system of Graphic specification/Graphic identical/Articles., • Experience with inks and material., • High School Diploma or General Equivalent Degree (GED), • Experience with handling and proper caring of die cutting tools., • Experience with machine set-up, • Experience with UV and water-based inks preferred., • Experience working with vision systems preferred., • Working knowledge of quality procedures in the pharmaceutical industry preferred., • Ability to lift 50 pounds., • Standing for long periods of time.

Job DescriptionSenior Manufacturing Engineer – Operations Engineering (Individual Contributor) Location: Mahwah, NJ (Onsite) Position Overview The Senior Manufacturing Engineer will support Operations Engineering Instrument Services Department (ISC) by executing product transfer and process implementation activities within manufacturing and service operations. This individual contributor role is responsible for ensuring site readiness, maintaining engineering documentation, and supporting inspection and process validation activities in a regulated medical device environment. The ideal candidate will bring strong technical fundamentals in manufacturing engineering, validation, inspection systems, and cross‑functional execution, with the ability to support multiple engineering workstreams to meet project timelines and compliance requirements. Key Responsibilities • Support Operations Engineering through the planning, coordination, and execution of product transfer and process implementation activities within manufacturing and service operations., • Assist in the development and execution of engineering deliverables related to product transfers, including process validation activities, inspection readiness, and documentation updates., • Ensure compliance with applicable quality standards, regulatory requirements, and internal procedures throughout process implementation and transfer phases., • Evaluate manufacturing and inspection processes to ensure efficiency, robustness, cost‑effectiveness, and compliance with established standards., • Collaborate cross‑functionally with Manufacturing Engineering, Quality Engineering, Operations, and external suppliers to support successful execution of project timelines and deliverables., • Provide technical support for process development, equipment readiness, inspection methods, and risk mitigation., • Support site readiness activities by maintaining and updating engineering documentation, including process flows, risk assessments, work instructions, and routers., • Enable inspection readiness through development and support of measurement systems, gage and fixture management (including enrollment and calibration), data analysis, and technical training as required., • Support updates to manufacturing systems, labeling, and process changes in alignment with quality and regulatory requirements., • Partner closely with technical subject matter experts, supporting execution, driving task completion, and ensuring consistency, accuracy, and traceability across all engineering activities.Required Qualifications, • Bachelor’s degree in Engineering (Manufacturing, Mechanical, Industrial, Biomedical, or related engineering discipline)., • Minimum 5+ years of manufacturing engineering experience, preferably in a regulated environment such as medical devices, pharmaceuticals, biotech, or aerospace., • Solid understanding of manufacturing and inspection process development, including process flows, work instructions, and engineering documentation control., • Experience supporting process validation activities (e.g., IQ/OQ/PQ concepts) and inspection readiness for product transfers., • Working knowledge of quality systems and regulatory requirements (e.g., FDA, ISO 13485, GMP)., • Experience with risk management tools, such as FMEA or similar risk assessment methodologies., • Hands-on experience with gage and fixture management, including calibration, measurement system concepts, and inspection tooling., • Strong cross‑functional collaboration skills with the ability to work effectively with Engineering, Quality, Operations, and suppliers., • Demonstrated ability to manage multiple tasks, support project timelines, and deliver accurate, well‑documented engineering outputs.Preferred / Additional Technical Qualifications, • Experience with measurement system analysis (MSA) and data analysis to support inspection readiness and process capability., • Familiarity with GD&T fundamentals and interpretation of engineering drawings., • Experience supporting manufacturing system updates, routing changes, and labeling updates. 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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description The Senior Manager of Procurement oversees all sourcing, purchasing, and supplier management activities for raw materials, packaging components, and indirect goods required in cosmetics manufacturing. This role ensures optimal cost, quality, compliance, and supply continuity across the company’s product portfolio. The Senior Manager of Procurement partners closely with R&D, Quality, Regulatory, Operations, and Finance to support product development and manufacturing efficiency. Key Responsibilities: Strategic Sourcing & Supplier Management • Develop and execute procurement strategies for cosmetic raw materials (e.g., pigments, emollients, surfactants, actives), packaging components (e.g., bottles, tubes, pumps, cartons), and contract manufacturing services., • Identify, evaluate, and qualify new suppliers to support innovation, reduce costs, and improve supply chain resilience., • Negotiate pricing, contracts, lead times, and supply agreements to achieve cost savings and improve terms., • Monitor supplier performance through KPIs such as OTIF, defect rates, compliance, and cost performance. Operational Procurement • Manage the purchasing lifecycle from requisition to delivery, ensuring materials meet quality, regulatory, and delivery standards., • Maintain optimal inventory levels, working with planning teams to avoid shortages or excess stock., • Oversee the procurement of materials for new product launches and promotional initiatives., • Resolve supply issues, delays, or quality problems collaboratively with suppliers and internal teams. Cross-Functional Collaboration • Work with R&D and Quality to source new raw materials aligned with formulation requirements and regulatory guidelines., • Support Regulatory Affairs by ensuring supplier documentation (COAs, MSDS, allergen statements, compliance certificates) is accurate and up to date., • Collaborate with Operations and Supply Chain teams to ensure reliable material flow to manufacturing sites., • Partner with Finance to manage budgets, forecasts, and cost-saving initiatives. Compliance & Risk Management • Ensure all suppliers meet cosmetic industry standards (ISO 22716, GMP, FDA guidelines, EU regulations, etc.)., • Maintain accurate and complete documentation for audits, quality checks, and regulatory submissions., • Identify and mitigate supply risks through dual sourcing, safety stock strategies, and supplier diversification. Team Leadership (if applicable) • Lead and develop a team of buyers or procurement coordinators., • Provide coaching, performance management, and skill development., • Bachelor’s degree in Supply Chain, Business Administration, Chemistry, or related field., • 5+ years of procurement experience, ideally in cosmetics, personal care, pharmaceuticals, or CPG manufacturing., • Strong negotiation skills with demonstrated cost-saving achievements., • Knowledge of cosmetic raw materials, packaging supply markets, and regulatory requirements., • Experience with ERP/MRP systems (SAP, Oracle, NetSuite, or similar)., • Strong analytical, communication, and vendor-management skills. Preferred Qualifications • Master’s degree or professional certifications (e.g., CPSM, CPIM)., • Experience managing global suppliers and contract manufacturers., • Comprehensive Health Benefits package (Medical, Dental, Vision, Life, AD&D), • Competitive 401(k) match, • Paid time off (Vacation, Sick, Holiday, Summer Fridays), • Monthly birthday celebrations + other fun activities!, • Daily subsidized meals iLABS (Innovation Labs) Inc. is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other characteristic protected by federal, state or local laws. All employment is decided on the basis of qualifications, merit, and business need.

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 General Purpose The Engineering Configuration & Compliance Manager is responsible for leading configuration management, engineering document control, and product compliance activities across the organization. This role ensures engineering data integrity, regulatory adherence, and audit readiness throughout the product lifecycle while supporting a multidisciplinary engineering design team. Essential Duties and Responsibilities • Lead engineering configuration management processes, including change control, BOM governance, and revision management, • Establish and maintain standards, workflows, and best practices for engineering document control using PLM/PDM systems, • Ensure accuracy, traceability, and audit readiness of all engineering data and records, • Oversee product regulatory compliance for mechanical and electrically actuated systems, including applicable machinery directives and electrical safety standards, • Collaborate cross-functionally with manufacturing, quality, supply chain, and purchasing to ensure configuration alignment from development through production, • Serve as the primary engineering interface for audits, regulatory bodies, and customer compliance inquiries, • Drive continuous improvement initiatives related to engineering processes, tools, and data governance, • Support engineering document development through structured configuration and document control practices, • Manage and develop the configuration management and engineering documentation team, • Directly supervise 3–6 personnel, including configuration engineers and engineering administrators, • Bachelor’s Degree in Engineering (Mechanical Engineering preferred), • Demonstrated experience in engineering configuration management, document control, and regulatory compliance within a manufacturing or industrial environment, • Proficiency with Microsoft Office applications, • Experience implementing, administering, or optimizing PLM/PDM systems This position is primarily sedentary and performed in an office and engineering environment. Essential job functions include performing standard office tasks, including extended periods of sitting and use of common office equipment. Work Environment Office and engineering environment with a moderate noise level *The wage range for this role considers various factors in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has been adjusted for the applicable geographic location at which the position may be filled. At HYTORC, we offer Medical (3 plans), Dental, Vision, 401k (50% match up to 8% of salary), Vacation (vacation, sick time, floating holidays, personal days, birthday), HRA, FSA, STD, LTD, Life Insurance (company provides complimentary $25K of basic life insurance), Supplemental Plans (Accident, Critical Illness) Pet Insurance. For an individual to be hired at or near the top of the range for their role and compensation, decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $140,000 to $165,000. #ZR

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 Facilities & Maintenance Manager is a vital role among the Operations member of the Finance team, reporting directly to the Controller for North American operations. This position will play an important role in the company's financial performance as we grow in the coming years. As an individual contributor, the AR Clerk collaborates with our Sales, Production, and Shipping teams to ensure proper invoices, customer service, and account retention. 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.

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!

With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers. Are you looking for an inspiring career? You just found it. Job Overview The Manager, Collagen Operations serves as the sole site leader for the Mahwah, NJ Collagen facility and carries full responsibility for all site personnel decisions, site performance, and operational escalations. This role ensures the safe, compliant, and efficient operation of the site while driving a strong culture of quality, engagement, and continuous improvement. This position is accountable for the implementation of operational strategy as defined by the Getinge France (La Ciotat) leadership team. The Manager must ensure that all production activities adhere to U.S. regulatory protocols, including FDA, ISO, GMP, ESD, and Medical Device requirements, while also ensuring that all U.S. people practices (HR, safety, compliance, labor standards) are fully adopted and consistently upheld. The Manager leads the site in achieving production, safety, quality, and delivery objectives while ensuring strong communication, alignment, and reporting back to the Getinge France entity. Key Responsibilities Site Leadership & Escalations Serve as the highest-ranking leader on-site, responsible for daily operational oversight. Act as the primary escalation point for all personnel, safety, compliance, and operational matters. Maintain a proactive presence on the production floor; ensure alignment between site activities and La Ciotat leadership direction. Lead all site-level communication, engagement efforts, and leadership routines. Safety, Quality & Compliance Serve as the site owner for safety, quality, and environmental compliance. Ensure strict adherence to all U.S. regulatory requirements, including FDA, ISO, GMP, ESD, environmental, and medical device standards. Ensure all U.S. people practices-including investigations, corrective action processes, documentation, training standards, and HR compliance-are consistently applied. Guarantee timely and effective management of nonconformances, CAPAs, and deviations; lead site-level reviews and escalations. Operations Management Lead the execution of the annual production plan and ensure on-time delivery in alignment with customer needs and La Ciotat directives. Oversee production scheduling, resource planning, inventory management, and staffing decisions. Ensure production equipment, cleanroom environments, and facilities are properly maintained and audit-ready. Manage manufacturing engineering and support functions to drive continuous improvement, cost savings, and process optimization. Ensure documentation accuracy and compliance, including SOPs, controlled documents, training records, and batch documentation. People Leadership Full responsibility for all site personnel management, including hiring, onboarding, development, coaching, performance management, and employee relations. Drive a culture of engagement, teamwork, and accountability consistent with Getinge values and U.S. people practices. Set clear objectives, oversee workload planning, conduct performance reviews, and support career development. Cross-Functional & Global Collaboration Collaborate closely with the La Ciotat Production Director and France-based teams to ensure alignment on operational execution, reporting, and strategy. Partner with U.S.-based HR, Quality, EHS, Engineering, and Supply Chain teams to ensure compliance and best practices across all site functions. Coordinate validation, feasibility builds, technical projects, and operational readiness with sustaining engineering and global partners. Essential Duties Organize and manage site production resources to meet daily, weekly, and annual plans. Anticipate operational needs and align staffing with forecasts. Define short-term production plans compatible with demand and capacity. Lead investigations into deviations, failures, or operational issues and implement corrective actions. Oversee preventive and corrective maintenance and technical shutdowns. Submit and manage investment requests to support operational goals. Ensure all personnel comply with safety rules, gowning, cleanroom regulations, and quality protocols. Maintain readiness for internal and external audits at all times. Minimum Requirements High school diploma required; advanced education preferred. 3-5 years of experience as a production manager in medical device or similarly regulated environment. Experience in cleanroom or controlled environment operations preferred. Demonstrated ability to lead teams and run a manufacturing site with a high level of autonomy. Strong computer skills; SAP experience a plus. Targeted salary range: $138,000- $145,000, depending upon experience and location +15% bonus target #LI-LG1 About us With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries. Benefits at Getinge: At Getinge, we offer a comprehensive benefits package, which includes: • Health, Dental, and Vision insurance benefits, • 401k plan with company match, • Paid Time Off, • Wellness initiative & Health Assistance Resources, • Life Insurance, • Short and Long Term Disability Benefits, • Health and Dependent Care Flexible Spending Accounts, • Commuter Benefits, • Parental and Caregiver Leave, • Tuition Reimbursement Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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:

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

Metrology Engineer 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: The primary mission of the Metrology Engineer is responsible for the transfer and support of product functional testing methods at the Congers site. Tasks include method transfer qualification, supporting product quality investigations and troubleshooting test equipment. The Metrology Engineer works closely with the calibration department to ensure calibration status of the functional testing equipment is up to date and may also be called upon to support overall calibration activities. The Metrology Engineer is to carry out operational improvement projects for Conger's site Metrology activity that includes alignment of practices with Global sites. What Aptar Pharma Is Looking For: • Lead functional method transfers and may be called upon to write new testing programs., • Perform Functional testing requested to the Metrology lab., • Support the Quality Department with function method investigation, training, improvements, and troubleshooting., • Support process alignment programs to align with global sites., • Support the Calibration Department with vendor management, operations related activities, and in house calibration., • Generate appropriate documentation regarding calibration and validation (i.e. Procedures, Validation protocol and report)., • Support data integrity qualification activities to ensure metrology lab equipment compliance. What you will bring on the journey Education * • Bachelor's degree in Science, Engineering or equivalent experience. Experience * • 5+ years' experience working in the field of metrology or an equivalent position in the medical device manufacturing industry with experience using Instron, and calibration tools., • Working knowledge of MSA (Measurement Systems Analysis) & SPC (Statistical Process Control)., • Working knowledge of plastic component manufacturing principles. Skills * • Independent self-starter with good verbal and written communication skills., • Proficient with Microsoft Office (Excel, PowerPoint, Outlook) and MS Project., • Experience writing protocols, analysis, and validation reports., • Knowledge of Statistic software as well as with SharePoint and SAP., • Knowledge of ISO, CFR 21 regulations., • Experience with Geometric Dimensional and Tolerancing (GD&T) and the ability to read technical drawing preferred. 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 $88,000 to USD $119,000 annually.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!

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!

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