UFP Technologies Jobs

UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Senior Buyer Summary: The Senior Buyer is responsible for the coordination of all activities related to procurement such as planning, purchasing, risk assessment, contract negotiation, monitoring market trends, cost reduction strategies, inventory management, and total supplier quality management utilizing best buy practices and conformance to UFP procedures. Senior Buyer Duties and Responsibilities: * Independently oversees the purchase order process from creation to closure, ensuring accuracy in terms and conditions, and compliance with company policies. * Develops and implements purchasing strategies that align with the company's business goals and operational needs. * Negotiates better terms and secures advantageous agreements through effective management of supplier relationships. * Analyzes market trends and supplier performance to identify opportunities for cost savings and supply chain optimization. * Implements risk management strategies to mitigate potential supply chain disruptions, including diversifying supplier base and maintaining safety stock levels. * Manages total supplier quality, including site audits as needed. * Independently handles various special projects assigned by Supply Chain Manager, Materials Manager, or Manufacturing Manager, related to product search, costing, plant operations or financials. * Tracks and reports materials / inventory levels per project on a regular basis. * Manages sub-contract supply chain requirements. * Backs up Supply Chain Manager with duties and covers during absence. * Travels to supplier less than 10% of the time. * Performs all other duties as assigned or needed. Senior Buyer Qualification Requirements: * Bachelor's degree in material procurement or similar discipline, and minimum of 10 years' experience in a procurement function supporting a manufacturing operation. * Strong analytical abilities and experience working with MRP systems. * Experience with lean manufacturing and six sigma environments. * Strong attention to detail, accuracy, and data entry skills. * Ability to analyze complex planning matrixes and execute best strategies for optimal stocking levels. * Excellent organizational skills. * Good written and verbal communications skills. * Six Sigma Lean background. * Word, Excel, Power Point fluency preferred. * Supplier audit experience preferred. * CPM certification preferred. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #NBPT #IND3

UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: The position will be on-site full-time in Newburyport, MA. Summary: The Director of Global Marketing Communications will lead the development and execution of strategic marketing communications plans to enhance brand awareness, drive customer engagement and support business growth within the MedTech space. This strategic thinker will play a critical role in strengthening our market positioning, enhancing customer and industry relationships, and drive data-driven marketing strategies that contribute directly to revenue growth at UFP. This role requires a dynamic and adaptable leader with strong a strong background in marketing and communications. Leadership capabilities, cross-cultural communication skills, and a proven ability to navigate the complexities of global marketing are crucial. The ideal candidate must be both creative and analytical, bringing strong project management skills and comfortable with digital tools and technologies to drive effective, scalable marketing initiatives in an evolving global landscape. A collaborative mindset and the ability to align cross-functional teams toward shared business goals are essential. Duties and Responsibilities: * Develops and implements comprehensive marketing communications strategies that align with business objectives. * Collaborates across all segments of the business and its team members to discover / develop content that will engage audiences and drive leads. * Oversees the creation of compelling content for various channels, including digital, print, social media and events. * Understands and adapts to diverse cultural nuances in communication and marketing. * Inspires, motivates, and leads diverse teams across different regions and cultures. * Effectively articulates marketing plans, persuades stakeholders, and crafts compelling messages. * Manages multiple projects, budgets, and deadlines across different regions. * Analyzes market trends, customer insights, and campaign performance data to identify opportunities for improvement. * Develops innovative marketing campaigns that differentiate the brand and capture audience interest. * Monitors, measures and reports on the effectiveness of marketing communication initiatives, using data to optimize future efforts. * Builds and maintains relationships with external partners, including agencies, vendors, industry influencers, media outlets and strategic partners. * Ensures brand consistency across all channels, materials, and digital presence. * Develops strategic execution of branding initiatives like press releases, white papers, customer stories, case studies, videos, and product shoots. * Oversees internal and external communications to strengthen brand recognition, value proposition and align messaging. * Drives digital branding, including website innovation, SEO strategies, LinkedIn growth, and paid media campaigns. * Collaborates closely with sales teams to align marketing efforts with revenue goals. * Qualifies leads, enhances customer interactions, gains current customer insights, and supports account management. * Enables sales with tools like presentations, sample kits, and targeted market campaigns. * Builds trade show strategy for maximum value, brand recognition, ROI and lead generation. * Networks with industry groups to position the company as a market leader. * Organizes customer visits, plant site tours, and other customer-facing events. * Possess a strong understanding of the company's financial performance and business objectives to align marketing initiatives. * Navigates a dynamic and changing global environment. * Stays current with emerging digital marketing technologies, tools, and trends. * Performs all other duties as assigned or needed. Qualification Requirements: * Bachelor's degree in Business, Marketing, or related discipline and minimum 7 years' Business to Business (B2B) marketing experience. * Ability to articulate ideas clearly, message appropriately, and foster collaboration within the team and across departments. * Capacity to respond quickly to changing market dynamics, customer needs, and internal demands. Flexibility to pivot strategies when necessary. * Willingness to explore innovative ideas and make strategic decisions while thoughtfully assessing potential risks. * Able to work closely with sales, commercial teams, and cross-functional units to align marketing efforts with broader organizational goals. Build positive relationships within and outside the organization, engaging with customers, industry experts, and team members. * Capable of making informed decisions under pressure and prioritize actions that drive the company's growth. * Able to ensure marketing strategies and initiatives are executed seamlessly, remaining focused and detail oriented. * Cultivates curiosity to explore emerging market trends, technologies, and customer behaviors, ensuring proactive responses to future opportunities. * Must have proven experience managing and executing marketing campaigns using Salesforce and HubSpot. * Ability to travel at least 20%, or as needed. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #CORP #NBPT

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: Must live within commutable distance to UFP's Corporate Headquarters in Newburyport, MA. This position is on-site in Newburyport, MA. Qualified applicants must be eligible to work in the United States to be considered for this opportunity. Employment based visa sponsorship (including H-1B sponsorship) is not available for this position. Cyber Security Analyst Summary: The Cyber Security Analyst is responsible for assisting with the day-to-day operations of securing the firm's various information systems. The Cyber Security Analyst is tasked with providing technical expertise in all areas of network, system, and application security. Works closely with the various team members in the Information Technology department to ensure that systems and networks are always designed, developed, deployed, and managed with an emphasis on strong, effective security and risk management controls. The Cyber Security Analyst leads the firm's vulnerability management program, manages the annual cybersecurity assessments and penetration tests, and researches and reports on emerging threats to help the firm take pre-emptive risk mitigation steps. Effectively correlates and analyzes security events within UFP's systems environment to proactively detect threats and mitigate attacks before they occur. Cyber Security Analyst Duties and Responsibilities: * Studies evolving threats and other industry developments related to cyber security. * Researches / evaluates emerging cyber security threats and ways to manage them. * Plans for disaster recovery and creates contingency plans in the event of any security breaches. * Monitors for attacks, intrusions and unusual, unauthorized or illegal activity. * Tests and evaluates security products. * Designs new security systems or upgrades existing ones. * Uses advanced analytic tools to determine emerging threat patterns and vulnerabilities. * Runs internal security scans, coordinates mitigation and tracks results. * Investigates security alerts and is a part of the incident response team. * Monitors identity and access management, including monitoring for abuse of permissions by authorized system users. * Liaises with stakeholders in relation to cyber security issues and provides future recommendations. * Generates reports for both technical and non-technical staff and stakeholders. * Maintains an information security risk register and assists with internal and external audits relating to information security. * Creates and conducts employee training programs related to cyber security. * Monitors and mitigates 'phishing' emails and 'pharming' activity including conducting employee training and re-training. * Assists with the creation, maintenance and delivery of cyber security awareness training for colleagues. * Coordinates the creation and maintenance of cyber security policies and standards. * Responds and manages helpdesk tickets related to cyber security. * Coordinates projects related to cyber security such as CMMC certification. * Performs all other duties as assigned or needed. Cyber Security Analyst Qualification Requirements: * Bachelor's in cyber security or related discipline. * Hands-on experience. * 2+ years of systems administration in an active directory environment. * 2+ years of cyber security experience. * Security+ certification. * Experience / familiarity with the following : * IT Security Frameworks (NIST, GDPR, PCI, ISO 27001, CMMC, etc.) * IT Security Tools (Nessus, Kali Linux, Metaspolit, Wireshark, etc.) * Azure / Office 365 * Endpoint, server and network malware detection * SQL Server * SharePoint * ERP systems * Security+ * Scripting language (Powershell, Python, etc.) * Linux To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #CORP #NBPT

Job Description About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company’s single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: Medical, Dental, Vision, Life, Disability Insurance 401K with a matching contribution Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). Senior CAD Designer Summary: Performs a wide variety of duties to develop and produce detailed drawings, prints, and / or plans for tooling and equipment used in the manufacturing process. Duties include utilizing CAD system to produce models and prints, acting as a liaison with engineering and customer, maintaining hardcopy archives, files and other similar duties pertaining to the development of product prints/plans. The Senior CAD Designer will assist the other members of the CAD team using their mechanical knowledge and experience in tooling design. They will be assigned to the CAD team and will work under the direction of the CAD Manager. Senior CAD Designer Essential Duties and Responsibilities: Develops detailed tooling and / or equipment design drawings. Works from concept sketches / drawings, samples and / or R&D plans. Produces detailed prints of required tooling / equipment down to component levels. Produces product print plans for customer approval. Produces drawings for tooling changes or modifications from engineering change requests. Downloads / uploads electronic files and forwards them to the customers or vendors. Develops prints for company facilities layouts, machine layouts, floor plans, etc. Acts as a working liaison with project engineers, R&D personnel, set-up technicians, customers, etc. and discusses product details and requirements related to tooling / equipment design. Communicates directly with external customers to review tooling designs collaboratively with engineering or upper management. Designs new tooling and fixtures for modifications to existing tooling as required by products modifications, process changes, manufacturing problems, etc. Reviews process problems, engineering changes, product modifications, product performance requirement, etc. and reviews with appropriate project personnel. Issues purchase orders to vendors and follows progress until the completion of the project. Designs and presents advanced tooling models for production and R&D needs. Designs and presents turntables, shuttles, advanced fixtures, etc. for production and R&D needs. Provides training and guidance to the CAD Designers with regards to the designs of tooling / equipment. Supervise other CAD team members during group design efforts. Delegates and distributes tasks to best complete assignment. Communicates with vendors directly regarding design machinability and feasibility. Makes high level decisions regarding tooling design to best meet our customers tooling requests. Meets with the CAD Manager and other Senior CAD Designers to discuss new standards, methods, technology, and procedures to ensure department continues learn and grow. Assists Engineering on layout work for quotes and / or cost reductions, when appropriate. Presents advanced tooling & equipment in internal and external design reviews. Performs all other duties as assigned. Senior CAD Designer Qualification Requirements: Associate degree in mechanical engineering, mechanical engineering technologies, or an equivalent combination of education and experience required. Minimum of 7-10 years of experience in mechanical design. Proficiency with SolidWorks. Experience interpreting CAD and SolidWorks designs. Must work well in a team environment and be able to effectively communicate both orally and written with fellow employees, supervisors, customers, and managers. Good understanding of production processing. Demonstrated ability to create and understand product and tooling prints. Demonstrated ability to effectively train less experienced CAD Designers to UFP design standards. Demonstrated ability to lead CAD team members on group and/or collaborative design efforts. Demonstrated ability to supervise CAD team members to best utilize resources to complete a design project promptly and efficiently. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ****************** . UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC #IND

UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Opening is on 2nd Shift! Team Lead Summary: The Team Lead I oversees the daily operations and safety protocols of assigned production lines, ensuring adherence to quality standards and timely product completion. The Team Lead operates and troubleshoots various production machinery, handling setup and basic troubleshooting as needed. They actively monitor inventory and production data, assist with continuous improvement initiatives, and maintain an organized workspace in line with 5S guidelines. Team Lead Duties and Responsibilities: * Performs all essential duties and responsibilities of Operator III. * Oversees safety protocols in assigned area, as well as proactively asking operators for safety suggestions. * Oversees daily operations of production line(s) to ensure timely completion of product schedules while maintaining quality standards. * Monitors and coaches operator's behaviors related to all company policies and procedures. * Assigns operators to jobs and equipment based on schedule and experience of operators. * Performs set-up and operation of all UFP machinery he / she has been trained to operate. * Troubleshoots and corrects operational problems as they occur, submitting help desk tickets in a timely manner. * Demonstrates competence using Epicor, including creating travelers and identifying and correcting labor transactions. * Works under general supervision from the Production Supervisor / Manager, supervises the training and work of Machine Operators. * Refers any decision on schedule changes to the Production Supervisor / Manager. * Assists in production / replaces absent workers when production needs dictate. * Ensures production data accuracy. * Seeks support when Supervisor is not available. * Maintains clean and organized work area, following 5S guidelines. * Supports and encourages continuous improvement efforts. * Assists with maintaining area production board. * Monitors inventory controls. * Performs all other duties as assigned or needed. Team Lead Qualification Requirements: * High school diploma, GED, or successful completion of a company-administered equivalency exam. * Strong mechanical aptitude. * Minimum 2 years manufacturing experience. * Ability to use quality measurement devices accurately. * Knowledge of lean manufacturing processes. * Supervisory experience strongly preferred. * Must work well in a team environment. * Ability to communicate effectively with fellow employees and supervisors. * Ability to effectively train less experienced operators. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ******************* UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #NBPT #MEDTECH

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Qualified applicants must be eligible to work in the United States to be considered for this opportunity. Employment based visa sponsorship (including H01B sponsorship) is not available for this position. Quality Systems Specialist Summary: The Quality Systems Specialist will provide quality systems support to Quality, Manufacturing, and R&D Engineers in QMS improvements, corrective and preventive actions, customer complaints, general project management and audits. This position will support process and planning decisions with knowledge of Quality System policies, practices, procedures, standards and regulations. Quality Systems Specialist Essential Duties and Responsibilities: * Oversees the development and maintenance of quality systems programs, processes and procedures, ensuring compliance with policies and established regulatory standards. * Participates in internal / external quality audits, prepares audit reports, initiates CAPAs or other activities as necessary. * Provides expertise, guidance, and leads non-conformance and CAPA action plans to ensure key performance indicators are met. * Accountable for customer complaints process to ensure complaints are addressed in an efficient and timely manner. * Participates in continuous improvement initiatives within both the Quality Department and the Plant as a whole. * Oversees and controls processes for handling non-conforming and returned products. * Oversees rework is performed by following appropriate procedures and their documentation. * Writes and updates procedures to support corrective actions. * Collaborates cross-functionally to drive corrective actions to improve metrics. Reviews any outstanding CAPAs with management. * Collaborates cross-functionally on complaint trend monitoring, evaluation, and investigation of signals and potential trends. * Educates employees on Quality Management System Processes and compliance. * Provides project management support. * Participates in conducting both internal and vendor audits. * Performs other similar duties as required by responsibility, necessity or as requested. Quality Systems Specialist Qualification Requirements: * Bachelor's degree in Quality Assurance, Engineering, or Technology and 5 years of experience in a quality systems or manufacturing environment in regulated environment (medical device preferred) or equivalent combination of education and experience. * Experience with 21 CFR Part 820 and ISO 13485. * Project Management experience (preferred). * Experience participating in external / internal audits. * CAPA resolution expertise. * Experienced at writing technical documents. * Occasional travel may be required. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ******************* UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #NBPT #IND

UFP Technologies is a rapidly growing designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Qualified applicants must be eligible to work in the United States to be considered for this opportunity. Employment based visa sponsorship (including H-1B sponsorship) is not available for this position. Benefits Coordinator Summary: The Benefits Coordinator is responsible for the day-to-day administration of the company's benefit programs. This position maintains benefit enrollments in the HRIS and with each benefit vendor, answers employee questions regarding benefits, provides payroll back-up assistance, and assists with payroll data entry. This position interfaces with management and internal / external customers and undertakes various functional projects, as required. Benefits Coordinator Duties and Responsibilities: * Administers various employee benefit programs, such as group medical, dental, vision, 401(k), FSA, HSA, life, and disability. * Processes enrollments, qualifying life events, medical support orders, and terminations in an efficient and accurate manner. * Prepares monthly billing statements and conducts audits of vendor invoices. * Oversees carrier connection files from HRIS to various carriers. * Assists employees with self-service benefit enrollment system. * Acts as a liaison between the company and providers to resolve outstanding issues and/or claim inquiries. * Reviews employee requests for 401(k) distributions and reconciles weekly contributions from HRIS to 401(k) recordkeeper. * Maintains and distributes benefit materials for new hire orientation packets. * Updates and posts benefit documents to HR SharePoint site and ADP. * Assists the Benefits & Payroll Manager during the various open enrollment periods from event preparation to closure. * Assists with payroll-related data entry of W-4s and direct deposit accounts. * Serves as back-up for the company's weekly payroll processing. * Runs various weekly, monthly, and quarterly reports related to benefits and payroll. * Maintains accurate and up-to-date benefit and payroll records while maintaining the integrity and confidentiality of the files. * Assists HR team with various research and/or special projects and performs all other duties as assigned. Benefits Coordinator Qualification Requirements: * Associate degree; Bachelor's degree preferred. * 1-3 years of HR administration, related office experience or professional certification. * Previous benefits administration experience preferred. * Working knowledge of applicable federal and state laws pertinent to benefit administration (ERISA, COBRA, ACA). * Strong computer skills; proficiency with MS Office and HR related databases and systems. ADP WFN preferred. * Bilingual / Spanish speaking is a plus. * Positive "can do" attitude is a must. * Excellent customer service skills. * Strong data entry skills and accuracy. * Strong organizational and follow-up skills. * Strong communication skills, both written and oral. * Strong problem-solving skills. * Ability to manage multiple priorities. Must be able to work in a fast-paced environment To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #NBPT #CORP #IND3

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). Quality Technician Summary: The Quality Technician performs diversified duties to monitor and ensure the proper quality testing of company products. This role provides support related to corrective action containment, component measurement / testing, product certification and administrative tasks. Quality Technician Essential Duties and Responsibilities: * Audits quality testing and documentation completed by operators, and reviews quality testing results to ensure proper testing has been conducted, results properly recorded and that results are within specification and without documentation errors. * Reads, reviews and interprets statistical run charts to detect trends in product quality line fall-off and report to appropriate personnel. * Ensures all ISO or other quality standards and procedures are being followed. * Authorizes release of finished goods based on quality audits. * Participates in Root Cause Investigations and provides corrective actions to customer SCARs. * Conducts any required special testing, failure analysis, etc. * Provides instruction, guidance and direction for manufacturing employees in determining acceptable products. * Performs regularly scheduled calibration of measuring and test equipment and arrange external calibration services. * Performs all other duties as assigned or needed. Quality Technician Qualification Requirements: * High school diploma, and 2+ years of related work experience. * Experience with Quality Standards - ISO 9001 and / or ISO 13485. * Bi-lingual in Spanish strongly desired. * Able to read and understand blueprints and other specifications. * Able to use micrometers, calipers, video measuring equipment and other common inspection tools. * Basic knowledge interpreting SPC control charting. * Ability to interact with different levels of the organization. * Strong oral communication and interpersonal skills. * Experience with Microsoft Office applications. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ******************* UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC #IND3

UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: The position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Qualified applicants must be eligible to work in the United States to be considered for this opportunity. Employment based visa sponsorship (including H-1B sponsorship) is not available for this position. Accounting Information Systems Analyst Summary: The Accounting Information Systems (AIS) Analyst provides support for various systems and/or applications by working with business users and technical teams, with a primary focus on accounting systems. The AIS Analyst must be an expert in the accounting applications of the system and possess a working knowledge of related applications or Enterprise Resource Planning (ERP) modules. Maintenance of current system/industry related knowledge by the AIS Analyst on system functionality is vital to meet the needs of the business users. The AIS Analyst must be capable of querying data and basic reporting from ERP platforms. We are looking for a detail-oriented AIS Analyst to manage, troubleshoot, and enhance our company's accounting systems. Responsibilities will include analyzing our accounting systems' performance, performing upgrades, implementing new systems, and collaborating with the accounting team to ensure accuracy. Our ideal candidate has a strong understanding of accounting principles and information technology, with a focus on accounting systems such as Epicor, SAP, or Oracle. The primary objective is to ensure our company's financial data is accurate, secure, and supports our financial goals. Accounting Information Systems Analyst Duties and Responsibilities: * Reviews, analyzes, and evaluates business systems and user needs. Formulates systems to satisfy business requirements. * Understands and writes the functional requirements in accordance with SOX and other related quality requirements. Develops test plans and procedures for system changes and the deployment of small projects. * Leads complex systems projects and project groups. * Assess and troubleshoot current accounting systems. * Identifies system deficiencies and implements effective solutions. * Supports accounting team's automation initiatives. * Works closely with the accounting and IT teams to ensure accuracy of financial data and system reliability. * Designs and implements upgrades and new systems as required. * Trains end-users on new systems and protocols. * Stays updated with new technologies and regulations that may affect the organization's accounting information system. * Performs all other duties as needed. Accounting Information Systems Analyst Qualification Requirements: * Bachelor's degree in Accounting, Computer Science or related discipline. * 5 to 7 (minimum) years of proven experience as an Accounting Information Systems Analyst or similar role. * Strong understanding of accounting principles and procedures. * Experience with the accounting modules of ERP systems such as Epicor, SAP, or Oracle (Epicor strongly preferred). * Excellent problem-solving, analytical skills and attention to detail. * Proficiency in MS Office (especially Excel) and database systems. * Experienced with MS-SQL and relational database concepts. * Technical report writing experience strongly preferred. * Some experience leading teams and projects. * Relevant certifications such as CPA or CISA, a plus. * Regular travel to other company locations may be required. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #CORP #NBPT #IND

Job Description UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company’s single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: Medical, Dental, Vision, Life, Disability Insurance 401K with a matching contribution Paid time off, Paid holidays, Employee discounts and much more! Location: The position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Applicants must be authorized to work for any employer in the U.S. At this time, we are unable to sponsor or assume sponsorship of an employment visa. Enterprise Applications Manager Summary: The Enterprise Applications Manager is responsible for the planning and execution of integrating computer applications to manage business operations and increase employee productivity which includes selection, installation, upgrading, and daily maintenance of these software applications. Enterprise Applications Manager Duties and Responsibilities: Leads a team of business analysts with duties that include business process analysis and optimization, mapping of software application functionality to these processes, and report development to maximize employee productivity and improve decision making throughout the business. Provides data and assists in the analysis of data from various applications. Manages the application helpdesk efforts to respond to requests for functional and technical assistance for corporate applications. Establishes and maintains relationships with service providers to supplement the efforts of the internal business analysis team. Continually optimizes the application environment and footprint to meet the changing needs of the business. Facilitates decisions to set priorities for application improvements and other assistance requests with application stakeholders and is then held accountable for following through on the agreed priorities. Manages the licensing of ERP and other corporate applications to ensure the business needs are met with the most cost-effective licensing strategy possible. Develops reports and other technical solutions. This is a hands-on managerial role that contributes to helpdesk and development efforts directly. Ensures cross training of the applications team to provide redundant knowledge across different members of the team. Provides Project Management for large and small ERP implementations and related projects. Performs all other duties as assigned or needed. Enterprise Applications Manager Qualification Requirements: Bachelor’s degree in computer science or business disciplines preferred but equivalent experience considered. Specialized training or demonstrated knowledge of ERP functionality. Previous supervisory or managerial experience preferred. Experience with managing and negotiating software license fees and maintenance. Technical abilities in data conversions, report writing and other techno-functional areas. SSRS and heavy MS-SQL experience highly preferred. Previous ERP implementation and upgrade experience. Willingness to travel. Up to 25% travel on average. Heavier at appropriate times during a remote project. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #CORP #NBPT #IND

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). Senior Quality Engineer Summary: The Senior Quality Engineer has the responsibility for the development and implementation of quality systems for sealed plastic film products in an ISO 13485 environment. This role will ensure that these products meet stringent quality and regulatory requirements across multiple industries. The Senior Quality Engineer will have a deep understanding of quality management systems, regulatory compliance, and manufacturing processes related to medical devices. Senior Quality Engineer Essential Duties and Responsibilities: * Oversees and approves IQ, OQ, PQ validation protocols, execution and reports on new and sustaining products. * Oversees PPAP activities and produces PPAP submittal packages on new and sustaining products. * Collaborates with Quality Technicians to resolve quality issues. * Participates as a member of the FMEA team related to primarily new and developing products. * Develops and documents control plans. * Conducts statistical capability studies and sets up SPC control charts. * Documents inspection procedures and test methods. * Performs regular audits of processes and materials to ensure that: Inspections, tests, and operations are being conducted and documented according to applicable specifications and standard operating procedures. Assures results of inspections and tests are in compliance with all applicable requirements. * Finalizes release of finished product based on above audits. * Monitors and interprets SPC charts to assure that processes remain in control. * Interfaces directly with production in the operator training process for quality issues. * Reviews reject reports and initiates corrective action as required. * Interfaces directly with other support departments as required. * Conducts special testing when required for failure analysis, validations, etc. * Sets up inspection / test equipment. * Develops and maintains Standard Operating Procedures. * Develops protocols, performs statistical analyses and writes reports for validations and formal product / process development. * Reviews and documents procedure changes for quality requirements and compliance with the quality system. * Provides audit support for third party audits, customer audits, and internal audits. * Observes all safety regulations and procedures. * Follows all department and company policies and procedures. * Performs other similar duties as required by responsibility, necessity or as requested. Senior Quality Engineer Qualification Requirements: * 4-year college degree in related field. * 3+ years' experience in a Quality Engineering Role (preferably in medical device manufacturing). * 3+ years' experience in the following: * Oversight and approval of validation activities (IQ, OQ, PQ, MSA) * Oversight of and submittal of PPAP packages * Participation in FMEA / PFMEA activities * Root Cause Analysis / CAPA * Internal Quality Audit * Supplier Quality * Software Validation * Good working knowledge of ISO 13485, PPAP, FMEA, AIAG Control Plan Methodology SPC, and Good Manufacturing Practices. * ASQC Certified Quality Engineer, preferred. * Proficiency in the use of Productivity Software such as Microsoft Office. * Ability to interact with all levels of the organization and with suppliers. * Strong written and oral communication skills. * Strong analytical skills in problem analysis and problem solving. * Strong leadership skills. * Occasional travel may be required. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ******************* UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC #IND

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: The position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Qualified applicants must be eligible to work in the United States to be considered for this opportunity. Employment based visa sponsorship (including H01B sponsorship) is not available for this position. Senior Manufacturing Engineer Summary: Applies advanced knowledge of continuous improvement engineering theory and methods to design, integrate, and improve companywide manufacturing systems or related processes and new process development. Work with designers, to refine product designs to increase manufacturability and decrease costs. Senior Manufacturing Engineer Essential Duties and Responsibilities: * Applies lean manufacturing techniques to reduce manufacturing waste. * Conducts time studies and adjusts production standards as required. * Designs and oversees the fabrication of manufacturing tooling and fixtures to support continuous improvement projects. * Coordinates fabrication of tools and fixtures to be used in production. * Continually monitors scrap rates and initiates projects reducing scrap cost in manufacturing. * Works with Team Leaders and production management to review shop order variances (material and labor) and initiates projects to eliminate variances and improve actual cost performance. * Trains work cell team members in continuous improvement, working with Team Leaders and Production Supervisors to create a culture of continuous improvement. * Monitors activities of Manufacturing Engineers and green belts offering support as needed. * Prepares work instructions to communicate the proper set-up and operation of manufacturing processes to meet customer requirements. * Trains production team members in the development and use of visual production tools to promote improvements to product quality and production efficiency. * Collects and utilizes data to make data driven decisions. * Provides reports summarizing problem solving and corrective action efforts to production teams and customers as required. * Ability to assist in the design, install and troubleshoot basic manufacturing equipment such as jigs, fixtures and gauges. * Utilizes six sigma tools and methodologies to determine root cause of failures using statistical methods and recommends changes in designs, tolerances, or processing methods. * Prepares estimates and proposals for projects to aid in the approval of continuous improvement projects through knowledge of UFP manufacturing capabilities and appropriate materials selection. * Submits capital projects for approval, as required. * Tracks continuous improvements projects and reports results monthly. * Prepares reports summarizing information or trends related to manufacturing performance. * Trains production personnel in new or existing methodology. * Supports new product transfer into production, working with our design team on new product designs to ensure that our processes are capable of meeting customer requirements. * Interacts with customers, account managers, manufacturing personnel, vendors and team members whenever necessary to satisfy project requirements. * Performs all other duties as assigned. Senior Manufacturing Engineer Qualification Requirements: * Bachelor's in Engineering or relevant discipline and 10+ years of continuous improvement experience in a manufacturing environment or an equivalent combination of education and experience. * Must have experience managing continuous improvement green belts and technical engineers responsible for continuous improvement. * Must have a proven track record in applying lean manufacturing and other continuous improvement manufacturing methodologies. Experience with GD&T, CAD, Minitab, MS Project strongly desired. * Proven track record applying statistical analysis to develop and control processes in a manufacturing environment. * Manufacturing experience must include heavy emphasis on assembly operations, tooling evaluation, vendor qualification, facilities engineering and cost savings through process improvement. * Basic Bridgeport, lathe and other machine shop equipment experience desired. * Occasional travel may be required. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ******************* UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #NBPT

Job DescriptionAbout UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company’s single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: Medical, Dental, Vision, Life, Disability Insurance 401K with a matching contribution Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). Manufacturing Engineer Summary: The Manufacturing Engineer applies knowledge of continuous improvement to enhance manufacturing quality, reliability, and cost-effectiveness. May design, or work with designers to refine product designs, to increase manufacturability, and decrease costs. Manufacturing Engineer Essential Duties and Responsibilities: Applies lean manufacturing techniques to reduce medical device manufacturing waste. Conducts time studies and adjusts production standards for medical device products as required. Understands regulatory and industry requirements for medical device manufacturing (GMP, RoHS, REACH, etc.). Provides direct production area support and identifies potential process improvements, efficiencies and safety issues. Continually monitors scrap rates and initiates projects to reduce scrap cost in manufacturing. Works with team leaders and production management to review shop order variances (material and labor) and initiates projects to eliminate variances and improve actual cost performance. Prepares work instructions to communicate the proper set-up and operation of manufacturing processes to produce products which meet customer requirements. Trains production team members in the development and use of visual production tools to promote improvements to product quality and production efficiency. Collects and utilizes data to make data driven decisions. Provides reports summarizing problem solving and corrective action efforts to production teams and customers as required. Ability to assist in the design, installation and troubleshooting of basic manufacturing equipment. Identifies root cause of failures using statistical methods and recommends changes in designs, tolerances, or processing methods. Prepares estimates and proposals for projects to aid in the approval of continuous improvement projects through knowledge of manufacturing capabilities and appropriate materials selection. Submits capital projects for approval, as required. Prepares reports summarizing information or trends related to manufacturing performance. Works to develop a detailed understanding of customer requirements for new product launches and product sustainment. Completes all documentation required for PPAP submittal (FAI, PFMEA, SOP, etc.). Properly drafts and submits ECRs and SICRs internally and externally to document changes to products or processes. Supports new product transfer into production, working with our design team. Interacts with customers, account managers, manufacturing personnel, vendors and team members whenever necessary to satisfy project requirements. Performs validations (IQ/OQ/PQ activities) on products to ensure proper performance to designated specifications. Drafts, executes, and reports validation protocols internally and externally. Preforms all other duties as assigned. Manufacturing Engineer Qualification Requirements: BS in Mechanical or Manufacturing Engineering and 3+ years’ work experience in the manufacturing industry. Experience with all medical device classes, preferred. Experience interpreting CAD and SolidWorks designs. Must have knowledge of lean manufacturing and other continuous improvement manufacturing methodologies. Proven track record applying statistical analysis to develop and control processes in a manufacturing environment. Manufacturing experience must include heavy emphasis on assembly operations, tooling evaluation, vendor qualification, facilities engineering and cost savings through process improvement. Must be available to work in the plant regularly to properly oversee projects and issues. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ****************** . UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC #IND

Job Description UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company’s single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: Medical, Dental, Vision, Life, Disability Insurance 401K with a matching contribution Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Opening is on 2nd Shift! Team Lead Summary: The Team Lead I oversees the daily operations and safety protocols of assigned production lines, ensuring adherence to quality standards and timely product completion. The Team Lead operates and troubleshoots various production machinery, handling setup and basic troubleshooting as needed. They actively monitor inventory and production data, assist with continuous improvement initiatives, and maintain an organized workspace in line with 5S guidelines. Team Lead Duties and Responsibilities: Performs all essential duties and responsibilities of Operator III. Oversees safety protocols in assigned area, as well as proactively asking operators for safety suggestions. Oversees daily operations of production line(s) to ensure timely completion of product schedules while maintaining quality standards. Monitors and coaches operator’s behaviors related to all company policies and procedures. Assigns operators to jobs and equipment based on schedule and experience of operators. Performs set-up and operation of all UFP machinery he / she has been trained to operate. Troubleshoots and corrects operational problems as they occur, submitting help desk tickets in a timely manner. Demonstrates competence using Epicor, including creating travelers and identifying and correcting labor transactions. Works under general supervision from the Production Supervisor / Manager, supervises the training and work of Machine Operators. Refers any decision on schedule changes to the Production Supervisor / Manager. Assists in production / replaces absent workers when production needs dictate. Ensures production data accuracy. Seeks support when Supervisor is not available. Maintains clean and organized work area, following 5S guidelines. Supports and encourages continuous improvement efforts. Assists with maintaining area production board. Monitors inventory controls. Performs all other duties as assigned or needed. Team Lead Qualification Requirements: High school diploma, GED, or successful completion of a company-administered equivalency exam. Strong mechanical aptitude. Minimum 2 years manufacturing experience. Ability to use quality measurement devices accurately. Knowledge of lean manufacturing processes. Supervisory experience strongly preferred. Must work well in a team environment. Ability to communicate effectively with fellow employees and supervisors. Ability to effectively train less experienced operators. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ****************** . UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #NBPT #MEDTECH

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position is based on-site in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). The position will be on-site full time. Process Engineer Summary: The Process Engineer applies advanced knowledge of materials, engineering theory and methods to design, integrate, and improve company wide manufacturing systems or related processes and new process development. Work with designers, to refine product designs to increase manufacturability and decrease costs. Oversees and assesses existing processes and workflows. Optimizes productivity by designing, implementing, and testing new procedures. Communicates findings and proposals to upper management. Tracks metrics to discover areas for improvement and monitor upgrades. Provides thorough instructions for successful implementation of process changes. Process Engineer Essential Duties and Responsibilities: * Applies lean manufacturing techniques to reduce manufacturing waste in a job shop environment. * Conducts time studies and adjusts production standards as required. * Reviews monthly Job Closes to analyses trends and opportunities for improvement per set performance goals. * Supports and manages (VIP) Value Improvement Program projects, costs analysis and project implementation. * Continually monitors scrap rates and initiates projects to reduce scrap cost in manufacturing. * Creates Value Stream Maps for critical products and processes. * Supports and trains employees in 5S practices. * Works with team leaders and production management to review shop order variances (material and labor) and initiates projects to eliminate variances and improve actual cost performance. * Trains work cell team members in continuous improvement working with team leaders and production supervision to create a culture of continuous improvement. * Collects and utilizes data to make data driven decisions. * Designs, installs and troubleshoots basic manufacturing equipment such as jigs, fixtures and gages. * Designs, develops and manufactures tooling and fixtures to support continuous improvement projects. * Utilizes six sigma tools and methodologies to determine root cause of failures using statistical methods and recommends changes in designs, tolerances, or processing methods. * Prepares estimates and proposals for projects to aid approval of continuous improvement projects through knowledge of UFP manufacturing capabilities and appropriate materials selection. * Tracks continuous improvements projects and reports results on a monthly basis. * Prepares reports summarizing information or trends related to manufacturing performance. * Documents improvement of processes and trains production personnel in new or existing methodology. * Manages new product transfer into production, working with the design team on new product designs to ensure that our processes are capable of meeting customer requirements. * Interacts with customers, account managers, manufacturing personnel, vendors and team members whenever necessary to satisfy project requirements. * Performs all other duties as assigned or needed. Process Engineer Education / Experience: * Bachelor's in Industrial or Mechanical Engineering or relevant discipline and 2-4 years in manufacturing engineering or an equivalent combination of education and experience. * Strong lean manufacturing experience, knowledge, and practitioner. * Must have a proven track record in applying lean manufacturing and other continuous improvement manufacturing methodologies. * Experience with CAD, MS Project strongly desired. * Proven track record applying analysis to develop and control processes in a manufacturing environment. * Manufacturing experience must include heavy emphasis on assembly operations, tooling evaluation, vendor qualification, facilities engineering and cost savings through process improvement. * Ability to persuade others to change existing practices. * Excellent verbal and written communication skills required. * Occasional travel may be required. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ******************* UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC #IND

Job Description UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company’s single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: Medical, Dental, Vision, Life, Disability Insurance 401K with a matching contribution Paid time off, Paid holidays, Employee discounts and much more! Location: The position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). Accounting Information Systems Analyst Summary: The Accounting Information Systems (AIS) Analyst provides support for various systems and/or applications by working with business users and technical teams, with a primary focus on accounting systems. The AIS Analyst must be an expert in the accounting applications of the system and possess a working knowledge of related applications or Enterprise Resource Planning (ERP) modules. Maintenance of current system/industry related knowledge by the AIS Analyst on system functionality is vital to meet the needs of the business users. The AIS Analyst must be capable of querying data and basic reporting from ERP platforms. We are looking for a detail-oriented AIS Analyst to manage, troubleshoot, and enhance our company’s accounting systems. Responsibilities will include analyzing our accounting systems’ performance, performing upgrades, implementing new systems, and collaborating with the accounting team to ensure accuracy. Our ideal candidate has a strong understanding of accounting principles and information technology, with a focus on accounting systems such as Epicor, SAP, or Oracle. The primary objective is to ensure our company’s financial data is accurate, secure, and supports our financial goals. Accounting Information Systems Analyst Duties and Responsibilities: Reviews, analyzes, and evaluates business systems and user needs. Formulates systems to satisfy business requirements. Understands and writes the functional requirements in accordance with SOX and other related quality requirements. Develops test plans and procedures for system changes and the deployment of small projects. Leads complex systems projects and project groups. Assess and troubleshoot current accounting systems. Identifies system deficiencies and implements effective solutions. Supports accounting team’s automation initiatives. Works closely with the accounting and IT teams to ensure accuracy of financial data and system reliability. Designs and implements upgrades and new systems as required. Trains end-users on new systems and protocols. Stays updated with new technologies and regulations that may affect the organization’s accounting information system. Performs all other duties as needed. Accounting Information Systems Analyst Qualification Requirements: Bachelor’s degree in Accounting, Computer Science or related discipline. 5 to 7 (minimum) years of proven experience as an Accounting Information Systems Analyst or similar role. Strong understanding of accounting principles and procedures. Experience with the accounting modules of ERP systems such as Epicor, SAP, or Oracle (Epicor strongly preferred). Excellent problem-solving, analytical skills and attention to detail. Proficiency in MS Office (especially Excel) and database systems. Experienced with MS-SQL and relational database concepts. Technical report writing experience strongly preferred. Some experience leading teams and projects. Relevant certifications such as CPA or CISA, a plus. Regular travel to other company locations may be required. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #CORP #NBPT #IND

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company's single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: * Medical, Dental, Vision, Life, Disability Insurance * 401K with a matching contribution * Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). Qualified applicants must be eligible to work in the United States to be considered for this opportunity. Employment based visa sponsorship (including H-1B sponsorship) is not available for this position. Senior CAD Designer Summary: Performs a wide variety of duties to develop and produce detailed drawings, prints, and / or plans for tooling and equipment used in the manufacturing process. Duties include utilizing CAD system to produce models and prints, acting as a liaison with engineering and customer, maintaining hardcopy archives, files and other similar duties pertaining to the development of product prints/plans. The Senior CAD Designer will assist the other members of the CAD team using their mechanical knowledge and experience in tooling design. They will be assigned to the CAD team and will work under the direction of the CAD Manager. Senior CAD Designer Essential Duties and Responsibilities: * Develops detailed tooling and / or equipment design drawings. * Works from concept sketches / drawings, samples and / or R&D plans. * Produces detailed prints of required tooling / equipment down to component levels. * Produces product print plans for customer approval. * Produces drawings for tooling changes or modifications from engineering change requests. * Downloads / uploads electronic files and forwards them to the customers or vendors. * Develops prints for company facilities layouts, machine layouts, floor plans, etc. * Acts as a working liaison with project engineers, R&D personnel, set-up technicians, customers, etc. and discusses product details and requirements related to tooling / equipment design. * Communicates directly with external customers to review tooling designs collaboratively with engineering or upper management. * Designs new tooling and fixtures for modifications to existing tooling as required by products modifications, process changes, manufacturing problems, etc. * Reviews process problems, engineering changes, product modifications, product performance requirement, etc. and reviews with appropriate project personnel. * Issues purchase orders to vendors and follows progress until the completion of the project. * Designs and presents advanced tooling models for production and R&D needs. * Designs and presents turntables, shuttles, advanced fixtures, etc. for production and R&D needs. * Provides training and guidance to the CAD Designers with regards to the designs of tooling / equipment. * Supervise other CAD team members during group design efforts. Delegates and distributes tasks to best complete assignment. * Communicates with vendors directly regarding design machinability and feasibility. * Makes high level decisions regarding tooling design to best meet our customers tooling requests. * Meets with the CAD Manager and other Senior CAD Designers to discuss new standards, methods, technology, and procedures to ensure department continues learn and grow. * Assists Engineering on layout work for quotes and / or cost reductions, when appropriate. * Presents advanced tooling & equipment in internal and external design reviews. * Performs all other duties as assigned. Senior CAD Designer Qualification Requirements: * Associate degree in mechanical engineering, mechanical engineering technologies, or an equivalent combination of education and experience required. * Minimum of 7-10 years of experience in mechanical design. * Proficiency with SolidWorks. * Experience interpreting CAD and SolidWorks designs. * Must work well in a team environment and be able to effectively communicate both orally and written with fellow employees, supervisors, customers, and managers. * Good understanding of production processing. * Demonstrated ability to create and understand product and tooling prints. * Demonstrated ability to effectively train less experienced CAD Designers to UFP design standards. * Demonstrated ability to lead CAD team members on group and/or collaborative design efforts. * Demonstrated ability to supervise CAD team members to best utilize resources to complete a design project promptly and efficiently. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ******************* UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC #IND

Job Description About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company’s single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: Medical, Dental, Vision, Life, Disability Insurance 401K with a matching contribution Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Newburyport, MA. The position holder will need to be within commuting distance (within 45 min). This position is for a 2nd shift schedule. Quality Technician Summary: Performs general Quality Assurance duties in support of our customers. Under the direction of the Quality Department Manager. The Quality Technician provides support related to corrective action containment, component measurement / testing, product certification and administrative tasks. Quality Technician Essential Duties and Responsibilities: Participates in Root Cause Investigations and provides corrective actions to customer SCARs. Performs FAIR – First Article Inspection Reports to support existing and new product development. Implements preventive action to prevent product failures. Reads blueprints/drawings. Performs Incoming, WIP, and FG inspections. May provide instruction, guidance and direction for manufacturing employees in determining acceptable products. Creates C of C documents for product shipments. Assist engineers with or perform gage and equipment calibration and maintenance. Maintains control system documents and performs general administrative tasks. Maintains organization of the NCM area. Performs all other duties as assigned or needed by department manager. Quality Technician Qualification Requirements: High school diploma or higher education. Some experience with Quality Standards – ISO 9001 or ISO 13485. Strong English and Math skills. Bilingual in Spanish preferred. Experience with Microsoft Office applications. A good understanding of the metric system, general metrology and statistics experience a plus. ASQ Certified Quality Engineer (CQE) or Certified Quality Technician (CQT) certificate/training a plus. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ****************** . UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #NBPT

Job Description About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered custom products. UFP is an important link in the medical device supply chain and a valued outsource partner to most of the top medical device manufacturers in the world. The Company’s single-use and single-patient devices and components are used in a wide range of medical devices and packaging for minimally invasive surgery, infection prevention, wound care, wearables, orthopedic soft goods, and orthopedic implants. UFP Technologies, Inc. offers a competitive benefits package, including but not limited to: Medical, Dental, Vision, Life, Disability Insurance 401K with a matching contribution Paid time off, Paid holidays, Employee discounts and much more! Location: This position will be on-site full-time in Chicopee, MA. The position holder will need to be within commuting distance (within 45 min). Senior Quality Engineer Summary: The Senior Quality Engineer has the responsibility for the development and implementation of quality systems for sealed plastic film products in an ISO 13485 environment. This role will ensure that these products meet stringent quality and regulatory requirements across multiple industries. The Senior Quality Engineer will have a deep understanding of quality management systems, regulatory compliance, and manufacturing processes related to medical devices. Senior Quality Engineer Essential Duties and Responsibilities: Oversees and approves IQ, OQ, PQ validation protocols, execution and reports on new and sustaining products. Oversees PPAP activities and produces PPAP submittal packages on new and sustaining products. Collaborates with Quality Technicians to resolve quality issues. Participates as a member of the FMEA team related to primarily new and developing products. Develops and documents control plans. Conducts statistical capability studies and sets up SPC control charts. Documents inspection procedures and test methods. Performs regular audits of processes and materials to ensure that: Inspections, tests, and operations are being conducted and documented according to applicable specifications and standard operating procedures. Assures results of inspections and tests are in compliance with all applicable requirements. Finalizes release of finished product based on above audits. Monitors and interprets SPC charts to assure that processes remain in control. Interfaces directly with production in the operator training process for quality issues. Reviews reject reports and initiates corrective action as required. Interfaces directly with other support departments as required. Conducts special testing when required for failure analysis, validations, etc. Sets up inspection / test equipment. Develops and maintains Standard Operating Procedures. Develops protocols, performs statistical analyses and writes reports for validations and formal product / process development. Reviews and documents procedure changes for quality requirements and compliance with the quality system. Provides audit support for third party audits, customer audits, and internal audits. Observes all safety regulations and procedures. Follows all department and company policies and procedures. Performs other similar duties as required by responsibility, necessity or as requested. Senior Quality Engineer Qualification Requirements: 4-year college degree in related field. 3+ years’ experience in a Quality Engineering Role (preferably in medical device manufacturing). 3+ years’ experience in the following: Oversight and approval of validation activities (IQ, OQ, PQ, MSA) Oversight of and submittal of PPAP packages Participation in FMEA / PFMEA activities Root Cause Analysis / CAPA Internal Quality Audit Supplier Quality Software Validation Good working knowledge of ISO 13485, PPAP, FMEA, AIAG Control Plan Methodology SPC, and Good Manufacturing Practices. ASQC Certified Quality Engineer, preferred. Proficiency in the use of Productivity Software such as Microsoft Office. Ability to interact with all levels of the organization and with suppliers. Strong written and oral communication skills. Strong analytical skills in problem analysis and problem solving. Strong leadership skills. Occasional travel may be required. To apply for this job please create a profile with us through our online application system. Click the "Apply" box in the upper right-hand corner to start the application process. Or, if you already have a social media account with LinkedIn, Google, or Facebook you can use your log in credentials to apply. For more information on UFP MedTech, visit ****************** . UFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled. #UFP #MEDTECH #CHIC #IND