Zimmer Biomet jobs in Denver, CO - 32 jobs

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** Paragon 28, a Zimmer Biomet Company focused on orthopedic medical devices for the foot and ankle, is hiring a National Accounts Manager to join our sales team. The National Account Manager is responsible for managing and nurturing relationships with Group Purchasing Organizations (GPOs), Ambulatory Surgery Centers (ASCs), Integrated Delivery Networks (IDNs), and hospital systems within their assigned region (East or West USA). Reporting to the Director of National Accounts, the National Account Manager will ensure the successful execution of strategic account plans, contract management, and sales growth in alignment with Paragon 28's business goals and customer needs. This position plays a key role in fostering long-term partnerships and ensuring client satisfaction. **How You'll Create Impact** Essential Responsibilities and Duties - Account Management: Build and maintain strong relationships with key decision-makers within GPOs, ASCs, IDNs, and hospital systems. Act as the primary point of contact for assigned accounts, ensuring consistent engagement and satisfaction. - Contract Execution: Assist in the negotiation, implementation, and management of contracts within the assigned region. Ensure compliance with Paragon 28's standards, pricing structures, and legal requirements. - Sales Growth: Support regional sales initiatives by identifying new business opportunities, upselling, and expanding relationships within existing accounts. - Customer Needs Assessment: Work closely with customers to understand their needs, challenges, and business objectives. Provide tailored solutions that align with Paragon 28's product offerings. - Performance Tracking: Track and report on account performance, including sales, renewals, and customer feedback. Ensure that regional goals and objectives are met. - Collaboration with Regional Director: Collaborate with the Director of Natioal Accounts to execute regional strategies, ensure alignment with organizational goals, and provide insight into customer trends and opportunities. - Problem Solving: Address and resolve any account-related issues, including billing, collections, or pricing challenges. Work with internal teams to provide timely and effective solutions. - Market Insight: Stay updated on market trends, competitor activities, and industry developments. Share relevant insights with the regional director and other stakeholders to support business growth. - Cross-Functional Collaboration: Work with internal teams (sales, marketing, finance, legal) to ensure smooth execution of contracts and to support account needs effectively. **Your Background** Qualifications - Bachelor's degree required. - Minimum of 2-3 years of experience in national account management or a related role in the medical device, healthcare, or orthopedic industry. - Proven ability to build and manage strategic customer relationships. - Experience with contract negotiation and account management within the healthcare sector. - Strong communication, problem-solving, and interpersonal skills. - Proficiency in MS Excel, MS Word, PowerPoint, and CRM systems. - Ability to work independently and as part of a team in a fast-paced, high-volume environment. - Strong sales skills with a focus on relationship building and customer satisfaction. - Valid driver's license and active vehicle insurance policy. Work Environment This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones and copy machines. When traveling, making calls on client organizations in office and hospital environments. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee is required to have close visual acuity to perform activities such as viewing a computer terminal for long periods of time. This role requires employee to physically travel to client organizations. The employee may be required to lift up-to 35 lbs. by themselves. Position Type/Expected Hours of Work This is a full-time position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined with Manager. **Travel Expectations** Up to 50% overnight travel. EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised. What You Can Expect The Sales Associate Rep plays a key support role within the Surgical commercial team, assisting in driving revenue growth, developing customer relationships, and advancing adoption of the company's surgical product portfolio. In this role, you will work closely with your territory team to provide expertise in the operating room, deliver superior customer service, and support territory strategy How You'll Create Impact * Meets or exceeds established quotas and objectives, advises customers about products, services and educational programs. * Builds relationships with customers to increase loyalty and customer experience. * Reviews market analyses to determine customer needs and forecast volume potential. * Analyzes sales / market data to assist in development of territory strategy. * Presents educational programs i.e. Lunch n Learns, plans and executes other educational events within assigned territory. * Utilizes sales process to understand customer needs and facilitate providing effective solutions. * Facilitates order processing, returns, and follows up as required. * Provides insight on market potential, territory/customer concerns, opportunities. * Represents the company as requested at trade association meetings or educational events to build relationships and promote products. * Coordinates liaison activities between the sales department and other business partners. * Assists other departments in preparation of manuals and technical publications. * Complies with company policies and procedures including compliance, safety, travel and expense reporting requirements. This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA. What Makes You Stand Out * Demonstrates strong goal orientation; results driven, highly competitive, and self- motivated with demonstrated successful sales track record * Strong interpersonal and relationship building skills. * Understanding of consultative sales process, experience with formalized sales training * Strong business acumen * Highly accountable, well organized with excellent planning skills * Strong hunter mentality * Available and able to work evenings and weekends * Demonstrated integrity with high ethical standards and practice * Ability to utilize a laptop computer with strong working knowledge of Microsoft Office including: Outlook, Word, Excel and PowerPoint. Your Background * Bachelor's degree in business, life sciences or related field, preferred. * Professional Selling Skills (PSS) experience, preferred. * Driver's License (Required). * A combination of education and experience will be considered. Travel Expectations * Up to 70% predominantly by car, depending on territory. * Up to 20% overnight travel may be required. This role has a base salary of $60,000 annually with additional earnings through commission and bonus opportunities + benefits. #LI-MB1 EOE/M/F/Vet/Disability

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** The Quality Inspector I - Temp is responsible for the inspection of materials, assemblies, work-in-progress, and finished medical devices, as well as the completion of documentation to determine conformance to specifications to release product for distribution and use. This position is onsite at our Paragon 28 location in Englewood, Colorado. **How You'll Create Impact** + Receiving Inspection of materials, work-in-progress, finished parts and assemblies and completion of associated paperwork for final release of product to the field + Visual inspections per documented specifications + Measurement of product features per documented specifications and inspection checklists + Generate accurate documentation of measured characteristics for non-conformance to specifications and identify product appropriately per procedures + Monitor calibration status of inspection equipment + On occasion, incumbents may also be asked to do the following: + Product labeling and packaging as needed + Verifying, scanning, and filing documents + Assist with identifying product status and organizing product + Other duties as assigned **Your Background** + High school diploma plus 1-2 years' quality experience; Associate degree preferred + Experience with dimensional measurement equipment such as micrometers, calipers, gage pins, dial indicators, etc. + Knowledge and experience with precision measuring equipment such as CMM, Vision Systems, + Basic understanding of print reading and GD&T per ANSY Y14.5 + Familiarity with 21 CFR 820/ISO13485, or other government/ISO standards preferred + Ability to follow standard operating procedures + Must have attention to detail and be able to work with small components + Good handwriting and communication skills + Basic computer skills (MS Word, Excel) + Knowledge of machined components is a plus **Work Environment** This job operates onsite in a professional laboratory and office environment. This role routinely uses standard office equipment such as computers, phones, copy machines, and basic laboratory equipment such as micrometers, calipers, drop indicators, and optical comparator. **Physical Demands** The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal to the organization. This role requires manual dexterity to work with small parts and write measurements. The employee frequently is required to move about the facility. The employee may be required to lift up-to 30 lbs. by themselves. **Position Type/Expected Hours of Work** This is a Temporary full-time position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined with Manager. **Compensation Data** Hourly Rate: $20.00-25.00 USD per hour depending on experience **Physical Requirements** **Travel Expectations** EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** The Distribution Coordinator works with various teams in the warehouse to receive, inspect, replenish, and/or ship surgical instrumentation and implants to healthcare facilities with impeccable attention to detail while maintaining inventory accuracy. **How You'll Create Impact** + Package product and materials ensuring contents are protected adequately for shipment. + Accurately prepare all necessary shipping documentation, including accurate addresses, and ensure that shipments contain the correct inventory + Receive incoming surgical trays, inspect instruments and implants, and restock inventory based on usage + Compare part numbers, lot numbers, and other information listed on the Pack Slip to verify accuracy of purchase order and shipping orders. + Compile data from sources such as purchase orders, invoices, requisitions, to maintain electronic record. + Assist with cycle counting of inventory when necessary + Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485. + Other duties as assigned + Shift: Monday through Friday 11am - 7:30pm **What Makes You Stand Out** As a Distribution Coordinator in the orthopedic medical device industry, you will ensure the efficient and accurate movement of critical medical products-from inventory management to order fulfillment and logistics coordination, committing to timely delivery that directly supports surgical teams and patient outcomes. This role bridges supply chain operations and customer service, helping maintain seamless access to life-changing orthopedic technologies. **Your Background** + High School Diploma or equivalent preferred. + 1+ year(s) related distribution or inventory control experience and/or training helpful + Ability to work effectively and efficiently in a team environment. + Strong attention to detail + Self-motivated with ability to achieve desired results independently + Aptitude for analyzing situations and resolving problems preferred **Compensation Data** $20 per hour + Opportunity to earn up to a 15% monthly bonus based on performance and established metrics. **Physical Requirements** **Travel Expectations** EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect Paragon 28, a Zimmer Biomet company focused on orthopedic medical device for the foot and ankle, is hiring a Quality Records and Release Coordinator to join our team in Englewood, Colorado. This role is responsible for review, final verification and scanning of Device History Records (DHR) for product release. These records include, but not limited to inspection records, labeling records, packaging records, material certifications, and Certificates of Conformance of finished medical devices. Additionally, this role will perform assigned incoming inspections on received product, primarily allograft and custom devices. This is a 100% onsite position. How You'll Create Impact Final verification of DHR documentation, including inspection records, certifications, purchase orders and engineering prints * Confirmation of physical product visual conformance with specifications prior to product release * Issuance of product release notifications * Product inspection of assigned parts * Scanning electronic DHR records as well as preparation of physical records/boxes and submit to Document Control to offsite * On occasion, incumbents may also be asked to do the following: o Support internal and external audits o Support Complaint and Non-Conformance investigations with DHR requests o Other duties as assigned Your Background Associate Degree and minimum of 5 years of experience in medical device inspection/ quality or a Bachelor's degree in technical discipline with 2 years of experience in medical device inspection/ quality. * Strong understanding of good documentation practices * Strong organizational skills * Detailed oriented * Ability to follow standard operating procedures * High proficiency in MS Office 365, Adobe Acrobat DC * Good written and oral communication skills * Prefer familiarity with 21 CFR 820/ISO13485, or other government/ISO standards * Experience in Electronic Records Management and/or AIIM training a plus Work Environment This job operates in an office/laboratory environment within a distribution facility. The role routinely uses standard office equipment such as computers, phones, copy machines, and filing cabinets. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee frequently is required to move about the facility. May be required to lift up-to 30 lbs. by themselves. Position Type/Expected Hours of Work This is a full-time, onsite hourly position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined by the supervisor and manager. Travel Expectations No overnight travel is required. EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** Paragon 28, a Zimmer Biomet Company, is hiring a Quality Engineer I - Production. The Quality Engineer has varied responsibilities to assist the Quality team in ensuring compliance to regulations and standards. This position is onsite at our Englewood, Colorado location. **How You'll Create Impact** - Create and revise components of the Quality System - Manage and complete CAPAs on the quality system - Perform internal audits, as needed - Assist Design Quality Engineers in completion of NCRs, Complaint investigations and other project related work as needed - Work with the supplier quality and purchasing departments to evaluate new suppliers and pre-production approvals - Assist in establishing receiving inspection criteria with input from Product Development, Engineering and QA - Execute equipment validations - Other duties as assigned **Your Background** - Bachelor's in Engineering or technical discipline and 2 years of related experience - Medical device experience preferred - Knowledge and experience with measuring equipment - Process Validation experience preferred - Experience reading and interpreting part drawings/GD&T and use of measuring equipment a plus - Familiarity with 21 CFR 820/ISO13485 and other government/ISO standards - Strong computer skills (MS Word & Excel) - Knowledge of Ti and SS machining a plus **Travel Expectations** Less than 10% overnight travel. **Compensation Data** Salary Range: $70,000 - $90,000 USD annually depending on skills and experience EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect Paragon 28, a Zimmer Biomet Company, located in Englewood, Colorado, is hiring a Marketing Materials Coordinator. The Marketing Materials Coordinator is responsible for shipping, auditing, and restocking marketing material products. Paragon 28 Marketing Materials include (but are not limited to): acrylics, show sets, lab (cadaveric/saw bone trays) sets, banners, sawbones, power, universal instruments, lab equipment (when needed, PPE and others), patient specific equipment, table cloths, and literature associated with Paragon 28's event types. Additional Marketing Materials may be added when necessary. Event types this position supports will vary from tradeshows, medical education courses, mobile labs, dinners, sales interactions, development/engineering labs, and/or educational lab sessions. Working in conjunction with the entire Medical Education team and Lab Manager, the Marketing Materials Coordinator is responsible for the show, cadaveric, and demo inventory to ensure every medical education opportunity and additional Paragon 28 event types are fully supported. This position is 100% onsite at our location in Englewood, Colorado. How You'll Create Impact * Contact for customers, field sales and distributor/agency reps through order entry and telephone support for the following duties: * Receive orders via SmartSheet, phone, and/or e-mail. * Process incoming and returned orders for products within the business day keeping inventory organized digitally using Google Sheets, SAP, and/or SmartSheets. * Schedule show, cadaver and demo sets to ensure lab/tradeshow coverage. * Ensure show, cadaver, and demo sets are returned promptly after event by the point of contact, cleaned, audited, and reset. * Track shipped orders and resolve late shipments. Send back up shipments as needed. * Notify accounting to bill for lost/damaged equipment. * Audit inventory and replenishment missing equipment from marketing material equipment. * Determine appropriate pricing, terms and shipping method for products by following Company guidelines. * Resolve issues with customers concerning order status, credit and shipping problems. Working closely with the event teams regarding shipping for large tradeshows. * Fulfill literature and other requests for information by working closely with the marketing and artwork team members. * Offsite and onsite temporary lab and marketing material set up. * Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. * Compares nomenclature, stock numbers, and other listed information on packing slips to verify accuracy of purchase orders and shipping orders. * Compiles information on receipt of disbursement of marketing material equipment and computes inventory balance, price, and cost. * Reconciles shipping and pack list discrepancies in a timely manner. * Prepare all necessary shipping documentation and ensure that shipments are tracked to destination. * Package materials and equipment ensuring that shipping documentation is accurate and materials are protected adequately for shipment. * Determine most efficient and economical routing and mode of transportation. * Initiate investigations into causes of misdirected shipments, damage or shortages in shipments or overcharges in freight cost. * Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485. * Assist in the development of processes and procedures for inventory, receiving, shipping, and administrative responsibilities resulting in cost and efficiency improvements for the marketing warehouse. * Maintains physical condition of warehouse by planning and implementing new design layouts; inspecting equipment; issuing work orders for repair and requisitions for replacement. * Support cross functionally including, but not limited to: Lab Manager or Medical Education Admin/Coordinators, Commercial, Events, Marketing, and Sales team members. * Other duties as assigned by the Manager. Your Background * High school diploma/GED plus 2-year related distribution or inventory control experience * Familiar with medical device industry, specifically foot and ankle is ideal. * Proficient in Microsoft Office. * Organized and attention to detail. * Must be able to establish and maintain relationships with outside vendors and P28 team members or sales agents. * Maintain a high level of professionalism with phone, email and in person interactions. * Ability to define problems, collect data, establish facts, and draw valid conclusions. * Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstracts and/or concrete variables. Work Environment * This job is performed in a distribution/warehouse environment. This role requires the handling of cadaveric specimens. Physical Demands * While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee frequently is required to move about the facility. The employee will regularly to lift up-to 50 lbs. by themselves. Position Type/Expected Hours of Work * This is a full-time position working four 10 hour shifts per business week. It may reasonably require additional hours during the week and weekend; specific requirements will be determined with Manager with advanced notice when possible. Travel Expectations 5% or more of overnight travel, only as needed to support offsite medical education labs or tradeshows Compensation Data Hourly Rate: $24.00-31.00 USD depending on skills and experience EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect Join the team shaping the future of foot and ankle orthopedics. Paragon 28, a Zimmer Biomet company, is seeking an energetic Associate Project Manager to help bring groundbreaking R&D ideas to life. The Associate Project Manager, R&D plays a key role in driving innovation by leading focused, single-discipline projects and supporting larger, cross-functional initiatives. In this role, you'll help guide new products from concept to commercial release-planning, reporting, executing, and controlling project activities through design control and established business processes. You'll ensure each project aligns with company strategy, delivers meaningful value, and launches on time and on budget. Medical Device industry experience is required. This position will be working at our location in Englewood, Colorado. How You'll Create Impact Project Management * Support the planning and implementation of single discipline and/or cross-functional projects. * Facilitate cross-functional collaboration with multiple internal functions including R&D, Quality, Regulatory, Clinical, Operations, and Marketing. * Support project goals and deliverables definition and team execution to exceed expectations. * Monitor and report on progress of the project to all stakeholders. * Present reports defining project progress, problems, and solutions. Budget Management * Support project budget and assess and manage project risk. Process Management & Improvement * Compliantly manage all aspects of the program's compliance matters. * Contribute to continuous improvement of Portfolio, Business, and Compliance processes. * Other duties as assigned Your Background * Bachelor's degree in Engineering or Science and 2+ years of solid knowledge and experience (or equivalent combination of education and experience) in managing projects. * Experience in people management, risk management, and change management. * Organizational skills with experience concurrently managing multiple tasks or activities. * Individual must be a motivated self-starter with the ability to work both independently and cross-functionally. * Medical device industry experience required. Travel Expectations Up to 15% overnight travel. Compensation Data Salary: $75,000 - $85,000 depending on skills and experience EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect Paragon 28, a Zimmer Biomet company focused on orthopedic medical devices for the foot and ankle, is hiring an EHS Specialist to join our team in Englewood, Colorado. The EHS Specialist ensures compliance with all local, state, federal, and corporate EHS standards, particularly those governed by OSHA, EPA, and FDA/cGMP regulations. The EHS Specialist will play a vital role in fostering a proactive, compliant safety culture among all employees and contractors. This position is onsite at our Englewood Colorado location. How You'll Create Impact * Advise management and take action to ensure compliance with OSHA, EPA, DOT, and company EHS regulations. * Conduct or coordinate required EHS inspections and regular facility-wide routine safety inspections at Grasslands Facility and assist with internal EHS auditing programs. * Develop, manage, and maintain critical EHS programs, including Lockout/Tagout (LOTO), Machine Guarding, Hazard Communication (HazCom), Powered Industrial Trucks (PIT), Bloodborne Pathogen and Emergency Response Plans for the Paragon28 Grasslands site. * Perform and document Job Hazard Analyses (JHAs) and Ergonomic Assessments for manufacturing and office tasks to minimize musculoskeletal injury risk. * Lead initiatives to promote environmental sustainability and reduce the company's environmental footprint. * Develop, customize, and deliver comprehensive EHS training modules for new hires, contractors, and existing employees. * Track, analyze, and report EHS Key Performance Indicators (KPIs) and compliance metrics to site and corporate leadership. * Assist with development, implementation, and revision of Paragon28 Grasslands site EHS procedures and promotional materials. * Coordinate a Safety Committee and promote EHS program at the Paragon28 Grasslands site through internal publications and encourage consideration of EHS impact during decision making process and integration of EHS responsibilities. * Responsible for oversight management of the Paragon28 Grasslands site Environmental Risk Management System Program. * Participate in new equipment installations and process move layouts for Paragon28 Grasslands site. * Other duties as assigned Your Background * Bachelor's Degree in Safety Management, Occupational Health and Safety, Environmental Engineering or equivalent combination of education and experience in a related field required. * Minimum 2 years of EHS experience, with direct experience in a manufacturing or production environment, preferably within the medical device, pharmaceutical, or similarly regulated industry. * Must possess strong written and verbal communication skills. * Microsoft Office Suite power user * Comprehensive knowledge of federal and state OSHA and EPA regulations. * Strong presentation skills for delivering effective training. * Professional certification such as Certified Safety Professional (CSP), Associate Safety Professional (ASP), Occupational Health or Safety Technician (OHST) preferred * OSHA 30-Hour General Industry Certification preferred Work Environment This job operates in an office and warehouse environment. This role routinely uses standard office equipment such as computers, phones and copy machines. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal to the organization. The employee is required to have close visual acuity to view a computer terminal and review reports. The employee may be required to lift up-to 15 lbs. by themselves. Position Type/Expected Hours of Work This is a full-time position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined with Manager. Travel Expectations Up to 10% travel Compensation Data Salary Range: $56,000 - $75,000 USD annually depending on skills and experience EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect Paragon 28-now part of Zimmer Biomet and a leader in foot and ankle orthopedic innovation-is looking for a driven Product Development Engineer to join our dynamic R&D team. As a Product Development Engineer I, you'll help bring new medical device concepts to life-leading targeted design and development tasks within a collaborative project team. With hands-on experience and growing autonomy, you'll make a tangible impact on projects that matter. This position is located at our Englewood, Colorado P28 headquarters. How You'll Create Impact Produce deliverables in support product development efforts from ideation to commercialization through entire product life cycle and on a given timeline, as directed by senior engineering staff, including: * Research and evaluate competitive product for performance characteristics * Conceptualization of new design ideas with some understanding of the inadequacy of existing designs * Parametric modeling and detail design of P28 implant and instrument development * Work within the P28 product development procedure to create design control documentation for P28 design history files and technical files. * Participate in development of testing protocols and assist in the testing process for new and existing products * Compile and comprehend test results and implement/recommend appropriate design changes * Participate in activities related to project phase gate design reviews * Interface with 3rd party suppliers, contractors, testing houses, etc. Assist the P28 Quality and Supply Chain departments to evaluate new suppliers for inclusion in the P28 approved supplier list Assist P28 quality team in developing inspection plans Observe surgery (live, cadaver, or video) on lower extremity pathology and formulate physician comments/ideas into meaningful design solutions. Document all notes. Work to become technical expert resource within specific product categories for sales support and other departments via phone and live product training. Assist on patent application preparation Assist with other development projects as additional resource when needed, while balancing own workload Other duties as directed by manager Your Background * Requires a bachelor's degree in Mechanical Engineering, Biomedical Engineering or related engineering discipline with 2-4 years of experience. * Prior experience in medical device development helpful. * Experience in taking medical device or similar product from ideation to commercialization helpful. * Understanding of medical device industry regulatory requirements preferred. * Experience with CAD. SolidWorks preferred. * High proficiency in MS Office * Effective communication and presentation skills with ability to convey information and respond to questions from groups of peers * Ability to work in a team environment Travel Expectations Up to 10% of overnight travel. Compensation Data SAlary: $80,000 - $105,000 USD annually depending on skills and experience. EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect Paragon 28, a Zimmer Biomet company focused on orthopedic medical devices for the foot and ankle, is hiring an International Distribution Supervisor. This will be a 100% onsite role at our location in Englewood, Colorado. The Supervisor of Distribution has overall responsibility for all day to day activities of the assigned Distribution team to meet departmental goals. This role also ensures staffing resources are properly utilized, all personnel are properly trained, and ensures clear communications to team members and management. How You'll Create Impact Essential Responsibilities and Duties * Partner with and develop Distribution Leads to ensure employees are properly utilized and each department within Distribution is sufficiently staffed. * Ensure employee compliance to protocols and standards. * Lead employees to meet the departmental and organizational expectations for productivity, quality, continuous improvement and goal accomplishment. * Coach, mentor and develop staff, including recruitment and onboarding, performance management and career development. * Train personnel in ERP system or other processes as needed. * Develop and drive implementation of processes and procedures to increase the efficient processing of inventory, customer fulfillment, receiving, and shipping. * Seek out opportunities for process improvement, develop possible solutions and partner with management and other departments as necessary to drive the process improvement for superior service levels to internal or external customers * Prepare reports, as necessary, to gain a deeper understanding of business successes and/or challenges, as well as, to communicate departmental performance to management as necessary. * Meet with the department on a regular basis to share relevant business updates, or other information as necessary. * Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485. * Knowledge of international customs documentation. * Ability to work with FedEx to clear international customs issues to ensure on time delivery. * Performs other duties as assigned by management Your Background Qualifications * Bachelor's degree preferred but not required * 3+ years Supervisory experience managing hourly employees * Previous operational medical device experience helpful * Demonstrated proficiency in supervising and motivating subordinates in a team environment. * Excellent written and oral communication skills. * Aptitude for analyzing situations and resolving problems * Self-motivated with the ability to achieve desired results with minimal supervision. * Proficient in Outlook, Word, Excel, and PowerPoint; SAP experience a plus * Ability to calculate figures, percentages and data. * Strong interpersonal and organizational skills, ability to influence others Work Environment This job is performed in a distribution/warehouse environment. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee frequently is required to move about the facility. The employee must occasionally lift and/or move up to 50 pounds by themselves. Position Type/Expected Hours of Work This is a full-time position which may require additional hours particularly at the end of the day to ensure orders are shipped. Travel Expectations No overnight travel required Compensation Data Salary: $60,000 - $78,000 USD annually depending on skills and experience. EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** Paragon 28, a Zimmer Biomet Company is hiring a Sr Supplier Quality Engineer. The Sr. Supplier Quality Engineer is a quality engineering position that has emphasis on developing and maintaining Paragon 28's supplier quality system and related quality activities specifically relating to product development, manufacturing, and supply chain of Paragon 28 orthopedic products for the Foot and Ankle. This is hybrid position located at our Englewood, Colorado location. **How You'll Create Impact** - Process Owner for Key Quality Processes: Supplier Management - Lead supplier qualification process. Interface with suppliers to ensure product compliance to specification and perform supplier audits as needed. - Develop measurement techniques for product release at suppliers. - Participating on project teams as a contributing member by providing supplier quality engineering support in the development of new suppliers and processes, and continuously improving company's products and suppliers. - Provide support for the manufacturing areas (external). Work with production personnel and supervision to determine and monitor quality metrics, samples plans and address non-conforming product issues. Lead corrective and preventive action investigations to resolve the root cause of problems. - Auditing suppliers on time and per schedule - Writing audit plans and audit reports for suppliers to all applicable standards and regulations - Writing and reviewing of procedures, plans, protocols and reports to ensure regulatory compliance. - Perform Mechanical Inspections and use typical equipment used in inspection. - Assist with Design Transfer for release of new product development projects. - Author and/or assist in the development and execution of process validations at suppliers - Perform statistical analysis for testing requirements and develop MSAs, TMQs, and inspection correlations. - Assist suppliers in completion of Supplier Corrective Actions per appropriate timelines - Assisting project teams on compliance with purchasing requirements per FDA QSR, European MDD/MDR, ISO 13485 and other applicable ISO/EN standards - Capture and calculate supplier metrics on a regular basis - Develop relationships with employees and suppliers to ensure team-oriented operation. - Accurately represents quality processes to 3rd party auditors (FDA, ISO 13485, MDSAP, etc.) - Other duties as assigned **Your Background** - Bachelor's degree in Engineering or technical discipline - 4+ years in related field, preferably medical device or manufacturing - Auditing experience, ISO 13485 preferred - Proficient in Machining methodologies (Titanium and Stainless-Steel experience best), knowledge of hardness, passivation, surface treatments, cleaning techniques etc. for communication with Suppliers and Engineers. - Familiarity with 21 CFR 820 and ISO 13485 and other Government / ISO Standards - Technical writing skills that include Quality Management Systems (QMS) and procedures - Proficient in Geometric Dimensioning and Tolerancing (GD&T) preferable - Process Validation experience - Basic Computer Skills (MS Office) **Compensation Data** Salary Range: $90,000 - $110,000 USD annually based on skills and experience **Travel Expectations** Travel should not exceed 50% of total time. Supplier travel will be needed for on-site audits and/or trouble shooting. EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect Paragon 28, a Zimmer Biomet company focused on orthopedic medical devices for injuries to the foot and ankle, is hiring a Supply Planner. The Supply Planner is responsible for the supply planning, procurement, and management of orders of medical devices and services from approved suppliers in alignment with forecasted net requirements. This role ensures cost, inventory, delivery, and service targets are met or exceeded through day-to-day supply chain management techniques in conjunction with identified improvement projects. This role interfaces with the Quality, Engineering, Marketing and Finance departments to align on and achieve organizational objectives. This position is 100% onsite at our facilities in Englewood, Colorado. How You'll Create Impact * Assess supplier capability, capacity, and cost to allocate annual spend to qualified suppliers optimizing for service, quality, and cost. * Manage basic and advanced planning parameters to ensure optimal net requirements planning. * Review net requirements against supply and demand; manage open order exceptions; negotiate price, delivery, and terms with external contract-manufacturing and other supply partners; place and manage purchase orders. * Regularly review KPIs; develop and execute strategies to address unfavorable results. * Identify and close business process gaps; collaborate with stakeholders to drive business process improvement for planning, procurement, and inventory. * Lead regular supplier production reviews to ensure needed capacity and on-time delivery. * Lead quarterly business reviews. * Monitor inventory levels to mitigate stockouts while maintaining cost effective operational expenses. * Support new supplier qualification activities. * Evaluate bids; negotiate to obtain the best quality, prices, and terms. * Act as a liaison between suppliers and internal departments such as Engineering, Quality, and Finance. * Visit existing and potential supplier facilities to evaluate manufacturing processes, capabilities, recent investments, potential for growth, performance trends, etc. * Other duties as assigned. Your Background * Bachelors degree preferred, may accept prior supply chain experience in lieu of degree * Minimum 3 years of experience in related field such as supply planning, purchasing, or supply chain required, preferably in medical device * APICS CSCP/CPIM certification preferred. * Proficient with MS Office, including advance level Excel skills. * Strategic Sourcing, opportunity analysis, and strong negotiation skills. * High volume purchasing/planning experience required. * Highly effective communication. * Strong analytical, decision-making, and problem-solving. * Experience working with detailed product line forecasts; familiarity with Sales & Operations business management process. * Demonstrated success in driving process improvement. * Strong decision-making, problem-solving skills, and time management skills with attention to detail. * Ability to work independently in a fast-paced environment, prioritize appropriately and handle multiple tasks and projects simultaneously. * SAP ECC or S4 experience preferred. * Previous medical device experience preferred. Travel Expectations Less than 25% of overnight travel Compensation Data Salary: $56,000 - $90,000 depending on skills and experience EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect The Distribution Coordinator works with various teams in the warehouse to receive, inspect, replenish, and/or ship surgical instrumentation and implants to healthcare facilities with impeccable attention to detail while maintaining inventory accuracy. How You'll Create Impact * Package product and materials ensuring contents are protected adequately for shipment. * Accurately prepare all necessary shipping documentation, including accurate addresses, and ensure that shipments contain the correct inventory * Receive incoming surgical trays, inspect instruments and implants, and restock inventory based on usage * Compare part numbers, lot numbers, and other information listed on the Pack Slip to verify accuracy of purchase order and shipping orders. * Compile data from sources such as purchase orders, invoices, requisitions, to maintain electronic record. * Assist with cycle counting of inventory when necessary * Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485. * Other duties as assigned * Shift - Monday through Friday 11am - 7:30pm MST What Makes You Stand Out As a Distribution Coordinator in the orthopedic medical device industry, you will ensure the efficient and accurate movement of critical medical products-from inventory management to order fulfillment and logistics coordination, committing to timely delivery that directly supports surgical teams and patient outcomes. This role bridges supply chain operations and customer service, helping maintain seamless access to life-changing orthopedic technologies. Your Background * High School Diploma or equivalent preferred. * 1+ year(s) related distribution or inventory control experience and/or training helpful * Ability to work effectively and efficiently in a team environment. * Strong attention to detail * Self-motivated with ability to achieve desired results independently * Aptitude for analyzing situations and resolving problems preferred Compensation Data * $22 per hour + Opportunity to earn up to a 10% Quarterly bonus based on performance and established metrics. Physical Requirements Travel Expectations EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** Paragon 28, a Zimmer Biomet company focused on orthopedic medical device for the foot and ankle, is hiring a Quality Records and Release Coordinator to join our team in Englewood, Colorado. This role is responsible for review, final verification and scanning of Device History Records (DHR) for product release. These records include, but not limited to inspection records, labeling records, packaging records, material certifications, and Certificates of Conformance of finished medical devices. Additionally, this role will perform assigned incoming inspections on received product, primarily allograft and custom devices. This is a 100% onsite position. **How You'll Create Impact** Final verification of DHR documentation, including inspection records, certifications, purchase orders and engineering prints · Confirmation of physical product visual conformance with specifications prior to product release · Issuance of product release notifications · Product inspection of assigned parts · Scanning electronic DHR records as well as preparation of physical records/boxes and submit to Document Control to offsite · On occasion, incumbents may also be asked to do the following: o Support internal and external audits o Support Complaint and Non-Conformance investigations with DHR requests o Other duties as assigned **Your Background** Associate Degree and minimum of 5 years of experience in medical device inspection/ quality or a Bachelor's degree in technical discipline with 2 years of experience in medical device inspection/ quality. · Strong understanding of good documentation practices · Strong organizational skills · Detailed oriented · Ability to follow standard operating procedures · High proficiency in MS Office 365, Adobe Acrobat DC · Good written and oral communication skills · Prefer familiarity with 21 CFR 820/ISO13485, or other government/ISO standards · Experience in Electronic Records Management and/or AIIM training a plus Work Environment This job operates in an office/laboratory environment within a distribution facility. The role routinely uses standard office equipment such as computers, phones, copy machines, and filing cabinets. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee frequently is required to move about the facility. May be required to lift up-to 30 lbs. by themselves. Position Type/Expected Hours of Work This is a full-time, onsite hourly position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined by the supervisor and manager. **Travel Expectations** No overnight travel is required. EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. What You Can Expect The Sr. Product Development Engineer leads the design of new products and improvements to existing products and systems, as part of a project team. This role also develops new product designs with firm grasp on design for manufacturing and customer need. This position is located in Englewood, Colorado at Paragon 28, a Zimmer Biomet Company focusing on orthopedic medical devices for the foot and ankle. How You'll Create Impact Essential Responsibilities and Duties * Lead product development efforts from ideation to commercialization through entire product life cycle, as part of a team, including: * Research and evaluate products, parts, processes for efficiency and reliability * Conceptualization of new design ideas while understanding the inadequacy of existing designs. * Parametric modeling and detail design of P28 implant and instrument development with a firm grasp on design for manufacturing * Assist junior Engineering staff with modeling and detailing methodology * Lead efforts of new product development in design control, including the management and implementation of P28 design history files. * Lead design efforts to minimize patient risk and adhere to regulatory requirements * Lead in development of testing protocols and assist in the testing process for new and existing products * Analyze test results and recommend appropriate design changes * Formulate complete test strategies and test reports with R&D and regulatory. Work with Marketing to determine how data or analysis could be used for education or as selling tool in abstract/poster or white paper. * Interface with 3rd party suppliers, contractors, testing houses, etc. * Assist the P28 Quality and Supply Chain departments to evaluate new suppliers for inclusion in the P28 approved supplier list * Assist P28 Quality team in developing inspection plans * Aide in publication efforts with Clinical Affairs team. * Lead surgical demonstrations (live, cadaver, or video) on lower extremity pathology and formulate physician comments/ideas into meaningful design solutions. * Provide sales support via phone and live training as "expert" technical resource within specific product categories. * Compile invention disclosures for patent applications and infringement evaluations * Participate in root cause analysis and corrective action development for design related issues in released product * Assist with other development projects as additional resource when needed, while balancing own workload * Other duties as directed by manager Non - Essential Responsibilities and Duties * Participate in clinical research projects or clinical trials. * Assist/ aide in skills development of junior engineers including: * Design for manufacturing * Develop testing strategies * Implementation of design control documentation * Validation and verification planning Your Background * Requires a bachelor's degree in Mechanical Engineering, Biomedical Engineering or related engineering discipline with 6+ years of experience * Prior experience in medical device development required. * Prior experience in taking a medical device or similar product from ideation to commercialization required. * Ability to read and interpret documents such as drawings, engineering specifications, testing standards, regulatory guidance documents, safety rules, company policy and procedure manuals. * Demonstrated ability to lead projects l autonomously as part of a cross-functional team (Supply Chain, Marketing, Quality, Regulatory, etc.) and deliver updates to senior management. * Experience with designing for manufacturability, inspection and assembly. * Proficient with design control activities and verification and validation activities with respect to medical device development. * Understanding of medical device industry regulatory requirements required. * Proficient with CAD. Solidworks preferred. * High proficiency in MS Office * Effective communication and presentation skills with ability to convey information and respond to questions from groups of peers * Ability to work in a team environment Work Environment This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones and copy machines. Occasional use of the development and quality labs necessary, adhering to all lab safety requirements. This position will work with cadaveric specimens. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee frequently is required to move about the facility. The employee is required to have close visual acuity to perform activities such as inspecting small parts, viewing computer terminal and drawings. The employee may be required to lift up-to 35 lbs. by themselves. Position Type/Expected Hours of Work This is a full-time position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined with Manager. Travel Expectations Up to 15% of overnight travel. Compensation Data Expected Salary Range: $93,000 - $125,000 USD annually EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** Paragon 28, a Zimmer Biomet company focused on medical devices for the foot and ankle, is hiring a National Accounts Manager to join our sales team. The National Account Manager is responsible for managing and nurturing relationships with Group Purchasing Organizations (GPOs), Ambulatory Surgery Centers (ASCs), Integrated Delivery Networks (IDNs), and hospital systems within their assigned region (East or West USA). Reporting to the Director of National Accounts, the National Account Manager will ensure the successful execution of strategic account plans, contract management, and sales growth in alignment with Paragon 28's business goals and customer needs. This position plays a key role in fostering long-term partnerships and ensuring client satisfaction. Essential Responsibilities and Duties **How You'll Create Impact** Essential Responsibilities and Duties - Account Management: Build and maintain strong relationships with key decision-makers within GPOs, ASCs, IDNs, and hospital systems. Act as the primary point of contact for assigned accounts, ensuring consistent engagement and satisfaction. - Contract Execution: Assist in the negotiation, implementation, and management of contracts within the assigned region. Ensure compliance with Paragon 28's standards, pricing structures, and legal requirements. - Sales Growth: Support regional sales initiatives by identifying new business opportunities, upselling, and expanding relationships within existing accounts. - Customer Needs Assessment: Work closely with customers to understand their needs, challenges, and business objectives. Provide tailored solutions that align with Paragon 28's product offerings. - Performance Tracking: Track and report on account performance, including sales, renewals, and customer feedback. Ensure that regional goals and objectives are met. - Collaboration with Regional Director: Collaborate with the Director of Natioal Accounts to execute regional strategies, ensure alignment with organizational goals, and provide insight into customer trends and opportunities. - Problem Solving: Address and resolve any account-related issues, including billing, collections, or pricing challenges. Work with internal teams to provide timely and effective solutions. - Market Insight: Stay updated on market trends, competitor activities, and industry developments. Share relevant insights with the regional director and other stakeholders to support business growth. - Cross-Functional Collaboration: Work with internal teams (sales, marketing, finance, legal) to ensure smooth execution of contracts and to support account needs effectively. **Your Background** Qualifications - Bachelor's degree required. - Minimum of 2-3 years of experience in national account management or a related role in the medical device, healthcare, or orthopedic industry. - Proven ability to build and manage strategic customer relationships. - Experience with contract negotiation and account management within the healthcare sector. - Strong communication, problem-solving, and interpersonal skills. - Proficiency in MS Excel, MS Word, PowerPoint, and CRM systems. - Ability to work independently and as part of a team in a fast-paced, high-volume environment. - Strong sales skills with a focus on relationship building and customer satisfaction. - Valid driver's license and active vehicle insurance policy. Work Environment This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones and copy machines. When traveling, making calls on client organizations in office and hospital environments. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee is required to have close visual acuity to perform activities such as viewing a computer terminal for long periods of time. This role requires employee to physically travel to client organizations. The employee may be required to lift up-to 35 lbs. by themselves. Position Type/Expected Hours of Work This is a full-time position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined with Manager. **Travel Expectations** Up to 50% overnight travel. **Compensation Data** Salary Range: $130,000-$150,000 USD annually depending on skills and experience. Eligibility for performance bonuses. EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** Paragon 28, a Zimmer Biomet Company, is hiring a Product Sustaining Engineer I for our team in Englewood, Colorado. This position is for someone who obtained their engineering degree and has at least 2 years of professional experience. The Product Sustaining Engineer has responsibility for leading projects that support legacy product systems and design and development of medical devices. This will be a hybrid position requiring onsite work at our Englewood, Colorado location. **How You'll Create Impact** **Essential Responsibilities and Duties** + Produce deliverables pertaining to sustaining engineering activities for legacy product systems, as directed by senior engineering staff including: o Review and evaluate product non-conformances for incoming legacy product o Review and evaluate product complaints + Update designs and device specifications for legacy products + Conceptualize new design ideas for legacy product systems and new development projects or line extensions + Use SolidWorks for parametric modeling and detailing designs of P28 implants and instruments + Create or update design control documentation for P28 design history files & technical files. o Create Engineering Change Requests (ECR) and manage through completion. + Ownership of development related CAPAs. Participation in root cause analysis to investigate issues. + Assist in documentation remediation efforts including: DHF documentation, risk documentation, inspection plans, protocols and reports. + Development of testing protocols and testing process for new and existing products o Participate in activities related to project phase gate design reviews o Assist with 3 rd party suppliers, contractors, testing houses, etc. + Assist in inspection of current and newly developed medical devices + Observe surgery (live, cadaver, or video) on lower extremity pathology. Document all notes. Participates in cadaveric labs to support assigned projects. + Other duties as directed by manager **Your Background** **Qualifications** + Requires a bachelor's degree in Mechanical Engineering, Biomedical Engineering or related engineering discipline with 2-5 years of experience. + Prior experience in medical device development helpful. + Understanding of medical device industry regulatory requirements preferred. + Experience with CAD. SolidWorks preferred. + Proficiency in MS Office + Effective communication and presentation skills with ability to convey information and respond to questions from groups of peers + Ability to work in a team environment **Work Environment** This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones and copy machines. Occasional use of the development and quality labs necessary, where lab safety must be adhered to. **Physical Demands** The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee is required to have close visual acuity to perform activities such as: viewing a computer terminal and design drawings as well as visual inspection involving small parts. The employee frequently is required to move about the facility. The employee may be required to lift up-to 35 lbs. by themselves. **Position Type/Expected Hours of Work** This is a full-time position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined with Manager. **Travel Expectations** 10% of overnight travel **Compensation Data** Salary Range: $70,000 - $90,000 USD annually depending on skills and experience **Physical Requirements** EOE

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** The Distribution Coordinator works with various teams in the warehouse to receive, inspect, replenish, and/or ship surgical instrumentation and implants to healthcare facilities with impeccable attention to detail while maintaining inventory accuracy. **How You'll Create Impact** + Package product and materials ensuring contents are protected adequately for shipment. + Accurately prepare all necessary shipping documentation, including accurate addresses, and ensure that shipments contain the correct inventory + Receive incoming surgical trays, inspect instruments and implants, and restock inventory based on usage + Compare part numbers, lot numbers, and other information listed on the Pack Slip to verify accuracy of purchase order and shipping orders. + Compile data from sources such as purchase orders, invoices, requisitions, to maintain electronic record. + Assist with cycle counting of inventory when necessary + Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485. + Other duties as assigned + Shift: Monday through Friday 11am - 7:30pm **What Makes You Stand Out** As a Distribution Coordinator in the orthopedic medical device industry, you will ensure the efficient and accurate movement of critical medical products-from inventory management to order fulfillment and logistics coordination, committing to timely delivery that directly supports surgical teams and patient outcomes. This role bridges supply chain operations and customer service, helping maintain seamless access to life-changing orthopedic technologies. **Your Background** + High School Diploma or equivalent preferred. + 1+ year(s) related distribution or inventory control experience and/or training helpful + Ability to work effectively and efficiently in a team environment. + Strong attention to detail + Self-motivated with ability to achieve desired results independently + Aptitude for analyzing situations and resolving problems preferred **Compensation Data** $20 per hour + Opportunity to earn up to a 15% monthly bonus based on performance and established metrics. **Physical Requirements** **Travel Expectations** EOE