HealthTronics jobs

Nashville, TN, United States Raleigh, NC, United States Tampa, FL, United States Atlanta, GA, United States This position is accountable for top line revenue generated by awareness and adoption of Hologic product portfolio in the US Healthcare Market. This individual is responsible for the development, management and guidance of all Strategic Sales and Client Success activities for Hologic Breast and Skeletal Health. This role oversees the execution of policies, procedures and programs to achieve maximum sales potential of capital, disposables, software and service revenue. Develops strategies and tactics for building sales pipelines, setting/achieving sales objectives and coordinating pipeline forecasting, budgets, and reports. Provides leadership and supervision of sales and client success colleagues. Also collaborates and executes strategies on converting competitive accounts. This person will have a passion for serving others and driving collaborative deals that benefit Hologic and our customers. **KEY RESPONSIBILITIES/DUTIES** (included but not limited to): + Collaborate with leadership to develop growth objectives, "go-to"market strategies and structure to proactively support achievement of those objectives and strategies. + Demonstrate medical device sales, sales management, team management and Corporate/National Account experience intuitively responding to strategic and tactical needs for market share protection and growth. + Partner with senior business leaders within Hologic Business Units to identify future business growth drivers and develop contracting strategies and tactics to support the execution of future growth. + Develop and update competitive databases aimed at gaining understanding of market potential, competitors, sales channels and sales/pricing strategies to ensure successful growth. In near term, develop a thorough understanding of the positioning of Hologic current products with specific IDNs/GPOs. + Develop a comprehensive understanding with National Accounts of the inner dealings of targeted IDNs, including their contracts and utilizes this knowledge to improve or enhance Hologic's business practices toward these accounts. + Execute against annual divisional sales initiatives and imperatives. + Develop and implement sales forecasts/marketing plans for targeted customers and keep management informed of critical issues through submission of regular updates and monthly success reports. + Help build and deliver training programs for the Business Unit sales team to ensure a high degree of GPO/IDN knowledge and Business/Finance Acumen. + Contribute and support acquisitions for positioning, implementation and sales success. + Work with operations to ensure complete and accurate information is used to forecast and communicate potential value of offerings to prospects. + Promote Hologic technology value prop to senior hospital executives who are decision makers and influencers related to supply chain. + Promote Hologic business model to senior hospital executives and applicable departmental leaders who are decision makers and influencers applicable to specific care models. + Provide effective leadership and supervision for sales staff members and internal teammates. + Recruit Strategic sales team members and onboard them to Hologic; coordinate necessary training and performance management functions. + Demonstrate the willingness to delegate goals, monitor progress, and drive team-oriented success. + Develop and maintain a pipeline of prospects. + Generate prospective sales lists and develop goals and strategies for selling. + Collaborate with marketing to coordinate and execute campaigns targeting specific Hologic categories. + Shepard the "due diligence" process to complete and communicate an assessment of the value Hologic can deliver, with a focus on complete and accurate projections of potential savings. + Collaborate with the corporate account team to ensure clarity of messaging and timing of contract awards. Support the implementation of GPO onboarding and identify opportunities for consulting, custom contracting, and other offerings and services. + Ensures high satisfaction and retention rates for Hologic customers. + Collaborate with Marketing to: + complete a market assessment (competitive offerings and share) + develop a business plan for pursuits + maintain information related to sales activity in Salesforce (or equivalent) + participate/plan for sales exhibits and trade shows, attend those pertinent to business + leverage marketing materials are reflective of current capabilities. + Contribute and support Annual Marketing Plan + Understand, support and plan for life cycle management to complement contract strategy and sales goals. + Top focus on the reps and managers in the field that you support and drive efficient, focused and solution-oriented strategies. + Build trust and credibility with applicable internal functions (Sales, Marketing, Finance, Offer Development, Contracting etc) to maintain and utilize information regarding value propositions to target the market. + Simplify the customer experience and create a "high touch" concierge experience while developing and nurturing relationships with health system/hospital stakeholders to communicate Hologic value propositions fiscally and clinically. + Lead collaboration efforts across Hologic divisions + Proactively evolve strategies based on business insight and direction + Develop mastery of the Women's Health Continuum of Care landscape; actively communicate and share this knowledge across Hologic + Prioritize selling capital, software, disposables and service and leveraging the full portfolio of Hologic to maximize a partnership for both the customer and Hologic with value based selling techniques. + Understand how stakeholders are connected and how their perceptions of value vary based on their role outlook + Develop best practices for communicating our mission and vision across stakeholders + Be able to relentlessly experiment with new selling concepts while maintaining an entrepreneurial mindset KNOWLEDGE, SKILLS & ABILITIES - + Intimate knowledge of healthcare provider market + Extensive knowledge of healthcare, GPO operations and/or Supply Chain/ Materials Management. + Knowledge and experience in sales strategies and selling skills + Effective communication (oral, listening, writing, and presentation skills) with a variety of stakeholders from executives to staff. + Demonstrated ability to work in a professional, multi-disciplinary, matrix reporting team as a group leader, facilitator, or participant + Demonstrated track record of success. + Demonstrated effective problem solving skills which include understanding issues, being able to simplify process and complex issues, while understanding the difference between critical details and unimportant facts. + Ability to work independently and handle stress appropriately. + Ability to handle multiple tasks effectively, prioritize appropriately, and adapt to changes in workload and work schedule. + Practice and adhere to the company's Code of Conduct philosophy, Mission/Vision, and Core Values. + Demonstrated successful project management experience with coordination and measurement of project deliverables. + Advanced computer skills with MicroSoft, PowerPoint, and Excel. Software skills with data warehouse and/or Micro Strategies highly preferred. Familiarity with SalesForce, Highspot, Definitive etc. EDUCATION + Bachelor's degree from an accredited College or University with concentration in business administration, economics, finance, or related field. Graduate degree (MBA or MHA) preferred. EXPERIENCE + 3-5 years cumulative relevant experience required, with at least three years of GPO or relevant sales and national account management experience in healthcare. 5+ years preferred. CERTIFICATE / LICENSE + None required but certification in Sales Training or Supply Chain viewed favorably. **Agency And Third Party Recruiter Notice** _Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered._ **_Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans._** **Additional Info:** + This role is based on a base salary and commission plan combination. On target compensation range for a highly successful individual may earn up to $250,000 annually. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, territory/ geography, education, business needs, market demand and performance versus quota. **OSHA CATEGORY -** The normal work routine involves no exposure to blood, body fluids, or tissues (although situations can be imagined or hypothesized under which anyone, anywhere, might encounter potential exposure to body fluids). Persons who perform these duties are not called upon as part of their employment to perform or assist in emergency care or first aid, or to be potentially exposed in some other way. \#LI-KM3

** The Therapeutic Area Medical Science Liaison (TA MSL) is a credible scientific partner responsible for providing clinical and health economic information related to disease states and the appropriate utilization of Genentech medicines (approved and pipeline). This field-based position will engage with healthcare providers, population health decision makers, and patients within their region(s), to further patient outcomes aligned with the overarching objectives of Genentech. In collaboration with their regional partners, TA MSLs are accountable for co-creating the local medical strategy and delivering for their customers. In addition, TA MSLs may be responsible for covering multiple medicines, as well as engaging in broad scientific discussions about patient outcomes and total cost of care, resulting in rich customer insights shared with key stakeholders across the organization. **Preferred States of Residence** FL, PR, GA, LA, MS, AR, AL, KY, and TN **Key Responsibilities** + Ensure end-to-end customer experience for TA specific customers in the region + Demonstrate deep scientific expertise in assigned molecules/products and therapeutic areas to exchange relevant information with thought leaders and healthcare decision makers + Build and leverage relationships with key external scientific and medical customers to understand evolving healthcare trends + Having proficiency in topics beyond scientific exchange, such as value/cost of care discussions and AE management + Continuous learning within the therapeutic area, active participation in upskilling programs, and adherence to guidelines and procedures. **Who you are** **Required Qualifications & Experience** + Advanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.). BSN with extensive field medical experience with a pharmaceutical company + Minimum of 5 years related work experience (clinical, managed care, or industry experience) + Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use) + Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry. **Preferred Experience** + Prior experience as a field medical science liaison + 2 or more years' clinical or health economic research experience (either in industry or in another, related setting) + 2 years' experience in therapy area + In-depth knowledge of Phase IV/post-marketing drug development **Location and Travel Requirements** This is a field based role + Overnight travel may be required. This position requires significant driving of either a company provided or personal vehicle as well as prolonged periods of sitting, both of which are part of the essential duties and responsibilities of the role. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business. + Business travel, by air or car, is required for regular external business meetings with customers and intermittent internal company meetings (up to 70% of time) + Applicants should reside within 30 miles of a major airport and should reside within 50 miles of the established territory. Preference will be given to applicants who reside within preferred states of residence listed above. The expected salary range for this position is $141,260-$262,340. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. **Benefits (****************************************************** **Relocation benefits are not available for this job posting.** Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants (***************************************************************************************************** .

Atlanta, GA, United States When presented with an obstacle, do you find another route? Are you a natural hunter who can seek opportunities? Are you passionate about medical diagnostics? If you answered yes to all the above, it sounds like our **Diagnostic Specialist** career opportunity is the next move for you! At Hologic we're driven by our purpose, promise and passion to empower people to live healthier lives everywhere, everyday. With ground-breaking technology at the core, our innovations are designed to achieve exceptional clinical results. Making it possible to detect, diagnose and treat illnesses and other health conditions earlier and more effectively. **What does your day to day look like?** + Effectively communicate and sell the benefits of the APTIMA product line, the ThinPrep Pap Test and adjunctive testing, to clinicians in an assigned geographic territory + Develop and execute a sales strategy within your assigned territory to meet and exceed sales goals. Insulate accounts against competition and regain lost customer accounts. + Accurately forecast and maintain an individual territory in accordance with a 90-day quota + Maintain ongoing business planning with your customers including business reviews with customer financial departments. + Maintain consistent and structured communication to District Sales Manager + Partner with our marketing department to support the development and execution of marketing programs and sales materials. + Attend local and national professional trade shows and events to promote products + Update and sync all relevant customer account information into Hologic's Data Management System daily. **Do you have what it takes?** Education: Bachelor of Arts/Science from an accredited university required Experience: We want to see your track record (at least 2 years) of delivering commercial success against assigned targets. You will be able to build meaningful relationships with new and existing customers, you will become a trusted partner at solution selling and can influence and negotiate. Due to the nature of our industry, you will need to understand and articulate complex scientific literature and use complex clinical data as a key factor in your sales process. Since this position requires extensive driving during the workday, a valid driving license and satisfactory driving record, as well as a serviceable vehicle available for work use is mandatory. **So why join Hologic?** We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and quarterly bonus structure, one of our talent partners can discuss this in more detail with you. From a benefits perspective, you will join our wide-ranging benefits policy including PTO, Employee Stock Purchase Plans, exciting Employee Wellness plans and many more! If you have the right skills and experience and want to join our team, apply today. We can't wait to hear from you! The total compensation range for this role is $130,000 to $140,000. This is based on a base salary and commission plan combination. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, territory/ geography, education, business needs, market demand and performance versus quota. **_Agency and Third Party Recruiter Notice:_** Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered. **_Hologic's employees are subject to third-party COVID-19 vaccination requirements, including from customers and governmental entities. Hologic is an equal opportunity employer and consistent with federal, state, and local requirements, will consider requests for reasonable accommodation based on disability or sincerely-held religious beliefs where it is able to do so without undue hardship to the company._** **_Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans._** \#LI-JM1 #LI-remote

At MIMEDX, our purpose starts with helping patients heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care products combined with a promising clinical pipeline, we are committed to making a transformative impact on the lives of patients we serve globally. Come see what it is like working with our Processing Operations team! POSITION SUMMARY: Perform any one or all of the routine processes (e.g. dissection, layout, cutting, and vialing) in laboratory, setting according to established procedures and guidelines. Produce high quality tissue products in an efficient manner. Ensure sterile processing and handling of tissue at all times. Perform regular inspection and cleaning of lab equipment to ensure equipment is in good, working order. Monitor equipment maintenance schedule to ensure routine and repair service is performed as needed. Perform data entry tasks. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Process human tissue in an aseptic processing environment (lab) according to standard operating procedures and work instructions using surgical instruments and machinery * Perform any one or all of the routine tissue processes (e.g. dissection, layout, cutting, and vialing), as per required specifications, within expected processing times in order to meet production schedules * Adhere to all policies and practices from the Quality Management System (QMS) based on company standards and regulatory standards for tissue processing * Document results of each process performed, supplies used, etc. to maintain integrity and traceability of donor * Enter relevant data from tissue processing record into company specific database * Monitor, maintain, and clean processing facility and equipment * Support and contribute new ideas to the continuous tissue processing improvement efforts * Monitor tissue processing supplies and notify management when supplies are needed; restock supplies EDUCATION/EXPERIENCE: * High School Diploma * Prefer BA/BS in Biology or Chemistry * Minimum 6 months - 1 year in biotech, pharma, medical or clean manufacturing * Prefer knowledge of Good Documentation Practice (GDP), Good Tissue Practice (GTP), Good Manufacturing Practice (GMP) and AATB regulations SKILLS/COMPETENCIES: * Excellent oral, written, listening, and interpersonal communication skills * Proficient in Microsoft Office (Word, Excel, etc.) * Solid organization skills to support the efficiency of the laboratory operations * Ability to effectively work and interact with all members of the laboratory, tissue processing, research & development, and tissue recovery functions * Must show aptitude to develop appropriate skills needed for the job WORK ENVIRONMENT: The work is typically performed in a controlled laboratory environment. Will have contact/exposure with biohazardous materials, chemicals, and blood and human tissue. Training will be conducted on the handling and safety practices necessary for the use and disposal of hazardous chemicals and potential biohazards. Will also be trained on all applicable equipment needed to perform the job. hourly manufacturing regenerative medicine biotech medical device lab pharmaceutical medical device sterile

At MIMEDX, our purpose starts with helping humans heal. We are driven by discovering and developing regenerative biologics to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care & surgical products combined with a promising clinical pipeline, we are committed to making a transformative impact on the lives of patients we serve globally. We are excited to add an Quality Control Technician to our Quality Control team! The position will pay between $20-28/hr based on previous relevant experience and other factors. POSITION SUMMARY: Perform various release criteria tests, using defined guidelines and Standard Operating Procedures (SOP's), to determine if materials/goods are acceptable for release. Compare test results for compliance with company and regulatory requirements, record results, and notify management of out-of-specification tests and trends. Inspect and ensure supplies received in the warehouse that are used in the production and/or packaging of tissue products and finished goods meet quality standards. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Perform well-defined, standardized microbial tests on donor culture samples, environmental samples and related supplies: * Microbiological identification of bacterial and fungal growth in/on both liquid and plate media; subculturing and identification of microorganisms to determine acceptability based on sample type * Media suitability tests (i.e. growth promotion and sterility) to ensure incoming media (both liquid and plate media) used to grow bacteria/fungi are not contaminated and are able to sustain microbial growth * Conduct physical inspections of raw materials (e.g. gowns, gloves, instruments, etc.) and finished goods (e.g. packaging, labels, marketing materials, etc.) received in the warehouse, per guidelines outlined in SOP's or material specifications * Compare findings of test results to established guidelines; identify reasons for failure and retest as permitted; initiate investigation for any failed test (i.e. out-of-specification result) * Assist in investigations, corrective actions/preventive actions (CAPA's), document changes, trending, etc. by providing requested information and implementing defined, corrective measures * Document and record results of tests in internal database * Perform preventive maintenance and equipment cleaning (e.g. incubators, refrigerators, carbon analyzers, etc.) used to perform quality control tests and/or in the manufacture of tissue products, as scheduled * Conduct well-defined, standardized testing of processing suites, water systems and manufactured products, such as: * Monitoring of controlled environmental areas (CEA), testing of air and surfaces for the presence of organisms and free-floating particulate to ensure required standards are met * Water tests to monitor levels of bioburden, total organic carbon, and conductivity from all water ports used in the manufacture/sterilization of tissue products and equipment * Residual moisture tests on tissue products to ensure moisture levels in products are at acceptable levels * For testing not conducted in-house, send samples to approved contract labs and review results for acceptability PROBLEM SOLVING: * Effectively identifies problems as they occur and takes appropriate steps to solve them in situations where the problem is not difficult or complex * Refers complex, unusual problems to supervisor or manager DECISION MAKING/SCOPE OF AUTHORITY: * Effectively identifies problems as they occur and takes appropriate steps to solve them in situations where the problem is not difficult or complex * Refers complex, unusual problems to supervisor or manager SPAN OF CONTROL/COMPLEXITY: * Fully functioning support role having greater responsibility to perform all (or most) of the standard work within the function; moderate impact to the department EDUCATION/EXPERIENCE: * Batchelor's degree in a science related field preferred * Minimum of 2 years of experience working within an FDA regulated environment; 5+ years of experience without a degree * Experience with microbiology related testing (e.g. microbiological techniques, micro identification, bioburden, sterility, endotoxin, ELISA, environmental monitoring, etc.) strongly preferred * Knowledge of AATB, FDA, and other state/federal regulations * Knowledge of USP, ISO, AAMI, ANSI, ASTM standards SKILLS/COMPETENCIES: * Strong written, verbal, and interpersonal communication skills * Proficient in Microsoft Office (Excel, Word, etc.) * Highly organized, detail-driven, and able to manage multiple priorities * Demonstrated ability to learn and apply new technical skills WORK ENVIRONMENT/EXPECTED BUSINESS TRAVEL: * Work is performed in laboratory settings, controlled environments, warehouse, and office spaces * Hands-on use of lab equipment and inspection tools is required * Reliable transportation is needed for travel between nearby facilities (approximately 8 miles) Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to, or requirements for, this job at any time.

At MIMEDX, our purpose starts with helping humans heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care & surgical products combined with a promising clinical pipeline, we are committed to making a transformative impact on the lives of patients we serve globally. We are excited to add an Art Director to our marketing team! The position will pay between $116,300 - $154,000 plus bonus' based on previous relevant experience, educational credentials, and location. POSITION SUMMARY: The Art Director is responsible for designing and leading graphic designers through the creative process supporting MIMEDX Marketing and Corporate initiatives; oversees and drives the concept, design and execution of product campaigns, marketing collateral, trade show graphics, digital applications, videos, etc. The Art Director acts as the critical bridge between strategic creative direction and hands-on execution, working closely with the Creative Director to develop leading-edge concepts and translate brand vision into exceptional visual experiences across all channels. The ideal candidate brings deep expertise in both digital and traditional design, and strong leadership capabilities. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Lead graphic designers, illustrators, animators, video production teams * Create compelling visual assets for digital platforms including websites, mobile applications, social media content, email campaigns, digital advertising, and interactive experiences * Ensure concept/design consistency across initiatives and mediums. * Design traditional marketing materials including print advertisements, brochures, catalogs, packaging, direct mail, trade show graphics, environmental signage, and large-format displays * Develop and maintain brand identity systems, style guides, and design standards to ensure consistency across all customer touchpoints * Produce presentation decks, sales materials, and internal communications that align with brand guidelines * Work well within the brand and creatively explore potential campaigns * Coordinate and prioritize design efforts across campaigns and teams. * Present concept/design decks and storyboards to stakeholders. * Prepare comprehensive production files with accurate specifications for both digital deployment and print vendors * Remain informed of all industry news, creative, and general activity. * Collaborate with Creative Director, designers, writers, other marketing team members, and internal stakeholders to ensure the appropriate concepts, themes, and messages are represented effectively and consistently for the business objective(s) and audience(s). * Ensure assignments adhere to the approved brand and messaging guidelines to maintain our corporate identity. * Prioritize and manage graphic design layouts/project communication requests; understand, communicate, and develop creative solutions that address specific goals, balancing creative expression and business objectives * Coordinate and assign the right graphic design resources to each job and ensure correct input/approvals are received throughout the design process * Engage, empower, and lead team to complete campaign/project requests using best practices for design, concept creation, visual innovation, and execution * Meet with marketing management to proactively plan for future projects and goals EDUCATION/EXPERIENCE: * 5+ years of art direction or senior graphic design experience within an internal or external agency. * Bachelor's Degree in Graphic Design, Visual Arts, or related field. * At least two years of experience leading the design of projects from concept to completion. * Proven track record managing projects from concept through completion across multiple media * Experience presenting creative work to clients or senior stakeholders * Demonstrated ability to work within established brand guidelines while bringing fresh creative thinking * Background in both digital-first and print production workflows * Strong portfolio demonstrating ability to concept and direct ideas, teams, and final product SKILLS/COMPETENCIES: * Excellent grammar, and oral, written, and interpersonal communication skills to effectively deal with individuals at all internal and external customers * Expert-level proficiency in Adobe Creative Suite (Photoshop, Illustrator, InDesign) * Strong working knowledge of digital design and prototyping tools (Figma, Sketch, Adobe XD, or similar) * Solid understanding of UI/UX principles for web and mobile design * Knowledge of HTML/CSS basics preferred but not required * Familiarity with project management and collaboration tools (Lytho, Asana, Monday.com, Slack, etc.) * Organized, flexible, and able to multi-task while maintaining a high level of accuracy, efficiency, and attention to detail * Ability to prioritize and respond with a sense of urgency to all inquiries and requests * Ability to make quick, sound decisions based on policy, past practices, and experience * Strong project management skills to direct resources and set priorities * Excellent analytical, problem-solving, and management skills * Ability to envision creative ways to leverage digital ideas and technologies. * High level of proficiency in branding, online marketing, and media concepts. * Able to integrate big ideas through all mediums. WORK ENVIRONMENT: The work is typically performed in a normal office environment. Role routinely uses standard office equipment. At MIMEDX, we are committed to fair and equitable pay practices. We pay our employees equitably for their work, commensurate with their individual skills and experience. Salary ranges and additional compensation, including discretionary bonuses and incentive pay, are determined by a rigorous review process. Salary ranges consider the experience, education, certifications, and skills required for the specific role, equity with similarly situated employees, as well as employer-verified US region specific market data provided by an independent 3rd party partner. Individual salaries vary depending on factors such as your experience, education, location and special skill set. In addition, MIMEDX offers competitive benefits including healthcare, 401k savings plan, ESPP, vacation, and parental leave. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to, or requirements for, this job at any time.

Find a Better Way... ...to use your skills and experience. This is the time to let your talent come to life. To maximize your knowledge and use it for the greater good. To work with the best professionals using state-of-the-art technology, and improve lives with your innovative ideas and ambitious dreams. Find a better way: the Sysmex Way. ...to improve the lives of others. Headquartered in Kobe, Japan, Sysmex is located in Lincolnshire, Illinois. Renowned worldwide for the very finest in quality, innovative diagnostic equipment and information-management systems, we apply science to enhance the quality of life on a global scale. Our agile, resourceful team is committed to realizing critical breakthroughs in laboratory diagnostics, information technology, workflow analysis and life sciences for the clinical laboratory. ...to build a promising future. Responsibilities We currently have a great opportunity for a Regional Field Service Technician. We currently have a great opportunity for a Field Service Technician. The Field Service Technician (FST) is responsible for developing the knowledge and expertise needed to move into a Service Engineer (SE) position and service the Sysmex product lines. The FST will undergo extensive training to prepare for future SE positions as they become available. During the training period, the FST will travel frequently throughout the U.S., when not attending formal training classes for the purposes of mentoring and job shadowing. Upon completion of the training program, the FST will be utilized to supplement existing territories, support emerging territories and other field needs until they assume a permanent assignment in a U.S. service district. This includes the opportunity for relocation. The FST is expected to move into an open SE position in a service district as they become available. Essential Duties and Responsibilities: Successfully complete all training to perform the duties of a Field Service Technician (FST). During training program, travel within their service districts to work with a mentor or assist with service-related tasks. Upon successful completion of the training program, provide service support in their respective service districts. Travel during the training period may be up to 50% within the United States. Accept an SE or related position after the successful completion of program. Demonstrate the ability to perform the following duties and responsibilities after training. Install, maintain, and repair Sysmex instruments and systems, including: Identifying and analyzing instrument problems. Repairing to meet specifications. Performing pre-installation site surveys, installations, scheduled maintenance, and approved modifications in accordance with Sysmex policies. Scheduling modifications as indicated in the Technical Service Bulletin (TSB) and Engineering Change Request (ECR) processes. Monitor and respond to communication devices during all scheduled times. Properly document all service-related activities in a timely and professional manner including inventory, service orders, expense reports, and all other required records. Perform duties within defined service standards, including but not limited to on-time and within labor hour goals for scheduled maintenance, demand service events, installations, and first-visit repair rates. Support and provide ownership of technical issues at existing customer sites. Work cross-functionally with other Sysmex Associates to ensure total customer resolution and maintain a highly satisfied customer base. Miscellaneous duties include: Maintain expenses within guidelines Maintain high level of customer account management and organization skills Maintain control of parts inventory and all company property Perform duties in such a manner as to develop confidence, promote goodwill, and maintain or improve credibility with regard to quality of products and customer service. Promote effective, positive, and productive communication and teamwork between all Sysmex personnel. Other duties as assigned Percentage of Travel: Up to 50% within the United States during training Physical Risk: Regular exposure to risk that may require alertness, but with minimal precautions. Physical Demands: Moderate physical activity. Routine handling of objects 21 to 50 pounds; continuous (at least 80% of time) walking or inspections, keyboard or CRT work. May require periods of moderate discomfort due to noise, dust, lighting and/or other conditions. For more information on our Field Service Technician Program, please visit ********************************************* Qualifications Associates degree or or 0-3 years required experience in Biomedical Engineering, Electronics, Clinical Laboratory Science which may include experience in the Armed Forces. Bachelor's degree preferred. Electronics and/or laboratory science. Completion of Sysmex-certified instrument training. A valid driver's license or ability to obtain one, within 90 days. Must be willing to relocate to any of our service districts throughout the U.S. General computer knowledge in a Windows environment is required. Basic knowledge of LIS systems and interfacing principles desirable. Demonstrated ability to explain in simple and understandable terms complex technical information associated with Sysmex instrument systems. Outstanding listening skills, patience and understanding. Demonstrated presentation and influence skills. Team orientation; demonstrated facilitation skills. Maintaining stable performance under pressure or opposition (such as time pressure or job ambiguity); handling stress in a manner that is acceptable to others and to the organization. Ability to maintain a high energy level and positive attitude. Excellent command of English, both verbal and written; second language desirable (Spanish, French or Portuguese). This job requires satisfaction of the credentialing requirements of Sysmex's customers, including hospitals and other healthcare facilities, which generally includes proof of current vaccinations for measles, mumps, rubella, varicella (chicken pox), and COVID-19. The hourly pay range for this role is $20.19 to $31.73, along with an overtime pay. Within this range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. The total compensation package for this position also includes a choice of health care plan(medical, vision, and dental insurance), an annual incentive bonus, paid time off, parental leave, bereavement leave and a 401(K) for all eligible employees. Sysmex is proud to be an EEO/Affirmative Action employer. All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, age, sex, sexual orientation, gender identity or expression, color, religion, national origin, genetics, disability status, protected veteran status or any other characteristic protected by law. We maintain a drug-free workplace and perform pre-employment substance abuse testing.

At MIMEDX, our purpose starts with helping humans heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care & surgical products, we are committed to making a transformative impact on the lives of patients we serve globally. Will you join us on this journey? We are excited to add a Processing Supervisor to our QOR team! This role will be a onsite. The position will pay between $74,000- $100,000 based on previous relevant experience and educational credentials. POSITION SUMMARY: Oversee the tissue processing operation ensures achievement of daily production goals achieved while meeting all product quality and compliance requirements. Supervise team members and facilitate completion of weekly schedule and accurate batch documentation submission to Quality Assurance. Guide and mentor team members on continuous improvements and knowledge of CFR 1271 HCP/T regulations as well as cGMP regulations included in CFR 210, 211, and 600. Manage conflicts, provide leadership and development to team members, and conduct performance reviews. Ensure all processing operations activities and initiatives comply with Company's policies and procedures and all applicable regulatory requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Oversee tissue processing operations and provide leadership and direct supervision to processing team members. * Areas of responsibility are Wet, Dry, VI and Dish room processes as assigned by manager. * Monitor work schedules to ensure adequate coverage and to meet daily production goals * Work closely with the Training team to ensure team members are cross trained in all relevant areas to successfully do their jobs. Implement and oversee professional development of team members. * Work with Engineering, Supply Chain and Quality to ensure product quality and production schedule attainment. * Assist with the development and implementation of policies, procedures and standards and ensure everyone is fully trained * Minimize safety incidents by proactively ensuring proper working and operations behaviors to eliminate potentially hazardous situations; complete incident/injury reports, as applicable * Drive continuous improvement efforts in all areas of operations using key performance indicators such as processing yields, performance to plan, and overtime management to identify areas of opportunity; lead cross-functional process improvement teams * Identify and implement Corrective Action/Preventive Actions (CAPA) and process non-conformances and complaint investigations related to processing areas * Provide routine performance feedback to team members, manage performance issues, and conduct annual performance reviews PROBLEM SOLVING: * Problems and issues faced are vague, but may be recognizable based on past solutions * Has autonomy to define solutions to non-routine problems within established operational policies and procedures DECISION MAKING/SCOPE OF AUTHORITY: * Ensures that work is performed consistently within the Companies Code of Conduct, and policies and procedures SPAN OF CONTROL/COMPLEXITY: * Typically supervises 20 or more support, production level employees (i.e. non-exempt) or entry level professionals. Heavily involved in day-to-day execution of results EDUCATION/EXPERIENCE: * BS/BA in related discipline or equivalent work experience * 3-5 years of cGMP experience in a production environment * 2 years of leadership / supervisory experience * Experience working with Quality Assurance in a cGMP regulated industry * Prefer knowledge of tissue processing and CFR 1271 HCP/T regulations * Understanding and application of lean manufacturing methodologies SKILLS/COMPETENCIES: * Excellent oral, written, and interpersonal communication skills with the ability to interact with individuals at all levels throughout the organization * Conflict management, resolution and ability to provide constructive feedback * Proficient in Microsoft Office (Excel, Word, etc.) * Ability to prioritize and respond with a sense of urgency to all inquiries and requests * Ability to manage time and workload effectively; organized, flexible, and able to multi-task while maintaining a high level of efficiency and attention to detail * Analytical and trouble shooting skills * Leadership skills with the ability to lead others to achieve desired results * Ability to make quick, sound decisions * Must show aptitude to develop appropriate skills needed for the job WORK ENVIRONMENT: The work is typically performed in a controlled laboratory and/or office environment. Will have contact/exposure with biohazardous materials, chemicals, and blood and human tissue. Training will be conducted on the handling and safety practices necessary for the use and disposal of hazardous chemicals and potential biohazards. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to, or requirements for, this job at any time.

At MIMEDX, our purpose starts with helping humans heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care & surgical products, we are committed to making a transformative impact on the lives of patients we serve globally. We are excited to add a Staff Accountant to our growing Accounting & Finance team! This role will pay between $60,000 - $80,000 based on experience and educational credentials. This is a hybrid position working in our Marietta, GA headquarters Monday & Wednesday each week. POSITION SUMMARY: The Staff Accountant will report to the Senior Accounting Manager and be responsible for supporting activities related to the Company's General Ledger accounting processes. The Staff Accountant will be heavily involved in the preparation and support of the recording of accounting entries, account reconciliations, and play a pivotal role in the Company's accounting processes. Finally, the Staff Accountant will assist in ad hoc, cross-functional finance projects which may arise from time to time. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Assist in the Company's month-end accounting close process through the preparation of journal entries and supporting documentation. * Prepare account reconciliations for general ledger accounts within assigned process areas. * Perform variance analysis, explaining month over month and quarter over quarter changes in account balances, and identify any potential issues. * Assist in the implementation of the Company's new Enterprise Resource Planning system, with input specific to the process areas over which the Staff Accountant has ownership. * Provide requested support to external auditors. * Implement new accounting processes as needs arise. * Devise and implement proprietary, innovative, and automated solutions to complement or supplant current manual processes. * Assist in the preparation and submission of various business license applications, indirect tax returns, census requests, and other required government forms to support the business. * Support the Company's internal control environment through the execution of certain control activities. * Collaborate with other departments on an as-needed basis for ad hoc projects. PROBLEM SOLVING: * Performs full range of standard professional level work that typically requires processing and interpreting, more complex, less clearly defined issues. Identifies problems and possible solutions and takes appropriate action to resolve * Demonstrates skill in data analysis techniques by resolving missing/incomplete information, inconsistencies/anomalies in more complex research/data DECISION MAKING/SCOPE OF AUTHORITY: * Nature of work requires increasing independence; receives guidance only on unusual complex problems or issues * Work review typically involves periodic review of output by supervisor and/or direct "customers" of the process SPAN OF CONTROL/COMPLEXITY: * Fully competent and productive professional contributor, working independently on larger, moderately complex projects/assignments that have direct impact on department results EDUCATION/EXPERIENCE: * BS or BA in Accounting or related field. * Familiarity of the full suite of Microsoft Office software solutions, particularly Microsoft Excel. * CPA License or CPA eligibility preferred * More than 1-2 years of relevant experience preferred * Familiarity with QAD preferred * Familiarity with computer programming languages, such as Python or R. preferred SKILLS/COMPETENCIES: * Strong interpersonal and communication skills. * Detail-oriented disposition with an ability to step back and see the big picture. * Satisfactory understanding of accounting and accounting processes. * Strong analytical and critical thinking skills. WORK ENVIRONMENT/EXPECTED BUSINESS TRAVEL: The work is typically performed in a normal office environment. Role routinely uses standard office equipment. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to, or requirements for, this job at any time.

Join our dynamic and forward-thinking team at IDEXX as a ServiceNow Application Analyst focused on IT Operations Management (ITOM) and Configuration Management Database (CMDB). Our team is currently working on projects to enhance our initial CMDB implementation by focusing on increasing the quality, comprehensiveness, and reliability of our CMDB. We believe the foundation of a resilient IT ecosystem begins with a mature and trusted CMDB, enabling streamlined security operations, proactive service delivery, and opportunities for further automation. In this ServiceNow Application Analyst role, you will be responsible for maintaining, optimizing, and ensuring the ongoing health, accuracy, and reliability of our CMDB. You will partner closely with technical stakeholders, data owners, and process managers across IT, Security, and Service Management to uphold the integrity of our CMDB and drive operational excellence. Your responsibilities will center on vigilant monitoring, proactive problem-solving, and hands-on maintenance, ensuring that the CMDB remains up to date and accurate for our key stakeholders of the platform. If you are passionate about empowering IT operations through a world-class CMDB and thrive in a collaborative, mission-driven environment, we welcome your application and look forward to advancing together. In this role, you will…. Monitor and maintain the ongoing health, accuracy, and completeness of the CMDB, ensuring it meets organizational standards and stakeholder needs. Perform day-to-day operational tasks, including data quality reviews, reconciliation, CI lifecycle management, and exception handling. Identify, diagnose, and resolve issues impacting the CMDB, either independently or in collaboration with ServiceNow developers and other technical teams. Partner with stakeholders across IT, Security, and Service Management to understand their requirements and help translate them into actionable CMDB use cases. Work with data owners and process managers to enforce proper CI ownership, data stewardship, and process adherence. Support ServiceNow discovery, integration, and automation processes to ensure accurate and timely CI data population. Provide guidance and training to stakeholders on CMDB best practices, data consumption, and reporting. Assist with audits, compliance reviews, and reporting related to CMDB data quality and configuration management processes. Document processes, procedures, and knowledge articles to support operational continuity and CMDB maturity. What You Will Need to Succeed… 3-5+ years of hands-on experience supporting and maintaining a ServiceNow CMDB in a large, complex IT environment. Strong understanding of CMDB data models, CI lifecycle, discovery, reconciliation, and data quality management. Experience with day-to-day CMDB operations, including troubleshooting, issue resolution, and stakeholder engagement. Familiarity with ServiceNow ITOM modules (e.g., Discovery, Service Mapping) and integration points. Excellent analytical and problem-solving skills, with keen attention to detail and data accuracy. Ability to communicate technical concepts to both technical and non-technical audiences. Experience partnering with IT, Security, and Service Management teams to deliver business value through CMDB insights and capabilities. Basic scripting or workflow automation skills (JavaScript, Flow Designer, or similar), a plus but not required. Location: 100% remote with the preference of EST or CST. What you can expect from us: Base annual salary target: $90000 to $100000 (yes, we do have flexibility if needed) Opportunity for annual cash bonus Health / Dental / Vision Benefits Day-One 5% matching 401k Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more! Why IDEXX? We're proud of the work we do, because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from diseases. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. #LI-REMOTE

At MIMEDX, our purpose starts with helping humans heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care & surgical products combined with a promising clinical pipeline, we are committed to making a transformative impact on the lives of patients we serve globally. We are excited to add a Director, Health Policy to our Health Policy team! The position will pay between $195,000 - $235,000 plus annual bonus and equity based on previous relevant experience, educational credentials, and location. This is a remote position with up to 15% travel. POSITION SUMMARY: Support the implementation and prioritization of proactive legislative and regulatory rulemaking initiatives that support key business objectives and drive business development opportunities. Play a key role in effecting favorable coverage decisions from all payers, with focus on Medicare, Medicaid and commercial payers. Formulate and execute strategies to maximize payer approval for existing and new products including but not limited to clinical and health economic data generation. Manage all health policy communications and relationships with all payers as well as other key stakeholders. Provide ongoing payer research to identify changes or updates in coverage of company products. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Create and implement strategies that influence a positive coverage decision for company products from payers; establish health policy coverage and awareness through negotiations with medical directors and/or medical policy committees * Identify and monitor changes in medical policy, trends in the US Healthcare system, and regulations that impact providers; seek legal guidance and/or team input as applicable * Participate in market access expansion efforts in the U.S. and global markets by completing product coverage requests, and submitting medical summaries and assessments to payers for review * Communicate with payer contacts to clarify coverage and reimbursement issues * Direct the education of the team members in product coding and medical coverage decisions of all payers and provide guidance on how to communicate new or existing information to affected departments * Communicate with key medical providers and sales team to proactively plan, implement, and strategize on market expansion of our products * Provide guidance to junior team members on prioritizing payer coverage policy initiatives; , define annual performance goals, conduct annual reviews and one-on-one team member meetings * Prepare assigned territory business plans, monthly activity reports, and other reports as requested EDUCATION/EXPERIENCE: * BS/BA in related discipline * 8+ years of experience in a directly related field including several years in a management/supervisory capacity, or verifiable ability. Certification is required in some areas * Prefer professional billing and coding experience and/or certification * Experience with pharmaceutical, biotechnology and/or device health policy and reimbursement * Demonstrated knowledge in securing coverage, coding and payment for medical products with government and commercial payers SKILLS/COMPETENCIES: * Excellent oral, written, and interpersonal communication skills * Ability to interact with all levels of management, both internal and external, third party payers, and customers * Ability to lead and inspire a team to meet organizational deliverables * Proficient in Microsoft Office (Excel, Word, etc.) * Organized, flexible, and able to multi-task while maintaining a high level of efficiency and attention to detail * Strong analytical and negotiating skills, clinical interests, strategic and technical analysis and problem solving skills * Ability to influence others to achieve desired results using tenacity and diplomacy * Strong research and presentation skills

At MIMEDX, our purpose starts with helping humans heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care & surgical products, we are committed to making a transformative impact on the lives of patients we serve globally. Will you join us on this journey? We are excited to add a Pilot Technician I to our Technology Transfer team! This role will be a on site position. The position will pay between $20.00-31.00 hourly based on previous relevant experience and educational credentials. POSITION SUMMARY: Perform any one or all of the routine processes (e.g. dissection, layout, lyophilization, cutting, vialing, and or visual inspection) in a clean room laboratory setting according to established procedures and/or protocol guidelines. Produce high quality tissue products in an efficient manner. Ensure sterile processing and handling of tissue at all times. Perform regular inspection and cleaning of lab equipment to ensure equipment is in good, working order. Monitor equipment maintenance schedule to ensure routine and repair service is performed as needed. Perform data entry tasks and/or data verification. . Perform custodial and administrative tasks to support co-tissue processors. Prepare, wash, and sterilize laboratory instruments, glassware, containers, etc. if required. Clean lab area, lab equipment, and handle hazardous waste removal, per standard operating and cleaning procedures. Ensure adequate supplies for gowning and sterile tissue processing are available in the lab at all times. Comply with all company policies, procedures, regulatory requirements and Good Documentation Practices (GDP). ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform a variety of clean room, dish room, and/or lab area tasks with a focus on providing a sterile processing environment and supplies Perform dish room duties such as preparing, washing, and sterilizing lab instruments, glassware, containers, etc. using a heated container for steam sterilization (i.e. autoclave) Perform custodial duties to ensure the cleanroom, dish room, and lab area are clean and orderly at all times and maintain cleaning logs, per company standards, policies, and procedures Provide assistance to co-processors as requested (e.g. empty trash, dispose of biohazardous waste, bring them supplies, clean work areas throughout the day, etc.) Monitor lab and clean room supply levels to ensure adequate supplies for gowning, tissue processing, and instrument sterilization are available at all times Inspect instruments and supplies for defects, lot numbers, and expiration dates; ensure equipment in all areas are in proper working order Perform in-processing (e.g. at various stages such as dissection, layout, cutout, etc.) and final chart review; ensure all required documentation is present, matching donor ID's and lot numbers, etc. and correct or obtain information, as needed, based on study design Answer telephone calls and/or texts to provide information regarding status of work Process human tissue in an aseptic processing environment (lab) according to standard operating procedures and work instructions using surgical instruments and machinery when required Process donors adhering to standard operating procedures, redlined procedures, and/or feasibility / protocol study designs Perform any one or all of the routine tissue processes (e.g. dissection, layout, cutting, and vialing), as per required specifications, within expected processing times in order to meet project timelines Adhere to all policies and practices from the Quality Management System (QMS) based on company standards and regulatory standards for tissue processing Document results of each process performed, supplies used, etc. to maintain integrity and traceability of donor Support and contribute new ideas to the continuous tissue processing improvement efforts Perform all tasks listed above within a team setting, with clear communication between teammates to ensure project timelines are achieved During downtime of pilot tasks (between studies), technicians are required to be an asset within operations to ensure demand is being met and aligning with company goals Helping Humans Heal EDUCATION/EXPERIENCE: High School Diploma Prefer BA/BS in Biology or Chemistry Minimum 6 months - 1 year in laboratory, biotech, pharma, medical or clean manufacturing Prefer knowledge of Good Documentation Practice (GDP), Good Tissue Practice (GTP), Good Manufacturing Practice (GMP) and AATB regulations SKILLS/COMPETENCIES: Excellent oral, written, listening, and interpersonal communication skills Proficient in Microsoft Office (Word, Excel, etc.) Solid organization skills to support the efficiency of the laboratory operations Ability to effectively work and interact with all members of the laboratory, tissue processing, research & development, and tissue recovery functions Must show aptitude to develop appropriate skills needed for the job WORK ENVIRONMENT: The work is typically performed in a controlled laboratory, dish room, and/or laboratory environment. Wil use an autoclave and industrial dishwashers when required. Will have contact/exposure with biohazardous materials, chemicals, and blood and human tissue. Training will be conducted on the handling and safety practices necessary for the use and disposal of hazardous chemicals and potential biohazards. Will also be trained on all applicable equipment needed to perform the job.

At MIMEDX, our purpose starts with helping humans heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care & surgical products, we are committed to making a transformative impact on the lives of patients we serve globally. Will you join us on this journey? We are excited to add a Sr. Distribution Associate to our Manufacturing Team! The position will pay between $20-25/hr based on previous relevant experience, educational credentials, and location. POSITION SUMMARY: Execute all distribution activities including, but not limited to, receiving/stocking, inventory reconciliation, processing pre/post sterilized inventory, Transfer donors/product between facilities and picking, packing & shipping orders to customers. Perform preventative maintenance on equipment to ensure equipment is in optimal working condition. Will utilize an inventory tracking system and is responsible for ensuring the system is maintained, with full quality and regulatory compliance. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Prepare and pack products for shipment to customers domestic and international * Maintain product tracking for all finished goods based upon donor and/or lot number * Ensure inventory transactions are completed between facilities * Cross-training must be at 75% or above. * Perform preventative maintenance on equipment as needed * Dependable and in good standing with Attendance * Highly-Motivate, responsive, and quality-driven professional * Have a strong understanding of job procedures * May assist in training new employees * Accurately completes inventory/cycle count and researches discrepancies * Process returned product * Verify customer shipments meet all regulatory requirements; prepare and execute all steps to facilitate and implement the shipment * Count and document raw materials, finished goods, and literature to ensure inventory accuracy * Send out tissues for sterilization; track their return in inventory database * Receive shipments from suppliers, inspect items for damage, verify quantities and items numbers, complete required paperwork (packaging slips/purchase orders) * Transport materials (manufacturing/office supplies, tissue, mail, placenta) between internal facilities as required * Track and manage inventory of returned goods and work with Customer Service to process Return Merchandise Authorizations (RMA's). * Move released items to available inventory in the warehouse PROBLEM SOLVING: * Selects correct processes from clearly prescribed rules, past practices, or instruction * Seeks advice and guidance on non-routine or problem areas from supervisor. Any deviations from the norm are cleared by the supervisor DECISION MAKING/SCOPE OF AUTHORITY: * Under close supervision, exercises limited latitude/independent judgement and decision making * Work typically involves detailed checks or close review of output by a senior coworker and/or supervisor SPAN OF CONTROL/COMPLEXITY: * Entry level support role requiring basic skills; can perform some of the basic tasks within the function; some impact at the job or department level EDUCATION/EXPERIENCE: * HS Diploma or GED * 4-5 years of experience in area of responsibility * Have a good overall understanding of DC workflow and can work with minimal guidance * Understanding of computerized inventory management systems * Prefer 4-5 years of inventory and/or materials management experience in a business involving both domestic and international distribution points * Must be able to work overtime when necessary and participate in all physical inventory * Must be a team player and demonstrate effective communication and problem-solving skills * Maintains a clean work area to ensure that product remains clean and help prevent work related injuries * Prefer experience working in a regulated industry * Prefer experience working in medical device industry or human donor tissue recovery and distribution industry (i.e. tissue banks) * Prefer experience working in an International Standards Organization (ISO) or Good Manufacturing Procedures (GMP) environment preferred * Knowledge of FedEx, UPS, and DHL shipping systems a plus SKILLS/COMPETENCIES: * Excellent oral, written, and interpersonal communication skills * Ability to interact with all levels of management, both internal and external, third party payers, and customers; with a focus on customer service * Proficient in Microsoft (Excel, Word) * Organized, flexible, and able to multi-task while maintaining a high level of efficiency and attention to detail * Proficiency with Material Requirements Planning (MRP) systems (QAD is preferred) WORK ENVIRONMENT: The work is typically performed in a warehouse and controlled lab environments.

At MiMedx, our purpose starts with helping patients heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care products combined with a promising clinical pipeline, we are committed to making a transformative impact on the lives of patients we serve globally. Will you join us on this journey? POSITION SUMMARY: Perform custodial and administrative tasks to support lab workers and tissue processors. Will launder employee scrubs on a daily basis and perform thorough cleaning tasks, per prescribed schedule. Update and maintain cleaning logs and ensure tasks are completed as required. Prepare, wash, and sterilize laboratory instruments, glassware, containers, etc. Clean lab area, lab equipment, and handle hazardous waste removal, per standard operating and cleaning procedures. Ensure adequate supplies for gowning and sterile tissue processing are available in the lab at all times. Comply with all company policies, procedures, regulatory requirements and Good Documentation Practices (GDP). ESSENTIAL DUTIES AND RESPONSIBILITIES: Will wash, fold, and put away work scrubs worn by operations employees on a daily basis Perform constant, custodial duties to ensure clean and sterile work environment in the lab and surrounding areas; update and maintain cleaning schedule logs as required Monitor and update records from electronic data logger equipment to internal database Assist with the following tasks: Perform dish room duties such as preparing, washing, and sterilizing lab instruments, glassware, containers, etc. using a heated container for steam sterilization (i.e. autoclave) Provide assistance to processors as requested (e.g. empty trash, dispose of biohazardous waste, bring them supplies, clean work areas throughout the day, etc.) Monitor lab and clean room supply levels to ensure adequate supplies for gowning, tissue processing, and instrument sterilization are available at all times Inspect instruments and supplies for defects, lot numbers, and expiration dates; ensure equipment in all areas are in proper working order Perform visual inspection of finished products and place products in appropriate packaging, following applicable guidelines and procedures Perform in-processing (e.g. at various stages such as dissection, layout, cutout, etc.) and final chart review; ensure all required documentation is present, matching donor ID's and lot numbers, etc. and correct or obtain information, as needed Answer telephone calls and provide information regarding status of work EDUCATION/EXPERIENCE: HS Diploma or GED Prefer previous lab assistant/aide experience in commercial or academic lab Prefer minimum 1 year experience with Good Laboratory Practices (GLP), proper lab techniques and practices (aseptic practices, sterile gowning and gloving), tissue packaging, assistance in tissue processing, and proper SOP documentation practices SKILLS/COMPETENCIES: Excellent oral, written, and interpersonal communication skills; good listener Proficient in Microsoft Office (Excel, Word, etc.) Organized, flexible; maintain a high level of efficiency and attention to detail Ability to handle time sensitive material and instructions Accuracy in record keeping and sorting, checking, counting, and verifying information and data; legible penmanship Must show aptitude to develop appropriate skills needed for the job WORK ENVIRONMENT: The work is typically performed in a controlled laboratory, dish room, and/or laboratory environment. Will use an autoclave and industrial dishwashers. Will have contact/exposure with biohazardous materials, chemicals, and blood and human tissue. Training will be conducted on the handling waste and safety practices necessary for the use and disposal of hazardous chemicals and potential biohazards. Will also be trained on all applicable equipment needed to perform the job.

As a Senior Automation SCADA and Controls Engineer, you will be joining a leader in veterinary medical device manufacturing that is driving the future of automation, data, and digital transformation in the industry. You'll be at the heart of IDEXX's smart manufacturing, Industry 4.0, and enterprise-wide Digital Transformation initiatives. This is your opportunity to shape the future of our SCADA and IIoT platforms, lead high-impact projects that elevate manufacturing efficiency, quality, and innovation-and grow your career at the intersection of automation, AI, and data. You'll work with cutting-edge automation and digital technologies in a smart manufacturing culture that values innovation, collaboration, and strong work-life balance. If you're ready to make a meaningful impact and help define the next generation of connected, data-driven factory systems, we want you on our team. What you'll do: * Automation & Controls Engineering: Perform automation controls engineering activities in support of production automation machinery and smart manufacturing, including machine automation controls, IIoT, PLC, HMI, SCADA, machine vision systems, industrial robots, computer networking, and other automation controls areas. * Software Development: Write, test, debug, modify, and implement automation applications, including PLC, HMI, SCADA, SQL, and Python. Platforms include Rockwell Studio 5000 and FactoryTalk View, Inductive Automation Ignition, OPC, MQTT, SQL Server, etc. * Smart Factory Integration: Build SCADA/MES solutions to digitally connect machines, equipment, and devices across the plant floor. Integrate with MES, CMMS, and other enterprise systems. * System Architecture: Define solution architecture, data strategies, and OT network/application cybersecurity. * Connectivity & Edge Devices: Evaluate and implement equipment connectivity options using PLCs, control devices, sensors, and IIoT edge technology. * Visualization & User Interfaces: Design intuitive HMIs and SCADA dashboards that provide real-time visibility into operations and equipment performance. * Troubleshooting & Support: Lead diagnostics, troubleshooting, and issue resolution for automation systems in production environments. What you'll need: * Bachelor's degree in Computer Science, Engineering, or related field-or equivalent experience. * 5+ years in automation/controls engineering, with proven expertise in PLC/HMI/SCADA development and troubleshooting. * Strong knowledge of Allen-Bradley PLCs and Rockwell Software. * Extensive knowledge and experience developing and implementing enterprise-level Industrial IoT, SCADA, and MES applications using Inductive Automation Ignition, including Perspective, Python, and SQL scripting. * In-depth understanding of IT and OT network architecture, including industrial communication protocols like Ethernet/IP, OPC, MQTT, Modbus, and TCP/IP. * Ability to provide innovative solutions to complex automation and data challenges. * Deep experience with connecting to and collecting data from industrial IoT devices, PLCs, manufacturing applications, and databases. * Strong project management skills with the ability to drive initiatives to completion with minimal guidance. * Travel 5% of the time. Preferred skills: * Experienced with process historians, SQL databases, time series databases, and SQL database programming. * Knowledge and experience with Data Engineering, Data Science, Artificial Intelligence (AI), Machine Learning (ML), and predictive analytics. * Programming experience in .NET, C#, Java, Node-RED, HTML, or full-stack development. * Experience with cloud platforms (AWS, Azure, Snowflake). * Knowledge and experience with Digital Transformation and Industry 4.0 frameworks. * Experienced with Data Analytics tools and software to process and visualize large data sets using tools like Tableau, Microsoft Power BI, Python, Plotty, and Dash. * Working knowledge of Unified Name Space (UNS) and ISA-95 * ISA/IEC 62443 OT Cybersecurity. Benefits: * Lead meaningful projects that directly impact manufacturing innovation in the veterinary medical device field * Grow your career at the intersection of automation, data, AI, and digital transformation * Lead innovation at an industry leader driving smart manufacturing initiatives * Enjoy a strong work-life balance in a safe, modern environment * Base salary: $110,000-$120,000 (dependent on experience) * Paid Time Off and competitive benefits * 401K Matching * Discounted Stock Purchasing * Yearly Merit Increases & Bonus Why IDEXX? We're proud of the work we do, because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. #LI-VR1

As a Senior Controls SCADA Engineer, you will be joining a leader in veterinary medical device manufacturing that is driving the future of automation, data, and digital transformation in the industry. You'll be at the heart of IDEXX's smart manufacturing, Industry 4.0, and enterprise-wide Digital Transformation initiatives. This is your opportunity to shape the future of our SCADA and IIoT platforms, lead high-impact projects that elevate manufacturing efficiency, quality, and innovation-and grow your career at the intersection of automation, AI, and data. You'll work with cutting-edge automation and digital technologies in a smart manufacturing culture that values innovation, collaboration, and strong work-life balance. If you're ready to make a meaningful impact and help define the next generation of connected, data-driven factory systems, we want you on our team. What you'll do: Automation & Controls Engineering: Perform automation controls engineering activities in support of production automation machinery and smart manufacturing, including machine automation controls, IIoT, PLC, HMI, SCADA, machine vision systems, industrial robots, computer networking, and other automation controls areas. Software Development: Write, test, debug, modify, and implement automation applications, including PLC, HMI, SCADA, SQL, and Python. Platforms include Rockwell Studio 5000 and FactoryTalk View, Inductive Automation Ignition, OPC, MQTT, SQL Server, etc. Smart Factory Integration: Build SCADA/MES solutions to digitally connect machines, equipment, and devices across the plant floor. Integrate with MES, CMMS, and other enterprise systems. System Architecture: Define solution architecture, data strategies, and OT network/application cybersecurity. Connectivity & Edge Devices: Evaluate and implement equipment connectivity options using PLCs, control devices, sensors, and IIoT edge technology. Visualization & User Interfaces: Design intuitive HMIs and SCADA dashboards that provide real-time visibility into operations and equipment performance. Troubleshooting & Support: Lead diagnostics, troubleshooting, and issue resolution for automation systems in production environments. What you'll need: Bachelor's degree in Computer Science, Engineering, or related field-or equivalent experience. 5+ years in automation/controls engineering, with proven expertise in PLC/HMI/SCADA development and troubleshooting. Strong knowledge of Allen-Bradley PLCs and Rockwell Software. Extensive knowledge and experience developing and implementing enterprise-level Industrial IoT, SCADA, and MES applications using Inductive Automation Ignition, including Perspective, Python, and SQL scripting. In-depth understanding of IT and OT network architecture, including industrial communication protocols like Ethernet/IP, OPC, MQTT, Modbus, and TCP/IP. Ability to provide innovative solutions to complex automation and data challenges. Deep experience with connecting to and collecting data from industrial IoT devices, PLCs, manufacturing applications, and databases. Strong project management skills with the ability to drive initiatives to completion with minimal guidance. Travel 5% of the time. Preferred skills: Experienced with process historians, SQL databases, time series databases, and SQL database programming. Knowledge and experience with Data Engineering, Data Science, Artificial Intelligence (AI), Machine Learning (ML), and predictive analytics. Programming experience in .NET, C#, Java, Node-RED, HTML, or full-stack development. Experience with cloud platforms (AWS, Azure, Snowflake). Knowledge and experience with Digital Transformation and Industry 4.0 frameworks. Experienced with Data Analytics tools and software to process and visualize large data sets using tools like Tableau, Microsoft Power BI, Python, Plotty, and Dash. Working knowledge of Unified Name Space (UNS) and ISA-95 ISA/IEC 62443 OT Cybersecurity. Benefits: Lead meaningful projects that directly impact manufacturing innovation in the veterinary medical device field Grow your career at the intersection of automation, data, AI, and digital transformation Lead innovation at an industry leader driving smart manufacturing initiatives Enjoy a strong work-life balance in a safe, modern environment Base salary: $110,000-$120,000 (with flexibility dependent on skillset and experience) Paid Time Off and competitive benefits 401K Matching Discounted Stock Purchasing Yearly Merit Increases & Bonus Why IDEXX? We're proud of the work we do, because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. #LI-VR1

At MIMEDX, our purpose starts with helping humans heal. We are driven by discovering and developing regenerative biologics utilizing human placental tissue to provide breakthrough therapies addressing the unmet medical needs for patients across multiple areas of healthcare. Possessing a strong portfolio of industry leading advanced wound care & surgical products, we are committed to making a transformative impact on the lives of patients we serve globally. Will you join us on this journey? We are excited to add CMC Project Manager to our Technology Transfer team! This role will be a onsite. The position will pay between $93,000 - 133,000k annually based on previous relevant experience and educational credentials. POSITION SUMMARY: MIMEDX is looking for a highly motivated and self-driven leader to join our dynamic and diverse Technology Transfer team of engineers and scientists. MIMEDX has a rapidly growing portfolio of healthcare products. To support this growth, the company is expanding the technology transfer team with talented individuals who will help develop and transition these products through the manufacturing and regulatory pipelines to patients. The successful candidate for this position will make an immediate impact on the development of our tissue product and medical device pipelines by integrating with the project team and planning and tracking projects to progress late-stage development and transfer activities. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Effectively manage the planning, development, and execution of projects supporting tissue products process development and medical device integration programs. * Collaborate with cross-functional teams to execute projects for biologic specific manufacturing processes, product characterization, and product testing. * Ensure that Protocols, methods, and procedures are reviewed and executed per regulatory requirements and business needs. * Track project timeline elements to ensure that functional deliverables are completed on time and according to relevant quality standards. * Plan and execute characterization studies during development for commercial supply chain(s) including review and approval of release testing plans. Review quality control plans and provide certification that design requirements meet specifications and are in compliance with cGMPs * Perform technical analysis of project data, including trending of data, root cause analysis, and predictive statistics. * Actively contribute to writing key tissue product and medical device development sections of regulatory documents and responses to regulatory authorities * Promote a culture of collaboration, cooperation, execution excellence, effective communication, and cross-functional problem-solving to enable a high-performing team. * Maintain productive and professional relationships with partners, collaborators, departments, contractors and customers. * Author/review technical protocols, reports and deliver presentations utilizing sound scientific reasoning and interpretation of the available data PROBLEM SOLVING: * Solutions require analysis and investigation * Knowledge around the various root cause determination techniques * Able to understand and implement statistical trending processes * Assesses issues thoroughly and solves complex problems quickly; removes roadblocks for the team * Able to define and communicate issue escalations to leadership per defined timing. DECISION MAKING/SCOPE OF AUTHORITY: * Achieves planned results by decisions and actions based on professional methods, business principles, and practical experience * May recommend/make decisions regarding existing or new programs/initiatives that have a significant medium to long-term impact to business operations/outcomes and carry potential consequences if unsuccessful SPAN OF CONTROL/COMPLEXITY: * Responsible for execution strategy and vison typically with a short-term operational focus on business results (e.g. 1 year) * Manage staff/administrative departments/areas * Manage business operations or technical departments/areas * Manage business functions/process EDUCATION/EXPERIENCE: * Bachelor's Degree in a related science/medical research field and minimum of ten (10) years of relevant work experience within a regulated field; or an appropriate combination of relevant education and experience. * Minimum of five (5) years of training or experience in the category or categories of tissue, medical device, or pharmaceutical manufacturing. * Must have a strong working knowledge of good documentation practices, cGMPs, design processes, and process development; monitoring and statistical analysis. * Must have strong knowledge of CAPA and root cause analysis. * Knowledge of the following: FDA, AATB, ISO, and other state/federal regulations and standards. SKILLS/COMPETENCIES: * Demonstrated effectiveness in project management disciplines (PMP certification preferred) * Demonstrated aptitude and proficiency in MS Word, MS Excel, MS project, Minitab, and Windows-based operating systems * Must be able to communicate ideas and information clearly, effectively, and frequently (oral and written) within a team, the company, and with outside consultants. * Must have strong technical writing skills and strong organization skills with attention to detail. * Ability to prioritize and respond with a sense of urgency to all inquiries and requests * Ability to manage time and workload effectively; organized, flexible, and able to multi-task while maintaining a high level of efficiency and attention to detail WORK ENVIRONMENT/EXPECTED BUSINESS TRAVEL: The work is typically performed in a normal office environment. Role routinely uses standard office equipment. Additional work will occur in laboratory and controlled environment areas. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to, or requirements for, this job at any time.

As a Senior Manufacturing Engineering Technician on the 3rd shift in our climate-controlled manufacturing area, you'll work with your own tool box (provided by IDEXX). You will have your own assigned desk, computer and cellphone. Our manufacturing is a dry plant and boiler-free environment. It's a medical device facility, it's very clean - you won't get dirty! Details: 3rd Shift Monday to Friday 9:30pm - 6:00am Benefits: Shift differential $3/hour $35.50/hr base pay with flexibility depending on skills and experience Paid Time Off 401K Matching Discounted Stock Purchasing Yearly Merit Increases Yearly Bonus $1000 credit to HAS account Safe location in a modern environment What you'll need: Your skill set includes experience in troubleshooting AC and DC electrical systems, as well as experience with motion control, conveyors, motors, pneumatics, sensors, and with PLC's (Allen Bradley controllers / Epson and Fanuc Robots experience is a plus) You can disassemble and re-assemble and troubleshoot complex mechanical systems You have 5+ years of experience working in a technical/Industrial Manufacturing Maintenance and repair capacity You'll be able to work overtime and/or on the weekends, if there is a business need. What you'll do: You will perform preventative and corrective maintenance on all manufacturing equipment, managed through a computerized maintenance management system (CMMS) You will troubleshoot and repair complex electro-mechanical systems including vision guided robots, motors, pneumatic pick and place, precision liquid dispensing, ultrasonic welding, and cam / indexer driven equipment When working to solve problems you will use root cause analysis, and recommend corrective action and you will analyze and compile engineering data to draw conclusions Your day-to-day activities will include working with engineering and production support to ensure the safe, efficient, and productive operation of the manufacturing equipment Why IDEXX? We're proud of the work we do, because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. #LI-VR1

NATIONWIDE- USA Join Our Talent Community for Radiologic Technologists At HealthTronics, we believe in staying ready-not just for today's needs, but for tomorrow's. That's why we're inviting talented Radiologic Technologists who want to make a difference in patient lives through mobile medical care to connect now. Upload your resume and stay connected! While we may not have an active opening in your area right now, we anticipate future needs as our teams grow and evolve across the country. If you're a licensed, mobile, and mission-minded Radiologic Technologist who wants to be first in line when a position opens near you-this is your invitation to raise your hand. Why Join the HealthTronics Talent Network? Get early access to future openings before they go public Be first in line for roles in your area or surrounding regions Connect with a recruiter who can guide your journey Learn about company culture, travel requirements, and growth paths Who We're Looking For: Licensed Radiologic Technologists (ARRT Certified) Professionals comfortable with mobile travel schedules Strong communicators with a patient-first mindset Those open to future opportunities across the U.S. Important Note: This is not an active job opening. Submitting your information to this Talent Network allows us to reach out directly when a role becomes available in your area. You're not applying for a specific position today-but you are taking the first step toward one. Apply today to stay on our radar. When the time is right, we'll be ready-and you'll already be at the top of the list. HealthTronics is committed to equal opportunity for all, without regard to race, religion, color, national origin, citizenship, sex, age, veteran status, disability, genetic information, or any other protected characteristic. HealthTronics will make reasonable accommodations for known physical or mental limitations of otherwise qualified employees and applicants with disabilities unless the accommodation would impose an undue hardship on the operation of our business. Visit our website and connect with us! Facebook | Twitter | Instagram| LinkedIn