Medical Device Assembler Salary in USA

Medical Device Assembler 1st Shift $18.50 Natick, MASchedule: 6:00 AM - 2:30 PM Monday - Friday Clean room environment!Your responsibilities include maintaining accurate production records and documentation, performing a variety of repetitive tasks with meticulous attention to detail, and adjusting to evolving procedures. Proficiency in manual dexterity and sharp eyesight are essential for effectively handling, manipulating, and inspecting small components.Qualifications:* High school diploma or GED (equivalent work experience considered).* Preferred experience in regulated manufacturing (e.g., medical, aerospace, or food packaging).* Proficiency in handling, manipulating, and inspecting small components.* Strong attention to detail and commitment to quality.* Proficient in spoken and written English.* Ability to commute to Natick, Massachusetts.Please email Jamie at: All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Company DescriptionWelcome to Express Employment Waltham/Framingham! We are a dedicated team focused on helping individuals find new roles or supporting hiring needs for businesses. Our mission is to serve you through every step of the process, ensuring your success.Role DescriptionOur client is a leading medical device company in Waltham, MA. This is a full-time role for a Manufacturing Manager overseeing Printed Circuit Board assembly. As the Manufacturing Manager, you will be responsible for overseeing the day-to-day operations of the PCBA production area. This includes production planning, quality control, and manufacturing operations management.Qualifications5+ years of management experience with SMT Printed Circuit Board assemblies and BGA TechnologyB.S/B.A Degree in technical or business disciplineStrong knowledge of SMT processes, equipment and industry best practicesKnowledge of PCB design and conceptsKnowledge of inventory control practices and manufacturing planningProven ability to lead and motivate team membersGood MS Office suite skillsAbility to manage multiple tasks and priorities in a manufacturing environment

Medical Device-Account Setup and Hospital Implementation SpecialistCharlotte, NC with up to 75% travelMedaxis carries the Negative Pressure Wound Therapy products manufactured by Medela LLC.Medaxis is seeking a Medical Device-Account Setup and Hospital Implementation SpecialistYou are a road warrior! This position is traveling up to 75% of the time.You have experience with medical devices and will be initiating the setup of medical device evaluations/implementations in hospitals.You are highly organized and are seen as someone who manages projects with efficiency.You are customer-focused and have experience in sales.You will drive the utilization of medical devices in the hospital.What We Offer our Medical Device-Account Setup and Hospital Implementation SpecialistExcellent salary and bonus potentialComprehensive benefits plan, which is affordable to our employees401K with matchPension Plan16-week Paid Parental LeaveGenerous PTO package, plus 14 paid holidaysA great place to work!Key Experience Needed: Medical Device-Account Setup and Hospital Implementation SpecialistBachelor’s degree in Business or related field preferredMinimum two years’ related experience and/or training, or equivalent combination of education and experienceMedical Device experienceStrong independent project management capabilities and organizational skills requiredExcellent verbal and written communication skillsAbility to manage multiple conflicting prioritiesComputer proficiency in MS Office programs (Word, Excel, Power Point)Experience working in an environment with global objectivesMust be able to read, understand and communicate in EnglishPosition Responsibilities: Medical Device,Account Setup and Hospital Implementation SpecialistInitiate new customer setup, NPWT education and product use training to ensure effective utilization of equipmentDrive utilization in key IDN’s with key cliniciansManage IDN relationship as Point of ContactCollaborate with BDM in managing evaluations/conversionsCollaborate w/ MedPro in supporting our key accountsResponsible for NPWT product in-servicing throughout hospital: surgeons, nurses, biomed, case management and otherProject management and rollout for multi-site facilitiesEmployee must meet vendor credentialing/compliance demands of accounts within given territory.This includes but not limited to: RepTrax, VendorMate, Status Blue, VCS, etc.For patient/customer safety purposes as part of the vendor credentialing process, Employee must satisfy account’s drug screening requirements, including but not limited to screening for marijuana use, regardless if use of marijuana is legal under applicable state law.For more information, please refer to the Drug and Alcohol Workplace Policy.Comply with all federal, state, and local laws and regulationsFollow all Company rules and regulations, including health and safety rulesSuccessfully interact with employees at all levelsRegular, reliable performance of all job dutiesTravel as may be required to meet business and customer expectationsPerform all other duties as assigned or as may be required from time to timePosition Salary: Starting at $80,000 per yearThis is not a job description. More details will be provided regarding the functions of this position.As an EEO/Affirmative Action Employer, all qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, citizenship, sex, protected veteran status, age, physical or mental disability, medical condition, HIV/AIDs status, marital status, domestic partner status, sexual orientation, gender identity (transgender status), weight, height or any other characteristic protected by federal, state, or local law or ordinance.https://mandatoryview.com/?LicenceId=e7c44cfe-6946-4b77-9939-493d186ba760&ProductType=OnlineApplicant&SubType=PG

Valued Team member: We are glad you are exploring new opportunities within Zimmer Biomet!What You Can ExpectUnder the direction of the Operations Manager, key responsibilities include the delivery and pickup of implants and instrumentation at hospitals within a defined geographic area, vehicle maintenance, on call rotation assignment relating to after-hour emergencies and office assistance on an as needed basis. Strong communication skills, attention to detail, as well as a valid driver's license with an acceptable drivers abstract are required.How You'll Create Impact Preparation, transport/delivery and pickup of implants and instrumentation to hospitals; obtain signature from customer to document proof of delivery. Maintain company vehicle assigned including alert to supervisor of repairs and servicing needs. Prepare daily drivers log to document vehicle safety inspection, track mileage, expenses and pickups and deliveries. On a monthly basis, reconcile purchases and process receipts utilizing Procurement card. Assist with warehouse and inventory as needed. This is not an exhaustive list of duties or functions and may not necessarily comprise all of the \"essential functions\".What Makes You Stand Out Ability to lift up to 50 pounds independently Organizational and time management skills are essential Demonstrated knowledge to identify Zimmer Biomet products by major product groupings and familiarity with product lines of other division. Must maintain professional and courteous demeanor with internal and external customers. Your Background High School Diploma, equivalent G.E.D, or equivalent experience Valid driver's license Acceptable driving record Vendor Credentialing possibly required Participation in an on-call schedule rotation Travel ExpectationsEOE/M/F/Vet/Disability

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages-from early development through approval-with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.Position Summary:The Quality Assurance Specialist III -Medical Device will provide advanced-level, hands-on support from a regulated systems perspective in a GxP laboratory services and kitting production environment. Activities include but are not limited to, product label control, internal auditing, and quality inspection & release of raw materials, in-process materials, finished products, and critical components. In addition, this position is responsible for providing backup for the document and record control system. Extended work hours may be necessary in order to meet business demands.Essential functions of the job include but are not limited to: Assist in maintaining established company wide GxP quality systems, actively managing assigned activities (including logging and tracking of events and outcomes), and working with end-users on thorough documentation of quality system events including:Non-ConformancesCustomer ComplaintsPlanned DeviationsChange ManagementCorrective and Preventive Action (CAPA)Audit ProgramsParticipating on the Material Review BoardAssist in scheduling, performing, and reporting internal audits, as well as supplier audits, and related activitiesAnalyze data resulting from monthly metrics and reporting tools for all aspects of quality systems, connecting data and forming conclusions regarding the compliance health of PFM, to include presentation of metric performance to management representatives and proposing durable solutionsRespond to supplier look-back notifications. Investigate and determine disposition of materialMonitor equipment calibration program to ensure timely and accurate completion of maintenanceManage the backroom during audits and inspections, review requested documentation and records, and assist in preparing subject matter experts for audit interviewsSupport departmental projects aimed operational process understanding efforts (process mapping)Act as a change-agent and QA lead during continuous improvement and global harmonization effortsProvide guidance to junior level QA specialistsClient-facing activities as assigned by department head such as leading client visits/audits and representing QA during project kick-off meetings and customer complaints for the CDx projectsCreate and conduct site-wide training for multiple disciplinesSupport validation activities, including review and approve validation protocols, reports, and final package documentationSupport the maintenance and review of DHF and actively participate in all Design Control activities pertaining to the CDx projectsAssist in the QA review and acceptance of customer specifications to conform to contractual requirementsGenerate and maintain label formats for manufactured and resale productsGenerate and maintain Certificates of Analysis for finished products and products for resaleInspect and approve all product labels generated by OperationsProvide support to other departments regarding requests, release status, regulatory requirements and other tasks as requestedWork with functional groups to develop correct documentation required to document evidence for the manufacturing/processing, testing and release of products and servicesMaintain filing and storage systems for document control, training and batch records for raw and finished productCollaborating with Project Management to plan upcoming quality deliverables and enforce compliance accountabilityInspect and release incoming raw material, critical components, packaging and labeling in accordance with individual specifications and standard operating proceduresPerform batch record review and release for finished product, raw materials, intermediate solutions, and servicesConduct product inspections, review repack recordsMiscellaneous:May participate actively on the safety committee, as neededAssist in training new and existing personnelParticipate in regulatory, notified body, and customer audits as neededProvide back-up coverage for other Quality SpecialistsCarry out other duties/projects as assignedQualifications:Minimum Required:Bachelor's Degree or equivalent combination of education and experience4 years of related experience in a life science, regulated environmentIn-depth knowledge of ISO 13485 and 21 CFR Part 820 standardsOther Required:Experience working in a Quality Department/Life Sciences-Regulated environment, including experience independently conducting internal audits, document review from a technical and quality perspective, batch release, incoming inspectionKnowledge of root cause analysis tools and application, identifying durable corrective/preventative actions, and participating in process improvementsAbility to meet deadlines and perform administrative functionsMicrosoft Office suite proficiency including Office Word, Excel, PowerPointAbility to organize tasks, work independently and adapt to changing prioritiesAbility to function independently within a minimally supervised environment with exceptional attention to detail requiredDemonstrated highly developed communication skills including well-developed writing skills and verbal and interpersonal skillsMust be able to read, write, speak, fluently and comprehend the English language

The Medical Device Process Technology Specialist provides manufacturing and technology support to the Albany ThermaCare production and packaging operations. The role focuses on authoring qualification documents that assist in improving process, technical, and technology capabilities. Success in the role is achieved through development of site Manufacturing Investigation Reports, QTS commitment execution, supporting development and execution of New Product Launch and technology transfer plans, IQ/OQ/PQ validation activities, and the authoring, execution andtraining of standard operating procedures. The selected candidate works in partnership with the site Operations, Engineering, Quality, Procurement, and Operational Excellence teams under the leadership of the site Process Technology Specialist to deliver integrated technical services to meet the site objectives.Role • Authors qualification documents in support of the site business strategy.• Resolves complex technical problems.• Identifies high-risk areas, areas of improvement and utilization of resources in specific production practices and processes. Determines the path forward through in-depth assessment, experimental testing, and complex data analysis. Develops and implements tactical solutions to mitigate impact and improve yield and effectiveness.• Works with continued process verification activities related to technology transfer of new products to the site as well as updates/optimization of existing commercial products.• Manages conflicting priorities of process improvements, production demands, compliance requirements, and time limitations.• Leads the execution of technical projects to accomplish management directives. Interprets process data for improvement opportunities and identifies and implements value-added solutions to mitigate risk and improve process capability and compliance.• Responsible for the implementation of validations and investigations within the manufacturing site.• Collaborates with various groups within Angelini during the various stages of new product development / technology transfer and develops / leads the site activities for qualification.• Collects and coordinates the combined input from different functional areas regarding the application of technologies that will optimize capital investment to provide robust, productive, and practical processes at a commercial scale.• Responsible for the implementation of Process Analytical Technologies enhancing monitoring and control.Professional Profile: • Bachelor's Degree in Business, Technical or Scientific Discipline or equivalent experience with continuous non-woven cell pack manufacturing.• Minimum of 3 years of successful and demonstrated experience supporting manufacturing in a GMP regulated environment.• Has strong subject matter expertise in relevant areas of continuous manufacturing operations, etc. or has broad technical knowledge of industrial operations. Keeps abreast of current developments and trends in areas of expertise. Assimilates and applies new job-related information that may vary in complexity within a reasonable timeframe.• Picks up on technical aspects; can learn new skills and knowledge; fast learner.• Excellent interpersonal, written, and verbal communication skills.• Knowledge in Lean and Six Sigma principles highly desirable.• Strong Customer service and communication skills.• Action oriented with a strong sense of urgency.• Must be well organized and detail oriented while applying sound judgment and decision-making skills to both routine and non-routine issues that arise.• Able to proactively manage multiple projects and priorities and organize time effectively.• Understands Regulatory and Production requirements inherent to medical device manufacturing.• Open minded and flexible, able to understand other cultures.Angelini Pharma is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity and/or expression, sexual orientation, national origin, genetics, disability, age or veteran status. About Us: Angelini is a medium size private international group, a leader in health and wellness in the field of pharmaceutical and consumer products. Born in Italy in the early twentieth century, the Angelini group has offices in 17 countries and worldwide distribution of products. Angelini Pharma Inc. is the US business unit, headquartered in Rockville, MD. In 2020 Angelini Pharma Inc. acquired the ThermaCare production facility in Albany, GA.

Job DescriptionAt Thermo Fisher Scientific team, you'll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe and delivering COVID-19 solutions. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building a fulfilling career with us.Location/Division Specific InformationMiddletown, VASpecialty Diagnostics Group (SDG)How will you make an impact?The Medical Device Complaint Handling Specialist III is responsible for managing and resolving complaints related to medical devices. This role involves investigating complaints, documenting findings, and ensuring compliance with regulatory requirements. The specialist will collaborate with cross-functional teams to address customer concerns and improve product quality.What will you do? The duties and responsibilities include, but are not limited to, the following:Receive and review complaints related to medical devices.Investigate complaints by gathering relevant information, analyzing data, and conducting root cause analysis.Ensure customer complaint investigations are complete, accurate and closed in a timely manner; includes meeting regulatory requirementsCollaborate with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Product Development, to resolve complaints.Connect with customers to address concerns and provide updates on complaint resolution.Supervise complaint trends and find opportunities for product improvement.Ensure compliance with applicable regulations and standards, such as FDA 21 CFR Part 820 and ISO 13485.Prepare for and participate in internal and external audits.Provides matrix/project leadership, training and guidance to junior team members.Ability to maintain accurate recordsParticipation in cross-functional business process improvement activities as the need arises.Keys to Success:EducationBachelor's degree in a relevant field, such as biomedical engineering, life sciences, or a related field required.Experience3 - 5+ years experience in an FDA regulated environment (drugs, biologics, medical devices or related products)Detailed knowledge of ISO 13485 and GMP regulations which govern a medical device and diagnostics manufacturing.Strong analytical and problem-solving skills required.Tracking and trending tools and reporting techniquesKnowledge, Skills, AbilitiesAble to create presentations, work with spreadsheets, prepare reports and write procedures utilizing MS Word, Excel and PowerPoint software applications.Lead meetings and obtain consensus among cross functional teamsExcellent communication and interpersonal skills.Ability to work independently and collaboratively in a team environment.Attention to detail and ability to manage multiple tasks simultaneously.Exercise independent discretion and judgment in execution of duties.BenefitsWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.comThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.Accessibility/Disability AccessJob Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Job DetailsJob Location: Corporate Office - Jacksonville, FLPosition Type: SeasonalEducation Level: High SchoolSalary Range: UndisclosedTravel Percentage: NoneJob Shift: DayDescription Job Summary Assist the Product Management Team with product lines or multiple product lines. Aid in the development of new products with maximum profitability. Assist in the improvement of products from existing ideas and the development of new ideas while gaining industry experience and contact with customers. Develop business and technical knowledge and demonstrate a high degree of work ethic in the accomplishment of assigned goals. Essential Functions, Duties, and Responsibilities Use professional verbal and written communication skills to explain technical product information to customers, salespeople, and other employees Prioritize activities and tasks based on set sales and development goals for the product line assist in publishing product education and product marketing media Research a product's market potential and develop a sales & price strategy Stay current on and cross reference competitive product offering and pricing Stay current on the standard of care and new technologies in the market in which the assigned product is applied Ensure the efficiency of products through product design and in collaboration with field inventory, warehouse inventory, and shipping key personnel Assist in completion of necessary documents for Product Development milestones & assist in the creation of regulatory submissions and inquiries during submissions Work on developing an in-depth knowledge of published clinical and internal testing & evidence for all marketing claims in the assigned product(s) Assist in managing the production of product development projects (PDSR/PVR) with manufacturing engineers Package & Ship products to the office or other field locations Complete, understand, and follow all required company policy trainings Understand KLS Martin Non-Disclosure Agreements and when to execute them Understand government regulations and company policy on expense activities Submit expenses for reimbursement following the company travel policy Complete Hospital Credentialing where necessary to perform essential duties Performs other related duties as assigned. Qualifications Educational and Experience Requirements Degree seeking student pursuing a 4 year college degree or masters degree. Preferred fields of study: Business, Marketing, or Engineering Previous experience or demonstrated ability to learn, Salesforce.com, SAP, Excel, Word, PowerPoint, Outlook, Concur, Paycom, iOS iPad & iPhone Knowledge, Skills, and Abilities Ability to develop and maintain collaborative relationships with all levels within the organization Plan and organize internal cross-department meetings to accomplish goals of the product line or project Ability to follow through on issues, make informed decisions that comply with policies and procedures, complete tasks and problem-solve Demonstrate the ability to work with minimal supervision and accomplish high level goals with minimal explicit instructions Skill Requirements Typing/computer keyboard Utilize computer software (specified above) Retrieve and compile information Maintain records/logs Verify data and information Organize and prioritize information/tasks Operate office equipment Advanced mathematical concepts (fractions, decimals, ratios, percentages, graphs) Verbal communication Written communication Public speaking/group presentations Research, analyze and interpret information Investigate, evaluate, recommend action Basic mathematical concepts (e.g. add, subtract) Abstract mathematical concepts (interpolation, inference, frequency, reliability, formulas, equations, statistics) Physical Requirements Sitting for extended periods Extended periods viewing computer screen Walking Reading Speaking Hear/Listen Maintain regular, punctual attendance Lifting/carrying up to 20 pounds various items Repetitive Motions Pushing/Pulling Bending/Stooping Reaching/Grasping Writing Hazards Normal office environment Toxic or caustic chemicals Electrical current Housekeeping and/or cleaning agents All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Job Summary Assist the Product Management Team with product lines or multiple product lines. Aid in the development of new products with maximum profitability. Assist in the improvement of products from existing ideas and the development of new ideas while gaining industry experience and contact with customers. Develop business and technical knowledge and demonstrate a high degree of work ethic in the accomplishment of assigned goals. Essential Functions, Duties, and Responsibilities Use professional verbal and written communication skills to explain technical product information to customers, salespeople, and other employees Prioritize activities and tasks based on set sales and development goals for the product line assist in publishing product education and product marketing media Research a product's market potential and develop a sales & price strategy Stay current on and cross reference competitive product offering and pricing Stay current on the standard of care and new technologies in the market in which the assigned product is applied Ensure the efficiency of products through product design and in collaboration with field inventory, warehouse inventory, and shipping key personnel Assist in completion of necessary documents for Product Development milestones & assist in the creation of regulatory submissions and inquiries during submissions Work on developing an in-depth knowledge of published clinical and internal testing & evidence for all marketing claims in the assigned product(s) Assist in managing the production of product development projects (PDSR/PVR) with manufacturing engineers Package & Ship products to the office or other field locations Complete, understand, and follow all required company policy trainings Understand KLS Martin Non-Disclosure Agreements and when to execute them Understand government regulations and company policy on expense activities Submit expenses for reimbursement following the company travel policy Complete Hospital Credentialing where necessary to perform essential duties Performs other related duties as assigned. Educational and Experience Requirements Degree seeking student pursuing a 4 year college degree or masters degree. Preferred fields of study: Business, Marketing, or Engineering Previous experience or demonstrated ability to learn, Salesforce.com, SAP, Excel, Word, PowerPoint, Outlook, Concur, Paycom, iOS iPad & iPhone Knowledge, Skills, and Abilities Ability to develop and maintain collaborative relationships with all levels within the organization Plan and organize internal cross-department meetings to accomplish goals of the product line or project Ability to follow through on issues, make informed decisions that comply with policies and procedures, complete tasks and problem-solve Demonstrate the ability to work with minimal supervision and accomplish high level goals with minimal explicit instructions Skill Requirements Typing/computer keyboard Utilize computer software (specified above) Retrieve and compile information Maintain records/logs Verify data and information Organize and prioritize information/tasks Operate office equipment Advanced mathematical concepts (fractions, decimals, ratios, percentages, graphs) Verbal communication Written communication Public speaking/group presentations Research, analyze and interpret information Investigate, evaluate, recommend action Basic mathematical concepts (e.g. add, subtract) Abstract mathematical concepts (interpolation, inference, frequency, reliability, formulas, equations, statistics) Physical Requirements Sitting for extended periods Extended periods viewing computer screen Walking Reading Speaking Hear/Listen Maintain regular, punctual attendance Lifting/carrying up to 20 pounds various items Repetitive Motions Pushing/Pulling Bending/Stooping Reaching/Grasping Writing Hazards Normal office environment Toxic or caustic chemicals Electrical current Housekeeping and/or cleaning agents All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered, and recognized.What You Can ExpectUnder the direction of the Operations Manager, key responsibilities include the delivery and pickup of implants and instrumentation at hospitals within a defined geographic area, vehicle maintenance, on call rotation assignment relating to after-hour emergencies and office assistance on an as needed basis. Strong communication skills, attention to detail, as well as a valid driver's license with an acceptable drivers abstract are required.How You'll Create Impact Preparation, transport/delivery and pickup of implants and instrumentation to hospitals; obtain signature from customer to document proof of delivery. Maintain company vehicle assigned including alert to supervisor of repairs and servicing needs. Prepare daily drivers log to document vehicle safety inspection, track mileage, expenses and pickups and deliveries. On a monthly basis, reconcile purchases and process receipts utilizing Procurement card. Assist with warehouse and inventory as needed. This is not an exhaustive list of duties or functions and may not necessarily comprise all of the \"essential functions\".What Makes You Stand Out Ability to lift up to 50 pounds independently Organizational and time management skills are essential Demonstrated knowledge to identify Zimmer Biomet products by major product groupings and familiarity with product lines of other division. Must maintain professional and courteous demeanor with internal and external customers. Your Background High School Diploma, equivalent G.E.D, or equivalent experience Valid driver's license Acceptable driving record Vendor Credentialing possibly required Participation in an on-call schedule rotation Travel Expectations Up to 5% EOE/M/F/Vet/Disability

Medical Device - Wound Care Sales - BiologicsMy medical device client is an innovative company that develops and manufactures regenerative therapies for wound and tissue repair. They are seeking to hire a Medical Sales Rep to cover and do new business development within an assigned territory. Responsibilities will include penetrating new business opportunities and managing clients. This position involves presentations to surgeons and being in wound care center settings.Profile:Medical Device Sales selling Biologics, Regenerative Medicine or Wound CareMust have experience/ relationships within hospitals within territory.Requirements:Bachelor's DegreeMin. 5+ years of Medical Sales experience preferably within Wound CareNew business development with ability to close large dealsExperience selling to hospitals, clinics and wound care centersKnowledge/Understanding of biotechnology industry and trendsKnowledge/Understanding of Healthcare reimbursement preferredAbility to develop and manage relationships amongst key decision makersDocumented Sales Success of meeting and achieving sales goalsAbility to multi-task and prioritizeStrong communication and presentation skillsAbility to travel as neededOffering:Base Salary $80,000 - $90,000 (based on experience/market)Year 1 @ plan $180,000 - $200,000Expenses (Auto, Phone)LaptopBenefits PackageDirect Sales Recruiting, LLC, (DSR) and DirectHR are National Recruitment organizations partnering with National, Regional and Local Clients to bring qualified candidates a career and a future. DSR offers over 50 years combined Recruitment, Sales and Management experience. We are, along with our clients, an Equal Opportunity Employer and are committed to hiring and supporting a diverse workforce. A M/F/D/V