35 jobs found in Nashville

A WebOps company is filling a position for a Telecommute Sales Engineer. Core Responsibilities Include: Collaborating across all departments to advance the technical dynamics of our GTM strategy Aligning with the product organization to ensure value proposition is fully represented Delivering compelling product demos and technical presentations to prospective customers and current clients Position Requirements Include: Customer-facing heads up capabilities BA/BS or equivalent experience 3-5+ years of sales engineering experience Drupal or WordPress experience

A bookkeeping company is searching for a person to fill their position for a Remote Accounting Specialist. Must be able to: Handle A/P, A/R, payroll and month-end closing services Perform other accounting related functions as requested by the client Prioritize and manage multiple client needs Qualifications Include: 3+ years performing full charge bookkeeping 2+ years using Quickbooks Software most recent experience on resume Demonstrated ability to handle multiple accounts simultaneously Exceptional attention to detail with excellent written and verbal communications skills

An insurance company is in need of a Telecommute Portfolio Business Analyst. Core Responsibilities Include: Preparing ad-hoc reports and analysis as requested Conducting user acceptance testing on new platforms Managing a portfolio of accounts to ensure the portfolio is generating expected outcomes Qualifications for this position include: Must have superior technical, analytic and decision making skills Must understand industry accepted policy management terms Minimum of 5 years of experience in insurance portfolio management Must understand how to use Excel, Tableau or other similar analytical and dashboard tools College degree or equivalent work experience Must be able to analyze data and present findings and alternatives

A translation and localization company is seeking a Telecommute Medical Subject Matter Expert. Must be able to: Translate various material Review user manuals Skills and Requirements Include: Proficient use of CAT tools, especially Worldserver Minimum 3 years experience in translation and/or editing of medical documents Ability to meet hourly throughput set at 1500 words/hour

An automating customer support provider is in need of a Telecommute Social Media Manager. Must be able to: Grow our influence and reputation in the world of small business on LinkedIn, Facebook, Twitter, and online Engage in conversations that yield positive engagement, promoting relevant content to our audience Influence and control major public-facing parts of the company Qualifications for this position include: Bachelor s degree in English, Journalism, Communication, or related fields 2+ years of managing social media accounts for businesses Experience using HootSuite, Buffer, or SproutSocial Experience using Photoshop or other photo editing tools Experience making GIFs from screenshots All other requirements necessary for this position

A revenue cycle management company is seeking a Telecommute Supply Coding and CDM Analyst. Individual must be able to fulfill the following responsibilities: Ensure quality and timeliness of proprietary content Coordinate and plan designated projects Evaluate and provide operational improvements in business processes Position Requirements Include: HighSchool Diploma or GED 3+ years of extensive clinical or CDM related experience or equivalent combination Extensive hospital experience or knowledge of hospital and Medicare coding Proficiency in main Microsoft applications Ability to interpret general business periodicals

A mobile application company is in need of a Remote Campus Director. Candidates will be responsible for the following: Organizing, staffing, and running free food booths for signups and brand awareness Recruiting, interviewing, and managing Brand Ambassadors Organizing and running events with sororities and fraternities Qualifications Include: Host biweekly meetings with Brand Ambassadors Must be entrepreneurial and creative Must be the queens and kings of campus Must be up to date on campus culture, events for collabs Must be able to thrive under pressure

A marketing company needs applicants for an opening for a Telecommute Full Stack Software Engineer. Candidates will be responsible for the following: Implementing and launching highly-visible end-user facing features Designing and developing large-scale web applications Creating robust high-volume production applications Qualifications Include: BS in Computer Science, or related technical field, or equivalent practical experience Software architecture and web application development experience Experience with AJAX, HTML and CSS Experience with JavaScript or Python Associated topics: algorithm, backend, c c++, c++, c#, devops, php, programming, sdet, software engineer

Work from Home - Avon Sales Representative About the Job Work when you want and where you want. - make your own schedule. Whatever your background, whether you come from Customer Service, Accounting, Marketing, Administrative or any other field or if you are just looking for a part-time career to supplement your current income, AVON is looking for you to become an Independent Sales Representative. Empower your life by starting your own Avon business. Avon is an iconic brand that is recognized and loved by millions. As a leader in beauty, anti-aging skin care, and fragrances, Avon makes it easy for you to sell and succeed, right from the start. Why Sell Avon? You have your own business You set your own hours Get your own free online store to sell and start earning Promote your Avon business through social media You determine your family/work/lifestyle balance Minimum start up investment No inventory required Exclusive Avon Opportunities Earn trips to great vacation destinations Access highly rated health, dental and vision insurance plans Enjoy education benefits & tuition discounts to keep your career moving Receive discounts on voice, data and WiFi service for all your digital devices Design, create and print business tools for free Free access to AVON U, featuring free tutorials and online courses to take your AVON Business to the next level Whether you're entering the workforce, returning after the kids are grown, want to be your own boss or looking for ways to supplement your current income, becoming an Independent AVON Sales Representative offers unlimited opportunities. Put your love of beauty, fashion and meeting people to good use with AVON. Join today!

An information technology company is filling a position for a Telecommute Cloud Financial Operations Principal Member. Core Responsibilities Include: Engaging regularly with Director and C-Suite level customers Overseeing the adoption and implementation of Cloudability s platform for customers Participating in deep architectural discussions Position Requirements Include: Travel as needed to ensure the success of critical customers Demonstrated public cloud knowledge and experience B.S. in Computer Science related field or equivalent experience Experienced in account management and/or technical client-facing support (2+ years) Proven experience navigating complex data sets and pull out insights using SQL or similar tools

A marketing company is searching for a person to fill their position for a Remote Product Designer. Core Responsibilities of this position include: Working with guide implementation Helping developers identify and accumulate UI patterns Must meet the following requirements for consideration: Experience translating wireframes into high fidelity interactive designs Experience designing and iterating on sketches, storyboards, information architecture blueprints and prototypes Experience with Sketch, Photoshop, Illustrator, InDesign, and/or other design tools

Job Description Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Senior Staff Regulatory Affairs Specialist to join our Joint Replacement Division to be in Mahwah, NJ or remotely anywhere in the US. Who we want Strategic. Creates alternative ways to proceed. Faced with any given scenario, can quickly spot the relevant patterns and issues. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Communicators. Articulates well and expresses ideas effectively. Learners. Great desire to learn and looks to continuously improve. Teammates . Supports, encourages, and inspires others. What you will do As the Senior Staff Regulatory Affairs Specialist, you will bring and sustain products on the market via pre-market submission activities with global Health Authorities. You will operate in a fast-paced environment and you will liaise with internal and external customers and establish strong relationships with Health Authorities. You will translate complex engineering or scientific principles into approachable content while educating others on Stryker products and processes. You will provide leadership and guidance to junior Regulatory Affairs professionals. Possess and apply advanced knowledge and understanding of the regulatory and legal frameworks, processes, and procedures to bring products to market and maintain compliance. Review progress with management; assist Management in training RA Specialists, Senior, or Staff Specialists as required. Identify requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.). Assist in the development of regulatory strategy and update strategy based upon regulatory changes. Evaluate proposed products for regulatory classification and jurisdiction. Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities. Prepare and submit regulatory submissions according to applicable regulatory requirements and guidelines. Help train stakeholders on current and new regulatory requirements to ensure organization-wide compliance. Author and update divisional SOPs, recommend timely changes to ensure regulatory compliance, and lead process improvements to maximize efficiencies. Provide regulatory input and technical guidance on global regulatory requirements to product development teams. Participate in New Product Development Teams throughout all phases to ensure US, EU, and other international regulatory requirements are incorporated as part of the development process. Demonstrate developing technical leadership skills interdepartmentally. Evaluate medical device regulations and develop strategies for bringing products to market. Author FDA submissions, EU design dossiers, and other regulatory documents to obtain approval to bring new or modified products to market. Partner with global regulatory affiliates and leverage Reconstructive product expertise to provide submission documentation for expedited international market access and sustaining support. Advise stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations. Provide regulatory information and guidance for proposed product claims/labeling. Monitor the progress of the regulatory authority review process through appropriate communications with the agency. Communicate and interact with regulatory authorities before and during the development and review of a regulatory submission through appropriate communication tools. Assess global impact of changes to launched products and support notifications/submissions as required. Review labeling and marketing literature for compliance with regulatory requirements. What you need A Bachelors Degree (B.S or B.A) in Engineering, Science or equivalent focus is required. A minimum of 7 years of experience in an FDA regulated industry required. A minimum of 5 years of Regulatory Affairs experience required. RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred. Experience authoring regulatory submissions for product approval and interacting with regulatory agencies required. Proven ability to develop, author and implement global regulatory strategies for new products. Ability to comply with constantly changing regulatory procedures and prioritize work effectively. Ability to analyze and resolve non-routine regulatory issues using independent judgment. Excellent analytical and writing skills. Excellent interpersonal, written and oral communication skills. Effective organizational skills. Advanced PC skills with proficiency in Microsoft office Suite, including Excel. Work From Home: YesTravel Percentage: Up to 25%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractors legal duty to furnish information. Associated topics: hematopathology, medical, mlt, molecular, pathology, sterile processing technician, technician i, technician iii, technician iv, toxicology

Job Description Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Senior Staff Regulatory Affairs Specialist to join our Joint Replacement Division to be in Mahwah, NJ or remotely anywhere in the US. Who we want Strategic. Creates alternative ways to proceed. Faced with any given scenario, can quickly spot the relevant patterns and issues. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Communicators. Articulates well and expresses ideas effectively. Learners. Great desire to learn and looks to continuously improve. Teammates . Supports, encourages, and inspires others. What you will do As the Senior Staff Regulatory Affairs Specialist, you will bring and sustain products on the market via pre-market submission activities with global Health Authorities. You will operate in a fast-paced environment and you will liaise with internal and external customers and establish strong relationships with Health Authorities. You will translate complex engineering or scientific principles into approachable content while educating others on Stryker products and processes. You will provide leadership and guidance to junior Regulatory Affairs professionals. Possess and apply advanced knowledge and understanding of the regulatory and legal frameworks, processes, and procedures to bring products to market and maintain compliance. Review progress with management; assist Management in training RA Specialists, Senior, or Staff Specialists as required. Identify requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.). Assist in the development of regulatory strategy and update strategy based upon regulatory changes. Evaluate proposed products for regulatory classification and jurisdiction. Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities. Prepare and submit regulatory submissions according to applicable regulatory requirements and guidelines. Help train stakeholders on current and new regulatory requirements to ensure organization-wide compliance. Author and update divisional SOPs, recommend timely changes to ensure regulatory compliance, and lead process improvements to maximize efficiencies. Provide regulatory input and technical guidance on global regulatory requirements to product development teams. Participate in New Product Development Teams throughout all phases to ensure US, EU, and other international regulatory requirements are incorporated as part of the development process. Demonstrate developing technical leadership skills interdepartmentally. Evaluate medical device regulations and develop strategies for bringing products to market. Author FDA submissions, EU design dossiers, and other regulatory documents to obtain approval to bring new or modified products to market. Partner with global regulatory affiliates and leverage Reconstructive product expertise to provide submission documentation for expedited international market access and sustaining support. Advise stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations. Provide regulatory information and guidance for proposed product claims/labeling. Monitor the progress of the regulatory authority review process through appropriate communications with the agency. Communicate and interact with regulatory authorities before and during the development and review of a regulatory submission through appropriate communication tools. Assess global impact of changes to launched products and support notifications/submissions as required. Review labeling and marketing literature for compliance with regulatory requirements. What you need A Bachelors Degree (B.S or B.A) in Engineering, Science or equivalent focus is required. A minimum of 7 years of experience in an FDA regulated industry required. A minimum of 5 years of Regulatory Affairs experience required. RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred. Experience authoring regulatory submissions for product approval and interacting with regulatory agencies required. Proven ability to develop, author and implement global regulatory strategies for new products. Ability to comply with constantly changing regulatory procedures and prioritize work effectively. Ability to analyze and resolve non-routine regulatory issues using independent judgment. Excellent analytical and writing skills. Excellent interpersonal, written and oral communication skills. Effective organizational skills. Advanced PC skills with proficiency in Microsoft office Suite, including Excel. Work From Home: YesTravel Percentage: Up to 25%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractors legal duty to furnish information. Associated topics: hematopathology, medical, mlt, molecular, pathology, sterile processing technician, technician i, technician iii, technician iv, toxicology

Job Description Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Senior Staff Regulatory Affairs Specialist to join our Joint Replacement Division to be in Mahwah, NJ or remotely anywhere in the US. Who we want Strategic. Creates alternative ways to proceed. Faced with any given scenario, can quickly spot the relevant patterns and issues. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Communicators. Articulates well and expresses ideas effectively. Learners. Great desire to learn and looks to continuously improve. Teammates . Supports, encourages, and inspires others. What you will do As the Senior Staff Regulatory Affairs Specialist, you will bring and sustain products on the market via pre-market submission activities with global Health Authorities. You will operate in a fast-paced environment and you will liaise with internal and external customers and establish strong relationships with Health Authorities. You will translate complex engineering or scientific principles into approachable content while educating others on Stryker products and processes. You will provide leadership and guidance to junior Regulatory Affairs professionals. Possess and apply advanced knowledge and understanding of the regulatory and legal frameworks, processes, and procedures to bring products to market and maintain compliance. Review progress with management; assist Management in training RA Specialists, Senior, or Staff Specialists as required. Identify requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.). Assist in the development of regulatory strategy and update strategy based upon regulatory changes. Evaluate proposed products for regulatory classification and jurisdiction. Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities. Prepare and submit regulatory submissions according to applicable regulatory requirements and guidelines. Help train stakeholders on current and new regulatory requirements to ensure organization-wide compliance. Author and update divisional SOPs, recommend timely changes to ensure regulatory compliance, and lead process improvements to maximize efficiencies. Provide regulatory input and technical guidance on global regulatory requirements to product development teams. Participate in New Product Development Teams throughout all phases to ensure US, EU, and other international regulatory requirements are incorporated as part of the development process. Demonstrate developing technical leadership skills interdepartmentally. Evaluate medical device regulations and develop strategies for bringing products to market. Author FDA submissions, EU design dossiers, and other regulatory documents to obtain approval to bring new or modified products to market. Partner with global regulatory affiliates and leverage Reconstructive product expertise to provide submission documentation for expedited international market access and sustaining support. Advise stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations. Provide regulatory information and guidance for proposed product claims/labeling. Monitor the progress of the regulatory authority review process through appropriate communications with the agency. Communicate and interact with regulatory authorities before and during the development and review of a regulatory submission through appropriate communication tools. Assess global impact of changes to launched products and support notifications/submissions as required. Review labeling and marketing literature for compliance with regulatory requirements. What you need A Bachelors Degree (B.S or B.A) in Engineering, Science or equivalent focus is required. A minimum of 7 years of experience in an FDA regulated industry required. A minimum of 5 years of Regulatory Affairs experience required. RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred. Experience authoring regulatory submissions for product approval and interacting with regulatory agencies required. Proven ability to develop, author and implement global regulatory strategies for new products. Ability to comply with constantly changing regulatory procedures and prioritize work effectively. Ability to analyze and resolve non-routine regulatory issues using independent judgment. Excellent analytical and writing skills. Excellent interpersonal, written and oral communication skills. Effective organizational skills. Advanced PC skills with proficiency in Microsoft office Suite, including Excel. Work From Home: YesTravel Percentage: Up to 25%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractors legal duty to furnish information. Associated topics: hematopathology, medical, mlt, molecular, pathology, sterile processing technician, technician i, technician iii, technician iv, toxicology

Job Description Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Senior Staff Regulatory Affairs Specialist to join our Joint Replacement Division to be in Mahwah, NJ or remotely anywhere in the US. Who we want Strategic. Creates alternative ways to proceed. Faced with any given scenario, can quickly spot the relevant patterns and issues. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Communicators. Articulates well and expresses ideas effectively. Learners. Great desire to learn and looks to continuously improve. Teammates . Supports, encourages, and inspires others. What you will do As the Senior Staff Regulatory Affairs Specialist, you will bring and sustain products on the market via pre-market submission activities with global Health Authorities. You will operate in a fast-paced environment and you will liaise with internal and external customers and establish strong relationships with Health Authorities. You will translate complex engineering or scientific principles into approachable content while educating others on Stryker products and processes. You will provide leadership and guidance to junior Regulatory Affairs professionals. Possess and apply advanced knowledge and understanding of the regulatory and legal frameworks, processes, and procedures to bring products to market and maintain compliance. Review progress with management; assist Management in training RA Specialists, Senior, or Staff Specialists as required. Identify requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.). Assist in the development of regulatory strategy and update strategy based upon regulatory changes. Evaluate proposed products for regulatory classification and jurisdiction. Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities. Prepare and submit regulatory submissions according to applicable regulatory requirements and guidelines. Help train stakeholders on current and new regulatory requirements to ensure organization-wide compliance. Author and update divisional SOPs, recommend timely changes to ensure regulatory compliance, and lead process improvements to maximize efficiencies. Provide regulatory input and technical guidance on global regulatory requirements to product development teams. Participate in New Product Development Teams throughout all phases to ensure US, EU, and other international regulatory requirements are incorporated as part of the development process. Demonstrate developing technical leadership skills interdepartmentally. Evaluate medical device regulations and develop strategies for bringing products to market. Author FDA submissions, EU design dossiers, and other regulatory documents to obtain approval to bring new or modified products to market. Partner with global regulatory affiliates and leverage Reconstructive product expertise to provide submission documentation for expedited international market access and sustaining support. Advise stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations. Provide regulatory information and guidance for proposed product claims/labeling. Monitor the progress of the regulatory authority review process through appropriate communications with the agency. Communicate and interact with regulatory authorities before and during the development and review of a regulatory submission through appropriate communication tools. Assess global impact of changes to launched products and support notifications/submissions as required. Review labeling and marketing literature for compliance with regulatory requirements. What you need A Bachelors Degree (B.S or B.A) in Engineering, Science or equivalent focus is required. A minimum of 7 years of experience in an FDA regulated industry required. A minimum of 5 years of Regulatory Affairs experience required. RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred. Experience authoring regulatory submissions for product approval and interacting with regulatory agencies required. Proven ability to develop, author and implement global regulatory strategies for new products. Ability to comply with constantly changing regulatory procedures and prioritize work effectively. Ability to analyze and resolve non-routine regulatory issues using independent judgment. Excellent analytical and writing skills. Excellent interpersonal, written and oral communication skills. Effective organizational skills. Advanced PC skills with proficiency in Microsoft office Suite, including Excel. Work From Home: YesTravel Percentage: Up to 25%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractors legal duty to furnish information. Associated topics: hematopathology, medical, mlt, molecular, pathology, sterile processing technician, technician i, technician iii, technician iv, toxicology

Job Description Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Senior Staff Regulatory Affairs Specialist to join our Joint Replacement Division to be in Mahwah, NJ or remotely anywhere in the US. Who we want Strategic. Creates alternative ways to proceed. Faced with any given scenario, can quickly spot the relevant patterns and issues. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Communicators. Articulates well and expresses ideas effectively. Learners. Great desire to learn and looks to continuously improve. Teammates . Supports, encourages, and inspires others. What you will do As the Senior Staff Regulatory Affairs Specialist, you will bring and sustain products on the market via pre-market submission activities with global Health Authorities. You will operate in a fast-paced environment and you will liaise with internal and external customers and establish strong relationships with Health Authorities. You will translate complex engineering or scientific principles into approachable content while educating others on Stryker products and processes. You will provide leadership and guidance to junior Regulatory Affairs professionals. Possess and apply advanced knowledge and understanding of the regulatory and legal frameworks, processes, and procedures to bring products to market and maintain compliance. Review progress with management; assist Management in training RA Specialists, Senior, or Staff Specialists as required. Identify requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.). Assist in the development of regulatory strategy and update strategy based upon regulatory changes. Evaluate proposed products for regulatory classification and jurisdiction. Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities. Prepare and submit regulatory submissions according to applicable regulatory requirements and guidelines. Help train stakeholders on current and new regulatory requirements to ensure organization-wide compliance. Author and update divisional SOPs, recommend timely changes to ensure regulatory compliance, and lead process improvements to maximize efficiencies. Provide regulatory input and technical guidance on global regulatory requirements to product development teams. Participate in New Product Development Teams throughout all phases to ensure US, EU, and other international regulatory requirements are incorporated as part of the development process. Demonstrate developing technical leadership skills interdepartmentally. Evaluate medical device regulations and develop strategies for bringing products to market. Author FDA submissions, EU design dossiers, and other regulatory documents to obtain approval to bring new or modified products to market. Partner with global regulatory affiliates and leverage Reconstructive product expertise to provide submission documentation for expedited international market access and sustaining support. Advise stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations. Provide regulatory information and guidance for proposed product claims/labeling. Monitor the progress of the regulatory authority review process through appropriate communications with the agency. Communicate and interact with regulatory authorities before and during the development and review of a regulatory submission through appropriate communication tools. Assess global impact of changes to launched products and support notifications/submissions as required. Review labeling and marketing literature for compliance with regulatory requirements. What you need A Bachelors Degree (B.S or B.A) in Engineering, Science or equivalent focus is required. A minimum of 7 years of experience in an FDA regulated industry required. A minimum of 5 years of Regulatory Affairs experience required. RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred. Experience authoring regulatory submissions for product approval and interacting with regulatory agencies required. Proven ability to develop, author and implement global regulatory strategies for new products. Ability to comply with constantly changing regulatory procedures and prioritize work effectively. Ability to analyze and resolve non-routine regulatory issues using independent judgment. Excellent analytical and writing skills. Excellent interpersonal, written and oral communication skills. Effective organizational skills. Advanced PC skills with proficiency in Microsoft office Suite, including Excel. Work From Home: YesTravel Percentage: Up to 25%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractors legal duty to furnish information. Associated topics: hematopathology, medical, mlt, molecular, pathology, sterile processing technician, technician i, technician iii, technician iv, toxicology

Job Description Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Senior Staff Regulatory Affairs Specialist to join our Joint Replacement Division to be in Mahwah, NJ or remotely anywhere in the US. Who we want Strategic. Creates alternative ways to proceed. Faced with any given scenario, can quickly spot the relevant patterns and issues. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Communicators. Articulates well and expresses ideas effectively. Learners. Great desire to learn and looks to continuously improve. Teammates . Supports, encourages, and inspires others. What you will do As the Senior Staff Regulatory Affairs Specialist, you will bring and sustain products on the market via pre-market submission activities with global Health Authorities. You will operate in a fast-paced environment and you will liaise with internal and external customers and establish strong relationships with Health Authorities. You will translate complex engineering or scientific principles into approachable content while educating others on Stryker products and processes. You will provide leadership and guidance to junior Regulatory Affairs professionals. Possess and apply advanced knowledge and understanding of the regulatory and legal frameworks, processes, and procedures to bring products to market and maintain compliance. Review progress with management; assist Management in training RA Specialists, Senior, or Staff Specialists as required. Identify requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.). Assist in the development of regulatory strategy and update strategy based upon regulatory changes. Evaluate proposed products for regulatory classification and jurisdiction. Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities. Prepare and submit regulatory submissions according to applicable regulatory requirements and guidelines. Help train stakeholders on current and new regulatory requirements to ensure organization-wide compliance. Author and update divisional SOPs, recommend timely changes to ensure regulatory compliance, and lead process improvements to maximize efficiencies. Provide regulatory input and technical guidance on global regulatory requirements to product development teams. Participate in New Product Development Teams throughout all phases to ensure US, EU, and other international regulatory requirements are incorporated as part of the development process. Demonstrate developing technical leadership skills interdepartmentally. Evaluate medical device regulations and develop strategies for bringing products to market. Author FDA submissions, EU design dossiers, and other regulatory documents to obtain approval to bring new or modified products to market. Partner with global regulatory affiliates and leverage Reconstructive product expertise to provide submission documentation for expedited international market access and sustaining support. Advise stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations. Provide regulatory information and guidance for proposed product claims/labeling. Monitor the progress of the regulatory authority review process through appropriate communications with the agency. Communicate and interact with regulatory authorities before and during the development and review of a regulatory submission through appropriate communication tools. Assess global impact of changes to launched products and support notifications/submissions as required. Review labeling and marketing literature for compliance with regulatory requirements. What you need A Bachelors Degree (B.S or B.A) in Engineering, Science or equivalent focus is required. A minimum of 7 years of experience in an FDA regulated industry required. A minimum of 5 years of Regulatory Affairs experience required. RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred. Experience authoring regulatory submissions for product approval and interacting with regulatory agencies required. Proven ability to develop, author and implement global regulatory strategies for new products. Ability to comply with constantly changing regulatory procedures and prioritize work effectively. Ability to analyze and resolve non-routine regulatory issues using independent judgment. Excellent analytical and writing skills. Excellent interpersonal, written and oral communication skills. Effective organizational skills. Advanced PC skills with proficiency in Microsoft office Suite, including Excel. Work From Home: YesTravel Percentage: Up to 25%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractors legal duty to furnish information. Associated topics: hematopathology, medical, mlt, molecular, pathology, sterile processing technician, technician i, technician iii, technician iv, toxicology

Overview The Occupational Therapy Assistant (COTA) in Home Health is responsible for providing occupational therapy to patients in their homes to restore them to their fullest physical ability. The Occupational Therapy Assistant performs his/her duties in accordance with policies and procedures and the established plan of care. LHC Group is the preferred post-acute care partner for hospitals, physicians and families nationwide. From home health and hospice care to long-term acute care and community-based services, we deliver high-quality, cost-effective care that empowers patients to manage their health at home. Hospitals and health systems around the country have partnered with LHC Group to deliver patient-centered care in the home. More hospitals, physicians and families choose LHC Group, because we are united by a single, shared purpose: It's all about helping people. Additional Details Under the supervision of an Occupational Therapist, is at all times responsible to follow all state specific laws governing theprovision of occupational therapy in home care, to follow the treatment set only as defined by the Occupational Therapist; to perform only those procedures that he/she is qualified and trained to perform and to make all recommendations for changes in the plan of care to the supervising Occupational Therapist. Following the plan of care, leads the patient in the use of therapeutic, creative, and self-care activities to improve functioning and safety. Observes, records, and reports to the supervising OT, the supervising nurse, and/or the physician the patient's response to treatment and changes in the patient's condition. Instructs patient, family, caregiver, and other members of the health care team in the areas of therapy in which they can participate to assist the patient. Visits patient according to Plan of Treatment; completes a progress note for each visit and submits progress notes per LHC policy. Participates in developing the Plan of Treatment. Participates in staff conferences and committees as necessary. All other duties as assigned. Qualifications License Requirements Current OTA licensure in the state of practice. Current CPR certification required. Current driver's license and vehicle insurance, and access to a dependable vehicle or public transportation. Company Description: Our company was founded over 20 years ago on the principle that its all about helping people, and we live by those words today. Its our mission to provide exceptional care and unparalleled service to patients and families who have placed their trust in us. We grow to fulfill this mission. When you become part of the LHC Group family, youre choosing a career path that will challenge you to grow both personally and professionally. Every day, all across the country, our LHC Group family is helping people. There are 10,000 of us, standing shoulder to shoulder, helping the patients in our care live, fuller, healthier lives. We do this because helping people is, quite simply, the reason we exist. Its our purpose. Associated topics: cht, certified occupational therapy assistant, cota, ffs, newborn care specialist, occupational, occupational therapist, occupational therapist ot, therapist, therapist ot

A webops platform has a current position open for a Telecommute Business Analyst. Individual must be able to fulfill the following responsibilities: Deliver

A business consulting and technology solutions provider is in need of a Remote Senior IT Director. Individual must be able to fulfill the following responsibilities