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Research And Development Manager
Bellisio Foods 4.1
Research and development specialist job in Columbus, OH
R&D Manager
The Research and Development (R&D) Manager at CP Foods North America will lead the planning, execution, and completion of new product development and existing product optimization projects, from concept through commercialization. This role requires a blend of scientific expertise, project management skills, and innovative thinking to ensure products meet market demands, quality standards, and regulatory requirements. The R&D Manager will foster a culture of innovation and collaborate closely with cross-functional teams including Marketing, Sales, Quality Assurance (QA), Operations, and Supply Chain.
Key Responsibilities
Product Development & Innovation: Drive the development of new and innovative food products and improve existing formulations to meet consumer needs and market trends.
Project Management: Oversee the R&D projects supported by the Columbus R&D team, ensuring projects are completed on time, within budget, and align with company objectives.
Team Leadership: Manage and mentor a team of food technologists and technicians, fostering a collaborative and innovative work environment.
Technical Expertise & Analysis: Provide technical leadership and support, including formulation, shelf-life stability testing, and sensory evaluation, for the projects supported by the R&D team. Strong knowledge of scientific process and application of experimental design in lab experiments and plant trials, including statistical analysis of results.
Scale-Up & Commercialization: Ensure trials have strong technical plans and are designed to ensure a seamless transition from lab to manufacturing. Partner with the Engineering, Quality and Operations teams to enable efficient start-up.
Quality & Regulatory Compliance: Work with quality and regulatory teams to ensure all products and processes comply with industry regulations and food safety standards (e.g., FDA, USDA, HACCP, GMPs, SQF).
Cross-Functional Collaboration: Partner with Marketing to translate consumer insights into project briefs, with Operations to ensure manufacturing feasibility, and with Procurement to source new ingredients and manage costs.
Documentation & Reporting: Maintain comprehensive documentation for product specifications, formulations, processing protocols, and project progress reports. Responsible for accurate documentation and protocol management for lab and pilot plant space in Columbus.
Qualifications & Skills
Education: Bachelor's or Master's degree in Food Science, Food Engineering, Culinary Science, or a related scientific field.
Experience:
Minimum of 5-10 years of R&D experience in the food manufacturing industry.
Proven experience managing R&D projects and leading cross-functional teams, experience with people management preferred.
Experience with commercializing products from concept to launch.
Technical Skills: Strong knowledge of ingredient functionality, food chemistry, processing techniques, and food safety systems.
Related Skills:
Excellent problem-solving, analytical, and critical thinking abilities.
Strong leadership, communication, and interpersonal skills.
Ability to manage multiple projects, prioritize tasks, and adapt to a fast-paced environment
Champions a “What If” attitude, searches and provides new ideas and solutions
Values collaboration and the power of team
Other job responsibilities as assigned
Location: Columbus, OH
Disclaimer
This job description indicates in general the nature and levels of work, knowledge, skills, abilities and other essential functions (as covered under the Americans with Disabilities Act) expected of an incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of an incumbent. Duties, responsibilities and activities may change at any time with or without notice.
$67k-104k yearly est. 2d ago
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Research Analyst (Remote)
Tilda Research
Remote research and development specialist job
About the Role
We are looking for candidates with excellent interpersonal and english communication skills, who can work in a Research Analyst role for our company. We are based in India and USA and this position will be fully remote, working from home.
You will have excellent email communication, document parsing and review skills to understand various clinical research related tasks and requirements. Some understanding of basic medical terminology is helpful, but not required. You will be a quick learner, with the ability to learn from online sources and get up to speed on various clinical research related topics like IRB interactions, Study Protocols, Delegation of Authority, inventory logs, etc.
We will provide some domain and job specific context, but we expect you to be able to learn on the job and be self‑motivated to perform.
Responsibilities
Interact with biotechnology and pharma clients over email and create specific regulatory and supporting documentation as required
Manage, fact‑check and enter data across various research related systems
Respond to any regulatory document requests by looking up the info in our local repository and sending emails back
Organize documentation, and get e‑Signatures from respective parties if required
Any administrative tasks which might come up
Requirements
MBA required
Excellent internet connection at home with video conference capability
Ability to work during late hours (1/2‑time overlap with US time zone)
Excellent spoken and written english communication
Ability to learn and use new technology and software
Attention to detail
About Tilda
The Tilda team has held various roles across all aspects of clinical trial management over the years. And during this time, we have often asked questions around clinical trial site management being so… inefficient, opaque, slow and broken. Our drive to find a solution, and our belief in technology to bridge the gap brought us together to build a new, ground‑up network of clinical trial sites, enabled by our technology platform. By investing in workflow automation, centralization and data integration across our sites, we are able to drive better study conduct metrics, and success for our physicians, pharma and CRO partners. We are inviting passionate individuals who can relate to our mission, to join our team of world‑class engineers, data scientists and clinical operations experts to reimagine the infrastructure for modern health innovation. We are a San Francisco based startup, backed by leading venture funds and industry leaders.
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$56k-94k yearly est. 19h ago
Market Development Specialist - Remote USA Position-Ameritas HQ is Lincoln, NE
Ameritas 4.7
Remote research and development specialist job
Back Market DevelopmentSpecialist #5660 Remote USA Position-Ameritas HQ is Lincoln, Nebraska, United States Apply X Facebook LinkedIn Email Copy Position Locations Remote USA Position-Ameritas HQ is Lincoln, Nebraska, United States Area of Interests Sales Full-Time/Part Time Full-time
Job Description
This individual will focus on securing new institutional and adopting employer sales for Ameritas. The position will establish new relationships as well as managing and driving greater sales within existing relationships. This position will have a heavy focus on the PEO, Association, MEP and PEP market.
The Market DevelopmentSpecialist is responsible for attaining the assigned annual sales goal by developing, supporting, and driving sales through key strategic relationships and increasing the number of adopting employers. These key relationships will include existing PEO/Association clients, PEO industry organizations (NAPEO, PACE, FAPEO), HRIS providers (PrismHR, iSolved), and other key intermediaries. In addition, this role will assist the Ameritas Retirement Plans Sales team with establishing new MEPs or PEPs, including coordinating the Sales paperwork and onboarding process.
Utilize verbal skills to communicate effectively to a wide array of distribution partners, while using effective listening and troubleshooting skills to help them solve for their problems. This role will be a good fit for someone who can demonstrate high levels of professionalism, sound judgment, strong analytical skills, prioritization and time management skills, and exemplary teamwork. To achieve the goals and priorities established the incumbent must exercise a great deal of personal discretion and judgment in maintaining objectivity among many groups/individuals, to communicate in a diplomatic manner, to effectively handle changing and/or stressful situations as well as to diffuse conflict and negotiate win-win outcomes.
This position is remote (within the U.S.A.) and does not require regular in-office presence.
What you do:
Partner with the Sales Director to prospect various distribution channels for institutional sales.
Develop and execute on client specific business plans for institutional sales designed to maximize results over time.
Proactively prospect and onboard new adopting employers for new and existing PEO, Association, MEP and PEP relationships.
Meet and exceed activity metrics as developed by VP of Sales.
Prepare and present proposals for Ameritas Retirement Plan products and services.
Partner with internal wholesaler (Regional Sales Consultant) and VP of Sales for development and execution of business strategy that produces maximum results.
Act as liaison between the client and Home Office as needed to ensure success.
Continuously enhance skills and retirement plan knowledge through professional development activities (Reading, formal/informal education, training classes, special projects/assignments).
Meet or exceed the annual sales objectives for the Institutional Sales team.
Communicate regularly with key internal partners, including but not limited to external sales reps, internal sales reps, relationship managers, and other key distribution personnel.
Develop/generate sales ideas and materials as needed to achieve results.
Gather and document competitive intelligence and industry insights for Senior Management and Field Partners.
Document all pertinent interaction and update any changes in the CRM system (SalesForce.com).
Maintain and update pipeline activity in CRM.
Perform other duties as assigned.
What you bring:
Bachelor's degree or equivalent combination of education and experience required.
4+ years of retirement plan industry and/or financial services industry knowledge and experience required.
Previous sales experience required. Proactive selling skills are very important.
Ability to analyze complex situations desired.
Life insurance license required. If not currently held, must be willing to obtain license within 6 months.
FINRA Series 6 or 7 licenses are required. If not currently held, must be willing to obtain licenses within 6 months.
Ability to travel nationally 25%-50% of the time is required.
What we offer:
A meaningful mission. Great benefits. A vibrant culture
Ameritas is an insurance, financial services and employee benefits provider Our purpose is fulfilling life. It means helping all kinds of people, at every age and stage, get more out of life.
At Ameritas, you'll find energizing work challenges. Flexible hybrid work options. Time for family and community. But dig deeper. Benefits at Ameritas cover things you expect -- and things you don't:
Ameritas Benefits
For your money:
* 401(k) Retirement Plan with company match and quarterly contribution.
* Tuition Reimbursement and Assistance.
* Incentive Program Bonuses.
* Competitive Pay.
For your time:
* Flexible Hybrid work.
* Thrive Days - Personal time off.
* Paid time off (PTO).
For your health and well-being:
* Health Benefits: Medical, Dental, Vision.
* Health Savings Account (HSA) with employer contribution.
* Well-being programs with financial rewards.
* Employee assistance program (EAP).
For your professional growth:
* Professional development programs.
* Leadership development programs.
* Employee resource groups.
* StrengthsFinder Program.
For your community:
* Matching donations program.
* Paid volunteer time- 8 hours per month.
For your family:
* Generous paid maternity leave and paternity leave.
* Fertility, surrogacy, and adoption assistance.
* Backup child, elder and pet care support.
An Equal Opportunity Employer
Ameritas has a reputation as a company that cares, and because everyone should feel safe bringing their authentic, whole self to work, we're committed to an inclusive culture and diverse workplace, enriched by our individual differences. We are an Equal Opportunity/Affirmative Action Employer that hires based on qualifications, positive attitude, and exemplary work ethic, regardless of sex, race, color, national origin, religion, age, disability, veteran status, genetic information, marital status, sexual orientation, gender identity or any other characteristic protected by law.
Application Deadline
This position will be open for a minimum of 3 business days or until filled.
This position is not open to individuals who are temporarily authorized to work in the U.S.
About this Position's Pay This is a sales position. The posted range reflects the base pay and variable compensation. The pay range posted reflects a nationwide minimum to maximum covering all potential locations where the position may be filled. The final determination on base pay for any position will be based on multiple factors including role, career level, work location, skill set, and candidate level of experience to ensure pay equity within the organization. This position will be eligible to participate in our comprehensive benefits package (see above for details). This position will be eligible to participate in our variable compensation program with a target defined by the applicable program. Job Details Pay Range Pay RangeThe estimated pay range for this job. Disclosing pay information promotes competitive and equitable pay.
The actual pay rate will depend on the person's qualifications and experience. $71,000.00 - $178,000.00 / year Pay Transparency Pay transparency is rooted in principles of fairness, equity, and accountability within the workplace. Sharing pay ranges for job postings is one way Ameritas shows our commitment to equitable compensation practices.
$51k-73k yearly est. 1d ago
Sterilization validation expert/R&D Microbiology(remote in Japan)
Environmental & Occupational
Remote research and development specialist job
We exist to create positive change for people and the planet. Join us and make a difference too! Job title: Technical Specialist and Scheme Manager (Microbiology)-relocation acceptable This role required to work in Japan or South Korea
Are you a Microbiologist, Sterilization Engineer, or Quality Manager looking for an interesting career change?
BSI hires qualified and experienced industry microbiologists to help clients navigate the areas of compliance within the areas of sterilization, packaging and microbiological testing outlined under ISO 13485. In this role you will have the opportunity to apply your sterile medical device experience to impact patient safety and help determine which new products go to market.
Technical Specialist Responsibilities:
* Responsible for planning, reporting and performing of audits of clients' management systems ensuring compliance with regulatory and voluntary requirements.
* Conduct comprehensive in-depth medical device reviews (including sterilization validation).
* Make recommendation whether to issue a certificate, based on objective evidence that the device is safe and effective.
The Technical Specialist - Microbiology role requires maturity to make difficult decisions regarding the benefits and risks of medical device products and whether to recommend certification. The individual must be able to clearly and confidently communicate with clients. Please carefully review the qualifications listed below and apply if you meet the criteria.
Education/Qualifications:
* A minimum of four (4) years' experience working as a microbiologist and/or sterilization engineer for a sterile medical device manufacturer
* Bachelor's degree (or higher) in Microbiology, Biology or related scientific degree
* Familiar with Gamma and EO sterilization
* Thorough knowledge of ISO 13485 quality standard and familiarity with Medical Devices Directive (MDD)/EU Medical Device Regulation (MDR)
* Quality management experience including significant participation in third party quality audits
* If you apply the role in Japan, then Native Japanese speaking required.
* If you apply the role in South Korea then Native Korean speaking required.
About Us
BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives.
Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments.
Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs.
Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society's critical issues - from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world.
BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.
$58k-93k yearly est. Auto-Apply 60d+ ago
Product Line Management II - (E2)
Applied Materials 4.5
Remote research and development specialist job
Who We Are Applied Materials is a global leader in materials engineering solutions used to produce virtually every new chip and advanced display in the world. We design, build and service cutting-edge equipment that helps our customers manufacture display and semiconductor chips - the brains of devices we use every day. As the foundation of the global electronics industry, Applied enables the exciting technologies that literally connect our world - like AI and IoT. If you want to push the boundaries of materials science and engineering to create next generation technology, join us to deliver material innovation that changes the world.
What We Offer
Salary:
$86,500.00 - $119,000.00
Location:
Austin,TX, Santa Clara,CA
You'll benefit from a supportive work culture that encourages you to learn, develop, and grow your career as you take on challenges and drive innovative solutions for our customers. We empower our team to push the boundaries of what is possible-while learning every day in a supportive leading global company. Visit our Careers website to learn more.
At Applied Materials, we care about the health and wellbeing of our employees. We're committed to providing programs and support that encourage personal and professional growth and care for you at work, at home, or wherever you may go. Learn more about our benefits.
Description
This role focuses on all research, development & engineering aspects of within Applied Materials Etch/SRP Service Business Unit (SBU) supporting Applied Materials' customer install base in the semi-conductor industry. This person will engage cross-functionally to drive product vitality including all new service product development and continuous improvement aspects of the business working to exceed customer and business expectations. Executes segment/functional business plans and contributes to the development of segment/functional strategy.
Responsibilities
* Responsible for program management of Research, Development and Engineering aspects of the Etch/SRP SBU including new service product development performance.
* Participate in developing service product roadmaps and managing product portfolios/investments.
* Leads customer application understanding and development to facilitate new product introduction.
* Accountable for the on-time delivery, cost and quality of new service products and technologies to support customer, operating plan and growth commitments of the Etch/SRP SBU.
* Participate in the development and execution of project management (PMP), product lifecycle processes (PLC), continuous improvement programs, ECO etc.
* Supports quality, productivity, spares and sustaining engineering initiatives partnering with customers and operations.
* Manages technology partners and supports new product related strategic sourcing needs partnering with strategic sourcing/supply chain.
* Leads sampling field quality processes working closely with field commercial resources Builds strong teams and cross-functional engagement across multiple geographies & external partners including Sales, Marketing, Operations, Finance, Legal etc. Communicates RD&E progress /execution to senior executives and stakeholders.
* Learn to troubleshoot tasks directly on hardware and system components. Understand and know how to operate basic mechanical and electrical tools (e.g., screwdrivers, torque wrenches, multimeters) for system setup and maintenance. Be able to learn how individual components interact within the overall system architecture.
Desired Skills, Competencies & Experience
* Bachelor's degree in a Science or Engineering discipline (Materials, Mechanical, Chemical, Physics, Electrical, or related field) required; Master's degree preferred. Prefer 2+ years of relevant experience. Prior experience with Etch and SRP processes is a plus.
* Experience and domain expertise in materials, deposition, plasma, and systems, along with proficiency in Tableau, Excel and other Microsoft Office applications.
* Semiconductor applications and services experience desired
* New product introduction experience with a performance-based track record
* Strong program management and product lifecycle management experience
* Customer focused - Voice of Customer (VOC) domain expertise and strong customer acumen
* Positive can-do hands-on entrepreneurial attitude that builds support for RD&E needs
* Strong communication skills and interpersonal presence that extends confidence and humility
* Ability to effectively manage and deliver to multiple Key Performance Indices (KPIs).
* Critical thinking and ability to influence and communicate effectively with cross-functional teams (Sales, finance, marketing, strategy, management).
* Highly organized and self-driven professional with a track record of successful project execution and superior time management
Additional Information
Time Type:
Full time
Employee Type:
Assignee / Regular
Travel:
Yes, 10% of the Time
Relocation Eligible:
Yes
The salary offered to a selected candidate will be based on multiple factors including location, hire grade, job-related knowledge, skills, experience, and with consideration of internal equity of our current team members. In addition to a comprehensive benefits package, candidates may be eligible for other forms of compensation such as participation in a bonus and a stock award program, as applicable.
For all sales roles, the posted salary range is the Target Total Cash (TTC) range for the role, which is the sum of base salary and target bonus amount at 100% goal achievement.
Applied Materials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.
In addition, Applied endeavors to make our careers site accessible to all users. If you would like to contact us regarding accessibility of our website or need assistance completing the application process, please contact us via e-mail at Accommodations_****************, or by calling our HR Direct Help Line at ************, option 1, and following the prompts to speak to an HR Advisor. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.
$86.5k-119k yearly Auto-Apply 6d ago
Lead R&D Data Scientist
Labcorp 4.5
Remote research and development specialist job
Labcorp Genetics (formerly Invitae) is dedicated to bringing comprehensive genetic information into mainstream medicine to improve healthcare for billions of people. Our team is driven to make a difference for the patients we serve. We are leading the transformation of the genetics industry, by making clinical-grade genetic information affordable and accessible to guide health decisions across all stages of life.
The genomics insights team leverages clinical genomic expertise, our massive genetics, laboratory and linked public/private datasets, and the latest AI/ML technologies to improve diagnosis, clinical care, and treatment options. We design and develop robust, quantitative, and scalable systems for variant interpretation and disease insights. Our research findings are broadly disseminated to improve testing guidelines, optimize reimbursement rates, and educate the healthcare ecosystem. We are seeking a Lead R&D Data Scientist to join our team and contribute to these initiatives.
Duties and Responsibilities:
Lead and deliver the translation of complex biological and clinical questions into actionable analysis plans.
Architect and implement robust data pipelines that integrate large-scale genomic, phenotypic, laboratory, and real-world clinical datasets.
Conduct repeatable data analysis and modeling with a high degree of scientific and statistical rigor, for complex tasks such as understanding patient trajectories, elucidating variant effect, and identifying genotype-phenotype associations.
Write clean, maintainable, and well-documented code following best practices for version control, testing, and scalability.
Prepare technical reports, peer-reviewed publications, and conference presentations to share research outcomes with internal stakeholders and the broader scientific community.
Collaborate closely with both internal and external stakeholders to drive impactful research and development initiatives.
Ensure high standards of data privacy, security, and compliance are maintained in all projects.
Qualifications:
Masters degree, or equivalent industry experience in Computer Science, Statistics, Data Science, Computational Biology, or a related field.
5+ years of hands-on experience in data science and statistical methods, as applied to large biomedical datasets.
Experience working within a collaborative technical team with strong software engineering practices.
Proficiency in modern programming languages (Python and SQL), shell scripting, and version control (Git).
Experience with data management, ETL, and business intelligence tools.
Excellent communication skills for presenting research findings to diverse audiences.
Preferred Qualifications:
Ph.D
Experience with big data technologies (Snowflake, Databricks, etc.) and visualization/dashboarding (Looker, Dash, etc.).
Experience with high performance computing (SGE etc.).
Experience in the development and validation of complex computational models for biological data, in particular machine learning and bioinformatics techniques.
Understanding of data privacy, security, and ethical considerations in clinical and biological research.
Previous published work in genetics, functional genomics, or clinical research.
This position is not eligible for visa sponsorship.
Application window closes: 02/14/2026
Pay Range: $100,000.00 - $155,000.00 a year
Schedule/Shift: M-F, 8-5 EST
All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.
The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers. Compensation may also include discretionary short- and long-term incentive packages.
Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.
$100k-155k yearly Auto-Apply 2d ago
Clinical Product Development Specialist
Gehc
Remote research and development specialist job
SummaryThe Clinical Product DevelopmentSpecialist will provide clinical input and expertise to the product development process. Works collaboratively with the engineering, design, clinical, and regulatory teams to ensure that product development addresses and solves clinical problems and that product performance meets the needs of users. Works in the early stages of data collection, algorithm tuning, and performance evaluations of new technologies. Provides sonographer input and support to engineering programs.Job Description
The GEHC Advanced Visualization Solutions (AVS) segment, a fast-growing business in GE HealthCare, includes ultrasound medical devices and solutions as well as image guided therapies. The portfolio spans the continuum of care to enable customers with ultrasound screening, diagnosis, treatment and monitoring of diseases. Our customers are seeking to improve efficiency in radiology and beyond and increase user confidence to provide better clinical outcomes continues to grow. Consequently, the need for AI, digital solutions, and automation, connecting devices and software in one seamless ecosystem continues to proliferate.
The Ultrasound AI COE team focuses on developing AI solutions for scan guidance and interpretation, to aid in early disease detection, improve workflow and productivity across many different ultrasound applications and care areas. The Clinical Product DevelopmentSpecialist is a key role on the Product team. This individual will leverage deep clinical expertise and ultrasound product experience to provide clinical input for development of breakthrough AI features.
Essential Responsibilities:
Work with product managers to identify opportunities for new technology developments and define requirements from a clinical perspective.
Provide clinical input as part of the product extended core team. Work with engineers to evaluate the performance of prototypes, provide input during defect management and risk mitigation processes.
Plan and execute clinical data collection to support engineering for both near and longer-term product developments.
Coordinate image and study labeling and analysis with sonographer and physician partners
Support needed in planning and executing validation tests
Plan and execute internal product verification and validation tests that require sonographer expertise
Design and support user training activities related to new product assessment
Identify continuous improvement activities by initiating the implementation of process and product quality improvement initiatives.
Support the regulatory and quality teams in validation components of design controls
Test the product with customers and analyze product feedback
Perform other duties as assigned
Required Qualifications:
Registered sonographer with relevant certifications.
At least 7 years of hands-on sonography experience including in clinical settings
Desired Characteristics:
10+ years' sonography experience, expertise in cardiac ultrasound strongly preferred
Industry experience in product development desired, including good technical understanding of ultrasound imaging systems and DICOM data handling.
Experience in conducting and managing medical imaging annotation for machine learning model development and testing a plus
Experience in teaching ultrasound or training of new users
Experience with formal clinical research protocols
Strong oral and written communication skills, excellent interpersonal and leadership skills.
Demonstrated ability to analyze and resolve problems.
Eligibility Requirements:
This position is based in the United States only. Legal authorization to work in the U.S. is required. GE HealthCare may agree to sponsor an individual for an employment visa now or in the future if there is a shortage of individuals with particular skills.
Must be willing to travel as required (up to 25% on occasion).
About Us
GE HealthCare is a leading global medical technology, pharmaceutical diagnostics, and digital solutions innovator, dedicated to providing integrated solutions, services, and data analytics to make hospitals more efficient, clinicians more effective, therapies more precise, and patients healthier and happier. Serving patients and providers for more than 100 years, GE HealthCare is advancing personalized, connected, and compassionate care, while simplifying the patient's journey across the care pathway. Together our Imaging, Ultrasound, Patient Care Solutions, and Pharmaceutical Diagnostics businesses help improve patient care from prevention and screening, to diagnosis, treatment, therapy, and monitoring. We are an $18 billion business with 51,000 employees working to create a world where healthcare has no limits.
We will not sponsor individuals for employment visas, now or in the future, for this job opening. For U.S. based positions only, the pay range for this position is $115,200.00-$172,800.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement.Additional Information
GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.
Relocation Assistance Provided: No
$115.2k-172.8k yearly Auto-Apply 60d+ ago
Product Development Analyst (Hybrid)
Concordance Healthcare Solutions Careers 3.5
Remote research and development specialist job
At Concordance Healthcare Solutions, we believe that each team member makes a difference in driving our purpose of positively impacting lives forward. Concordance is committed to our guiding principles of financial stewardship, accountability, forward thinking, aligned relationships and an inclusive culture. This is done through maintaining an unwavering amount of respect and commitment with our employees and customers, being authentic to who we are and operating with the highest levels of integrity. Through our dedicated staff of over 750 employees, working in strategically-located distribution centers across the country, we offer dynamic supply chain solutions to the entire healthcare continuum.
We have a job opening and exciting opportunity for a full-time Product Development Analyst in our Tiffin, OH location. The Product Development Analyst supports the design, development, and launch of new and existing products within Concordance Healthcare Solutions' portfolio. This role bridges clinical knowledge, market insight, and operational execution to ensure products meet customer needs, regulatory standards, and strategic growth objectives. The Specialist partners closely with Marketing, Sourcing, Sales, and Supplier Relations teams to drive private-label product initiatives from concept through commercialization.
Essential Functions:
Assist in product design, packaging artwork, and labeling to ensure compliance, consistency, and brand alignment.
Collaborate with suppliers to gather technical specifications, Instructions for Use (IFUs), and regulatory documentation.
Support the Product Approval Team (PAT) process and facilitate timely product launches.
Evaluate substitute products and cross-reference alternatives to optimize availability and support conversions.
Apply clinical knowledge to assess product usability, performance, and healthcare applicability.
Support Sales and Marketing teams with product knowledge and training.
Conduct product performance analysis, usage tracking, and competitive benchmarking.
Provide data-driven insights and ROI reporting to guide sourcing and sales strategies.
Deliver professional presentations to internal teams, suppliers, and customers.
Act as a liaison between Marketing, Sourcing, and vendor partners to ensure project alignment.
Partner with cross-functional stakeholders to identify growth opportunities and streamline processes.
Timely completion of product development and launch milestones.
Accuracy and compliance of product artwork and IFU documentation.
Successful execution of cross-reference projects and substitute product identifications.
Sales team satisfaction with product support and analytics.
Contribution to private-label (HCS) growth and category expansion.
Other duties as assigned.
What You Will Need To Be Successful:
Bachelor's Degree or higher in Business, Healthcare Administration, Marketing or a related field or equivalent combination of education and experience.
Clinical background or exposure to medical products required.
2-4 years of experience in product development, sourcing, or healthcare distribution preferred.
Familiarity with FDA, AAMI, and other healthcare regulatory requirements a plus.
Prior experience in packaging, labeling, or artwork review strongly desired.
Knowledge of healthcare distribution, clinical products, and regulatory requirements a must.
Strong analytical and problem-solving skills with a data-driven mindset.
Ability to communicate effectively across technical, clinical, and commercial audiences.
Presentation and training delivery skills.
Proficiency with Microsoft Office Suite (Excel, PowerPoint, Word) and data visualization tools.
Strong organizational and project management skills with the ability to prioritize tasks effectively.
Successfully pass a pre-employment (post-offer) background check and drug screening.
Work Location:
This role is located in Tiffin, OH.
With the possibility of a work from home hybrid model (in office part of the week and remote part of the week).
We offer great benefits and competitive pay!
Health, Life, Dental, Vision Insurance
Paid Vacation and Paid Sick Leave, Paid Holiday
401K Retirement Plan - Company match
Company paid Short Term & Long Term Disability
Concordance Healthcare Solutions, LLC is committed to being the most respected, innovative, national, multi-market healthcare solutions company earning the highest level of trust by operating with integrity, unwavering commitment and exceptional service through our culture of excellence. Through our dedicated staff of over 900 employees, working in strategically-located distribution centers across the country, we offer dynamic supply chain solutions to the entire healthcare continuum.
Concordance Healthcare Solutions is proud to provide Equal Employment Opportunities to all individuals for employment and prohibits any kind of discrimination on the basis of race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, or any other characteristic protected by federal, state or local laws.
Consistent with the Americans with Disabilities Act, our organization is committed to providing reasonable accommodation to qualified applicants and employees as requested. If reasonable accommodation is necessary for the interview process, please contact hr-admin@concordancehs.com.
Position will remain open until filled. Interested applicants should apply on-line at http://www.concordancehealthcare.com/careers. Internal employees should apply on-line through UKG Pro by selecting Menu > Myself > My Company > View Opportunities
$55k-84k yearly est. 60d+ ago
Specialist - Research-Fixed Term
MSU Careers Details 3.8
Remote research and development specialist job
The Education Policy Innovation Collaborative (EPIC) at Michigan State University (MSU) is seeking a researchspecialist to join EPIC leadership to work on externally-funded multi-year projects. EPIC is a policy lab located within the College of Education. EPIC partners with state and local education leaders to produce rigorous and objective multi-method research with consequence that strengthens evidence-based decision-making for practice and policy in Michigan, with implications for historically underserved students throughout the country. The researchspecialist will join the EPIC team in a leadership role to work on one or more externally-funded EPIC research projects. The EPIC team includes Dr. Madeline Mavrogordato, Faculty Director, Emily Mohr, Managing Director, Dr. Tara Kilbride, Associate Director, postdoctoral researchers, research staff, affiliated faculty, and doctoral students.
Duties for the researchspecialist will include some or all of the following:
Leading center-wide, partner-driven research projects that examine the impact of policies and programs using large-scale longitudinal administrative data from the State of Michigan, as well as survey and interview data collected by EPIC Acting as a representative of EPIC and MSU to research partners at state agencies, local school districts, and education organizations.
Providing expertise in quantitative methodologies that includes substantial experience conducting statistical/econometric analysis and quasi-experimental design using panel data in STATA Writing, editing, and guiding the development of clear and concise publications, including manuscripts for academic journal articles, stakeholder-facing research reports and policy briefs, and presentation materials appropriate for both academic and general audiences.
Providing oversight, mentoring, training, and professional development to other EPIC researchers;
Responding to ad hoc data and analysis requests, both internal and external Representing EPIC by fielding media requests and conducting interviews.
Giving presentations to academic and policy stakeholder audiences.
Assisting with the development of grant proposals Producing data summaries, tables and visualizations.
Other duties as appropriate based on the specific interests and expertise of the selected candidate.
The researchspecialist will oversee doctoral research assistants and collaborate with EPIC staff to ensure all research products are timely, accurate, and actionable. We are seeking a person who is excited to be a member of a dynamic and motivated group, and who is driven by a desire to produce both rigorous and policy-relevant research aimed at driving improvements for Michigan students. The position, which includes benefits, is a fixed term annual, 100% time position beginning January 5, 2026 with the potential for annual renewals in the College of Education.
Equal Employment Opportunity Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, age, disability or protected veteran status.
Required Degree
Doctorate -Education, public policy, economics, statistics, social science or a similar field
Minimum Requirements
A Ph.D. in education, public policy, economics, statistics, social science or a similar field Significant expertise with STATA statistical software.
Expertise in standard econometric models and techniques.
Experience with large-scale quantitative data management and analysis.
Experience planning and executing quality assurance on complex analyses using large-scale data sets.
Demonstrated knowledge and interest in partner-orientated education research.
Extreme attention to detail and strong organizational skills.
Proficiency in Microsoft Office Suite products.
Ability to manage multiple projects and competing priorities with little supervision, as well as maintain flexibility.
Excellent interpersonal, verbal, and written communication skills.
Desired Qualifications
Research project management experience, including developing and maintaining project timelines with contingency plans, supervising and coordinating the work of others and ensuring project deliverables are met to a high standard for quality and accuracy.
Experience with data collection and analysis activities across a large team.
Experience presenting research products to a wide variety of audiences.
Required Application Materials
Interested candidates should send:
1) a letter of application stating qualifications for and reasons for interest in this position;
2) current resume or curriculum vitae;
3) the names and contact information for three references,
4) a writing sample produced for an academic audience,
5) a research product designed for a research partner (e.g., policymaker, practitioner) audience.
Special Instructions
Questions can be directed to Emily Mohr at emohr@msu.edu.
Review of Applications Begins On
10/24/2025
Remote Work Statement
MSU strives to provide a flexible work environment and this position has been designated as remote-friendly. Remote-friendly means some or all of the duties can be performed remotely as mutually agreed upon.
Website
https://epicedpolicy.org/
MSU Statement
Michigan State University has been advancing the common good with uncommon will for more than 160 years. One of the top research universities in the world, MSU pushes the boundaries of discovery and forges enduring partnerships to solve the most pressing global challenges while providing life-changing opportunities to a diverse and inclusive academic community through more than 200 programs of study in 17 degree-granting colleges.
$53k-80k yearly est. 60d+ ago
Growth Product Lead, Loyalty
Trafilea
Remote research and development specialist job
Trafilea is a Consumer Tech Platform for Transformative Brand Growth. We're building the AI Growth Engine that powers the next generation of consumer brands.
With over $1B+ in cumulative revenue, 12M+ customers, and 500+ talents across 19 countries, we combine technology, growth marketing, and operational excellence to scale purpose-driven, digitally native brands.
We own and operate our own digitally native brands (not an agency), with presence in Walmart, Nordstrom, and Amazon, and a strong global D2C footprint.
Why Trafilea
We're a tech-led eCommerce group scaling our own globally loved DTC brands, while helping ambitious talent grow just as fast.
🚀 We build and scale our own brands.
🦾 We invest in AI and automation like few others in eCom.
📈 We test fast, grow fast, and help you do the same.
🤝 Be part of a dynamic, diverse, and talented global team.
🌍 100% Remote, USD competitive salary, paid time off, and more.
Job Responsibilities
We're looking for a creative and results-oriented Growth Product Lead to design and deliver hands-on, value-driven experiences that customers engage with on a recurring basis.
Our Subscriptions Tribe is responsible for scaling programs like Shapermint Club, Autoship, ShaperBox, and Credits into sustainable, high-performing initiatives that drive recurring revenue, increase order share, and maximize customer lifetime value.
As Product Lead - Subscriptions & Loyalty, you will partner closely with Product Manager Camila Rodríguez and the Subscriptions Tribe to execute initiatives that strengthen retention, optimize subscription funnels, and deliver measurable improvements in churn, repurchase rate, and LTV.
Own subscription growth experiments across Club, Autoship, Shaperbox, and Credits, turning hypotheses into MVPs and quick-win pilots.
Map and optimize subscription journeys (onboarding, renewal, cancellation) to reduce friction and improve retention.
Execute data-driven initiatives with clear KPIs (churn, RR45D, LTV uplift) and share insights through dashboards and reports.
Collaborate daily with Product, Marketing, CX, BI, and Tech to align on roadmap priorities and manage dependencies.
Design bold retention mechanics and personalization flows based on customer feedback, cohort analysis, and behavioral signals.
Drive influencer/ambassador-style engagement by ensuring community-driven and loyalty mechanics connect with customer needs.
Run agile practices (sprints, stand-ups, retros) to keep squads accountable and reduce operational load for Tribe leadership.
Prioritize and scale successful pilots into playbooks for global markets (US, CA, UK, AU), fueling recurring revenue growth.
Job requirements
2-4 years of experience in Growth/Product, ideally in e-commerce or SaaS.
Strong growth-marketing mindset: designs hypotheses, tests quickly, iterates weekly.
Fluent in cohort analysis, dashboards, churn, and retention metrics.
Execution-driven: hands-on with no-code pilots, flow-building, and CRM triggers.
Strong collaboration in cross-functional squads.
Clear communication: async documentation and storytelling with data.
Exposure to subscriptions or loyalty; deeper technical/financial skills to be built on the job.
Basic agile methodology knowledge with willingness to own squad leadership practices.
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$69k-93k yearly est. 60d+ ago
R&D Technician
Mindlance 4.6
Research and development specialist job in Columbus, OH
Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at *************************
Job Description
Major Responsibilities: Responsible for implementing and maintaining the effectiveness of the quality system. · Weighs ingredients, prepares batches, and supports production at the product research
center · Submits samples for analysis and consolidates/tabulates results ·
Organizes non-routine testing, completes these tests and summarizes results
B.S. in Food Science and Technology, Chemistry or Sciences preferred. 0 - 3
years technical work experience, preferably in developing food/nutritional
products The candidate should also demonstrate the ability to handle multiple
priorities as well as a good work ethic
Qualifications
B.S. in Food Science and Technology, Chemistry or Sciences preferred. 0 - 3
years technical work experience, preferably in developing food/nutritional
products
Additional Information
Thanks & Regards
___________________________________________________________________________
Riya Seth | Team Recruitment | Mindlance, Inc. | W: ************
$59k-80k yearly est. 60d+ ago
Clinical Development Scientist - Lilly Gene Therapy, Sensory
Eli Lilly and Company 4.6
Remote research and development specialist job
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Organization Overview
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Role Overview
The Clinical Development Scientist is a clinical trialist with clinical trial experience responsible for management of clinical supply (in collaboration with Supply Chain) and implementation of clinical supply/device trainings (in collaboration with other functional areas) for global clinical programs. They will be responsible for development of training materials and ensure timely planning and implementation of clinical supply/device trainings.
The Clinical Development Scientist will also collaborate cross-functionally to support the clinical and scientific execution of all Lilly Gene Therapy clinical and preclinical programs, as needed. They will ensure timely planning, implementation, management, and reporting of clinical studies and trials. The successful candidate will collaborate cross-functionally to support all Lilly Gene Therapy Sensory clinical programs and provide clinical/scientific support to clinical trial sites and CROs.
Responsibilities:
Develop and manage updates of trial documents related to clinical supplies
Develop training materials for clinical supply training sessions for clinical trial sites and CROs (if applicable) and manage the training material updates
Collaborate both internally and externally to facilitate clinical trial site activities to ensure sites are ready for dose administration at site activation and throughout the trial
Lead the efforts to conduct training sessions related to clinical materials and supplies
Serve as the clinical development representative to work with Clinical Supply Management in supply management, demand forecasting, shipment operation/logistics, etc.
Serve as the clinical/scientific representative for assigned clinical trials, as well as program teams, and facilitate the clinical/scientific execution of clinical and preclinical programs, as needed
Support the clinical operations team, including clinical trial manager, in achieving trial deliverables, including adherence to budget and timelines, and developing trial documents, procedures, and plans
Support authorship and review of clinical/regulatory documents (
e.g
., clinical protocols, Investigator Brochures, clinical study reports, briefing packages, etc.); collaborate cross-functionally in planning regulatory strategy and communications
Other duties as assigned or as business needs require
Basic Qualifications:
Bachelor's degree in the Life Sciences required
A minimum of two (2) years of pharmaceutical and/or clinical experience
Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization and/or visas for this role
Additional Skills / Preferences:
Master's or higher level degree preferred (ie. PharmD, PhD, etc,..)
Global clinical trials in the rare disease area
Clinical/investigational pharmacy with gene therapy products or clinical supply management
Prior pharma/biotech or academic experience in rare disease, otology, audiology, gene therapy, cellular therapy, and/or medical device preferred
Proven track record of successfully conducting/supporting clinical trials and associated development activities
Comprehensive understanding of the drug development and approval processes, and clinical trial design
Strong interpersonal skills required
Strong problem-solving skills, including the ability to identify and evaluate the critical factors of obstacles or opportunities; given background, experience, and judgment, able to understand potential causes and deliver potential solutions
Ability to plan and think strategically and critically; intellectually curious, willing to take ownership of the assigned tasks and support clinical/pipeline programs, as needed
Ability to critically evaluate and analyze scientific data and literature
Strong communication skills (written and verbal) including the ability to express oneself clearly and concisely, and to message and document key progress and challenges appropriately; excellent presentation skills required
Capable of representing Lilly Gene Therapy professionally with external global opinion leaders, investigators, vendors, regulatory agencies, and others
Ability to work effectively cross-functionally, and to serve as clinical resource within the company
Self-motivated and detail-oriented with ability to prioritize and handle multiple projects
Additional Information:
Travel may be up to 15%, including international travel
Location: USA Remote
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$63,000 - $154,000
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
$63k-154k yearly Auto-Apply 6d ago
Product Development Analyst I- P&C
Emergent Holdings Career Section
Research and development specialist job in Westerville, OH
Product Development Analyst I is responsible for the oversight and development of new and updated products, working closely with leaders from Underwriting, Claims, Compliance, General Counsel, and Corporate Underwriting.
This position assists the Manager of Product Development and Compliance in developing, maintaining, and reviewing bureau coverage forms and endorsements to provide Specialty Lines business units with access to quality policy language and products.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
Coordinating the Product Development process for Specialty Lines, including:
Reviewing current policy forms and endorsements to analyze and identify unforeseen or unanticipated liabilities.
Reviewing forms for new products to identify gaps and limitations in proposed policy language.
Researching legal and statutory requirements by state for new and existing products.
Maintains the historical record of Specialty Lines forms and collaborating with Corporate Underwriting to update and maintain the AF Group Forms Library for Specialty Lines.
2. Collaborating with Underwriting and Claims to ensure consistency in policy language and claim-
handling. This includes:
Working with Claims to ensure underwriters are kept apprised of potentially unforeseen or unanticipated liabilities due to policy form and endorsement language, as well as emerging claim and legal trends.
Prepares draft forms and revisions for existing products and exposures for presentation to Leadership.
Communicating the publishing of new or updated policy forms and endorsements to floor underwriters.
3. Coordinating Underwriting compliance for all Specialty Lines, including:
With Management, responding to the states regarding Underwriting and Compliance complaints.
Reviewing bulletins and circulars from trade organizations and the states to assess for applicability to Specialty Lines products and processes and referring as necessary.
4. Keeping abreast of external industry developments, including in the legislative and judicial arenas. This includes:
Assisting in the review ISO, AAIS and other bureau-driven circulars and products. Referring recommended form and product changes to Management to align with AF Group's strategic direction across Specialty Lines organizations.
5. Product Development and Product Compliance
Reviewing recommended form and product changes to align with Specialty Lines strategic direction, recommend implementation options, and lead prioritization of coverage enhancements across the Division.
Preparing, monitoring, drafting, and obtaining regulatory approval of rates, rules, and forms utilized by admitted products within Specialty Lines.
With Management, developing responses to objections to admitted products within Specialty Lines.
EDUCATION AND EXPERIENCE
Relevant combination of education and experience may be considered in lieu of degree.
Bachelor's degree required.
CPCU or ARM preferred.
Three (3) to five (5) years of experience in P&C Underwriting, Product Management, or Product Development required.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
OTHER SKILLS AND ABILITIES
Extensive knowledge of insurance and underwriting environment across all lines of business (Casualty / Property - Admitted / Non-Admitted - Assigned Risk).
Ability to analyze and synthesize information for broad consumption.
Technical acumen and the ability to command technical content for various audiences.
Ability to effectively exchange information, in verbal or written form, by sharing ideas, reporting facts and other information, responding to questions, and employing active listening techniques.
Ability to work effectively in a team environment and individually.
Good communication (written and verbal), organizational, and planning skills.
ADDITIONAL INFORMATION
The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. This does not constitute a contract for employment.
WORKING CONDITIONS
Work is performed in office with minimal hazards. Travel may be required, with occasional overnight stay. Ability to lift and carry computer equipment weighing up to 35 lbs. Driver's license is required.
The qualifications listed above are intended to represent the minimum education, experience, skills, knowledge and ability levels associated with performing the duties and responsibilities contained in this job description.
Pay Range - Actual compensation decision relies on the consideration of internal equity, candidate's skills and professional experience, geographic location, market, and other potential factors. It is not standard practice for an offer to be at or near the top of the range, and therefore a reasonable estimate for this role is between $56,700 and $94,900.
We are an Equal Opportunity Employer. We will not tolerate discrimination or harassment in any form. Candidates for the position stated above are hired on an "at will" basis. Nothing herein is intended to create a contract.
#LI-TM1 #CIG
$56.7k-94.9k yearly Auto-Apply 11d ago
Product Development Analyst I- P&C
Emergent Holdings, Inc.
Research and development specialist job in Westerville, OH
Product Development Analyst I is responsible for the oversight and development of new and updated products, working closely with leaders from Underwriting, Claims, Compliance, General Counsel, and Corporate Underwriting.
This position assists the Manager of Product Development and Compliance in developing, maintaining, and reviewing bureau coverage forms and endorsements to provide Specialty Lines business units with access to quality policy language and products.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
Coordinating the Product Development process for Specialty Lines, including:
Reviewing current policy forms and endorsements to analyze and identify unforeseen or unanticipated liabilities.
Reviewing forms for new products to identify gaps and limitations in proposed policy language.
Researching legal and statutory requirements by state for new and existing products.
Maintains the historical record of Specialty Lines forms and collaborating with Corporate Underwriting to update and maintain the AF Group Forms Library for Specialty Lines.
2. Collaborating with Underwriting and Claims to ensure consistency in policy language and claim-
handling. This includes:
Working with Claims to ensure underwriters are kept apprised of potentially unforeseen or unanticipated liabilities due to policy form and endorsement language, as well as emerging claim and legal trends.
Prepares draft forms and revisions for existing products and exposures for presentation to Leadership.
Communicating the publishing of new or updated policy forms and endorsements to floor underwriters.
3. Coordinating Underwriting compliance for all Specialty Lines, including:
With Management, responding to the states regarding Underwriting and Compliance complaints.
Reviewing bulletins and circulars from trade organizations and the states to assess for applicability to Specialty Lines products and processes and referring as necessary.
4. Keeping abreast of external industry developments, including in the legislative and judicial arenas. This includes:
Assisting in the review ISO, AAIS and other bureau-driven circulars and products. Referring recommended form and product changes to Management to align with AF Group's strategic direction across Specialty Lines organizations.
5. Product Development and Product Compliance
Reviewing recommended form and product changes to align with Specialty Lines strategic direction, recommend implementation options, and lead prioritization of coverage enhancements across the Division.
Preparing, monitoring, drafting, and obtaining regulatory approval of rates, rules, and forms utilized by admitted products within Specialty Lines.
With Management, developing responses to objections to admitted products within Specialty Lines.
EDUCATION AND EXPERIENCE
Relevant combination of education and experience may be considered in lieu of degree.
Bachelor's degree required.
CPCU or ARM preferred.
Three (3) to five (5) years of experience in P&C Underwriting, Product Management, or Product Development required.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
OTHER SKILLS AND ABILITIES
Extensive knowledge of insurance and underwriting environment across all lines of business (Casualty / Property - Admitted / Non-Admitted - Assigned Risk).
Ability to analyze and synthesize information for broad consumption.
Technical acumen and the ability to command technical content for various audiences.
Ability to effectively exchange information, in verbal or written form, by sharing ideas, reporting facts and other information, responding to questions, and employing active listening techniques.
Ability to work effectively in a team environment and individually.
Good communication (written and verbal), organizational, and planning skills.
ADDITIONAL INFORMATION
The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. This does not constitute a contract for employment.
WORKING CONDITIONS
Work is performed in office with minimal hazards. Travel may be required, with occasional overnight stay. Ability to lift and carry computer equipment weighing up to 35 lbs. Driver's license is required.
The qualifications listed above are intended to represent the minimum education, experience, skills, knowledge and ability levels associated with performing the duties and responsibilities contained in this job description.
Pay Range - Actual compensation decision relies on the consideration of internal equity, candidate's skills and professional experience, geographic location, market, and other potential factors. It is not standard practice for an offer to be at or near the top of the range, and therefore a reasonable estimate for this role is between $56,700 and $94,900.
We are an Equal Opportunity Employer. We will not tolerate discrimination or harassment in any form. Candidates for the position stated above are hired on an "at will" basis. Nothing herein is intended to create a contract.
#LI-TM1 #CIG
$56.7k-94.9k yearly Auto-Apply 11d ago
Advisor, Supply Chain Product Management
Cardinal Health 4.4
Research and development specialist job in Dublin, OH
What does Supply Chain Product Management contribute to Cardinal Health
Operations is responsible for materials handling and product distribution in a distribution or manufacturing environment. Includes warehousing and fulfillment of materials and products, transportation, inventory management as well as demand, supply and manufacturing planning. Supply Chain Product Management is responsible for identifying, recommending, designing and implementing new solutions for the Supply Chain organization including new technology features, practices, processes, metrics or models. Supply Chain Product Management develops the strategic vision, supporting business case, delivering product timeline, and financials for new products.
The Cardinal Health Supply Chain Product Management team delivers products and services that create a differentiated experience for customers while relentlessly improving speed, reliability, and cost through supply chain optimization. We enable growth through effective and efficient movement of over 45 million shipments for Cardinal Health customers. This includes the flow of materials and products between suppliers, manufacturers, and customers.
As an Associate Product Manager / Advisor on the Supply Chain Product Management team, you will play a key role in supporting efforts to enable end to end supply chain system flows for transportation, inventory, and/or warehouse management activities and business processes. Working with supply chain functional business partners, your focus will be on successful execution of holistic solutions for the Pharmaceutical Supply Chain. You will be a critical contributor in the delivery of innovative, market leading solutions that drive operational efficiencies, reduce costs, enhance customer experience and satisfaction. Your work will contribute towards the end vision of a connected supply chain product portfolio with cognitive capabilities that optimize the Pharma supply chain through automated processes along with the ability to predict trends or unexpected events, react in real-time, and provide insights to the business to ensure the best possible service to Cardinal Health customers.
Responsibilities
Attends and actively participates in agile ceremonies, asking questions of both business and IT to understand business needs and solutions (how and what), and explores product and solution analytics for understanding
Collaborates with Product Manager in the exploration of new / innovative technologies and participates in product discovery efforts and leads smaller discovery sessions for enhancements
Partners with enterprise IT on day to day execution, participates in daily Agile / SCRUM ceremonies owning documentation, updates tickets and statuses regularly, recap notes, and communication to stakeholders.
Works cross functionally and collaborates with Customer Service, Transportation Operations, and Sales team members to research, define, and create user personas, business processes, and user journey maps.
Refines backlog of product backlog items (user stories, tasks) that are prioritized and ready for the next sprint cycle, identifies trade-offs and determines path forward with support as needed from manager; takes action to resolve challenges at team level, communicates blockers in timely fashion
Uses analytics to lead backlog refinement, planning, and to measure progress against product strategy.
Responsible for the publishing and maintenance of product metrics dashboards and communications to stakeholders.
Supports the Product Manager in measuring success of products deployed, through the co-creation of Key Performance Indicators, target adoption rates, and financial impact targets.
Understands how their product/solution contribution to value within the overall portfolio and program, contributes to defining OKRs, collaborates with cross-functional teammates to articulate requirements for solutions
Ensures high-quality solution delivery by participating in product launch activities, such as pre-UAT testing and validation and rollout communication/training
Qualifications
Bachelor's Degree in Business, Supply Chain or related field, or equivalent work experience, preferred
3+ years of experience in Inventory Management, Supply Chain, or Business roles preferred
Sharp analytical and problem-solving skills
Outstanding communication, presentation, and leadership skills
Strong proficiency with Microsoft Office products
Professional level business writing skills: a writing sample will be requested as part of the interview process
Knowledge of Agile processes and principles is a plus
What is expected of you and others at this level
Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects
May contribute to the development of policies and procedures
Works on complex projects of large scope
Develops technical solutions to a wide range of difficult problems
Solutions are innovative and consistent with organization objectives
Completes work independently; receives general guidance on new projects
Work reviewed for purpose of meeting objectives
May act as a mentor to less experienced colleagues
Anticipated salary range: $80,900 - $92,400
Bonus eligible: No
Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
Medical, dental and vision coverage
Paid time off plan
Health savings account (HSA)
401k savings plan
Access to wages before pay day with my FlexPay
Flexible spending accounts (FSAs)
Short- and long-term disability coverage
Work-Life resources
Paid parental leave
Healthy lifestyle programs
Application window anticipated to close: 3/13/2026 *if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.
To read and review this privacy notice click
here
$80.9k-92.4k yearly Auto-Apply 4d ago
Chemistry R&D Lab Technician (Pharmaceuticals)
Actalent
Research and development specialist job in Columbus, OH
We are hiring for a Chemistry Lab Technician in the Pharmaceutical industry here in the Columbus, Ohio area. This is a long-term career opportunity for someone looking to grow in the sciences. This role will primarily be supporting the research and development team by performing testing on generic pharmaceutical products. An ideal candidate for this role will have a Bachelors Degree in a scientific field - with a strong preference for Chemistry, Biochemistry, or Pharmaceutical Science degrees.
Shift: 1st shift, Monday - Friday, 8am - 4:30pm
Job Description
This role will primarily be performing R&D laboratory testing on generic pharmaceutical products. Testing will primarily be chemistry focused and job duties will include:
* Conducts chemical and physical analyses in support of the development of a manufacturable multisource pharmaceutical product. Provides analytical support for the release of registration materials in support of regulatory submissions. Assists analytical method validation and transfer activities.
* Performs the assigned analytical tasks in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with cGXP's, and company practices and procedures.
* Follows work instructions, SOPs and company practices. Documents analytical activities and results accurately, in a timely manner and right-first time and maintains integrity of data.
* Follows written analytical procedures. Identifies execution challenges of analytical methods and support trouble shooting activities.
Bench Work will include:
* Sample prep
* Standard weighs
* Wet Chemistry
* Dilutions
* Titrations
* HPLC
* NGI testing
* Admitted dose testing
* May perform other chemistry testing as needed.
Qualifications:
* Bachelor's degree in a science field with strong chemistry coursework
Job Type & Location
This is a Permanent position based out of Columbus, OH.
Pay and Benefits
The pay range for this position is $24.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Columbus,OH.
Application Deadline
This position is anticipated to close on Jan 19, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
$24-24 hourly 10d ago
APP Primary Care Marion Barks Rd
Ohio Health 3.3
Research and development specialist job in Marion, OH
We are more than a health system. We are a belief system. We believe wellness and sickness are both part of a lifelong partnership, and that everyone could use an expert guide. We work hard, care deeply and reach further to help people uncover their own power to be healthy. We inspire hope. We learn, grow, and achieve more - in our careers and in our communities.
Summary:
The Advanced Practice Providers (APP), Physician Assistant (PA) or Advanced Practice Registered Nurse (APRN) including Clinical Nurse Specialist (CNS) or Nurse Practitioner (NP), work in collaboration with the physician in the outpatient setting (in-person or Telehealth). Primary care offices or clinics can include family medicine, pediatrics, or internal medicine. The Primary Care APP may perform minimally invasive procedures and generally works with a stable patient population.
Responsibilities And Duties:
Works under direction and in consultation/collaboration with physician and may perform services authorized by the supervising/collaborating physician that are part of the physician's normal course of practice and expertise. Promotes quality outcomes and initiatives. Must have a Supervision Agreement (SA) or Standard Care Arrangement (SCA) with a physician in like practice. Practices within applicable state laws, appropriate boards, and in accordance with his/her/their SA/SCA and delineation of privileges.
Minimum Qualifications:
Master's Degree (Required) AANP - American Association of Nurse Practitioners - American Association of Nurse Practitioners Certification Board, BLS - Basic Life Support - American Heart Association, CNP - Certified Nurse Practitioner - American Association of Nurse Practitioners Certification Board, RN - Registered Nurse - Ohio Board of Nursing
Additional Job Description:
Work Shift:
Day
Scheduled Weekly Hours :
40
Department
PCP Barks Rd
Join us!
... if your passion is to work in a caring environment
... if you believe that learning is a life-long process
... if you strive for excellence and want to be among the best in the healthcare industry
Equal Employment Opportunity
OhioHealth is an equal opportunity employer and fully supports and maintains compliance with all state, federal, and local regulations. OhioHealth does not discriminate against associates or applicants because of race, color, genetic information, religion, sex, sexual orientation, gender identity or expression, age, ancestry, national origin, veteran status, military status, pregnancy, disability, marital status, familial status, or other characteristics protected by law. Equal employment is extended to all person in all aspects of the associate-employer relationship including recruitment, hiring, training, promotion, transfer, compensation, discipline, reduction in staff, termination, assignment of benefits, and any other term or condition of employment
$59k-90k yearly est. Auto-Apply 24d ago
Specialist, Product Development
Scotts Miracle-Gro Company
Research and development specialist job in Marysville, OH
Here at Scotts Miracle-Gro there is no such thing as a typical day. Our culture is constantly energized by new and exciting growth opportunities and at a rapid pace. Below are details on an open job. If the role interests you and you would like to be considered we encourage you to apply!
We are seeking a creative and motivated Biology Specialist to join the Research & Development Innovation Team. This role will focus on the testing, development and characterization of novel products and formulations for the consumer lawn and garden category for Scotts Miracle-Gro. Key responsibilities include following established methods and protocols to evaluate new and emerging technologies, collecting appropriate data, clearly summarizing and communicating results, writing reports and making recommendations on next steps to fellow members of R&D and cross functional partners to advance the key innovation focus areas for all of our core business units which include Gardens (Miracle-Gro), Lawns (Scotts, Turf Builder) and Controls (Ortho, Tomcat). The Biology Specialist will align technologies with consumer and business needs, work cross functionally with the innovation team and business unit partners to advance the technolgies to the next phase of development.
The majority of time will be spent independently following established standard operating procedures, methods and protocols to evaluate various technologies on common lawn and garden plants. The remaining time will be spent documenting, analyzing and reporting data to cross-functional teams, peers, and leadership making recommendations on path forward to multiple business units, collaborating closely with innovation team, subject matter experts and business unit partners to ensure alignment on project goals and maximize efficient use of resources versus milestones and commercialization schedules and providing technical support and advice to cross functional partners for new and current products and technologies.
Target Skills: self- starter that's action oriented, scientific curiosity and rigor, motivated to identify opportunities and increase their overall contributions, attention to detail and accuracy, networking and relationship building, excellent written and oral communication, adaptability and flexibility to work independently as well as in a team environment, computer experience such as spreadsheets, presentations, documents, data analysis
Education: Bachelor's Degree in Biology, Microbiology, Agronomy or other related scientific fields would be considered
Experience: 0-2 years, experience handling, maintaining and testing biological materials or products and experience or knowledge of gardening, lawn care or pesticide control products is welcome
The starting budgeted pay range for this role will generally fall between $52,500.00 - $61,800.00 per year. Scotts will consider various factors in determining the actual pay including your skills, qualifications, experience, and geographical location.For remote roles where the final candidate resides in Alaska, California, Colorado, Illinois, New York, Oregon or Washington, state required pay thresholds will be factored into base salary.
Here at ScottsMiracle-Gro, we believe providing an enriching and engaging employee experience is what sets us apart from other organizations. We recognize our employees are so much more than just their job title so we offer programs and benefits that support them in all aspects of their lives. Wondering how we do it? Below is a glimpse of our highlight reel…
* Our Live Total Health program provides you with options to align to your personal needs. Selections range from medical, dental and vision coverage for you, your spouse/domestic partner and dependents to an outstanding wellness reimbursement program to an unbelievable 401K match (up to 7.5%) as well as a 15% discount on company stock and much more
* We know our talent is our most precious asset and your unique development contributes to our organization's success now and in the future. Career growth at our company is not always a ladder. It's much more like a rock climbing adventure. Grow through exploration and experiences rather than a predictable linear path.
* We value the importance of family. We provide access to Maven Family Planning and up to $30,000 to accommodate for adoption, fertility and surrogacy.
* Be part of something bigger by joining one of our Employee Resource Groups focusing on diversity and inclusion, family, education and sustainability: Scotts Women's Network, Scotts Black Employees' Network, Scotts Veterans Network, Scotts Young Professionals, Scotts Pride Network (GroPride), Scotts Associates for a Greener Earth (SAGE), Scotts Family TREE and our Associate Boards.
* Join a company with a strong belief in giving back to the communities where we live and work. We have a shared passion for service and volunteerism and believe participating in community service benefits our communities and strengthens our team.
Not interested in this role? Stay up to date on future opportunities by joining our ScottsMiracle-Gro and Hawthorne Gardening talent communities.
Scotts is an EEO Employer, dedicated to a culturally diverse, drug free workplace.
EEO/AA Employer/Minority/Female/Disability/Veteran/Sexual Orientation/Gender Identity
Notification to Agencies:
Please note that the Scotts Miracle-Gro company does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, the Scotts Miracle-Gro company will not consider or approve payment regarding recruiter fees or referral compensations.
$52.5k-61.8k yearly Auto-Apply 5d ago
Specialist, Product Development
The Scotts Miracle-Gro Company
Research and development specialist job in Marysville, OH
Here at Scotts Miracle-Gro there is no such thing as a typical day. Our culture is constantly energized by new and exciting growth opportunities and at a rapid pace. Below are details on an open job. If the role interests you and you would like to be considered we encourage you to apply!
We are seeking a creative and motivated Biology Specialist to join the Research & Development Innovation Team. This role will focus on the testing, development and characterization of novel products and formulations for the consumer lawn and garden category for Scotts Miracle-Gro. Key responsibilities include following established methods and protocols to evaluate new and emerging technologies, collecting appropriate data, clearly summarizing and communicating results, writing reports and making recommendations on next steps to fellow members of R&D and cross functional partners to advance the key innovation focus areas for all of our core business units which include Gardens (Miracle-Gro), Lawns (Scotts, Turf Builder) and Controls (Ortho, Tomcat). The Biology Specialist will align technologies with consumer and business needs, work cross functionally with the innovation team and business unit partners to advance the technolgies to the next phase of development.
The majority of time will be spent independently following established standard operating procedures, methods and protocols to evaluate various technologies on common lawn and garden plants. The remaining time will be spent documenting, analyzing and reporting data to cross-functional teams, peers, and leadership making recommendations on path forward to multiple business units, collaborating closely with innovation team, subject matter experts and business unit partners to ensure alignment on project goals and maximize efficient use of resources versus milestones and commercialization schedules and providing technical support and advice to cross functional partners for new and current products and technologies.
Target Skills: self- starter that's action oriented, scientific curiosity and rigor, motivated to identify opportunities and increase their overall contributions, attention to detail and accuracy, networking and relationship building, excellent written and oral communication, adaptability and flexibility to work independently as well as in a team environment, computer experience such as spreadsheets, presentations, documents, data analysis
Education: Bachelor's Degree in Biology, Microbiology, Agronomy or other related scientific fields would be considered
Experience: 0-2 years, experience handling, maintaining and testing biological materials or products and experience or knowledge of gardening, lawn care or pesticide control products is welcome
The starting budgeted pay range for this role will generally fall between $52,500.00 - $61,800.00 per year. Scotts will consider various factors in determining the actual pay including your skills, qualifications, experience, and geographical location.For remote roles where the final candidate resides in Alaska, California, Colorado, Illinois, New York, Oregon or Washington, state required pay thresholds will be factored into base salary.
Here at ScottsMiracle-Gro, we believe providing an enriching and engaging employee experience is what sets us apart from other organizations. We recognize our employees are so much more than just their job title so we offer programs and benefits that support them in all aspects of their lives. Wondering how we do it? Below is a glimpse of our highlight reel…
Our
Live Total Health
program provides you with options to align to your personal needs. Selections range from medical, dental and vision coverage for you, your spouse/domestic partner and dependents to an outstanding wellness reimbursement program to an unbelievable 401K match (up to 7.5%) as well as a 15% discount on company stock and much more
We know our talent is our most precious asset and your unique development contributes to our organization's success now and in the future. Career growth at our company is not always a ladder. It's much more like a rock climbing adventure. Grow through exploration and experiences rather than a predictable linear path.
We value the importance of family. We provide access to Maven Family Planning and up to $30,000 to accommodate for adoption, fertility and surrogacy.
Be part of something bigger by joining one of our Employee Resource Groups focusing on diversity and inclusion, family, education and sustainability: Scotts Women's Network, Scotts Black Employees' Network, Scotts Veterans Network, Scotts Young Professionals, Scotts Pride Network (GroPride), Scotts Associates for a Greener Earth (SAGE), Scotts Family TREE and our Associate Boards.
Join a company with a strong belief in giving back to the communities where we live and work. We have a shared passion for service and volunteerism and believe participating in community service benefits our communities and strengthens our team.
Not interested in this role? Stay up to date on future opportunities by joining our ScottsMiracle-Gro and Hawthorne Gardening talent communities.
Scotts is an EEO Employer, dedicated to a culturally diverse, drug free workplace.
EEO/AA Employer/Minority/Female/Disability/Veteran/Sexual Orientation/Gender Identity
Notification to Agencies:
Please note that the Scotts Miracle-Gro company does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, the Scotts Miracle-Gro company will not consider or approve payment regarding recruiter fees or referral compensations.
$52.5k-61.8k yearly Auto-Apply 37d ago
Provider Research Specialist
Bluecross Blueshield of Tennessee 4.7
Remote research and development specialist job
Join Our Team as a Provider ResearchSpecialist with Provider Operation Process Support!
Are you passionate about ensuring accuracy and efficiency in healthcare operations? BlueCross BlueShield of Tennessee's Provider Operation Process Support team is looking for a detail-oriented ResearchSpecialist to join our mission of improving healthcare access and affordability.
In this role, you will:
Audit incoming applications to ensure all required information is documented or attached.
Handle multiple applications simultaneously with using BPM, Cactus, CAQH, and Facets
Communicate effectively with providers and internal teams to resolve any issues and ensure smooth operations.
Preferred skills include:
Strong multitasking abilities and proficiency in using multiple applications.
Excellent communication skills for interacting with providers and internal teams.
Back office or auditing experience.
Experience with credentialing software such as Cactus and familiarity with Facets.
If you are a strategic thinker with exceptional analytical skills, we want to hear from you. Help us shape the future of healthcare by enrolling providers to work with BCBST, making a meaningful difference in the lives of our members.
Job Responsibilities
Monitors provider system data files and creates and maintains contract fact sheets for each contracted provider, including but not limited to: participation in all BCBST networks, special arrangements, and reimbursement data in all BCBST systems.
Works closely with Provider Relations and Provider Service Organization staff to resolve provider and member problems or complaints related to provider participation status.
Investigates all information associated with contract(s) to ensure accuracy and completeness (i.e., profile form, change forms, provider leaving group forms, signature pages, reimbursement schedules, escalation, incentive, pre-application information, credentialing information and electronic commerce information).
Works closely with the provider community to get corrected data needed from the research of the contracts and forms received prior to having contract data entered and maintained in the FACETS system.
Job Qualifications
Education
High School Diploma or equivalent
Experience
3 years - Experience in a Support function or Customer Service, experience with the military, or coursework towards a related degree.
Skills\Certifications
Proficient in Microsoft Office (Outlook, Word, Excel and PowerPoint)
Proficient oral and written communication skills
Proficient interpersonal and organizational skills
This position is a BBNE, Grade 09, Incentive AEP
Must have BCBST ResearchSpecialist experience
Number of Openings Available
1
Worker Type:
Employee
Company:
BCBST BlueCross BlueShield of Tennessee, Inc.
Applying for this job indicates your acknowledgement and understanding of the following statements:
BCBST will recruit, hire, train and promote individuals in all job classifications without regard to race, religion, color, age, sex, national origin, citizenship, pregnancy, veteran status, sexual orientation, physical or mental disability, gender identity, or any other characteristic protected by applicable law.
Further information regarding BCBST's EEO Policies/Notices may be found by reviewing the following page:
BCBST's EEO Policies/Notices
BlueCross BlueShield of Tennessee is not accepting unsolicited assistance from search firms for this employment opportunity. All resumes submitted by search firms to any employee at BlueCross BlueShield of Tennessee via-email, the Internet or any other method without a valid, written Direct Placement Agreement in place for this position from BlueCross BlueShield of Tennessee HR/Talent Acquisition will not be considered. No fee will be paid in the event the applicant is hired by BlueCross BlueShield of Tennessee as a result of the referral or through other means.
$44k-62k yearly est. Auto-Apply 4d ago
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