Css Scientific Jobs in Usa
1,743 positions found — Page 97
Key Responsibilities:
Job Description
We are seeking a skilled Matlab Simulink Developer with expertise in Matlab Model-Based Development to design moderately complex algorithms using model-based design tools. The ideal candidate will have a strong understanding of the principles, techniques, and procedures used in Matlab and Simulink.
Responsibilities
- Design and develop algorithms using Matlab and Simulink for model-based development.
- Create and maintain appropriate design documentation for review purposes.
- Utilize mathematical models and computer-aided engineering/scientific design tools such as Matlab/Simulink and Math CAD to simulate steady state, dynamic, and transient operation of embedded controls.
- Perform product-level testing to ensure system functionality and reliability.
- Develop Matlab Simulink models to produce embedded software for generator set and automatic transfer switch controllers.
- Apply knowledge of electrical systems in the power generation industry, including distributed/embedded power generation, conventional centralized power generation, and islanded/standalone power systems.
Essential Skills
- Proficiency in Matlab and Simulink for model-based development.
- Experience in performance simulation using mathematic models and computer-aided engineering/scientific design tools.
- Ability to create and review design documentation.
- Experience in product-level testing of embedded controls.
Additional Skills & Qualifications
- Understanding of electrical systems in the power generation industry.
Job Description
- Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol.
- Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide patient teaching regarding administration. Maintains investigational drug accountability. -In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
- Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities.
- Maintains regulatory documents in accordance with SOP and applicable regulations.
- Participates in required training and education programs. Responsible for education of clinic staff regarding clinical research.
- May collaborate with Research Site Leader in the study selection process.
- Additional responsibilities may include working directly with other research bases and/or sponsors.
- Identify quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
- May be responsible for compiling and reporting protocol activity, accrual data, and research financial information to practice administration and physicians.
- May oversee the preparation of orders by physicians to assure that protocol compliance is maintained. Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting.
- Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
Qualifications
- Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
- Minimum five years of experience in a clinical or scientific related discipline required.
- SoCRA or ACRP certification preferred.
OR
- Graduate from an accredited program for nursing education (BSN preferred). Minimum 3 years of nursing experience. Experience in clinical research preferred. Current licensure as a registered nurse in state of practice. Current BLCS or ACLS certification required. OCN, SoCRA or ACRP certification preferred.
We are seeking a highly analytical and strategic individual to serve as the primary quantitative leader for our Digital Marketing organization. As the Senior Marketing Science Analyst, you will build and own the growth analytics function, setting the foundation for how we measure, model, and make decisions across the entire digital business - building the predictive models (Retention/Churn, CLV) and incrementality frameworks (MMM/Geo-Lift/DDA) that dictate how we spend our next million dollars. As a direct report to the VP, you are not just a reporter of performance—you are a strategist who uses advanced mathematics to engineer growth and operationalize insights across every digital touchpoint.
This is a high-impact, performance-based role designed to move beyond standard reporting. While we have established baseline infrastructure, you are expected to take our capabilities to the next level—building the predictive and causal models that directly engineer profitable growth. You will serve as the "analytical architect," responsible for unlocking deep customer insights, increasing the validity and speed of our KPIs, and translating complex data into clear, actionable strategies for the VP and broader marketing team. This individual will effectively exhibit JD Finish Line’s core values of Customer, People, Winning, Community, and Financial Responsibility in everything they do by performing the following main duties:
Growth & Performance Architecture
- Strategic Partnership: Act as the primary analytical partner for paid and retention channel owners to optimize performance and unlock channel-level efficiencies.
- Full-Funnel Ownership: Build and own the marketing analytics function, establishing how we measure the core drivers of the business and the impact of our actions on those drivers.
- Advanced Attribution: Transition the organization from baseline models to sophisticated Multi-Touch Attribution (MTA) and Market Mix Modeling (MMM) to drive profitable acquisition.
- Incrementality Testing: Design and lead "Scientific Lift" studies (e.g. Geo-tests) to measure the true causal impact of Meta, Google, and Brand campaigns.
- Market Mix Modeling (MMM): Maintain the statistical model that advises the VP on quarterly budget shifts between Paid, Owned, and Earned media.
- Full-Funnel Attribution: Manage the transition from basic last-click reporting to a multi-touch, data-driven attribution (DDA) model.
Customer Science & Program Development
- Model Development: Lead the development of programs that target customers across the full lifecycle using advanced statistical modeling, machine learning, and propensity scoring.
- Predictive Insights: Build and maintain predictive models (Churn, CLV, Next-Best-Action) that allow the CRM/retention team to automate 1-to-1 personalization.
- Data Harmonization: Collect, harmonize, and review data across disparate sources (Commerce Tools, Looker/Big Query, Meta, GA4, Braze) to ensure a unified view of the customer.
Strategic Partnership & Team Enablement
- Paid Media/Acquisition: Provide the Paid Media team with data-driven insights on bid optimization, budget allocation, and target audiences derived from MMM, MTA and CLV forecasts to lower blended Customer Acquisition Cost (CAC) while scaling volume.
- CRM/Retention: Collaborate closely with the CRM/Lifecycle team to operationalize models by feeding predictive scores directly into segmentation and personalization engines (e.g., Braze) to maximize conversion and retention rates.
- Executive Insight: Serve as the strategic analytical consultant to leadership, translating complex mathematical findings into clear, concise, and actionable business recommendations for investment decisions.
- Data Strategy: Partner with Data Engineering and IT teams to architect and ensure the integrity, governance, and flow of data from raw sources (E-commerce platform, Ad Platforms, appsflyer, etc) into the cloud data warehouse for modeling purposes.
Experimentation & Rigorous Analysis
- Scientific Testing: Design and execute rigorous experiments (A/B, Multivariate, and Geo-Lift) to isolate the true causal impact of marketing initiatives.
- Visual Storytelling: Formulate key insights, charts, and reports for high-level presentations to the VP and executive leadership, turning complex coefficients into business narratives.
- KPI Visibility: Increase the transparency and accuracy of core business metrics, ensuring the team is making decisions based on "valid" and "real-time" data.
Requirements
- Education: B.S. or M.S. in a quantitative field (Statistics, Economics, Mathematics, or Data Science).
- Professional Experience: 4-8 years in Marketing Analytics or Data Science, with at least 3 years in a high-volume Retail/E-commerce environment.
- Strategic Acumen: Proven ability to translate complex data into business strategy and present to executive-level stakeholders. Experience working independently on analytical tasks, building, and optimizing ‘big data’ pipelines, architectures, and data sets
- Experience developing and delivering exec-level presentations using insights derived from analytics
- Strong working knowledge of Microsoft PowerPoint and Excel
- Coding & Data Science: Expert proficiency in SQL and Python
- Web Analytics & BI: Expert experience with Google Analytics 4 (GA4) and a major BI/Visualization platform (preferably Looker).
- Marketing: Direct working experience with the data output of a major CRM/E-commerce platform (e.g., Commercetools, Braze, etc).
- Visualization: Mastery of Looker to build executive-level dashboards.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Sit for more than 6 hours per shift
- Use hands to finger, handle and feel
- Reach with hands and arms
- Talk and/or hear
- Stand for up to 2 hours at a time regularly
- Walk or move from one location to another regularly
- Periodically may need to climb, balance, stoop, kneel, or crouch
- Lift and/or move up to 10 pounds regularly and up to 50 pounds occasionally
- Punctuality and regular attendance consistent with the company’s policies are required for the position.
- Average workweek is 40 hours, which can vary depending on business need.
- The work environment for this position is a moderately noisy office setting.
#LI-DNI
Project Manager 2 / Superintendent 3
Compa Industries is searching for qualified candidates for a Project Manager 2 / Superintendent 3 position at Los Alamos National Laboratory (LANL) in Los Alamos, NM.
Salary: $62/hr - $67/hr
Location: Los Alamos, NM (TA-55 Plant, on-site 100%)
Citizenship: US Citizenship Required
Work Schedule: 4/10s with anticipated overtime; must be willing to work days, nights, weekends, and potentially graveyard shifts
Clearance: Ability to obtain a Q Clearance needed.
Mandatory Experience Requirement – Read Before Applying
Candidates must have the following before applying:
- Ability to obtain a Q Security Clearance
- Nuclear facility experience
- Willingness and ability to support graveyard shifts
Applications lacking these qualifications will not be considered.
Impact
Join a mission-critical team at Los Alamos National Laboratory responsible for overseeing construction projects essential to national security. As a Project Manager 2 / Superintendent 3, you will lead construction efforts, ensuring safety, budget compliance, and schedule performance in a high-security nuclear facility. Your work will directly support scientific advancement and federal mission delivery in one of the nation's most unique operational environments.
Responsibilities and Duties
- Lead and manage projects up to $500k and oversee Superintendent 2s
- Serve as Control Account Manager (CAM), managing budget, schedule, and scope performance
- Present project performance updates to federal sponsors
- Conduct investigations into abnormal events/incidents and assist in corrective action plans
- Perform variance analysis and develop corrective action plans for cost/schedule variances
- Lead constructability reviews and interface with stakeholders
- Ensure compliance with safety, security, and configuration management requirements
- Promote teamwork and open communication across trades and departments
Minimum Qualifications
- At least 10 years of experience in engineering, procurement, or construction
- 5+ years managing construction projects with scope, schedule, and budget oversight
- Demonstrated experience in Earned Value Management Systems (EVMS)
- Experience in construction within a nuclear environment
- Ability to interpret technical documents, blueprints, schematics
- Strong communication and leadership skills
- Able to meet physical demands: lifting, standing, stair climbing
Desired Skills
- Experience leading teams under collective bargaining agreements
- Proficiency in risk identification and mitigation strategies
- Experience using computerized work management systems
- Strong understanding of lock-out/tag-out policies and facility control systems
- Demonstrated customer engagement and issue resolution capabilities
Education and Experience Requirements
- Recognized degree in engineering, scientific discipline, or project management preferred
- Equivalent combination of education and relevant experience will be considered
Why Work at COMPA Industries?
We strive to provide careers, not just jobs. For over 30 years, COMPA has supported the DOE and national security missions with technical expertise and innovation. We offer competitive compensation, a collaborative culture, and the chance to make a real difference. Be part of a mission-focused team solving complex challenges in nuclear facilities.
COMPA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration without regard to age, race, color, religion, sex, national origin, sexual orientation, disability, or protected Veteran status.
Note: COMPA's policy may disqualify applicants with certain criminal histories from specific positions.
Location: Irvine, CA
Join a trailblazing startup founded by a renowned Professor in transforming the future of water and air. As a Senior R&D Scientist, you'll be at the heart of pioneering technologies for atmospheric water harvesting and CO2 capture, driving innovations that make a global impact.
Why You Should Apply
- Lead cutting-edge research in atmospheric water harvesting.
- Competitive salary and benefits package.
- Collaborate with top-tier scientists and engineers.
- Play a crucial role in the commercialization of breakthrough technologies.
- Contribute to sustainability and environmental solutions.
- Work with the head of Product Engineering to scale up MOF/COF-based technologies.
- Collaborate with R&D scientists on technical and functional specifications.
- Design and develop heat management systems, optimizing components like heat exchangers and thermal storage.
- Scale technologies from prototype to commercial stage.
- Optimize system parameters to enhance performance, efficiency, and safety.
- Evaluate and manage sourcing of materials and components.
- Set up QC/QA processes and procedures for production.
- Maintain detailed electronic notebooks and contribute to intellectual property.
- Report periodically to management and participate in technical meetings.
- PhD in mechanical engineering or a similar field with a strong research background.
- Proficient in thermodynamics, fluid mechanics, and heat transfer.
- Over 5 years of industrial R&D experience.
- Skilled in designing system-level prototypes and using simulation tools.
- Familiar with health and safety procedures in production.
- Excellent teamwork, problem-solving, and communication skills.
We'd love to see your resume, but we don't need it to have a conversation. Send us an email to and tell us why you're interested. Or, feel free to email your resume. Please include Job#19433.
Company Overview
Mundell & Associates (MUNDELL) is a group of passionate professionals working together to discover, clean and protect our earth. We are in search of a key team member to help provide focused leadership. Headquartered in Indianapolis, Indiana, (locally owned and operated) Mundell & Associates, Inc. was founded in 1995 to provide professional earth and environmental consulting services for commercial companies, Fortune 500 firms, municipalities, engineering firms, and the legal community. We are experienced project engineers, scientists, program directors, senior technical consultants and expert witnesses who have worked throughout the United States, Canada, Mexico, South America, Europe and Asia.
Our specialties include the quantitative stratigraphic, geotechnical, geochemical, geophysical and hydrogeological characterization of the subsurface; quantitative analysis and engineering design of remediation systems; groundwater modeling and contaminant transport analysis, water resources evaluations, as well as environmental and engineering geophysics.
MUNDELL personnel believe that the proper scientific or engineering analysis of any site communicated in easily understandable terms will provide its clients with the guidance and direction they need to accomplish their goals. We believe that our pleasant demeanor, our high level of enjoyment in what we do and how we do it, and our passion for providing a high-quality product creates an atmosphere in our work environment that is collaborative and attractive to those seeking employment.
Job Description
Oversee, manage, and collaborate with the geophysics team to deliver high quality outcomes for clients by implementing efficient project deliverables. Establish and maintain positive relationships with clients. Participate in business development opportunities in the geophysics service area. Assist with other service areas by using multi-disciplinary experience.
Position Overview
A successful candidate for this position will be team-focused, responsive, accountable, an expert in their technical specialty, and possess an entrepreneurial mindset. This position is essential to the current and future success of MUNDELL. This position must maintain positive relationships and outcomes for external stakeholders while developing new business opportunities. The candidate will lead, manage, and mentor the Geophysics service area to tackle complex issues for our clients by providing leadership, technical guidance, and expertise for Geophysical services. This candidate will also be expected to provide assistance in other MUNDELL service areas as they arise including, but not limited to: environmental reporting, remediation activities, and litigation work.
Responsibilities
- Review, develop and direct: proposals and scope of work for geophysical surveys, data acquisition, processing, and reports.
- Assist in review and technical oversight of engineering plans, environmental reports and litigation projects as needed.
- Main point of contact for Geophysics clients to ensure high quality deliverables are on budget and on time.
- Create and manage sales and marketing goals by building strong relationships with key clients and develop new client opportunities to support the growth of MUNDELL services.
- Manage and mentor staff to maintain company billable standards, implement company policy, and develop key skill sets of the team for current and future needs of our client base.
- Provide high level strategy for client projects. Develop a deep and broad understanding of client challenges to ensure the team can provide positive solutions.
- Evaluate geophysical equipment and software.
- Maintain working knowledge of area of expertise and expand knowledge in other areas for MUNDELL growth opportunities.
- Provide ongoing input to company operations to develop and maintain company growth and culture
- Represent MUNDELL at industry events, conferences, and networking functions.
- Participate in professional societies and deliver presentations and papers at national and local seminars and symposiums.
Requirements
- B.S. degree (M.S. or PhD preferred) scientific or engineering discipline from an accredited university.
- Registration as a professional engineer, (PE), or professional geologist (PG) in the state of Indiana.
- A minimum of five (5) years of progressive consulting experience.
- Advanced technical knowledge in the geophysics discipline; familiarity with geophysical field methods; excellent surveying and mapping skills; advanced knowledge of geophysical equipment including operation, maintenance, and troubleshooting; strong project management and organizational skills; multidisciplinary environmental project experience.
- Strong PC skills and experience with method specific geophysical software including GPR, EM, magnetics, seismic, resistivity and borehole logging.
- Supervisory experience leading a team of professionals.
- A record of developing new client opportunities.
- Excellent verbal/written communication, presentation, and negotiation skills; experience working with engineers, scientists, developers, contractors, law firms, insurance carriers, state/federal regulators, industry experts and the public.
- Maintain 40-HAZWOPER training with yearly 8-Hour refresher.
- Valid driver's license in good standing
- The ability to travel to project sites and work in outdoor conditions is required.
- Ability to lift and carry up to 50lbs.
- Must be authorized to work in the U.S.
Benefits
· Health Insurance (multiple PPO and HDHP available)
· Dental Insurance
· Vision insurance
· Company provided Basic Life and AD&D Insurance
· Company provided Long-Term and Short-Term Disability coverage
· Supplemental insurance offerings
· Paid Time Off
· Paid Holidays
· 401(k) with company match
· Flexible work environment
· Paid Parental Bonding Leave
· Employee Assistance Program
· Cell phone reimbursement
· Allowance for Professional Materials
/company/careers/
We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Why Us?
We want the best and brightest people to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life.
Job Description Summary
SUMMARY OF POSITION:
The Sr. Director, Quality is responsible for a broad range of duties/functions that includes all Quality functions at the St. Louis Plant, and the Centers of Excellence for Microbiology, Elemental Impurities, and Validation, to support the Generics Business
The Sr. Director, Quality is responsible for ensuring cGMP compliance and product quality at the Saint Louis, MO facility while supporting broader site quality initiatives aligned with company objectives. This role provides strategic leadership in the development, implementation, and oversight of site quality systems to ensure that all manufacturing, testing, packaging, storage, and distribution activities meet regulatory standards and deliver the highest product quality. The Sr. Director leads and mentors quality assurance and quality control teams, oversees daily quality operations, and serves as a key partner to site leadership by providing guidance on quality and compliance across the organization.
Job Description
St Louis Plant Quality
Responsible for and will develop, establish and maintain quality systems programs, policies, processes, procedures and controls ensuring that performance and quality of products conform to established standards and agency guidelines to ensure customer satisfaction. Provide expertise and guidance in interpreting governmental regulations, agency guidelines and internal policies to assure compliance. May serve as liaison between the company and the various governmental agencies. Work directly with operating entities to ensure that inspections and audits are conducted on a continuing basis as specified to enforce requirements and meet specifications.
Establish and ensure appropriate Quality Systems are implemented and maintained, including ongoing data analysis of product and process outputs to ensure early detection and response to quality concerns, and prevention of quality issues. Establish and ensure compliance with cGMPs, good housekeeping practices, employee hygiene and equipment sanitation; analyze plant error, salvage, spoilage reports and process statistics for significant findings and conclusions; work with Research and Development during new product start-ups, and establish key checkpoints for new products and processes
Centers of Excellence for Microbiology, Elemental Impurities, and Validation
The Sr. Director is responsible for Centers of Excellence for Microbiology, Elemental Impurities, and Validation to support the Generics Business. Will develop policy, create systems, develop strategies and minimize costs while striving for excellence in customer service. Establishes and maintains positive and mutually rewarding relationships with internal and external customers of the department. The Sr. Director will be also responsible for oversight and management of the training department to include all NEO, CBT and OJT systems in alignment with company policies and procedures.
ESSENTIAL FUNCTIONS:
St Louis Plant Quality Departments
- Manages all aspects of plant Quality Systems including, CAPA, Supplier Quality, Change Control, in-process Quality Assurance, Quality Control, complaint management and validation functions.
- Support an aggressive Quality program which instills personal accountability for accuracy, consistency and completeness for all operations and departments according to site and corporate policies. Create and maintain an environment of excellence, world-class quality and continuous improvement throughout the entire plant.
- Responsible to make fact-based, scientifically sound, quality decisions regarding products manufactured at the St. Louis Plant facility. These decisions must be made within the requirements of cGMPs and applicable regulatory/industry guidance documents.
- Manage approval or rejection of starting materials, packaging materials, and intermediate, bulk and finished products per the appropriate regulations and documents.
- Ensure the evaluation of batch records and that all necessary testing is carried out.
- Approve specifications, sampling instructions, test methods and other QC procedures.
- Ensure the authorization of all controlled documents, including records retention.
- Ensure the monitoring and control of the manufacturing and Quality Control environments.
- Ensure compliance with cGMP standards.
- Ensure the appropriate process, equipment and facility validations meet expectations for validations, process capability, corrective actions and general compliance both for Corporate and for applicable regulatory agencies.
- Coach and develop the team to High Performance while fostering a culture of team ownership.
- Ensure team compliance with all policies, procedures and site/company regulations.
- Set clear vision by ensuring goals and objectives are aligned with site strategies and managing each team member’s performance management.
- Exhibit accountability and responsibility for an area or process in order to affect change and lead efforts and ideas to completion.
- Provide leadership for employee relations through effective communications, coaching, training and development and eliminate roadblocks in order for the team to move forward.
- Supply the highest level of internal and external customer service while having the ability to diplomatically challenge established procedures and systems.
- Lead team in continuous improvement activities and take control when faced with adversity while incorporating team input.
- Ensure proper maintenance and cleanliness of the department, premises and equipment.
- Measure and communicate team’s progress against individual, team and site goals and Key Performance Indicators (KPI’s).
- Lead and/or support investigations. Author, approve and/review area quality and safety exceptions and investigation reports. Ensure on-time completion of all corrective action items assigned to area.
Centers of Excellence for Microbiology, Elemental Impurities, and Validation
- Develop policy, create systems, develop strategies and minimize costs while striving for excellence in customer service.
- Establish and maintain positive and mutually rewarding relationships with internal and external customers of the department. T
- Responsible for oversight and management of the training department to include all NEO, CBT and OJT systems in alignment with Mallickrodt policies and procedures.
General
- Budget creation and management for Quality, and Traing Departments (>$15MM).
- Defines requirements of department personnel and works with Human Resources to hire such personnel.
- Acts as subject matter expert and lead with internal and external regulatory inspections and audits of manufacturing sites in the area of Quality Systems, and Training.
- Interfaces with FDA and regulatory agencies outsite the US for events that include but are not limited to: manufacturing site inspections, Field Actions, and Recalls.
MINIMUM REQUIREMENTS:
Education:
Bachelor's degree in chemistry, microbiology or similar life sciences or technical field such as engineering, mathematics, etc.
Experience:
- Minimum of 15 years of pharmacuetical industry experience in a Quality Assurance and/or Regulatory Affairs function including experience in manufacturing and control of bulk drug substances, and solid dosage form drug products.
- Minimum 5 years managerial experience in a pharmaceutial quality/regulatory affairs environment.
Preferred Skills/Qualifications:
- Previous experience serving as a pharmaceutical manufacturing site leader of a significant quality function (Total Plant population >500 persons, Quality Function >100 persons).
- Exceptional oral and written communication skills. Strong managerial and excellent negotiating skills in order to obtain balanced results from direct and indirect reports.
- Knowledge of FDA and International regulations and guidances in the area of Quality Systems for pharmaceutical products and medical devices.
- Experience interacting with regulatory agencies such as the FDA and EU regulatory bodies as an inspection host.
- Strong patient and customer focus.
Skills/Competencies:
- Strong writing skills to effectively communicate technical/clinical information to others.
- Ability to use various software programs (Word, Excel, Power Point, Access) and a willingness to expand and increase these competencies.
- Superior verbal communication skills including impeccable telephone etiquette.
- Scientific literature searching and evaluation skills.
WORKING CONDITIONS:
This Position works primarily in an office environment. Ability to sit for long periods of time and lifting of up to 10 pounds may occasionally be required. Will require occasional periods in the manufacturing areas and walking throughout the plants. Manufacturing areas are not climate controlled. During summer months, building exhaust fans provide ventilation but remain warm. When in manufacturing areas, PPE is required to be worn
Approximately 10 to 15% travel (mainly domestic, but some international) will be required for manufacturing site visits and off-site business meetings and professiona training seminars and conference.
DISCLAIMER:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Job Title: Representative, Technical Sales
Reports To: Director, Sales
Position Location: Charleston, SC
FLSA Status (Exempt/Non-Exempt): Exempt
Position Summary:
Grows key accounts and reactivates inactive customers within assigned areas. Communicates value propositions by offering product and services. Works to establish effective business relationships with multiple levels. Identifies new business opportunities with account and actively closes on leads, quotes, etc. Maintains minimum expected call and meeting frequencies and keeps information on file.
Key Responsibilities:
- Drives revenue growth in territory by developing and maintaining strategic long-term trusting relationships to accomplish organic growth and long-term company objectives
- Build strong customer allegiance and partnership and create the overall strategy’s day tactics for account growth and margin improvement
- Negotiating price agreements with key clients and meeting established deadlines for the fulfillment of each clients’ long-term goals
- Coordination of all sales and marketing activities associated within these accounts to ensure profitable growth
- Conduct quarterly business reviews with key stakeholders within target accounts
- Evaluate and lead all new business development opportunities
- Coordinate contract renewal price strategies and commercial initiatives with pricing , finance and appropriate senior executives to drive growth targets
- Measure, track, analyze and report key account metrics
- Planning and presenting reports on account progress, goals, and quarterly initiatives to share with team members, stakeholders, and possible use in future case studies or company training
- Ensure that databases are current and updated with accurate customer information
- Performs other duties as assigned
Education:
- Bachelor’s Degree in a science related fieldfrom an accredited higher learning institution strongly preferred or an equivalent combination of education and experience.
Experience:
- 3+ years of related sales or technical product experience in related product categories strongly preferred.
Minimum Requirements/Qualifications:
- Proficiency in Excel and MS office applications is required and strong database experience is desirable.
- Interpersonal skills to build relationships with and to conduct professional and courteous phone conversation with internal and external customers.
- Must be results oriented and self-motivated; strives to achieve targets and goals; is assertive and proactive.
- Excellent technical and analytical skills as well as the ability to learn, to gain sufficient knowledge of product lines to participate in promotions and probe effectively and to analyze data and compile reports as needed. Must be able to assimilate data and draw conclusions.
- Must possess a customer focused mentality to meet and exceed our customer expectations.
- Ability to manage and execute multiple projects concurrently to successful completion, meet deadlines, and follow-up in a timely manner through excellent organizational, planning, prioritization and multi-tasking skills.
- Ability to work independently and be able to work in a team atmosphere.
- Strong selling and negotiation skills and be confident and poised to independently negotiate and manage a relationship with various customers as well as execute key sales strategies.
- Thrives in a fast-paced, collaborative environment, efficiently works under pressures, within deadlines or other time essential constraints.
- Excellent communication skills, both written and verbal, to clearly and concisely communicate to all levels of the organization.
- Strong work ethic and an ability to excel within a rapidly changing and growing organization.
- Ability to travel for customer meetings, training & team meetings; up to 50%
Compensation & Benefits:
- Salary Range: $65,000-$80,000, depending on location, experience, and qualifications.
- Sales-Incentive Plan (SIP): $24,000-$30,000
- Benefits coverage begins day 1, including the following:
- Medical, Dental, Vision Insurance
- Disability Insurance
- Life Insurance
- 401(k) company match
- Paid Time Off (15 days annually)
- Paid Holiday time (10 company-designated days)
- Tuition Assistance
- Additional benefits available with company package
This position has not been approved for Relocation Assistance.
The above statements are intended to describe the general nature and level of the work being performed by people assigned to this job. They are not an exhaustive list of all of the duties and responsibilities associated with it.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.
POSITION OVERVIEW
The Territory Account Manager contributes to the Company’s success by developing, maintaining, and expanding sales within the assigned territory. The incumbent creates and executes a strategic business plan to maximize net sales of assigned products in alignment with commercial leadership and all Company guidelines, policies, and objectives.
SUMMARY OF KEY RESPONSIBILITIES
• Creates a business plan to maximize territory sales and generate revenue.
• Develops, implements, and continuously builds knowledge of territory, market dynamics, products, competitors, and disease states.
• Achieves sales goals, conducts day-to-day activities including submitting timely and accurate reports (expenses, business plans, etc.) while adhering to ethical sales practices, compliance guidelines, and promotional regulations.
• Develops and maintains superior relationships with target audience (MDs, RNs, NPs, PAs, PharmDs, MAs, staff, etc.)
• Effectively educates target audience on products using Company approved resources, sales materials, and promotional initiatives as identified by sales leadership.
• Maintains accurate records of all sales activities, including sales calls, presentations, targets/leads database, and follow-up activities.
• Regularly participates in local and regional professional events, industry conferences, annual meetings, and other Company-wide meetings.
• Successfully collaborates with cross-functional team members, including Sales Operations, Field Medical Affairs, Marketing, and Market Access.
• Maintains sufficient supply of sales literature and educational materials.
• Organizes and executes territory-specific events, such as speaker bureau presentations, lunch-and-learn programs, etc.
• Participates in special projects or sales-related activities, as deemed necessary.
• Shares market intelligence to optimize brand strategy and execution.
• Works within assigned expense budget by exercising sound judgment regarding general operating, travel, and promotional expenditures.
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REQUIRED QUALIFICATIONS AND SKILLS
• B.S. / B.A. in business, scientific, or other related discipline.
• Minimum of five (5) years’ experience in specialty pharmaceutical sales. Experience in transplant, nephrology, and/or rare/orphan (specialty product) experience is preferred.
• Proficiency in working with specialty drugs via a HUB distribution model is preferred.
• Demonstrates in-depth scientific, therapeutic, product, and competitor knowledge; recognized as an expert resource by all relevant stakeholders.
• Excellent communication, presentation, and organizational skills.
• Consistently displays positive attitude through challenges and change.
• Proficiency in MS Office (Outlook, Word, Excel, PowerPoint).
• Meets all requirements for health care industry representative (HCIR) credentialing to gain entry into facilities and organizations that are in the assigned territory.
• A valid driver’s license and a driving record that meets Company standards.
We’re Hiring: Medical Representative – Women’s Health (UTI Support Supplement)
Location: Atlanta, GA (Home Base)
Territory: New York + Texas + National and Regional Medical Conferences
Travel: 60–70%
At Pharmatoka, we are reshaping prevention-first care in women’s urinary health. With more than 20 years of scientific expertise and over 15 years in the U.S. market, our clinically supported, non-prescription supplement is trusted globally for recurrent UTI support. As we continue to expand across key U.S. regions, we are seeking a driven, science-focused Medical Representative to strengthen HCP adoption and accelerate territory growth.
This position reports directly to the Director of E-Commerce and Marketing.
How You’ll Make an Impact
HCP Engagement & Reactivation
Re-engage inactive referrers and convert cold/warm leads into consistent product recommendation.
HCP Education & Product Adoption
Deliver clear, evidence-based education on clinical data, and patient outcomes to drive long-term adoption.
Territory Expansion
Build and grow recommending accounts across three regions by nurturing strong relationships within women’s health and urology practices.
Multi-Channel Outreach
Connect with HCPs through in-person visits, lunch-and-learns, regional conferences, phone, email, and professional social channels to maintain engagement.
Market & Account Insight
Research practices, validate contacts, understand patient demographics, and identify high-potential centers of influence.
Scientific Communication
Confidently discuss clinical studies, outcomes, and positioning within prevention pathways in a credible, compliant manner.
Medical Conferences
Represent Pharmatoka at national and regional medical meetings, including booth setup, product promotion, and engagement with healthcare professionals.
Field Reporting & Insights
Track activities and conversions through CRM and share insights from the field to support ongoing strategy refinement.
Qualifications
Required
- BA/BS degree
- 4+ years of successful HCP-facing sales experience (healthcare, pharma, medical device, or nutraceuticals)
- Strong understanding of sales processes, healthcare products, and industry dynamics
- Proven ability to interpret and communicate clinical evidence clearly and confidently
- Excellent communication, presentation, and facilitation skills
- Strong analytical thinking, business acumen, and problem-solving capability
- Motivational and persuasive interpersonal skills
- Team-oriented with leadership qualities
- Demonstrated record of sustained high sales performance
- Exceptional planning, prioritization, and territory management
- A proactive, accountable, “ownership” mindset
- Proficiency in Microsoft Office Suite
Work Conditions
- Work performed both in the Atlanta office and in the field; regular travel required across the assigned territory and to conferences
- Occasional lifting of up to 50 lbs (materials, booth setup, product samples, etc.)
- Frequent standing, walking, and presenting in clinical environments
Compensation
- Base Salary: $95000
- Performance bonus
- Full reimbursement of travel expenses
Benefits
- Medical insurance
- Generous PTO (Vacation, Sick, and national holidays)
- 401(k) with immediate eligibility, company match, and annual employer contribution from day one.
This job description reflects the general nature and level of work expected. It is not an exhaustive list of all responsibilities, duties, or skills required, and additional tasks may be assigned as needed.
All qualified applicants will receive consideration without regard to race, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.