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Global RTR Process Design Lead
Job Description
Join the team behind iconic brands like Huggies®, Kleenex®, Cottonelle®, Scott®, Kotex®, Poise®, Depend®, and Kimberly-Clark Professional®.
At Kimberly-Clark, it’s all here for you—innovation, growth, and the chance to make a real impact.
You were made to create Better Care for a Better World: as a person, you’re a problem-solver – a connector – someone who thrives on creating order from complexity and driving continuous improvement.
You see the big picture while mastering the details, ensuring that every product, process, and partnership flows with precision and purpose.
You live your life in alignment with the highest values of integrity, efficiency, and collaboration, always working to turn today’s challenges into tomorrow’s success stories.
In this role, you’ll help us deliver better care for billions of people around the world It starts with YOU.
As Kimberly-Clark forms a strategic partnership with Suzano to create a world-class international tissue and professional products company, this role is proposed to transfer to the new venture once the transaction closes, anticipated in mid-2026, subject to consultation and other applicable legal requirements.
This is a rare opportunity to help shape a new global leader backed by two industry powerhouses.
You’ll be part of a high-potential business that combines Kimberly-Clark’s iconic brands and commercial excellence with Suzano’s industrial and sustainability leadership.
About You
In one of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.
We are recruiting for a Global RTR Process Design Lead in Krakow who will serves as the Global Record to Report (RTR) Process Architect, responsible for driving global standardization, simplification, and continuous optimization of RTR processes.
It defines global RTR process standards, designs future‑state processes, and supports the Associate Director of RTR by resolving complex and ad‑hoc RTR issues and ensuring consistent adoption of the global RTR operating model across regions
Duties & Responsibilities:
* Define, standardize, and continuously optimize global Record to Report (RTR) processes in line with the global process vision
* Own and maintain global RTR process architecture, standards, and documentation (L2–L4), ensuring alignment to the global template
* Evaluate AS‑IS process performance, identify design gaps, and develop TO‑BE process solutions with minimal customization
* Act as a key support and escalation partner to the Associate Director of RTR on complex, non‑standard, or ad‑hoc RTR process and design issues
* Partner with the Global Process Owner, regional finance teams, and GBS organizations to drive adoption of standardized RTR processes
* Support global initiatives such as system enhancements, finance transfo...
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Type: Permanent Location: Krakow, PL-MA
Salary / Rate: Not Specified
Posted: 2026-05-09 08:14:23
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Sr.
HR Operations Enablement Specialist
Job Description
Únete al equipo detrás de marcas icónicas como Huggies®, Cottonelle®, Kotex®, Poise® y Depend®.
En Kimberly-Clark, todo está aquí para ti: innovación, crecimiento y la oportunidad de generar un impacto real.
No eres la persona que se conforma con cualquier puesto.
Nosotros tampoco.
Porque queremos crear una Mejor Atención para un Mundo Mejor, y eso requiere un tipo de persona y equipos comprometidos con marcar la diferencia.
Aquí aportarás tu experiencia profesional, talento y motivación para construir y gestionar nuestro portafolio de marcas icónicas e innovadoras.
En este puesto, nos ayudarás a ofrecer una mejor atención a miles de millones de personas en todo el mundo.
TODO COMIENZA CONTIGO.
Acerca de ti
En este rol profesional, te centrarás en ganar con los consumidores y el mercado, poniendo la seguridad, el respeto mutuo y la dignidad humana en el centro.
Coordinar y ejecutar los procesos de operaciones de Recursos Humanos, soporte a auditorías, compensación y bienestar, garantizando alineación con las políticas corporativas, el cumplimiento del marco legal de la sugregión y la estrategia que permitirán apalancar los objetivos del negocio.
Todo empieza contigo.
* Auditar el servicio prestado por el vendor de share services, generando propuestas de mejora y propiciando la mejora continua.
* Garantizar estandarización de procesos ajustados a los SLA y KPI
* Controlar las migraciones hacia al sistema de payroll a través de reportes de sincronizaciones de novedades de nómina.
* Evaluar las oportunidades de mejora en los procesos creando proyectos que garanticen la estandarización y la eficiencia a nivel de la región.
Ideas kaizen.
* Mantener actualizados y mapeados los procesos de acuerdo a las legislaciones de cada país y políticas internas.
* Llevar a cabo las tareas cotidianas relacionadas con la administración y manejo de extranjeros, logística de movilidad en la subregión y mantener actualizados los sistemas de notificación de cada país de la subregión
* Completar todas las tareas relacionadas con la administración de vacaciones, la logística local
Para tener éxito en este puesto, necesitarás las siguientes calificaciones:
* Profesional en las carreras de Administración, Ingeniería, Psicología o afines.
* Experiencia superior a 3 años en posiciones similares.
* Experiencia en servicio al cliente, resolución de problemas y análisis de métricas.
* Conocimiento Gestión del Talento Humano, Legislación laboral.
* Conocimiento en Workday u otros sistemas de HR.
* Conocimiento en Service Now.
* Inglés Avanzado B2-C1.
La posición tiene contacto con USA.
* Excel Básico.
Guiado por un propósito.
Impulsado por ti.
Beneficios totales
Creemos que nuestros empleados son nuestro mayor activo y estamos comprometidos a proporcionarles los recursos que ne...
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Type: Permanent Location: Belen, CR-SJ
Salary / Rate: Not Specified
Posted: 2026-05-09 08:14:17
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EHS Manager -מנהל.ת בטיחות
Job Description
הצטרפו לצוות שמאחורי מותגים אייקוניים כמו Huggies®, Kleenex®, Kotex®, Depend® ו-Kimberly-Clark Professional® בקימברלי-קלארק, הכל כאן בשבילכם- חדשנות, צמיחה והזדמנות לעשות השפעה אמיתית.
אתה לא האדם שיסתפק בכל תפקיד.
גם אנחנו לא.
כי אנחנו שואפים ליצור טיפול טוב יותר לעולם טוב יותר, וזה דורש סוג מסוים של אנשים וצוותים שאכפת להם לעשות שינוי.
כאן תביאו את המומחיות המקצועית, הכישרון והדחף שלכם לבניית וניהול תיק המותגים האיקוניים והפורצי דרך שלנו.
בתפקיד זה, תסייעו לנו לספק טיפול טוב יותר למיליארדי אנשים ברחבי העולם.
זה מתחיל איתך.
תחומי אחריות עיקריים :
* הסמכות המקצועית המפעלית בתחום הבטיחות והגהות.
חבר הנהלת המפעל.
* מימוש דרישות החוק ודרישות החברה בתחום הבטיחות והגהות התעסוקתית.
* הטמעת תרבות בטיחות ושמירה על בטיחות ובריאות העובדים.
* הובלת הלמידה מאירועי הבטיחות ופעולות מתקנות למניעת הישנות האירועים.
* הובלת פרואקטיביות בבטיחות לצמצום חשיפת העובדים לסיכונים והעלאת המודעות לבטיחות.
* הכנת תוכנית ניהול בטיחות שנתית ומימושה כולל הגדרת מטרות ויעדים שנתיים.
* עדכון סקרי הסיכונים לעמדות העבודה ווידוא הדרכת העובדים.
* עדכון תיק המפעל ושמירת כשירות צוותי החירום המפעליים.
* חניכת נאמני הבטיחות ופיתוחם המקצועי.
* מוכנות המפעל לעמידה בדרישות תקן 45001.
דרישות התפקיד:
* משרה מלאה.
עדיפות לבעלי תואר ראשון.
* ממונה בטיחות עם תעודת כשירות בתוקף.
* ממונה בטיחות בגז טבעי – יתרון.
* ניסיון מעשי בחברה גלובאלית – יתרון.
* שליטה טובה מאוד באנגלית (דיבור, קריאה, כתיבה).
הטבות
אנו מאמינים שהעובדים שלנו הם הנכס הגדול ביותר שלנו, ואנו מחויבים לספק להם את המשאבים שהם צריכים כדי להצליח.
אם אתם מחפשים קריירה מתגמלת בחברה שאכפת לה מהעובדים שלה, קימברלי-קלארק הוא המקום בשבילכם.
גמישות שעובדת בקימברלי-קלארק
אנו מאמינים שעבודה נהדרת מתרחשת כשאנשים מתאחדים במטרה.
לכן אנו מציעים מודל עבודה גמיש שמשלב עבודה מרחוק עם שיתוף פעולה פרונטלי מכוון — עוזר לכם להתחבר, לצמוח ולחדש תוך שמירה על האיזון שאתם מעריכים.
ולבסוף, האותיות הקטנות....
כדי שקימברלי-קלארק תגדל ותשגשג, עלינו להיות ארגון כוללני שמיישם את החוויות והתשוקות המגוונות של חברי הצוות שלו למותגים שמשפרים את חייהם של אנשים ברחבי העולם, ולכן אנו שואפים לבנות כוח עבודה שמקיף את חוויות הצרכנים שלנו.
כשאתם מביאים את המחשבה המקורית שלכם לקימברלי-קלארק, אתה מזין את ההצלחה המתמשכת של המיזם שלנו.
אנו מעסיקים מחויבים לשוויון הזדמנויות, וכל המועמדים המוסמכים יקבל התייחסות לעבודה ללא קשר לגזע, צבע, דת, מין, מוצא לאומי, סטטוס נכות, מעמד ותיק מוגן, נטייה מינית, זהות מגדרית, גיל, הריון, מידע גנטי, סטטוס אזרחות או כל תכונה אחרת המוגנת על פי חוק.
ההצהרות לעיל נועדו לתאר את הטבע הכללי ורמת העבודה שבוצעו על ידי עובדים המוקצים לסיווג זה.
הצהרות אינן מיועדות להתפרש כרשימה ממצה של כל החובות, האחריות והכישורים הנדרשים לתפקיד זה.
Primary Location
Gilboa
Additional Locations
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
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Type: Permanent Location: Afula, IL-Z
Salary / Rate: Not Specified
Posted: 2026-05-09 08:14:05
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Applications due by: June 5th
Pay Range DOE: $19.29/hour
Work Schedule: Various shifts – 1st shift - 6:00 am to 2:45 pm; 2nd shift - 2:45 pm – 11:00 pm; 3rd shift - 11:00 pm to 6:00 am.
Work Location: Various
This position is eligible for Paid Sick and Safe Time (PSST) under the Healthy Families and Workplaces Act.
All employees may also make pre-tax or post-tax (Roth) contributions to our retirement plan – must be 18 years of age to participate.
Goodwill of Colorado is a Public Service Loan Forgiveness Program (PSLF) eligible employer.
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*This is a temp-to-hire with the eligibility of full-time permanent placement.
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JOB SUMMARY:
The Unarmed Security Officer is tasked with protecting client property and personnel by maintaining security, promoting safety, and deterring illegal activity through a visible on-site presence.
* Maintains a visible presence to deter criminal, prohibited, or suspicious activity in both public and restricted areas, including main and auxiliary buildings, grounds, parking lots, stairwells, and other assigned areas.
* Responds promptly and effectively to both emergency and non-emergency situations, including working in high-activity environments involving trespassing, drug activity, or similar issues.
* Provides verbal crisis intervention by quickly assessing situations, establishing rapport, recognizing emotional or cognitive limitations, and offering appropriate support or direction.
* Performs physical intervention during crisis situations when necessary and authorized.
* Escorts individuals and assists client personnel as required.
* Remains consistently alert and vigilant to conditions or activities that may result in personal injury, property damage, or loss.
* Prepares accurate, clear, and legible incident and activity reports.
* Maintains positive and professional working relationships with coworkers, client staff, and other vendors.
* Demonstrates functional knowledge of the assigned facility and, when applicable, multiple facilities.
* Enforces and complies with all client policies, procedures, and guidelines.
* Performs additional duties as directed by Security leadership or other authorized personnel.
* Completes other related tasks as assigned.
QUALIFICATIONS:
Qualifications & Requirements
To perform this position successfully, an individual must be able to carry out each essential duty satisfactorily.
The qualifications below represent the knowledge, skills, and abilities required.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role.
Education
* High school diploma or equivalent is required.
* Preferred qualifications include a college degree in criminal justice or a related security field, graduation from a police academy, or rele...
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Type: Permanent Location: Aurora, US-CO
Salary / Rate: Not Specified
Posted: 2026-05-09 08:06:27
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Thank you for your interest in a career at NeighborHealth, formerly East Boston Neighborhood Health Center!
As one of the largest community health centers in the country, NeighborHealth is proud to serve the greater Boston area with a strong commitment to the health and well-being of our patients and communities.
Whether you're a nurse or physician providing direct care, a manager leading dedicated teams, or part of the essential support staff who keep our operations running smoothly — every role at NeighborHealth is vital.
Together, we’re advancing medicine and delivering the best care experience for our patients and community!
Interested in this position? Apply online and create a personal candidate account!
Current Employees of NeighborHealth- Please use our internal careers portal to apply for positions.
To learn more about working at NeighborHealth and our benefits, please visit out our Careers Page.
Time Type:
Full time
Department:
Quality
All Locations:
10 Gove Street – Taylor Building, 151 Orleans Street, 20 Maverick Square – Cradock Building, 300 Ocean Avenue – Revere, 79 Paris Street
Position Summary:
NeighborHealth is seeking a Population Health Coordinator to join our team, where you will have the opportunity to make a profound impact on the lives of underserved individuals and families.
You will provide a critical role by successfully supporting the quality improvement, outreach, clinical operations, and population health efforts of key strategic initiatives within our department and across the health center.
This role is ideal for a professional with knowledge of clinic operations and patient facing care who is looking to grow in quality improvement, population health, and using data to inform decisions to improve patient outcomes and/or workflows.
* $The role requires a combination of patient outreach and quality improvement work.
You will work with patients to identify barriers to care, solve these barriers, and communicate with care teams across the organization.
In addition, you will learn evidence-based tools in quality improvement, process improvement, and data usage to improve patient outcomes.
The successful candidate will be able to perform the following responsibilities:
* Lead or support clinical operations workflow development and iterative improvement as assigned.
* Demonstrate the ability, willingness, and motivation to learn and apply population health and quality improvement principles.
* Support Quality Improvement/Population Health Managers with meeting preparation, data collection and analysis, clinical operations activities, quality improvement initiatives, and workflow development.
* Build and maintain relationships with key stakeholders across the enterprise as needed or directed.
* Collaborate with key stakeholders to drive improvements in patient care and patient outcomes as directed.
* Assist with implementing and monitoring workflow and/or scr...
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Type: Permanent Location: East Boston, US-MA
Salary / Rate: Not Specified
Posted: 2026-05-09 08:05:01
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Thank you for your interest in a career at NeighborHealth, formerly East Boston Neighborhood Health Center!
As one of the largest community health centers in the country, NeighborHealth is proud to serve the greater Boston area with a strong commitment to the health and well-being of our patients and communities.
Whether you're a nurse or physician providing direct care, a manager leading dedicated teams, or part of the essential support staff who keep our operations running smoothly — every role at NeighborHealth is vital.
Together, we’re advancing medicine and delivering the best care experience for our patients and community!
Interested in this position? Apply online and create a personal candidate account!
Current Employees of NeighborHealth- Please use our internal careers portal to apply for positions.
To learn more about working at NeighborHealth and our benefits, please visit out our Careers Page.
Time Type:
Full time
Department:
Quality
All Locations:
10 Gove Street – Taylor Building, 151 Orleans Street, 20 Maverick Square – Cradock Building, 300 Ocean Avenue – Revere, 79 Paris Street
Position Summary:
NeighborHealth is seeking an experienced Quality analyst.
This role is ideal for a professional with deep expertise in data management, EMR (Epic) reporting, dashboard build and management, data analysis, and Quality/Process improvement, with an ability to work collaboratively in cross-functional teams and translate data into actionable steps.
The Quality Analyst plays a key role in advancing the health center’s strategic projects on quality, population health, and performance improvement.
This position is responsible for collecting, validating, analyzing, and reporting clinical and operational data to support organizational priorities.
Working closely with senior leadership, the analyst produces dashboards, supports UDS and regulatory reporting, and provides actionable insights that drive improvements in patient outcomes and overall performance.
The successful candidate will be able to perform the following responsibilities:
Quality Measurement & Reporting
* Develop, maintain, and analyze quality performance reports including UDS, HEDIS, PCMH, CMS, and internal quality measures.
* Extract, validate, and manage data from Epic using Reporting Workbench and other internal reporting tools.
What You’ll Bring
* Bachelor’s degree in Public Health, Healthcare Administration, Data Analytics, or related field.
* 1–3 years of experience in healthcare quality, data analysis, or population health.
* Strong proficiency in Microsoft Excel.
* Experience with data visualization (charts, graphs, dashboards).
* Familiarity with quality improvement methodologies.
* Knowledge of SQL.
* Experience with Epic Reporting Workbench, Slicer Dicer, or other Epic reporting tools.
* Understanding of UDS, HEDIS, PCMH, and other clinical quality metrics.
Preferred
* Epic Cogito cert...
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Type: Permanent Location: East Boston, US-MA
Salary / Rate: Not Specified
Posted: 2026-05-09 08:04:55
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What you’ll do as a Senior Subcontracts Administrator
* Deliver Cradle-to-Grave subcontracts support from solicitation through subcontract closeout
* Collaborate with Subcontract teammates and Program Managers (PMs) to identify and define subcontracting requirements, provide guidance concerning the required subcontract type (FFP, CPFF, T&M, etc.), and complete of all backup documents required to initiate and execute subcontract actions
* Ensure subcontracts are consistent with legal requirements, customer specifications, and government regulations
* Provide training to PMs and Division Administrators on subcontract requirements
* Prepare and disseminate information to appropriate employees regarding subcontract status, compliance, modification, deviation, negotiation, and termination
* Stay up to date on subcontracting standards, legislation, plans and policies
* Develop solutions to complex problems which require the regular use of ingenuity and innovation
* Build positive relationships with division partners and subcontractors by maintaining excellent internal and external customer service standards
* Mentor Junior Subcontract Administrators, as needed
* Assist in Small Business Subcontract Plan Reporting
Senior Subcontracts Administrator Requirements
* Demonstrated knowledge/experience working in a cradle-to-grave federal subcontracting environment, from the solicitation phase through subcontract closeout
* Demonstrated knowledge/experience in FAR/DFAR requirements
* Demonstrated expertise in negotiation and development of subcontracts
* Experience with government subcontract file documentation, including CPSR requirements for federal acquisitions
* Experience in a high-volume subcontract administration environment
* Experience with various contract types, including CPFF, FFP, T&M, and CR
* Ability to create and edit files in Microsoft Word, Adobe Acrobat, Excel to create and edit documents
* Demonstrated understanding and successful application of principles, theories, concepts and techniques in the preparation of competitive and non-competitive subcontracts, evaluation and negotiation of cost/price and terms and conditions, post-award subcontract management, and closeout activities
Senior Subcontracts Administrator Preferences
* Advanced SharePoint experience
* Experience using Deltek and/or Costpoint
Education and Experience
* Bachelor’s degree in Business Administration or equivalent
+ 5 –7 years of related experience with a Bachelor’s degree
+ 3-5 years of related experience with a Master’s degree
+ 8 years minimum of related experience in lieu of a degree
REMOTE WORK NOTICE: This position is available for fully remote or hybrid work consideration at or near the Washington, DC, Raleigh, NC or Albuquerque, NM areas.
Company & Division Information
Applied Research Associates, Inc....
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Type: Permanent Location: Albuquerque, US-NM
Salary / Rate: Not Specified
Posted: 2026-05-09 07:53:05
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Provides direct case management services to residents and/or aftercare clients based on individual treatment plans.
Serves as primary counselor for residents and/or aftercare clients.
Serves as primary resource for the coordination of service needs of residents and/or aftercare clients.
Performs individual counseling, group co-facilitation, crisis intervention, weekly treatment planning reviews, psycho-social assessments, and required documentation.
Type: Permanent Location: Toledo, US-OH
Salary / Rate: Not Specified
Posted: 2026-05-09 07:43:49
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General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
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Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2026-05-08 08:48:11
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Technician – Bacterins
As a technician – Bio/Pharm Production, you will be part of the manufacturing team supporting vaccine production at the Fort Dodge site.
In this role, you’ll be responsible for operating and troubleshooting production equipment, executing aseptic processes, and ensuring all activities meet cGMP, safety, and quality standards.
Your Responsibilities:
• Perform aseptic manufacturing activities including weighing, measuring, sampling, and batch record execution in compliance with cGMP standards
• Operate, monitor, and troubleshoot production equipment; ensure materials and equipment are ready and released for use
• Execute production processes, cleaning, environmental monitoring, and in-process quality checks
• Complete documentation including batch records, SOP updates, and deviation reports using electronic systems
• Follow safety protocols and contribute to continuous improvement initiatives, including LEAN practices
What You Need to Succeed (minimum qualifications):
• Education: Bachelor’s degree in microbiology or related field, OR associate’s degree with 2+ years of experience, OR High School Diploma/GED with 4+ years of relevant experience
• Experience: Experience in manufacturing, biological production, or regulated environments
• Top 2 skills: Strong attention to detail and ability to follow GMP procedures + basic technical troubleshooting and equipment operation
What will give you a competitive edge (preferred qualifications):
• Experience with biological manufacturing equipment (e.g., fermentation, centrifuge, concentration units)
• Familiarity with ERP or electronic inventory management systems
• Experience in regulated environments (cGMP, USDA, OSHA)
• Ability to write SOPs, deviations, and support documentation
• Exposure to LEAN or continuous improvement initiatives
Additional Information:
• Travel: Minimal
• Location: Fort Dodge, IA – Onsite Manufacturing Role
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identit...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2026-05-08 08:43:11
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Tu Rol: Associate-Quality Control (Contrato Temporal)
Como Associate-Quality Control, formarás parte del equipo de Calidad para garantizar que las materias primas, materiales de empaque y productos terminados cumplan con las especificaciones establecidas.
En este rol, serás responsable de ejecutar procesos analíticos, documentales y de inspección, asegurando el cumplimiento regulatorio local y los estándares de calidad de Elanco.
Tus Responsabilidades:
* Ejecutar análisis fisicoquímicos, manejo de muestras y aplicaciones en SAP para materias primas, productos a granel y estudios de estabilidad.
* Gestionar los procesos relacionados con la validación y el desarrollo de métodos analíticos en cumplimiento con las normativas locales.
* Realizar el muestreo e inspección de materiales de empaque y productos fabricados para asegurar que cumplen con los atributos físicos de calidad.
* Gestionar y dar seguimiento a los eventos de calidad relacionados con los materiales de empaque en coordinación con los proveedores.
* Apoyar en procesos administrativos de cumplimiento regulatorio, como programas de estabilidades, validación de procesos y auditorías.
Lo que necesitas para tener éxito (requisitos mínimos):
* Título Universitario (Licenciatura en Química, Farmacia, Ingeniería Química o campo afín).
* Un mínimo de 2 años de experiencia en Control de Calidad, análisis fisicoquímicos o laboratorios dentro de la industria farmacéutica.
* Experiencia práctica en validación de métodos analíticos y manejo del sistema SAP.
Lo que te dará una ventaja competitiva (requisitos preferibles):
* Conocimiento sólido de las normativas regulatorias locales y estándares de calidad farmacéutica.
* Experiencia en inspección de materiales de empaque y evaluación de atributos físicos (impresión, hermeticidad, aspecto).
* Habilidad comprobada para gestionar eventos de calidad y trato directo con proveedores.
* Capacidad analítica y atención al detalle en la documentación de procesos.
* Nivel de inglés intermedio.
Información Adicion...
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Type: Permanent Location: Ecatepec de Morelos, MX-MEX
Salary / Rate: Not Specified
Posted: 2026-05-08 08:43:09
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Join the dynamic and diverse team at La Jolla Beach & Tennis Club, Inc., where tradition meets opportunity.
Our family of properties includes the iconic La Jolla Beach & Tennis Club, a private oceanfront club with world-class tennis courts and direct beach access; the inviting La Jolla Shores Hotel, a beachfront getaway beloved for its relaxed coastal charm; and the internationally acclaimed Marine Room, celebrated for its fine dining and dramatic surfside views.
These landmark destinations are cherished La Jolla institutions, built on a legacy of family values, exceptional service, and a deep commitment to our community.
As part of our team, you’ll enjoy a supportive and collaborative work environment, competitive pay, outstanding benefits, and the chance to grow your career in a setting as inspiring as the coastline we call home.
Whether you’re starting your career or ready to take it to the next level, we’re passionate about helping our employees thrive in one of California’s most beautiful destinations.
What we offer:
* Free daily meal and salad bar
* Benefits including: Medical, Dental, Vision, 401K (based on employment status)
* Paid vacation, sick, and holiday time
* Dining discounts for employees (and up to 6 guests) at the Marine Room, The Shores Restaurant, and our Club Dining!
* Property retail shop and hotel discounts
* $500 referral bonus for referring new employees to The La Jolla Beach & Tennis Club
What we ask:
* Consistently provide professional, attentive, and genuinely friendly service
* Promote and follow LJBTC, Inc's Signature Service standards and requirements to ensure a lasting impression of exemplary service resulting in satisfied and loyal members and guests
Hourly Rate
$23.00
Summary
Guard's hotel, club and restaurant properties against fire, theft, vandalism, and illegal entry by performing the following duties.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
* Must have a San Diego County EMT certification.
* Be able to administer advanced medical treatment in line with EMT certification.
* Stands guard at designated post. Permits authorized persons to enter property.
* Regulates vehicle and pedestrian traffic at property entrances to maintain orderly flow.
* Patrols buildings and grounds of the property to ensure the safety and security of members, guests, visitors, and employees.
* Examines doors, windows, and gates to determine that they are locked and secure.
* Warns violators of rule infractions, such as loitering, smoking, trespassing, or carrying forbidden articles. Escorts persons engaging in suspicious or criminal acts off property.
* Inspects equipment and machinery to ascertain if tampering has occurred.
* Watches for and reports irregularities such as fire hazards, leaking water pipes, and security doors left unlocked.
* Observes departing personnel to guard against theft of company p...
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Type: Contract Location: La Jolla, US-CA
Salary / Rate: Not Specified
Posted: 2026-05-08 08:02:00
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
At Roche, we believe precision medicine radically improves lives.
Our Global CAP/CLIA laboratories are the "heartbeat" of diagnostic innovation, bridging the gap between early research and life-saving commercial diagnostics.
As a Laboratory Manager, you aren't just overseeing a facility; you are leading a team that transforms complex biological data into the insights clinicians need to treat patients with cancer and other life-altering diseases.
We are seeking a high-caliber Laboratory Manager (m/f/d) to oversee our dual-specialty pathology and immunoassay laboratory.
This role requires a unique blend of technical expertise in tissue-based diagnostics and immunoassay automated testing.
You will be responsible for the operational excellence of the lab, ensuring that both the Histology/Pathology and Immunoassay/Chemistry departments function at peak efficiency while maintaining total compliance with ISO15189, CAP (College of American Pathologists) and CLIA regulations.
The Opportunity
You will oversee a dual-specialty laboratory at the forefront of the industry.
Your leadership will span two critical domains:
* Anatomic Pathology: Managing high-complexity tissue-based diagnostics, including advanced Immunohistochemistry (IHC) and In Situ Hybridization (ISH)
* Immunoassay Excellence: Driving peaks of operational efficiency in our automated immunoassay tracks on state-of-the-art cobas® platforms
You will also be a key driver in our Digital Pathology transformation, integrating whole-slide imaging and AI-based image analysis into routine clinical workflows to set new standards for diagnostic precision.
Your key responsibilities:
* Visionary Operational Leadership: Supervise the daily "rhythm" of the lab, synchronizing pathology and immunoassay workflows to ensure competitive turnaround times (TAT)
* Guardian of Quality: Maintain an "inspection-ready" culture, serving as the primary lead for CAP/CLIA and ISO 15189 audits
* Champion of People: Lead, mentor, and inspire team of Laboratory scientists, fostering a culture of continuous learning and technical excellence
* Strategic Technical Oversight: Manage the validation and implementation of new assays and novel pla...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-05-08 07:44:52
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Ready to lead complex energy projects that shape the future of sustainable development?
At ERM, we’re looking for a strategic thinker and hands-on leader to join our Upper Midwest team as a Managing Consultant, Environmental Permitting.
This is your opportunity to influence high-profile energy infrastructure projects across North America—while driving compliance, innovation, and environmental stewardship.
Why This Role Matters
Energy development is evolving rapidly, and regulatory compliance is critical to success.
As a Managing Consultant, you’ll be at the forefront of guiding clients through environmental permitting and impact assessments for transformative projects—ranging from renewable energy to midstream oil and gas and electric transmission.
Your expertise ensures these projects meet federal, state, and local requirements while advancing sustainable solutions.
What Your Impact Is
* Lead environmental permitting strategies for major energy projects regulated by FERC and state siting agencies.
* Shape project outcomes by managing complex, multi-site initiatives on time and within budget.
* Build trusted client relationships and drive business development opportunities.
* Mentor and develop junior consultants, fostering technical excellence and leadership within ERM.
What You’ll Bring
Required:
* Bachelor’s or Master’s degree in environmental studies, environmental science, planning, or a related field, or equivalent relevant experience.
* 4+ years (5+ years preferred) of experience in environmental impact assessment, siting, and permitting for energy projects.
* Strong knowledge of NEPA, Clean Water Act, Endangered Species Act, and state siting regulations (i.e., Minnesota Public Utilities Commission).
* Proven ability to manage projects, lead teams, and communicate effectively with clients and regulatory agencies.
* Excellent technical writing and interpersonal communication skills.
* Proficiency in MS Office Suite.
* This position is not eligible for immigration sponsorship.
Preferred:
* Familiarity with permitting processes in the Upper Midwest (ND, SD, MN, WI, IA).
* GIS and mapping experience (National Wetland Inventory, USGS, aerial photography).
Key Responsibilities
* Manage single or multi-site projects, ensuring scope, budget, and timelines are met.
* Prepare siting and permit applications for federal, state, and local authorities.
* Develop environmental plans (erosion control, stormwater, spill prevention).
* Collaborate with ERM teams on impact assessments, routing studies, and facility siting.
* Engage with regulatory agencies and stakeholders to secure approvals.
* Generate technical proposals and support business development initiatives.
* Oversee QA/QC processes and mentor junior staff.
For the Managing Consultant, Environmental Permitting position, the anticipated annual base pay is $90,000 – $104,...
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Type: Permanent Location: Minneapolis, US-MN
Salary / Rate: Not Specified
Posted: 2026-05-08 07:34:33
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your role:
We have an exciting opportunity to join a dynamic Biopharma Technical Development team at Elanco, where you will play a key role in the development and scale-up of innovative biopharmaceutical and vaccine products.
Working in a collaborative, inclusive and innovation-driven environment, you will contribute to bringing new therapies from concept through to commercialization — making a real impact on animal health globally.
This is a hands-on laboratory role with strong technical ownership, offering the chance to work across global R&D projects, mentor others, and influence key scientific and business decisions.
Your responsibilities:
As a Consultant Scientist, you will take ownership of downstream purification process development for large molecule projects, supporting activities from early-stage development through to commercialization.
Your responsibilities will include:
* Lead downstream (protein purification) development across project phases
* Design, execute and evaluate experiments using sound scientific and statistical approaches
* Apply Quality by Design (QbD) principles to develop robust processes and control strategies
* Drive scale-up activities and support pilot plant operations in Speke
* Lead and support technical transfers and process implementation
* Ensure successful delivery of materials for clinical trials (IVP/CT) and registration
* Ensure high-quality, data-driven outputs across projects
* Develop and maintain strong experimental strategies and documentation
* Deliver clear and impactful technical reports
* Partner with cross-functional and global teams to support product development
* Act as a technical expert across the Elanco network
* Contribute to commercialization strategies and innovation initiatives
* Mentor and support junior scientists
* Foster a collaborative and knowledge-sharing team culture
* Identify new technologies and support future capability building
* Contribute to scientific and technical strategy within the function
What You Need to Succeed (minimum qualifications):
...
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Type: Permanent Location: Liverpool, GB-LIV
Salary / Rate: 60000
Posted: 2026-05-07 08:17:04
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Reporting & Analysis Analyst III (Global Business Services)
Job Description
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Main Responsibilities:
Financial Accounting and Regional Management Reporting
* Prepare and coordinate the consolidation of financial statements and financial reviews of Kimberly-Clark Asia Pacific entities to facilitate efficient, timely, and accurate reporting of results, reviews, and projections as needed, in accordance with local and US GAAP requirements
* Compilation, submission and reporting of the financial results and other financial information and reporting schedules for Asia Pacific affiliates in accordance with US GAAP to senior stakeholders in the GBS, Record to Report team and Regional Finance Teams
* Ensure that corporate governance is met, taking accountability for effective operation of relevant financial reporting controls
* Assist in better business decisions by provision of financial expertise and insightful analysis
Reconciliation and Integrity of Statutory Financial Statements
* Ensure the integrity of monthly statutory financial statements is maintained by through relevant detailed account reconciliations and variance analysis to ensure the financial records accurately reflect the status of transactions and events.
Stakeholder Engagement
* Partners with stakeholders in GBS & across countries in APAC to ensure timely submission of financial reporting deliverables along with building knowledge and expertise in understanding and explaining key business drivers to aid financial reviews and commentary preparation.
Continuous Improvement
* Champion ways to improve financial reporting processes via sustainable and scalable automation, simplification, and standardization initiatives.
* Continuously review and improve financial reporting controls and streamline processes under area of responsibility.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact.
We’re founded on 151 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2026-05-07 08:10:15
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The Missions, Concepts and Capabilities (MCC) division of Applied Research Associates, Inc.
(ARA) Applied Research Associates, Inc.) is looking to hire a full-time Chemical Analyst.
The successful candidate will provide general knowledge and subject matter expertise as a Chemist in support of the Defense Threat Reduction Agency (DTRA).
The candidate will work closely with other members of the multi-disciplinary Reachback team.
The successful candidate will be team-oriented and possess strong multi-tasking abilities.
In addition, this position requires the use of models in all areas of CBRNE.
Tasks also include the presentation of modeling results and decision support aids to both internal and external customers in the form of written reports and oral presentations.
This person will perform complex engineering and scientific modeling and analyses and providing scientific reports and technical assessments to military decision makers.
Essential Functions:
* Review current research in various and potentially diverse subject areas for familiarity and relevance
* Providing general knowledge and chemical-related subject matter expertise to government agencies and first responders
* Assist in the development of program plans, timelines, and technical documents
* Attend technical and programmatic meetings in which you coordinate responses from scientific community members and review the assembled materials for technical accuracy, consistency, and completeness.
* Willingness to be cross-trained to provide modeling and information across the CBRNE spectrum.
Required Qualifications:
* MS in Chemistry or a related field with 1 year of experience
* Candidate should be able and willing to work rotating shifts in support of 24/7/365 operations
* Must be a US Citizen
* Active US DoD Secret or above clearance
* Strong communication skills, both orally and verbally, technical presentation, teamwork mentality, graphic visualization and Microsoft Office proficiency skills are required
Desired Qualifications:
* Experience working with organizations within DTRA or the DoD as well as other government agencies
* Experience in Combating WMD threats or CBRN threats (primarily through modeling and simulation and/or test experience)
* Experience in CBRNE/WMD with a focus on chemical weapons, hazardous chemicals, and other toxic industrial materials
* Experience with modeling and simulation
COMPANY INFORMATION:
Applied Research Associates, Inc.
is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems in the physical sciences.
The company, founded in Albuquerque, NM, in 1979, currently employs 1100 professionals.
ARA offices throughout the United States and Canada provide a broad range of technical expertise in defense technologies, civil technologies, computer software and simulation, systems...
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Type: Permanent Location: Fort Belvoir, US-VA
Salary / Rate: Not Specified
Posted: 2026-05-07 07:54:15
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ABOUT THE ROLE
Quality Auditors who will be responsible for all phases of inspection and quality audits. The Quality Auditor ensures conformance to blueprint as appropriate, customer specific and internal procedure requirements for all products, and processes.
This is an afternoon shift direct-hire opportunity, 11:00 pm - 7:00 am, with overtime and weekends as needed. This position offers a 15% Shift Premium.
WHAT YOU’LL DO
* Perform receiving, in process and final audit inspection as directed
* Record attribute and variable data on in process inspection record according to parts-specific dynamic control plans
* Verify that procedures are being followed and inspections performed by operators
* Responsible for supporting the team efforts of set up and operation of stamping presses as related to inspection tools, etc.
* Perform final audit inspection which requires tagging parts and dunnage properly for storage in work in process areas or for shipment to the customer
* Responsible for notifying press and/or production if non-conforming material is detected, suspect material is to be identified and isolated.
Assist in identification of “Clean Point”.
* Communicate findings, regarding trends or nonconforming parts or processes to appropriate personnel and participate in corrective action process
* Perform First piece and in-process inspections and log in process inspection record, as applicable, including contamination testing, as applicable
* Perform Last Off inspections, including provide part data to assist in tooling repairs on last off report
* Generate reports of nonconforming material or product(s)
* Identify nonconforming material and quarantine
* Assist in root cause analysis and problem-solving tasks as assigned
* Assist in Gage R&R’s and Part Capability Studies as assigned
* Identify trends using basic statistical process control techniques
* Other duties as assigned
* Communicates to next shift personnel
WHAT YOU’LL NEED TO SUCCEED
* All inspection work requires proficient use of measuring equipment (scales, micrometers, calipers) and checking fixtures, and metrology tools (surface testers, CMM’s, )
* Must be computer literate and have working knowledge of other workplace machinery such as a SAP hand held scanners calculators and printers
* Must be able to read blueprints as appropriate
* Possess working knowledge of IATF16949, ISO 14001, and Q1 Compliance Criteria
WHAT’S IN IT FOR YOU
* Employee Stock Ownership Plan
* Incentive Bonus
* Medical, Vision, Dental
* Prescription Drug Plan
* Pet Insurance Plans
* 401K
* Paid Vacation & Holidays
* Tuition Reimbursement
* Short Term Disability
* Health and Wellness Reimbursement
* Employee Recognition
* Discount Programs
WHAT ELSE YOU’LL NEED TO KNOW
* Excellent communication skills, both verbal...
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Type: Permanent Location: Sterling Heights, US-MI
Salary / Rate: Not Specified
Posted: 2026-05-07 07:46:12
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Westminster Woods on Julington Creek is the Natural Choice in active living.
We are a five star facility located on beautiful Julington Creek in Northwest St.
Johns County.
Our employees work with excellence and serve with heart.
We are currently seeking a Speech Therapist to work PRN.
This position will provide patient/resident assessment, care planning, direct treatment and consultation to a general rehab caseload.
Participate in the Interdisciplinary team process.
Provide teaching and training to care giver staff.
Involvement in clinical program development.
EOE, DFWP - "We honor those who have served."
SPEECH THERAPIST ESSENTIAL DUTIES AND RESPONSIBILITIES:
1.
Evaluate, diagnose and treat cognitive, swallowing, speech & language disorders or communication efficiencies following MD orders.
2.
Conduct assessments and screens to determine therapy needs.
Enter in the system Plan of Care that meets resident’s needs.
3.
Develop and provide Caregiver Training to current staff.
4.
Maintain timely and accurate documentation and enter information into the system.
5.
Perform Resident’s screening during the admission process, quarterly & annual screening to determine the need for therapy.
SPEECH THERAPIST ESSENTIAL QUALIFICATIONS:
Master of Science degree in Speech Language Pathology and Professional Licensure where required by state law; two years clinical experience preferred.
Candidates should demonstrate effective verbal and written communication skills; utilize effective time management skills.
Candidates should also demonstrate the ability to function effectively in multi-faceted systems and to interact effectively with all levels of staff and customers.
Candidates that are available to work weekends are a plus!
Applicants can learn more about Florida background screening requirements at https://info.flclearinghouse.com/.
When applying to this opportunity, please upload a cover letter, current resume, and any applicable licenses or certifications.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2026-05-07 07:43:10
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Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world's most in demand and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life's essentials - and creates lasting value for its colleagues, customers, and other stakeholders.
Learn more about the company's Customized Polymer, Sustainable Fiber, Durable Metal, and Integrated Solutions at www.greif.com and follow Greif on Instagram and LinkedIn.
OUR VISION:
Being the customer service company in the world.
OUR PURPOSE:
Creating packaging solutions for life’s essentials.
Job Requisition #:
034083 Account Manager Mill (Open)
Job Description:
The Junior Area Sales Manager supports revenue growth by managing a defined portfolio of smaller or lower complexity accounts while also qualifying, advancing, and closing sales opportunities.
This role combines proactive prospecting, pipeline management, and account expansion responsibilities, operating with oversight and collaboration from senior sales leadership.
The Junior Area Sales Manager owns opportunities within defined deal size and margin parameters and serves as a key feeder and partner to Area Sales Managers.
Key Responsibilities
Sales & Opportunity Management
* Manage inbound and outbound customer interactions to qualify leads and advance opportunities through the sales funnel.
* Own opportunities within defined complexity, deal size, and pricing thresholds; progress deals from discovery to close.
* Maintain a robust and accurate pipeline in CRM, ensuring timely updates to opportunity stages, probabilities, close dates, and next steps.
* Prepare standard quotes and proposals using approved tools and templates; coordinate pricing exceptions to ensure margin discipline.
* Forecast sales results for assigned accounts with accuracy and consistency.
Account & Territory Support
* Manage a small territory or portfolio of accounts with oversight; execute call plans to expand share of wallet and retain customers.
* Build and maintain relationships with purchasing and operational contacts to secure reorders and identify upsell opportunities.
* Monitor account health metrics (win rate, cycle time, retention) and take corrective actions to improve performance.
* Support targeted campaigns for whitespace, dormant, or underpenetrated accounts through structured outreach and follow‑up.
Customer Engagement & Solutions Development
* Build relationships to understand customer needs, applications, and decision criteria; align Mills value propositions accordingly.
* Coordinate product demos, sampling, trials, or technical discussions with internal resources as needed.
* Use standardized talk tracks, value‑based selling techniques, and objection handl...
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Type: Permanent Location: Delaware, US-OH
Salary / Rate: Not Specified
Posted: 2026-05-06 09:21:17
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The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Essential Duties:
Scientific/General
* Ensure reports are compliant with current procedures.
* Ensure final reports accurately reflect the data, results, and conclusions of the testing.
* Act as a final signature for assigned studies.
* Collaborate on Customer Specification Sheets (CSS) etc.
as assigned.
* Ensure sample and data traceability are maintained throughout testing.
* Ensure calculations and statistics accurately reflect the raw data.
* Ensure accuracy of raw data.
* Ensure test controls and monitors are accurately recorded and reviewed.
* Collaborate within the Quality Event (QE) process.
* Read and maintain an understanding of validation procedures.
* Collaborate with document owners on Standard Test Procedures (STP) as assigned.
Regulatory Compliance
* Know and follow applicable regulatory requirements (GMP, GLP, ISO, etc.).
* Know and follow company policies and procedures.
* Ensure that test procedures are approved, communicated to, and followed by analysts.
* Ensure all data are accurately and concurrently recorded.
* Ensure unforeseen circumstances or events are recorded and that corrective action is taken.
* Complete required training on time.
Customer Service
* Uphold the NL service standard.
* Communicate regularly with sponsors as needed to relay study updates and CSS details.
* Meet or exceed sponsor expectations.
* Collaborate with the Sales department on testing quotes.
* Maintain a general understanding of company pricing and credit policies.
* Review and update study information in CRM and/or other laboratory systems.
Project Management
* Coordinate workflow to ensure sponsor expectations are met.
Professionalism
* Keep current with technical and scientific information.
* Ensure analysts understand testing performed on behalf of the study director.
* Attend work regularly and reliably.
* Adhere to all policies and procedures.
* Perform other duties as assigned
Education and experience requirements:
* B.S.
degree (li...
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Type: Permanent Location: Taylorsville, US-UT
Salary / Rate: Not Specified
Posted: 2026-05-06 09:16:56
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DataVoice, a division of Harris; is seeking a Support Analyst.
The DataVoice Support Specialist provides timely, professional, and customer-focused technical support for DataVoice customers.
This role assists customers with software, application, and operational support issues while building knowledge of DataVoice products, customer environments, support processes, and internal tools.
The DataVoice Support Specialist is responsible for documenting support activity, troubleshooting assigned issues, communicating clearly with customers and internal teams, and escalating more complex or higher-impact issues as needed.
This role plays an important part in helping maintain stable customer environments, supporting service continuity, and delivering a positive customer experience.
This remote role welcomes candidates anywhere in Canada and the US.
Travel is required as needed, approximately 5%.
Candidates must hold a current, valid passport and be legally eligible to travel internationally.
This includes either passport based visa exemption or possession of any required travel visas for entry into Canada, the United States, and the Caribbean.
Preference will be given to candidates who can work in CST, but are open to PST/EST timezone.
Department: Customer Support — DataVoice
Reports To: Director, Customer Support
Salary:
48K - 60K
What your impact will be:
* Respond to customer support requests in a timely, professional, and customer-focused manner.
* Assist with troubleshooting software, application, data, integration, and basic system-related issues.
* Document customer issues, troubleshooting steps, communications, and resolutions clearly in the ticketing system.
* Monitor assigned tickets and follow up as needed to support timely ticket progression and resolution.
* Escalate customer-sensitive issues to senior team members, leadership, or internal technical teams as appropriate.
* Communicate clearly with customers regarding issue status, next steps, expected follow-up, and resolution progress.
* Partner with internal teams to help investigate issues, gather technical details, and support effective problem resolution.
* Assist with maintenance, upgrade, testing, and other operational support activities as assigned.
* Help identify customer-impacting issues, recurring problems, documentation gaps, or process concerns and share feedback with the team.
* Follow established support processes, service expectations, and escalation procedures to help ensure consistent customer service.
* Maintain and update support documentation, knowledge base content, standard procedures, and internal notes as needed.
* Build knowledge of DataVoice products, customer workflows, system configurations, support tools, and common troubleshooting practices over time.
* Support operational readiness by helping ensure assigned work is documented, organized, and appropriately escalated when needed.
...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2026-05-06 09:12:33
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Partner Software, a division of Harris; is seeking a Support Specialist provides timely, professional, and customer-focused support for Partner customers.
This role is responsible for assisting customers with software-related questions and issues, documenting support activity, and working with internal teams to help resolve problems.
The Support Specialist plays an important role in delivering a positive customer experience while building knowledge of support processes, products, and tools.
This remote role welcomes candidates anywhere in Canada and the US.
Travel is required as needed, approximately 5%%.
Candidates must hold a current, valid passport and be legally eligible to travel internationally.
This includes either passport based visa exemption or possession of any required travel visas for entry into Canada, the United States, and the Caribbean.
Preference will be given to candidates who can work in EST timezone.
Salary:
35K - 45K
What your impact will be:
* Respond to customer support requests in a timely and professional manner.
* Assist with troubleshooting software, application, and basic system issues.
* Document customer issues, troubleshooting steps, and resolutions in the ticketing system.
* Escalate more complex or higher-impact issues to senior team members or other internal teams as needed.
* Communicate clearly with customers and internal teams regarding issue status, next steps, and resolution progress.
* Follow established support processes and service expectations to help ensure consistent customer service.
* Assist with software updates, testing, and other support-related activities as assigned.
* Maintain and update support documentation, knowledge base content, and internal procedures.
* Monitor assigned tickets and follow up as needed to support timely resolution.
* Identify recurring issues or documentation gaps and share feedback with the team to support continuous improvement.
* Build knowledge of Partner products, support tools, and customer workflows over time.
What we are looking for:
* Associate’s degree, technical certification, or equivalent professional experience in a related field.
* 1+ years of experience in customer service, help desk, technical support, or a related role preferred.
* Strong communication and interpersonal skills with a customer-focused approach.
* Basic problem-solving skills and willingness to learn technical concepts and support processes.
* Ability to stay organized and manage multiple tasks in a fast-paced environment.
* Attention to detail and ability to document information clearly and accurately.
* Basic computer proficiency and comfort learning new software systems and tools.
What we can offer:
* 3 weeks’ vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision paid 100% by Harris starting from your first day of employment
* Employee stock ownership...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2026-05-06 09:12:32
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Our Business
Adare Pharma Solutions is a global Contract Development and Manufacturing Organization (CDMO) with locations across North America and Italy.
We offer a wide range of manufacturing, packaging, and research and development services.
Our clients range from growing biotech firms advancing groundbreaking clinical trials to established pharmaceutical companies producing high volumes of approved, widely used medicines.
By combining top talent from the life sciences industry with modern research and manufacturing technologies, Adare enables clients to deliver potentially lifesaving medicines in more easily consumable formats - particularly for patients such as infants or the elderly.
This is the meaning behind “Transforming Drug Delivery – Transforming Lives.”
Our Culture
When it comes to being an employee of Adare, although we are located across multiple countries and come from diverse backgrounds, we work together toward a common purpose.
Supported by leadership that is experienced and highly regarded in the industry, we are paving the way for a brighter and better future by attracting top talent from both within and beyond the CDMO space.
In addition to delivering high-quality results for our external clients, we foster a collaborative, client-centric culture internally - one where employees support one another, share knowledge, and encourage each other to bring their best selves to work each day.
Why Come to Adare?
Adare is Private Equity owned and poised for growth.
Employees are provided with internal development opportunities to progress within the organization, enhancing their professional skills and industry knowledge through Adare’s investment in their growth.
We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry, formulations, analytical research and development, finance, supply chain, sales, marketing, project management, human resources, and environmental health and safety.
Our benefits package is highly competitive, offering medical, dental, and vision coverage; a retirement plan with company match, paid time off and company holidays, tuition reimbursement with no waiting period, life insurance, pet insurance, Flexible Spending Accounts (medical and dependent care), and disability coverage.
Position
Formulation Technician
Location
Vandalia, Ohio
Summary
The Formulation Technician I, II, or III will assist the R&D Formulations staff with product development activities from small scale to commercial batch production. The Formulation Technician should be someone with a keen interest in life sciences or drug manufacturing. This is a developmental role where training is provided, offering an opportunity to learn various techniques of drug manufacturing including dispensing, blending, granulation, compression and coating.
Responsibilities
* Assist in running projects associated with product development, product and process optimization batches, a...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2026-05-06 07:58:34
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We are currently seeking School Psychologists in the following areas:
Goshen, NY; Wappinger, NY; Sugar Loaf, NY; Ulster County
Liberty POST is currently seeking a motivated and energetic School Psychologist for per diem employment to work with children who are birth-5 years old through Early Intervention and Preschool Special Education programs.
Immediate positions are available.
Liberty POST has offered its clients a range of high-quality and individualized services since 1994.
Backed by Liberty Resources Inc.
and part of a large social services circle, originally POST was a speech-language practice in Syracuse NY and has grown to provide a range of services throughout all of New York State and New Jersey.
We employ over 500 professionals in a variety of settings and offer a collaborative team approach to provide evaluation, direct therapy, and family education through child-directed play.
We are focused on the importance of a child’s natural learning environment, a family’s unique strengths and needs and the diverse population we serve.
Job Duties and Responsibilities:
* Evaluate, monitor and track child’s progress and adjust treatment plans accordingly.
* Test and evaluate child’s abilities to determine realistic goals.
* Record information on the initial evaluation, treatment, and progress in a timely manner using Electronic Medical Record system.
* Proficient at writing detailed analysis and reports.
* Effectively organize and maintain confidentially of child’s records and other documentations.
* Follow all state laws and regulations as it pertains to Early Intervention, CPSE/CSE special education.
Qualifications, Knowledge and Experience:
* Master's degree in School Psychology required
* Minimum of two years working with children in special education required
* Certification in NYS as a School Psychologist required
* Knowledge and experience administering standardized testing in the following areas: cognitive, achievement, behavioral/social-emotional and adaptive skills.
* Experience using Frontline (formerly IEP Direct) to assist in developing IEPs.
Benefits for this position:
* Health Benefits and Retirement packages available for FT positions
* Accrual of sick time based on NYS Sick time Laws
* Mentoring is offered to all providers
* Access to unlimited CEU courses offered that are accredited through ASHA, AOTA, APTA and CTLE
* Flexible scheduling
* Work with a team of professionals that care about making a difference
* Payment is biweekly with direct deposit
Job Type: Per Diem
Pay Rate:
* Evaluations - Psychological: $180
* Social History: $125
* Observation: $40
* CPSE meetings: $25
Liberty POST is an equal opportunity employer.
We offer equal employment opportunities to all persons without regard to race, color, ethnicity, religion, sex, sexual orientation, national origin,...
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Type: Permanent Location: Goshen, US-NY
Salary / Rate: Not Specified
Posted: 2026-05-06 07:40:07
