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Team Coordinator jobs in United States

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חברה
אופי המשרה
קטגוריות תפקיד
שם תפקיד (1)
United States
אזור
עיר
נמצאו 1,935 משרות
24.11.2025
E

Ebay Warehouse Incubation Team Member United States, New Jersey

Limitless High-tech career opportunities - Expoint
Unpack, review, and sort inventory to verify product condition and authenticity. Catalog inventory with detailed titles and key attributes that pertain to filters on our platforms. Store, putaway, and maintain...
תיאור:

What you will accomplish:

  • Unpack, review, and sort inventory to verify product condition and authenticity

  • Catalog inventory with detailed titles and key attributes that pertain to filters on our platforms

  • Store, putaway, and maintain organized storage areas for inventory accuracy and accessibility

  • Pack, label, and ship items within 48 hours of payment date according to established processes and carrier requirements

  • Collaborate with multiple departments to ensure items are processed safely and efficiently

  • Own individual projects while adapting daily to changing tasks and priorities, contributing to all warehouse operations as needed

  • Assist with developing and improving standard operating procedures (SOPs) for receiving, stowing, cataloguing and shipping

  • Support testing or pilot programs for new tools, systems, or operational workflows in the incubation environment

What you will bring:

  • Enthusiasm and willingness to learn warehouse processes and the collectibles industry

  • Strong project problem-solving skills

  • Ability to meet hard deadlines (Overtime needed depending on auction cycle)

  • High School Diploma or GED

Qualification Preferences:

  • 1+ year of warehouse experience (shipping, sorting, picking, cataloguing)

  • Working knowledge of the collectibles space in (sports, TCG, pop culture, etc.) preferred by not required

  • Ability to lift 30-50 lbs consistently

The base pay range for this position is expected in the range below:

$30,800 - $52,900
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23.11.2025
BS

Boston Scientific Team Lead Production Supervisor - Weekend Shift United States, Minnesota

Limitless High-tech career opportunities - Expoint
Produce high quality products, safely, on time for the customer at the lowest cost. Facilitate and partner with a cross functional production team of production, quality and manufacturing engineering team...
תיאור:

:

Your Responsibilities will Include:

  • Produce high quality products, safely, on time for the customer at the lowest cost
  • Facilitate and partner with a cross functional production team of production, quality and manufacturing engineering team members to achieve annual safety, quality, service and cost goals while maintaining a high engagement & high-performance culture
  • Identify customer requirements to deliver the right products at the right time
  • Be responsive & flexible to customer demands
  • Achieve & exceed product cost goals
  • Support new product development readiness activities for the line team
  • Manufacture products to the highest quality standards and ensure compliance to all Boston Scientific policies and regulations
  • Promote safety, quality & compliance among the team while maintaining Good Manufacturing Practices
  • Foster teamwork and enable a culture of Operational Excellence throughout the entire cross-functional team
  • Ensure effective two-way communication between the production line team and cross-functional support teams
  • Manage, motivate, develop, and involve product builders through coaching and performance management
  • Embed the company values through demonstration & recognition of individual & team behaviors
  • Utilize production area planning tools to ensure all resources are in place to achieve team commitments such as Direct Labor Staffing, Equipment Capacity, Support Team, and Space
  • Ensure product builder training is effective & efficient and maintain training versatility across entire team
  • Utilize leader standard work to ensure lines are meeting standards and escalate appropriately
  • Lead & create team engagement around continuous improvement goals for safety, quality, service, cost and space through the utilization of lean and operational excellence tools and best practices
  • Benchmark and share best practices
  • Partner with materials management team for build planning and material delivery systems and tools
  • Analyze build plan requirements and provide forward looking monthly production commitments
  • Anticipate requirements and position resources to meet & exceed the customer needs
  • Provide appropriate input into the long-term planning of the production area


Required Qualifications:

  • Bachelor’s Degree or equivalent combination of education and experience will be considered in lieu of degree
  • 4 years’ minimum of manufacturing and/or engineering experience
  • 4 years’ minimum of supervisor/management experience
  • Solid computer skills required including Microsoft Excel, Word, and PowerPoint
  • Demonstrated Lean tools/systems experience

Preferred Qualifications:

  • Experience in a regulated environment
  • Medical device industry experience
  • Strong written and verbal communication skills with the ability to communicate at all levels of the organization
  • Ability to be flexible and agile
  • Ability to be a self-starter

Maximum Salary: $ 156900

Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).


For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.

Show more

משרות נוספות שיכולות לעניין אותך

22.11.2025
WP

West Pharma Product Analysis Coordinator United States, Arizona, Scottsdale

Limitless High-tech career opportunities - Expoint
Receive, log, and organize all incoming packages, ensuring proper documentation and maintaining order throughout the entire complaint workflow process. Maintains processes and procedures for receiving handling, storage, and disposition of...
תיאור:
Job Summary

In this role, you will be under the direction of the Product Analysis Manager to support activities related to product root-cause failure investigations on electro-mechanical drug delivery devices in a biohazard laboratory. You will additionally drive investigation process lean initiatives, manage communication with internal and external customers, train team members on new devices and assist with coordinating work for the lab technicians.

Essential Duties and Responsibilities
  • Receive, log, and organize all incoming packages, ensuring proper documentation and maintaining order throughout the entire complaint workflow process
  • Maintains processes and procedures for receiving handling, storage, and disposition of returned devices according to regulations and company standards.
  • Maintains the product analysis lab including supplies, calibration, equipment maintenance, safety adherence, capacity improvements, and access
  • Coordinate lean process improvements for device investigations, lab procedures, and daily productivity as needed.
  • Communicates with customers regarding product issues and returned devices.
  • Creates and maintains a clean, neat, and safe work environment through identifying and resolving potential safety hazards.
  • Promotes teamwork and collaboration between departments to optimize processes and resolve problems.
  • Monitor upcoming deadlines and ensure all tasks are assigned and completed on time.
  • Demonstrates a “Customer Service” approach to all activities and assignments.
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
  • Complies with the company’s safety and quality policies at all times, including proper handling of biohazard materials and components.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Complies with site and enterprise safety procedures when handling biohazard materials/components and potent drug compounds.
Work Experience
  • 0 - 3 years of experience required
  • Experience working in a laboratory or cGMP/pharmaceutical environment preferred
  • Laboratory administrative/Coordinator/Analyst role preferred
Preferred Knowledge, Skills and Abilities
  • Experience in conducting root cause investigations of field units.
  • Experience in laboratory test equipment operation and maintenance such as Instron, CT scanner, oscilloscope, power supply, multi-meter, and microscopes.
  • Background in Microsoft excel for the purposes of trending complaint data.
  • Background in medical device or pharmaceutical industry.
  • Knowledge of lean manufacturing and operational excellence concepts.
  • Able to comply with the company’s safety policy at all times.
Physical Requirements
Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.
Additional Requirements
  • Must be able to stand for long periods of time
  • Use hands to finger, handle, feel or operate objects, tools or controls and reach with hands and arms
  • Physical ability and willingness to wear proper gowning for work in an ISO 5 compliant particulate cleanroom environment
  • Must be able to communicate effectively with written and oral skills, make quick decisions, interpret data, read and write, speak in front of groups, express and exchange ideas, understand direction and adhere to procedures
  • Organizational skills will enable planning, prioritization and achievement of goals especially of importance for the successful execution of related activities
  • Read and interpret data, information and documents
  • Must maintain the ability to work well with others in a variety of situations
  • Must be able to follow directions, multi-task, work under time constraints, problem solve, and prioritize
  • Ability to make independent and sound judgments
  • Observe and interpret situations, analyze and solve problems
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משרות נוספות שיכולות לעניין אותך

22.11.2025
BS

Boston Scientific Senior Quality Assurance Engineer - Field Action Team Lead United States, Minnesota

Limitless High-tech career opportunities - Expoint
Lead all phases of project management for Field Actions—planning, execution, monitoring, and closure—to ensure team accountability and on-time delivery. Prepare and manage project schedules, budgets, and deliverables using tools such...
תיאור:

About the role:

As the Field Action Team Lead within Global Quality Systems at Boston Scientific, you will play a critical role in managing and executing the Field Action process including Product Recalls, Field Safety Corrective Actions, and Safety Alerts. This position leads cross-functional Field Action teams, coordinating execution across multiple business units while ensuring compliance with internal quality procedures and external regulatory requirements.

This highly visible role requires strong project management, communication, and collaboration skills to effectively guide stakeholders including Business Unit Leaders, Quality Business Process Leads, Regional Field Action Coordinators, and other team members. You will oversee multiple Field Actions at various stages of completion, minimizing risks and ensuring timely, compliant execution.

Your responsibilities will include:

● Lead all phases of project management for Field Actions—planning, execution, monitoring, and closure—to ensure team accountability and on-time delivery.

● Prepare and manage project schedules, budgets, and deliverables using tools such as Microsoft Project; define and track key project tasks.

● Assign responsibilities, monitor progress, assess risks, and implement contingency plans to maintain quality and project integrity.

● Communicate project status through regular updates and meetings; collaborate across departments to address and resolve issues.

● Lead postmortem evaluations to document lessons learned and identify future improvement opportunities.

● Develop and maintain project plans for product changes and field action development, reporting key progress to senior leadership.

● Coordinate, finalize, and ensure compliance of all Field Action communications with internal and regulatory requirements.

● Support continuous improvement initiatives within the Field Action process.

Required qualifications:

● Bachelor’s degree and a minimum of 4 years' experience in a regulated industry (e.g., medical device, pharmaceuticals, or biotechnology); or Master’s degree with a minimum of 3 years' relevant experience.

● Minimum of 4 years' experience managing cross-functional projects, including scope, schedule, and budget.

● Strong background in post-market, field action (recall), and quality system processes.

● Proficiency in Microsoft Office and project management tools (e.g., Teams, PowerPoint, Excel, MS Project, Visio).

● Ability to travel 0–10%.

Preferred qualifications:

● Bachelor’s degree in communications, technical writing, or a related field such as science, health, or engineering.

● Effective communication skills, including experience engaging regulators, clinicians, and cross-functional stakeholders.

● Strong writing, editing, and presentation capabilities.

● Demonstrated problem-solving skills and ability to synthesize complex technical inputs.

● Strong organizational skills, attention to detail, and multitasking abilities.

● High emotional intelligence, situational leadership, and ability to influence across teams.

● Proactive, results-oriented mindset with a focus on quality and continuous improvement.

Maximum Salary: $ 156900

Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).


For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.

Show more

משרות נוספות שיכולות לעניין אותך

22.11.2025
WP

West Pharma Production Team Leader United States, Pennsylvania, Williamsport

Limitless High-tech career opportunities - Expoint
Take over information at shift change, using Excel to prepare shift change papers. Perform basic troubleshooting, cleaning, and maintenance tasks on molding and finishing equipment as directed. Utilize Intouch for...
תיאור:
Job Summary

Assists the Production Supervisor in the daily operations of the Direct Labor Department. Coordinates all activities of the weekend workforce. In addition, this position requires performing all essential duties for all direct labor positions.

Essential Duties and Responsibilities
  • Take over information at shift change, using Excel to prepare shift change papers.
  • Perform basic troubleshooting, cleaning, and maintenance tasks on molding and finishing equipment as directed.
  • Utilize Intouch for production scheduling, tracking, and capturing data.
  • Prepare production shop packets and labels. Review completed shop packets for accuracy.
  • Issue non-conforming material reports when defective lining material, bags, etc. are found.
  • Basic use of SAP: checking inventory balances, locating products and materials.
  • Responsible for Central Stores activities as needed.
  • Conditional Release Procedure - S.O.I. 13.3.2
  • Maintain a routine presence on the production floor to monitor and support all activities.
  • Give break(s) as required.
  • Work on special projects as directed by the Production Supervisor.
  • Monitor alarm systems for the facility and facilitate emergency response activities as designated.
  • Accident response, reporting, and investigation.
  • Ensure policies, rules, regulations, and procedures are followed. Report and document incidents.
  • Edit Kronos.
  • Follow call-in instructions on off-shifts and weekends to obtain coverage for all essential production activities.
  • Contact department managers if circumstances arise that require their input.
  • Train new hires in job functions in addition to certifying on procedures.
  • Actively participate and comply with all West HSE programs and regulations.
  • Maintain a neat and orderly work environment in accordance with West 5S program.
  • Maintains methods/procedures and all supporting documentation to meet the requirements of Quality Systems ISO 13485:2016
  • Performs additional duties at the request of the direct supervisor.
Education
  • High School Diploma or equivalent required and
  • Bachelor's Degree or working towards preferred
Work Experience
  • 5+ years’ production experience; with 2-year lead experience
  • Knowledge of Good Manufacturing Practices (GMP) requirements would be an advantage.
Preferred Knowledge, Skills and Abilities
  • Exhibits qualities of a leader, owning the responsibility and desiring to help the department to meet its goals.
  • Work in a manner that promotes good working relationships throughout the department.
  • Safeguard all corporate or plant confidential information.
  • Must have good verbal reasoning, numerate ability and mechanical aptitude skills.
  • Must have good communication skills, both written and oral.
  • Must have good organizational skills.
  • Must be able to work in a team environment.
  • Basic knowledge and understanding of a computer.
  • Must be willing to work in a controlled environment, which involves the wearing of a gown, cap and relevant personal protective equipment.
Physical Requirements
Heavy-Exerting up to 100lbs/45kg of force occasionally and/or up to 50lb/22kg of force frequently, and/or up to 20lbs/9kg of force constantly to move objects.
Show more

משרות נוספות שיכולות לעניין אותך

21.11.2025
R

Red hat Event Coordinator United States, Florida, Venice

Limitless High-tech career opportunities - Expoint
Develop and customize AEM Guides components, templates, and workflows to meet specific documentation and publishing requirements. Design and implement DITA-OT plugins, specific schematron rules, specific post-processing pipelines in AEM. Configure...
תיאור:

Job Summary

In this role, you will work closely with technical writers, content strategists, and other stakeholders to ensure a seamless and powerful content authoring and publishing experience for our users.

What you'll do

  • Develop and customize AEM Guides components, templates, and workflows to meet specific documentation and publishing requirements.

  • Design and implement DITA-OT plugins, specific schematron rules, specific post-processing pipelines in AEM.

  • Configure and maintain the AEM publishing pipelines using DITA-OT for various output formats (PDF and HTML5) and optimize content in the Java Content Repository (JCR).

  • Implement and manage content standards and a structured authoring environment, focusing on reuse, metadata, and file structure to improve content consistency across teams.

  • Integrate AEM Guides with other internal systems and part of the Adobe stack with various APIs and web services.

  • Configure and maintain AEM instances, including dispatcher configurations, user permissions, OSGi services, and system maintenance.

  • Develop and implement strategic plans for the content platform that align with the larger Red Hat content vision and roadmap.

  • Troubleshoot, debug, and optimize AEM performance and resolve technical issues related to content implementation and delivery.

  • Document technical specifications, architecture, and development processes for knowledge sharing and future reference.

What you'll bring

  • Proven experience as an AEM Developer, including custom component development and integration

  • Expertise in AEM architecture and building blocks, including Sling Models, OSGi bundles, custom workflows, templates, and components.

  • Familiarity with converting structured, topic-based source (in formats such as DITA/XML or AsciiDoc) to HTML and experience applying content architecture concepts like content reuse, metadata, single sourcing content, applying conditional values, and information architecture in a CMS.

  • Knowledge of creating custom DITA-OT plugins and deploying them in the AEM Guides environment is preferred but not required.

  • Advanced research and analytical skills for complex problem-solving and troubleshooting cross-functional issues.

  • Ability to develop and implement strategic technical plans that fit into a larger content vision and roadmap.

  • Experience with development tools such as Maven, Git, JIRA, Slack, and experience in operating in an Agile/Scrum methodology.

  • Excellent written and verbal communication skills, with the ability to effectively convey technical concepts to both technical and non-technical stakeholders.

  • Experience working in a complex, cross-functional technology organization.

  • Ability to manage multiple assignments at once and good project management skills.

The salary range for this position is $116,270.00 - $191,840.00. Actual offer will be based on your qualifications.

Pay Transparency

● Comprehensive medical, dental, and vision coverage

● Flexible Spending Account - healthcare and dependent care

● Health Savings Account - high deductible medical plan

● Retirement 401(k) with employer match

● Paid time off and holidays

● Paid parental leave plans for all new parents

● Leave benefits including disability, paid family medical leave, and paid military leave

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משרות נוספות שיכולות לעניין אותך

21.11.2025
BS

Boston Scientific Production Coordinator - 3rd Shift United States, Minnesota

Limitless High-tech career opportunities - Expoint
Understands safety SQDC daily/monthly goals, submits safety improvement ideas. Encourages and supports a safety and quality first culture – ensures manufacturing personnel are following SOPs. Partners with supervisor or peers...
תיאור:

Your responsibilities will include:

  • Understands safety SQDC daily/monthly goals, submits safety improvement ideas
  • Encourages and supports a safety and quality first culture – ensures manufacturing personnel are following SOPs
  • Partners with supervisor or peers to set VSP staffing plans and communicates downtimes to ensure a smooth flow of production
  • Monitors daily performance, escalates equipment and component downtimes in a timely manner
  • Executes the training plan set by the production supervisor
  • Leads by example, submitting continuous improvement ideas and encourages team members to do the same
  • Participates in kaizen activities, aware of lean tools
  • Able to use various forms of communication (in-person, Microsoft Teams, email)
  • Effectively onboards new team members
  • Sustains and leads by example with BSC’s Core Values & Behaviors to enable a positive work culture

Required qualifications:

  • 1 year of manufacturing experience with a High School Diploma or an equivalent combination of education/work experience

Preferred qualifications:

  • Experience in a regulated environment and/or Medical device industry

Maximum Salary: $ 63856

Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).


For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.

Show more

משרות נוספות שיכולות לעניין אותך

Limitless High-tech career opportunities - Expoint
Unpack, review, and sort inventory to verify product condition and authenticity. Catalog inventory with detailed titles and key attributes that pertain to filters on our platforms. Store, putaway, and maintain...
תיאור:

What you will accomplish:

  • Unpack, review, and sort inventory to verify product condition and authenticity

  • Catalog inventory with detailed titles and key attributes that pertain to filters on our platforms

  • Store, putaway, and maintain organized storage areas for inventory accuracy and accessibility

  • Pack, label, and ship items within 48 hours of payment date according to established processes and carrier requirements

  • Collaborate with multiple departments to ensure items are processed safely and efficiently

  • Own individual projects while adapting daily to changing tasks and priorities, contributing to all warehouse operations as needed

  • Assist with developing and improving standard operating procedures (SOPs) for receiving, stowing, cataloguing and shipping

  • Support testing or pilot programs for new tools, systems, or operational workflows in the incubation environment

What you will bring:

  • Enthusiasm and willingness to learn warehouse processes and the collectibles industry

  • Strong project problem-solving skills

  • Ability to meet hard deadlines (Overtime needed depending on auction cycle)

  • High School Diploma or GED

Qualification Preferences:

  • 1+ year of warehouse experience (shipping, sorting, picking, cataloguing)

  • Working knowledge of the collectibles space in (sports, TCG, pop culture, etc.) preferred by not required

  • Ability to lift 30-50 lbs consistently

The base pay range for this position is expected in the range below:

$30,800 - $52,900
Show more
תכננו את מהלך הקריירה הבא שלכם בתעשיית ההייטק עם אקספוינט! הפלטפורמה שלנו מציעה מגוון רחב של משרות Team Coordinator באזור United States, ומעניקה לכם גישה לחברות הטובות ביותר בתחום. בין אם אתם מחפשים אתגר חדש או שינוי נוף, אקספוינט תקל על מציאת התאמת העבודה המושלמת עבורכם. עם מנוע החיפוש הקל לשימוש שלנו, תוכלו למצוא במהירות הזדמנויות עבודה ולחבור לחברות מובילות. הירשמו היום ועשו את הצעד הבא בקריירת ההיי-טק שלכם עם Expoint.