Jobs at Abbott (Now Hiring) — 2,754 open — Page 33

Abbott

Clinical Trial Associate I

Madison, Wisconsin, United States · On-site

$51k–$101k/yr

Entry level$20B raised

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnost…

Skills: Clinical trials, Administrative support, Project management, Trial Master File, Regulatory compliance

Abbott

Crew Leader Logistics - NEW Altavista, VA Warehouse - 1st Shift

Altavista, Virginia, United States · On-site

$20/hr–$41/hr

Entry level$20B raised

Skills: Logistics, Warehouse operations, Team leadership, Inventory management, Power industrial equipment

Abbott

Project Manager

Portland, Oregon, United States · On-site

$78k–$156k/yr

Senior$20B raised

Skills: Project management, Cross-functional collaboration, Process improvement, SmartSheet, Microsoft Project

Abbott

Lab Manager; Microbiology - Nutrition Manufacturing - Casa Grande AZ

Casa Grande, Arizona, United States · On-site

$99k–$199k/yr

Senior+$20B raised

Lab Manager; Microbiology - Nutrition Manufacturing Abbott Nutrition in Casa Grande, AZ is seeking a Lab Manager for our Microbiology Department. The Lab Manager is responsible for providing support and/or oversight in t…

Skills: Microbiological Testing, CAPA, GMP, FDA Regulations, Laboratory Management

Abbott

Clinical Sales Specialist, Electrophysiology (Upstate New York)

Buffalo, New York, United States · Remote OK

$61k–$123k/yr

Mid level$20B raised

Skills: Clinical support, Sales support, Electrophysiology, Structural heart, Interventional cardiology

Abbott

QC Specialist I

Shanghai, Shanghai, China · On-site

Entry level$20B raised

职位目标 Job Purpose: 根据适用的法规、公司政策及风险管理结果建立、落实及完善产品实现过程中的检测体系，确保检验测试活动合规、高效运行。 Establish, implement and improve the inspection and testing system in the product realization process in accordance with applicable regulations, …

Skills: GMP, GDP, EHS, SOP, Laboratory Management

Abbott

Sales Representative/Account Manager

Capital City of Prague, Prague, Czechia · On-site

Senior$20B raised

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott…

Skills: Sales, Account management, Market development, Laboratory diagnostics, Biochemistry

Abbott

Manager, Histology

Madison, Wisconsin, United States · On-site

$99k–$199k/yr

Senior$20B raised

Skills: Histology, Laboratory management, Team leadership, Quality assurance, Regulatory compliance

Abbott

Associate Laboratory Director - Remote

Phoenix, Arizona, United States · Remote Solely

$113k–$227k/yr

Senior+$20B raised

Skills: Clinical laboratory oversight, Regulatory compliance, Quality management, Strategic planning, Research and development

Abbott

Energy Center Technician - Powerhouse - Night Shift, Altavista

Altavista, Virginia, United States · On-site

$24/hr–$49/hr

Mid level$20B raised

Energy Center Operator Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career developmen…

Skills: Boiler operation, Air compressor maintenance, Ammonia refrigeration, Chiller maintenance, Cooling tower operation

Abbott

Lean and Flow Transformation Project Specialist

Madison, Wisconsin, United States · On-site

$78k–$156k/yr

Senior$20B raised

Skills: Lean, Flow, Six Sigma, Process Improvement, Change Management

Abbott

Brand Manager, HCP Web

Alameda, California, United States · On-site

$114k–$228k/yr

Mid level$20B raised

Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international…

Skills: Digital marketing, Website management, Content marketing, Project coordination, Stakeholder management

Abbott

Clinical Specialist - Orange County, CA

Irvine, California, United States · On-site

$61k–$123k/yr

Mid level$20B raised

Skills: Cardiac rhythm management, Clinical support, Engineering, Technical support, Relationship building

Abbott

Clinical Laboratory Director

Madison, Wisconsin, United States · On-site

$149k–$299k/yr

Senior+$20B raised

Skills: Clinical laboratory management, CLIA compliance, Molecular pathology, Genomic technologies, Risk assessment

Abbott

Multi-Skilled Maintenance Technician

Witney, England, United Kingdom · On-site

Mid level$20B raised

JOB DESCRIPTION: Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. Joining us, you c…

Skills: Preventive maintenance, Fault finding, Problem solving, Precision assemblies, Machine tools

Abbott

Account Sales Executive

Washington, District of Columbia, United States · Remote OK

$78k–$156k/yr

Mid level$20B raised

Skills: B2B sales, Capital sales, New business acquisition, Pipeline management, Strategic sales

Abbott

Warehouse Specialist - 12-Hour Night Shift

Columbus, Ohio, United States · On-site

$17/hr–$34/hr

Entry level$20B raised

Skills: Forklift operation, Warehouse operations, Material control, Data entry, Shipping and receiving

Abbott

Pediatric Sales Specialist - Chesapeake, VA

Chesapeake, Virginia, United States · Remote OK

$61k–$123k/yr

Mid level$20B raised

Skills: Sales, Hospital negotiations, Contracting, Clinical knowledge, Product promotion

Abbott

Medical Representative

China · Remote OK

Mid level$20B raised

JOB DESCRIPTION:日常拜访：每周应该保证4.5天的正常拜访时间。每天的面对面有效拜访人数不应该少于12人。应该保证对A,B级客户的正确覆盖率和拜访频率。VIP拜访：每月至少一次对固定区域内重要医院的主管院长、药剂科主任、药事委员会成员、重要学科带头人进行拜访，以获得最大的支持。产品介绍会：每周至少召开一次产品介绍会，以扩大医生对产品的进一步了解。绩效发展：每月初应根据公司下达指标对自己负责的固定区域进行规划，并且每周跟踪进…

Skills: Sales, Territory management, Product presentation, Customer relationship management, Market analysis

Abbott

Facilities Admin

Pleasanton, California, United States · On-site

$22/hr–$45/hr

Mid level$20B raised

Skills: Facilities administration, Maintenance coordination, Infor EAM, Windchill, Ariba

JOB DESCRIPTION:

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

Career development with an international company where you can grow the career you dream of.

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

An excellent retirement savings plan with a high employer contribution

Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Madison, WI location in the Cancer Diagnostics division. This position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support. This position will coordinate with all members of the Clinical Affairs team and internal and external stakeholders to successfully execute the clinical study plans of the company.

What You’ll Work On

Include, but are not limited to, the following:

Collect essential documents and review for completeness and compliance with Standard Operating Procedures, the protocols, and appropriate regulations; review Trial Master File (TMF) inventory for missing and expiring documents.

Interact with clinical study sites to support study start-up, execution, and close-out activities.

Create and maintain study related trackers, including but not limited to, enrollment, study supplies, receipt of samples, and site information.

Coordinate the ordering, tracking, and accountability of clinical supplies, including investigational product materials, equipment, and special-order items as requested.

Review for completeness and route legal documents for execution. File all versions in document management database.

Draft study documents (study trackers, templates, presentations, etc.) as requested.

Support case report form (CRF) development, participate in user acceptance testing (UAT) for electronic data systems and review related data management documents, as applicable.

Represent Exact Sciences as a customer advocate/liaison both internally and externally.

Coordinate study start-up, execution, and close-out activities, or Investigator Meetings, as requested.

Responsible for completing assigned tasks to support study timelines and metrics with minimal ongoing direction.

Identify and report problems, investigate alternatives, and make recommendations for resolution and process improvements.

Responsible for organizing cross-functional project meetings. Distribute agendas, take and distribute meeting minutes.

Provide follow-up support and data collection for Research and Development teams to advance project objectives.

Initiate purchase requests liaise with Accounts Payable and vendors as needed.

Provide support to Clinical Trial Manager for clinical study budget review, tracking, and maintenance.

Must be able to work both independently and collaboratively as part of the clinical study team to meet study objectives and timelines.

Author and provide input to Clinical Affairs business processes.

Maintain a working understanding of current SOPs, work instructions, applicable regulations, and guidance documents, such as FDA Code of Federal Regulations (CFR) and International Council on Harmonisation (ICH), Guideline for Good Clinical Practices (GCP).

Maintain applicable clinical study data in Clinical Trial Management System.

Ability to organize, present, and convey problems or issues.

Strong verbal and written communication skills.

Effective presentation skills.

Ability to interface and work effectively within team and department with changing priorities.

Ability to frequently and accurately communicate with co-workers, customers, and vendors, via the telephone or by email.

Ability to exercise judgment and determine appropriate action to a variety of problems of varying complexity.

Ability to manage multiple deadlines.

Analytical, problem solving and decision-making skills.

Excellent attention to detail and organizational skills.

Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.

Support and comply with the company’s Quality Management System policies and procedures.

Maintain regular and reliable attendance.

Ability to act with an inclusion mindset and model these behaviors for the organization.

Ability to work designated schedule.

Ability to work nights and/or weekends.

Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.

Ability to travel 5% of working time away from work location, may include overnight/weekend travel.

Required Qualifications

Bachelor’s degree in the life sciences or related field; or Associates degree in the life sciences or related field and 2 years of relevant experience in lieu of Bachelor’s degree.

General knowledge of applicable clinical research principles and requirements, including GCP and ICH guidelines.

Proficient in using basic software applications including Microsoft Office (Word - generate documents and tables, Excel - create and modify spreadsheets, create complex formulas, etc., Email – preferably Outlook) and various search engines for conducting Internet searches.

Demonstrated ability to perform the essential duties of the position with or without accommodation.

Authorization to work in the United States without sponsorship.

Preferred Qualifications

1+ year of experience in a clinical research setting (Clinical Trial Assistant, Study Coordinator, or similar).

Experience in a healthcare, clinical, or science related field.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.

The base pay for this position is

In specific locations, the pay range may vary from the range posted.

Jobs at Abbott (Now Hiring) — 2,754 open — Page 33

Clinical Trial Associate I

Crew Leader Logistics - NEW Altavista, VA Warehouse - 1st Shift

Project Manager

Lab Manager; Microbiology - Nutrition Manufacturing - Casa Grande AZ

Clinical Sales Specialist, Electrophysiology (Upstate New York)

QC Specialist I

Sales Representative/Account Manager

Manager, Histology

Associate Laboratory Director - Remote

Energy Center Technician - Powerhouse - Night Shift, Altavista

Lean and Flow Transformation Project Specialist

Brand Manager, HCP Web

Clinical Specialist - Orange County, CA

Clinical Laboratory Director

Multi-Skilled Maintenance Technician

Account Sales Executive

Warehouse Specialist - 12-Hour Night Shift

Pediatric Sales Specialist - Chesapeake, VA

Medical Representative

Facilities Admin

Clinical Trial Associate I

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