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Omnicell Careers

Be the Solution. Imagine the Impact.

Since 1992, Omnicell (NASDAQ: OMCL) has been inspired to create safer and more efficient ways to manage medications and supplies across all care settings. As a leader in medication and supply dispensing automation, central pharmacy automation, IV robotics, analytics software, and medication adherence and packaging systems, Omnicell is focused on improving care across the entire healthcare continuum—from the acute care hospital setting, to post-acute skilled nursing and long-term care facilities, to the patient’s home.

Over 4,000 customers worldwide use Omnicell® automation and analytics solutions to increase operational efficiency, reduce medication errors, deliver actionable intelligence and improve patient safety.

Omnicell’s innovative medication adherence solutions, used by over 32,000 institutional and retail pharmacies in North America and the United Kingdom, are designed to improve patient adherence to prescriptions, helping to reduce costly hospital readmissions.

Recent Omnicell acquisitions, including Ateb, add distinct capabilities, particularly in central pharmacy, IV robotics, and pharmacy software, creating the broadest medication management product portfolio in the industry.


Quality Assurance Engineer III


Description

Quality Assurance Engineer III

Reporting to the Senior Manager Production Quality and located at the Omnicell Thornhill facility located in Warrendale, PA, the Quality Assurance Engineer II will plan, execute, and report on supplier audits, ensuring performance to Omnicell quality standards and regulatory requirements.

Responsibilities:

  • Data collection and review of supplier failure data for analysis and trending using industry tools such as fishbone diagram, FMEA, etc.  Assist in creation and presentation of metric reports
  • Work with Manufacturing and Procurement teams to initiate, communicate, and monitor Supplier Corrective Actions
  • Participate/coordinate root cause failure analysis of nonconforming material with Manufacturing Engineering and the supplier to determine product quality (including situations where limits may not be clearly defined)
  • Develop a program to hold Quarterly Business Reviews (QBR) with top suppliers providing first-hand knowledge on quality issues and performance
  • Participate in domestic and international supplier qualifications for prospective suppliers as part of Supply Chain sourcing strategy or new product introduction projects. Develop Supplier Quality Agreements with the procurement team
  •  Support the on-going maintenance and improvement of Supplier QA processes for assessment and performance monitoring
  • Determine requirements for part qualifications and maintain incoming inspection levels
  • Perform process planning, documentation, and procedures to support product quality requirements
  • Conduct root cause analysis through facilitating brainstorming, use of fishbone diagrams, 8D methodologies, CAPA and design of experiments, etc.

Additional Responsibilities:

  • Support the Quality Department objectives and goals by managing or participating in Quality projects
  • Manage and/or participate in CAPAs as required
  • Act as a liaison between Quality and other Omnicell functional departments
  • Lead or participate in Quality Management Review meetings

 

Required Skills/Knowledge:

  • Ability to effectively interface and communicate with multiple constituents, including senior management, customers, consultants, vendors, and employees of all level
  • Ability to work collaboratively with peers and team members
  • Change agent who accepts and supports new ideas and processes
  • Strong written and verbal communication skills to all levels of an organization
  • Refined multi-tasking and time management skills
  • Ability to consistently balance sense of urgency with diplomacy/empathy
  • Ability to make decisions and execute directives
  • Attention to detail
  • Commitment to cost reduction/controls
  • Strong organizational and project management skills
  • Ability to work under tight deadlines and handle multiple detail-oriented projects
  • Proficient with common MS office programs (Word, Excel, PowerPoint, Project)
  • Excellent oral, written and presentation communication skills
  • Team builder, self-starter, organized, analytical and decisive

Work Conditions:

  • Office Environment
  • May travel up to 25%

Basic Qualifications:

  • Bachelor of Science degree in Engineering
  • Minimum 5 years’ experience in an FDA regulated Medical Device Engineering role
  • Experience working with complex electro-mechanical systems
  • Specific training and demonstrated success in applying quality problem-solving methods such as fishbone diagrams, FMEA, process capability analysis, 8D methodologies, CAPA, DoE, SPC, etc.
  • Experience with broad variety of measurement and quality data analytic techniques

Preferred Qualifications:

  • ISO13485 auditor certification

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.

Omnicell will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.





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