Inspired by Care

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 Engineer III


Quality Assurance Engineer III


Omnicell is seeking to fill a Quality Assurance Engineer III at our  Thornhill facility located in Warrendale, PA.  This role will report to the Senior Manager Production Quality and will be responsible for Production Quality activities.  Their primary responsibilities will be to prepare and maintain necessary documentation, monitor production quality performance to identify opportunities for improvements, act as a liaison between manufacturing and quality inspectors, and promote quality awareness.



  • Assist in the establishment of quality acceptance criteria and activities including but not limited to incoming, in-process and final inspection
  • Participate as Material Review Board member and assist in disposition of non-conforming materials.
  • Work with manufacturing to document, markup, and communicate changes to parts and assemblies within change control process
  • Collaborate with design quality and engineering personnel to determine critical part features and review manufacturability of design 
  • Participate in change control activities
  • Prepare, supervise and report suitable and effectual
  • Support new product introductions to ensure QMS requirements are followed
  • Ensure compliance to internal QMS documentation and ISO 13485
  • Provide input into Process Validation activities


Additional Responsibilities:

  • Oversee/Coordinate internal rework activities
  • Support development of design and process FMEAs
  • 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 Knowledge and Skills:

  • 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
  • Strongly demonstrated written and verbal communication and presentation 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
  • Strongly demonstrated attention to detail
  • Commitment to cost reduction/controls
  • Strongly demonstrated organizational and project management skills
  • Demonstrated proficiency with common MS office programs (Word, Excel, PowerPoint, Project)
  • Ability to work under tight deadlines and handle multiple detail-oriented projects
  • Team builder, self-starter, organized, analytical and decisive


Basic Qualifications:

  • Bachelor degree
  • Minimum five (5) years’ experience in a quality production environment
  • Experience working with complex electro-mechanical systems
  • Experience with broad variety of measurement and quality data analytic techniques


Preferred Qualifications:

  • ISO 13485 or FDA regulated medical device experience
  • Robotics experience
  • SAP  experience


Work Conditions:

  • Office Environment
  • May travel up to 10%



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.

Are you a returning applicant?

If you've applied online with us before, we already have your information on file! Login using your email address and password to update your profile and apply to this job instantly.

Previous Applicants:

If you do not remember your password click here.

Back to Search Results

New Search