Home › Companies › Elrj Fa Us2 Oraclecloud Com CX 9001 › Supplier Quality Engineer II
Supplier Quality Engineer II
Elrj Fa Us2 Oraclecloud Com CX 9001 · Warrendale, PA, United States · Hybrid · Active · Oracle Recruiting Cloud / Fusion HCM
Job facts
| Field | Value |
|---|---|
| Company | Elrj Fa Us2 Oraclecloud Com CX 9001 |
| Title | Supplier Quality Engineer II |
| Normalized title | - |
| Department / team | Quality |
| Location | Warrendale, PA, United States |
| Work model | Hybrid / Hybrid |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-06-04 / 2026-06-06 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Elrj Fa Us2 Oraclecloud Com CX 9001. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Warrendale. | Open |
| Department jobs | Active postings in Quality. | Open |
| Work model jobs | Active Hybrid postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Elrj Fa Us2 Oraclecloud Com CX 9001 |
| Source | 1e86b782-0b35-4934-ae0f-bceeffbd9e50 |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
Description
Description
Supplier Quality Engineer (SQ Engineer II) - 5322
Reporting to the Senior Manager of Global Supplier Quality, this individual will be based out of an Omnicell US Manufacturing Facility. This role’s primary function is to ensure quality standards are implemented and effective throughout Omnicell’s Manufacturing and Service Supplier’s. This SQE department member will also closely work with Global Supply Chain, Development and Manufacturing Engineering personnel at Omnicell to understand current product quality issues and assist with root cause and corrective action with suppliers.
Responsibilities:
Data collection, analysis, and trending of supplier performance data from ERP system and PLM database. Creation of metric reports and presentations for Internal, Supplier QBRs and Management Review. Lead SCAR activities for supplier product and process quality issues, ensuring all facets of CAPA activities are addressed including effectiveness. Work with existing and new suppliers by planning and executing audits to ensure performance to Omnicell quality standards and regulatory requirements are be met. Ability to develop, communicate & implement strategies for improving performance of Omnicell’s Manufacturing & Service suppliers. Partner with New Product Introduction teams to support successful component qualifications at suppliers. Work closely with other QA departments within the Omnicell Global Factory Network on assigning and monitoring effectiveness of Supplier Corrective Actions in a timely manner. Provides supplier quality support of Omnicell’s suppliers engaged in the production of components. Review and approve Supplier IQ/OQ/PQ Protocols and Final Reports, verifying that sampling sizes are statistically valid. Work with suppliers to establish and maintain controlled manufacturing processes utilizing Control Plans and PFMEA’s and PPAPS.
Additional Responsibilities:
Act as a change agent who accepts and supports new ideas and processes. Commitment to cost reduction/controls. Support the ongoing maintenance and continual improvement of Supplier Quality processes. Update/creation of internal procedures as required. Participate in corporate quality improvement projects as required.
Required Knowledge and Skills:
Proven working knowledge of auditing methodologies associated with ISO 9001 or ISO 13485 standards. Quality concepts/tools (Pareto, fishbone diagram, FMEA, PPAP, etc.). Proficient understanding of engineering and manufacturing terminology and processes. Excellent comprehension of engineering drawings and specifications. Proactive, self-motivated, and empathetic work ethic in a fast-paced work environment. Ability to effectively interface and communicate with multiple constituents, including senior management, suppliers, consultants, and employees of all levels. Ability to work collaboratively with peers and team members. 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. 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. Self-starter, organized, analytical and decisive.
Basic Qualifications:
Minimum (3) years quality/manufacturing experience BS Degree in Engineering or Technical Science
PREFERRED QUALIFICATIONS
ISO 13485 or FDA regulated medical device experience ISO 9001, ISO 14001, 21CFR820 experience Certified Lead Auditor
WORK CONDITIONS
Hybrid environment working out of our Warrendale, PA location (15086) May travel up to 30% (Including international)
COMPENSATION
85,000-95,000K
Organization
Omnicell is dedicated to fostering an inclusive workplace. We welcome applications from all individuals, valuing a wide range of perspectives and backgrounds. As an equal opportunity employer, we do not discriminate based on race, gender, religion, sexual orientation, gender identity, national origin, veteran status, or disability. We are committed to making our recruitment process accessible to everyone. We offer support and reasonable adjustments for individuals with disabilities during our hiring process. If you need assistance, please contact us at [email protected] .
At Omnicell, respect for privacy and confidentiality is paramount. We adhere to strict policies to prevent discrimination or retaliation against those who engage in open conversations about compensation. However, employees privy to compensation information as part of their job role are expected to maintain confidentiality, except in specific circumstances outlined by law, such as during formal complaints, investigations, or as required by legal obligations.
Please note that Omnicell reserves the right to modify job roles and responsibilities as needed to meet our organization's evolving needs and drive our mission forward.
Company
Since 1992, Omnicell has been committed to transforming pharmacy care through outcomes-centric innovation designed to optimize clinical and business outcomes across all settings of care. We strive to be the healthcare provider’s most trusted partner by our guiding promise of “Outcomes. Defined and Delivered.”
Our comprehensive portfolio of robotics, smart devices, intelligent software, and expert services is helping healthcare facilities worldwide to improve business and clinical outcomes as they move closer to the industry vision of the Autonomous Pharmacy.
Our guiding principles inform everything we do:
As Passionate Transformers , we find a better way to innovate relentlessly.
Being Mission Driven, we consistently deliver on our promises.
Our Entrepreneurial spirit makes the most of EVERY opportunity for innovation.
Understanding that Relationships Matter creates synergies that yield the greatest benefits for all.
Intellectually Curious, eager to think deeper to learn and improve.
In Doing the Right Thing , we lead by example in ALL we do.
We are deeply committed to Environmental, Social, and Governance (ESG) initiatives. Our ESG efforts focus on creating an inclusive culture and a healthier world. This includes our Employee Impact Groups, which foster inclusion and belonging, as well as our learning and well-being programs that support personal and professional growth. We also prioritize sustainability in our operations, aiming to reduce our environmental footprint and promote responsible business practices. Join us in transforming the pharmacy care delivery model, making patient care safer and smarter for all.
Full job record
| Job ID | 445009b9dbf66e8466d444a3482153e1f660b669 |
| Org ID | 135106d9-00ec-41a9-970f-33caba63b949 |
| Source ID | 1e86b782-0b35-4934-ae0f-bceeffbd9e50 |
| Board ID | 1e86b782-0b35-4934-ae0f-bceeffbd9e50 |
| Provider | oracle_hcm |
| Provider Job Key | 5322 |
| Title | Supplier Quality Engineer II |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Warrendale, PA, United States |
| Department | Quality |
| Team | — |
| Employment Type | full_time |
| Workplace Type | hybrid |
| Remote Policy | hybrid |
| Country | United States |
| Region | PA |
| City | Warrendale |
| Salary Raw | Description Supplier Quality Engineer (SQ Engineer II) - 5322 Reporting to the Senior Manager of Global Supplier Quality, this individual will be based out of an Omnicell US Manufacturing Facility. This role’s primary function is to ensure quality standards are implemented and effective throughout Omnicell’s Manufacturing and Service Supplier’s. This SQE department member will also closely work with Global Supply Chain, Development and Manufacturing Engineering personnel at Omnicell to understand current product quality issues and assist with root cause and corrective action with suppliers. Responsibilities: Data collection, analysis, and trending of supplier performance data from ERP system and PLM database. Creation of metric reports and presentations for Internal, Supplier QBRs and Management Review. Lead SCAR activities for supplier product and process quality issues, ensuring all facets of CAPA activities are addressed including effectiveness. Work with existing and new suppliers by planning and executing audits to ensure performance to Omnicell quality standards and regulatory requirements are be met. Ability to develop, communicate & implement strategies for improving performance of Omnicell’s Manufacturing & Service suppliers. Partner with New Product Introduction teams to support successful component qualifications at suppliers. Work closely with other QA departments within the Omnicell Global Factory Network on assigning and monitoring effectiveness of Supplier Corrective Actions in a timely manner. Provides supplier quality support of Omnicell’s suppliers engaged in the production of components. Review and approve Supplier IQ/OQ/PQ Protocols and Final Reports, verifying that sampling sizes are statistically valid. Work with suppliers to establish and maintain controlled manufacturing processes utilizing Control Plans and PFMEA’s and PPAPS. Additional Responsibilities: Act as a change agent who accepts and supports new ideas and processes. Commitment to cost reduction/controls. Support the ongoing maintenance and continual improvement of Supplier Quality processes. Update/creation of internal procedures as required. Participate in corporate quality improvement projects as required. Required Knowledge and Skills: Proven working knowledge of auditing methodologies associated with ISO 9001 or ISO 13485 standards. Quality concepts/tools (Pareto, fishbone diagram, FMEA, PPAP, etc.). Proficient understanding of engineering and manufacturing terminology and processes. Excellent comprehension of engineering drawings and specifications. Proactive, self-motivated, and empathetic work ethic in a fast-paced work environment. Ability to effectively interface and communicate with multiple constituents, including senior management, suppliers, consultants, and employees of all levels. Ability to work collaboratively with peers and team members. 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. 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. Self-starter, organized, analytical and decisive. Basic Qualifications: Minimum (3) years quality/manufacturing experience BS Degree in Engineering or Technical Science PREFERRED QUALIFICATIONS ISO 13485 or FDA regulated medical device experience ISO 9001, ISO 14001, 21CFR820 experience Certified Lead Auditor WORK CONDITIONS Hybrid environment working out of our Warrendale, PA location (15086) May travel up to 30% (Including international) COMPENSATION 85,000-95,000K Organization Omnicell is dedicated to fostering an inclusive workplace. We welcome applications from all individuals, valuing a wide range of perspectives and backgrounds. As an equal opportunity employer, we do not discriminate based on race, gender, religion, sexual orientation, gender identity, national origin, veteran status, or disability. We are committed to making our recruitment process accessible to everyone. We offer support and reasonable adjustments for individuals with disabilities during our hiring process. If you need assistance, please contact us at [email protected] . At Omnicell, respect for privacy and confidentiality is paramount. We adhere to strict policies to prevent discrimination or retaliation against those who engage in open conversations about compensation. However, employees privy to compensation information as part of their job role are expected to maintain confidentiality, except in specific circumstances outlined by law, such as during formal complaints, investigations, or as required by legal obligations. Please note that Omnicell reserves the right to modify job roles and responsibilities as needed to meet our organization's evolving needs and drive our mission forward. Company Since 1992, Omnicell has been committed to transforming pharmacy care through outcomes-centric innovation designed to optimize clinical and business outcomes across all settings of care. We strive to be the healthcare provider’s most trusted partner by our guiding promise of “Outcomes. Defined and Delivered.” Our comprehensive portfolio of robotics, smart devices, intelligent software, and expert services is helping healthcare facilities worldwide to improve business and clinical outcomes as they move closer to the industry vision of the Autonomous Pharmacy. Our guiding principles inform everything we do: As Passionate Transformers , we find a better way to innovate relentlessly. Being Mission Driven, we consistently deliver on our promises. Our Entrepreneurial spirit makes the most of EVERY opportunity for innovation. Understanding that Relationships Matter creates synergies that yield the greatest benefits for all. Intellectually Curious, eager to think deeper to learn and improve. In Doing the Right Thing , we lead by example in ALL we do. We are deeply committed to Environmental, Social, and Governance (ESG) initiatives. Our ESG efforts focus on creating an inclusive culture and a healthier world. This includes our Employee Impact Groups, which foster inclusion and belonging, as well as our learning and well-being programs that support personal and professional growth. We also prioritize sustainability in our operations, aiming to reduce our environmental footprint and promote responsible business practices. Join us in transforming the pharmacy care delivery model, making patient care safer and smarter for all. |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://elrj.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/agency/job/5322 |
| Apply URL | https://elrj.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/agency/job/5322 |
| First Seen At | 2026-06-06 11:02:12Z |
| Last Seen At | 2026-06-06 19:34:12Z |
| Last Checked At | 2026-06-06 19:34:12Z |
| Last Changed At | 2026-06-06 11:02:12Z |
| Inactive At | — |
| Source Posted At | 2026-06-04 20:42:08Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=elrj.fa.us2.oraclecloud.com|CX_9001/date=2026-06-06/2026-06-06T19-34-03-895Z-7942997c5900e73c78b464a11d3c4d1d8b37cc654ea59e0065ec7bca690230fa.json |
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"ExternalDescriptionStr": "<p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"><strong>Supplier Quality Engineer (SQ Engineer II) - 5322</strong></span></span></p><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Reporting to the Senior Manager of Global Supplier Quality, this individual will be based out of an Omnicell US Manufacturing Facility. This role’s primary function is to ensure quality standards are implemented and effective throughout Omnicell’s Manufacturing and Service Supplier’s. This SQE department member will also closely work with Global Supply Chain, Development and Manufacturing Engineering personnel at Omnicell to understand current product quality issues and assist with root cause and corrective action with suppliers.</span></span></p><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"><strong>Responsibilities: </strong></span></span></p><ul style=\"list-style-type: disc;\"><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Data collection, analysis, and trending of supplier performance data from ERP system and PLM database. </span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Creation of metric reports and presentations for Internal, Supplier QBRs and Management Review.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Lead SCAR activities for supplier product and process quality issues, ensuring all facets of CAPA activities are addressed including effectiveness. </span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Work with existing and new suppliers by planning and executing audits to ensure performance to Omnicell quality standards and regulatory requirements are be met. </span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Ability to develop, communicate & implement strategies for improving performance of Omnicell’s Manufacturing & Service suppliers.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Partner with New Product Introduction teams to support successful component qualifications at suppliers.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Work closely with other QA departments within the Omnicell Global Factory Network on assigning and monitoring effectiveness of Supplier Corrective Actions in a timely manner. </span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Provides supplier quality support of Omnicell’s suppliers engaged in the production of components.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Review and approve Supplier IQ/OQ/PQ Protocols and Final Reports, verifying that sampling sizes are statistically valid.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Work with suppliers to establish and maintain controlled manufacturing processes utilizing Control Plans and PFMEA’s and PPAPS.</span></span></li></ul><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"> </span></span></p><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"><strong>Additional Responsibilities: </strong></span></span></p><ul style=\"list-style-type: disc;\"><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Act as a change agent who accepts and supports new ideas and processes.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Commitment to cost reduction/controls.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Support the ongoing maintenance and continual improvement of Supplier Quality processes.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Update/creation of internal procedures as required.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Participate in corporate quality improvement projects as required.</span></span></li></ul><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"> </span></span></p><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"><strong>Required Knowledge and Skills:</strong></span></span></p><ul style=\"list-style-type: disc;\"><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Proven working knowledge of auditing methodologies associated with ISO 9001 or ISO 13485 standards.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Quality concepts/tools (Pareto, fishbone diagram, FMEA, PPAP, etc.).</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Proficient understanding of engineering and manufacturing terminology and processes.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Excellent comprehension of engineering drawings and specifications.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Proactive, self-motivated, and empathetic work ethic in a fast-paced work environment. </span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Ability to effectively interface and communicate with multiple constituents, including senior management, suppliers, consultants, and employees of all levels.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Ability to work collaboratively with peers and team members.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Strongly demonstrated written and verbal communication and presentation skills to all levels of an organization.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Refined multi-tasking and time management skills.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Ability to consistently balance sense of urgency with diplomacy/empathy.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Ability to make decisions and execute directives.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Strongly demonstrated attention to detail.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Strongly demonstrated organizational and project management skills.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Demonstrated proficiency with common MS office programs (Word, Excel, PowerPoint, Project).</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Ability to work under tight deadlines and handle multiple detail-oriented projects.</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Self-starter, organized, analytical and decisive.</span></span></li></ul><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"> </span></span></p><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"><strong>Basic Qualifications: </strong></span></span></p><ul style=\"list-style-type: disc;\"><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Minimum (3) years quality/manufacturing experience</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><p><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">BS Degree in Engineering or Technical Science </span></span></p><p><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"> </span></span></p></li></ul><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"><strong>PREFERRED QUALIFICATIONS</strong></span></span></p><ul style=\"list-style-type: disc;\"><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">ISO 13485 or FDA regulated medical device experience</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">ISO 9001, ISO 14001, 21CFR820 experience</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Certified Lead Auditor </span></span></li></ul><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"> </span></span></p><p style=\"background-color: white; line-height: normal;\"><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"><strong>WORK CONDITIONS </strong></span></span></p><ul style=\"list-style-type: disc;\"><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">Hybrid environment working out of our Warrendale, PA location (15086)</span></span></li><li style=\"background-color: white; color: rgb(51, 51, 51); line-height: normal;\"><span style=\"font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">May travel up to 30% (Including international)</span></span></li></ul><p> </p><p><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\"><strong>COMPENSATION</strong></span></span></p><ul><li><span style=\"color: rgb(51, 51, 51); font-family: Helvetica, sans-serif;\"><span style=\"font-size: 10.5pt;\">85,000-95,000K </span></span></li></ul><p> </p>",
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"OrganizationDescriptionStr": "<p>Omnicell is dedicated to fostering an inclusive workplace. We welcome applications from all individuals, valuing a wide range of perspectives and backgrounds. As an equal opportunity employer, we do not discriminate based on race, gender, religion, sexual orientation, gender identity, national origin, veteran status, or disability. We are committed to making our recruitment process accessible to everyone. We offer support and reasonable adjustments for individuals with disabilities during our hiring process. If you need assistance, please contact us at <a href=\"mailto:[email protected]\" target=\"_blank\" rel=\"nofollow\"><u>[email protected]</u></a>. </p>\n<p>At Omnicell, respect for privacy and confidentiality is paramount. We adhere to strict policies to prevent discrimination or retaliation against those who engage in open conversations about compensation. However, employees privy to compensation information as part of their job role are expected to maintain confidentiality, except in specific circumstances outlined by law, such as during formal complaints, investigations, or as required by legal obligations. <br/></p>\n<p>Please note that Omnicell reserves the right to modify job roles and responsibilities as needed to meet our organization's evolving needs and drive our mission forward.</p>\n<p></p>\n<style></style>\n<style></style>",
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