Technology & Software Openings

Drive ongoing development efforts for Peak Health portals, applications, mobile apps, and communications by liaising with IT support teams within McGriff/MMA and external teams.. Lead all Peak Health technology improvement projects.. Submit and maintain tickets through the Service Now system for McGriff / MMA Support as needed to support Business Operations.. Help maintain GoAnywhere MFT for all file transfers in and out.. Technical / development experience with Microsoft Access, SQL Server, and.net

Oversee the SQA roadmap, projects, and team to ensure timely delivery of high-quality platform releases within budget. 5+ years of experience leading SQA teams in a Supervisory or Managerial capacity. Familiarity with COTS (commercial off-the-shelf) tools such as JIRA, qTest, Confluence, Perforce/GitHub. Gaming industry experience preferred. Proficient in coaching and guiding SQA engineers on effective test methods and emerging technologies

Proficient in using measuring tools consisting of calipers, height gages, radius gages, micrometers, scales, surface plates, compression/tension load testing, profilometer, hardness testing equipment (Rockwell, Brinell, Webster, durometer, etc.). At Dover Fueling Solutions (DFS), we are taking fueling and convenience retail to the next level.. DFS is part of a legacy of leadership that spans back generations, made up of some of the most trusted, leading-edge brands in the industry.. Providing advanced fuel-dispensing equipment, including clean energy solutions, systems and payment, automatic tank gauging and wet stock-management solutions, DFS comprises the product brands of Wayne Fueling Systems, OPW Fuel Management Systems, ClearView, Tokheim, ProGauge, Fairbanks, LIQAL, AvaLAN, and Bulloch Technologies.. Headquartered in Austin, TX, DFS has a significant technology development and manufacturing presence worldwide, including facilities in Brazil, China, India, Italy, Poland, the Netherlands, the United Kingdom and the United States.

We make our medicines at internal and external sites around the world and coordinate all aspects of production of Roche medicines in all disease areas and dosage forms.. To ensure readiness for a step-change in the standard of care that Roche delivers in the area of Cardiovascular, Renal and Metabolism (CVRM), PT will construct a new manufacturing site in the U.S. in Holly Springs, North Carolina.. As the Head of Quality Assurance you are initially accountable for providing Quality oversight for the design, qualification and ramp-up of the green field high volume facility’s operations, including strategic workforce planning, hiring the respective personnel, setting up the organization, all relevant processes and documentation (e.g. SOPs).. You are responsible for ensuring timely ramp-up to support the overall project timelines including the project management activities, IT systems and definition of the processes in compliance with GMP/Quality requirements.. You will transition to local full time on-site work once the site buildings are built and equipment delivered.

5) Work with functional areas to improve the lifecycle of Test Sample Plan review cycle times and batch release dates.. 7) Responsible for the review and approval of laboratory investigations, deviations, and CAPAs∯*∯ (5%) 8) Attend relevant operational meetings in support of disposition activities.. BS in scientific field with 15+ years' experience or MS and 10+ years' experience in a QA cGMP regulated environment within biopharmaceuticals or equivalent.. Experience with quality systems to include batch release review, batch disposition of biopharmaceuticals, and lab investigations and deviations.. Ability to apply concepts of basic algebra and statistics.

The Quality Assurance Manager is responsible for the Leadership and Management of the Quality Assurance Department, as well as all aspects of QA related compliance, regulatory certifications management, customer relationships, and overall product quality.. Assist the plant manager with the implementation of the site safety systems.. Notify the plant manager of any safety systems malfunctions or violations.. Bachelors' degree in Textiles, Chemical Engineering, or a similar field, with an MS in QA or QC desired. 2 to 5 years of past work as a Quality Assurance Manager in an Industrial Environment- work in continuous process industry is a plus

Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat opioid use disorder (OUD).. The scope of responsibilities includes Quality Systems, Compliance, Supplier Management, Document Control, Annual Product Quality Reviews (APQR), Quality Technical Agreements, Inspections, Validation and Final Product dispositions.. Manage the Document Management System; create, review, and approve documents including SOPs, WIs and protocols.. Provide regulatory expertise to the technology transfer process, as needed.. Minimum ten (10) years of experience in pharmaceutical manufacturing required

Carver Living Center is hiring a Quality Assurance LPN or RN with the primary purpose of this position to ensure the highest quality of care for the residents of our facility by monitoring, auditing, and evaluating the services being provided.. Quality Assurance protocols and implementation must be in accordance with current federal, state, and local standards, guidelines, and regulations that govern our facility, and as may be required by the Director of Nursing Services, to ensure that the highest degree of quality care is always maintained.. Active/unencumbered LPN / RN License in the state of North Carolina. Minimum 3 years’ experience in long term care. must be knowledgeable with critical thinking skills of nursing and medical practices and procedures, as well as state, federal, and regulatory requirements that pertain to long-term care.

Title: QA Contractor, GMP Quality Assurance. The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality Assurance, or designee, will be responsible for assisting in the management of Client's Quality Management System (QMS) and will strongly support Client's Culture of Quality.. Provide timely support of Learning Management System, Change Control, Deviation Management Systems, or other QMS based customer requests.. 3+ experience working within a pharmaceutical/biotech Quality Management system, such as Trackwise, ZenQMS, Veeva, is a requirement. Experience in analytical method validation and QC testing, especially in the fields of mammalian cell culture and Gene Therapy/Biologics based potency testing, is preferred.

Truist Audit Manager is responsible for providing a leadership role in the delivery of high-risk, complex and value-added independent and objective risk-based internal audit assurance and advisory services.. The Audit Manager will proactively coach junior team members by providing candid and constructive feedback.. Experience in auditing and issue validations reviews (examples of key areas include wealth management, enterprise risk management, credit and information technology). Possess appropriate professional certification such as Certified Internal Auditor (CIA), Certified Public Accountant (CPA), Certification in Risk Management Assurance (CRMA) and Certified Information Systems Auditor (CISA).. Depending on the position and division, this job may also be eligible for Truist's defined benefit pension plan, restricted stock units, and/or a deferred compensation plan.

RBC Bank Georgia, N.A. is a US subsidiary of Royal Bank of Canada with a passion to provide US Banking services for Canadians living, working and travelling in the United States.. RBC Bank's "Cross-Border" solutions are designed to meet the unique needs and challenges Canadians face south of the border including but not limited to the ability to access and link their Canadian and US Banking accounts, perform Cross Border Transfers and leveraging their Canadian credit standing and existing banking relationships with RBC for purposes of obtaining credit/loans in the US. RBC Bank Operations is located in Raleigh, NC.. Completes HMDA data integrity scrub and partners with business units to ensure Regulatory Compliance HMDA. Prepares and monitors reports relating to risk management, fair lending and controls oversight for COO and RBC Bank senior management review and internal governance forums. Provides general mortgage compliance support by monitoring REFCO's support mailbox

The Director, Product Quality Assurance (QA) will be responsible for leading the product quality assurance group at Beam's manufacturing facility in RTP, North Carolina.. The position will have quality oversight for manufacturing, testing, and validation/qualification at the RTP facility.. The position is an onsite role in RTP NC and will report into Beam's VP, Product QA.. Lead and support the Beam Quality Assurance organization and will help define, communicate, and drive the Quality vision and mindset of the entire company in close collaboration with the VP, Product QA.. Review and oversee QA aspect of validation Commissioning, Qualification, and Validation (CQV) effort of the various startup and buildout phases of the facility build.

Summary: Perform tactical work and review a variety of documents, protocols, and reports. Oxford will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. Oxford provides supplemental medical (we do not offer major medical), dental, vision, life, and disability benefit plans along with a 401(k) Retirement Savings Plan. Paid holidays based on eligibility and paid sick leave for applicable jurisdiction, as required. Oxford is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. We will make a determination on your request for reasonable accommodation on a case-by-case basis.

Truist Audit Manager is responsible for providing a leadership role in the delivery of high-risk, complex and value-added independent and objective risk-based internal audit assurance and advisory services. The Audit Manager will proactively coach junior team members by providing candid and constructive feedback. Experience in auditing and issue validations reviews (examples of key areas include wealth management, enterprise risk management, credit and information technology).. Possess appropriate professional certification such as Certified Internal Auditor (CIA), Certified Public Accountant (CPA), Certification in Risk Management Assurance (CRMA) and Certified Information Systems Auditor (CISA). Depending on the position and division, this job may also be eligible for Truist’s defined benefit pension plan, restricted stock units, and/or a deferred compensation plan.

Coordinates the activities of the FoodSafety &QualityAssurance (FSQA) teamforimplementationof quality and food safety programs(HACCP and SSOP)and procedures. Complete additional tasks as directed by QA Manager orQA Superintendent. Managetheteam of hourly/SNE QA Technicians includingmanagingKronos Timekeeping System. Must have an understanding of USDA and OSHA regulations. Able to work independently and exhibit PPC’s values to uphold the Quality Pillar and FSQA Programs.

We're looking for top-tier talent and offer the flexibility you need to thrive and deliver lasting impact.. This includes defining API standards, taxonomy, governance, and best practices.. + 3+ years' progressive experience in Technical Product Management and/or Software Engineering within the tech or telecom industry, specifically working with digital platforms, developer portals, and APIs.. + Technical knowledge and understanding of API design principles (REST, GraphQL, Even Driven APIs), microservices architecture, cloud platforms, and relevant development technologies.. + Experience with digital platforms, enterprise customer portals, and/or complex web applications, coupled with strong working knowledge of web development technologies, user experience design & research, modern software development methodologies (Agile, DevOps), and analytics tools & techniques.

The WEP Clinical Quality Assurance Manager will be responsible for the leadership and operational execution of the site quality assurance function regarding the distribution and manufacturing (secondary packaging & labelling) activities.. The Quality Manager will also act as a primary expert and interface between supply chain and logistics, project management, and other departments to drive delivery of client solutions with respect to Post Approval Named Patient/Expanded Access Program and Clinical Trial supply service lines for the site.. Complete critical warehouse reviews as the Responsible Person, Deputy Responsible Person or Equivalent Delegate verifying warehouse maintenance programs have been completed (e.g. pest control, cleaning reports, calibration reviews).. Strong understanding of fundamental principles for core Quality Management System processes (e.g. risk assessments, deviations, change control, supplier/customer management).. Market Access and Commercialization

V-Soft Consulting is currently hiring for a Program Director - Senior (Remote) for our premier client.. Project Management Institute Certification (PMP, PgMP, PfMP, ACP, etc.). Scrum Alliance (CAL, CSP, CSM, CSPO, or advanced certs).. Scaled Agile Framework Certification (SAFe – SA or SAFe – SPC).. Bachelor’s or master’s degree in computer science, information systems, business administration or related field with seven or more years’ experience in combined (waterfall and agile) environments along with applicable certifications such as (not all are required)

Activities include, but not limited to general Product Development / Design Control customer input, specification development, verification and validation testing, manufacturing transfer, risk assessment, usability, design change control, etc. Quality activities for medical device manufacturing and Design & Development activities throughout all stages of the device development process (e.g. general Product Development / Design Control customer input, specification development, verification and validation testing, manufacturing transfer, risk assessment, usability, design change control). R&D quality oversight of preclinical and clinical planning and readiness activities. Certification(s) – ASQ Certified Quality Engineer or equivalent.. Experience with FDA, European agency regulations, cGMP regulations, and Quality Management software is highly preferred.

Lead the development of cutting-edge embedded software solutions for a next-generation infusion pump platform.. Oversee the design, development, and maintenance of software for the infusion pump platforms.. Champion Agile methodologies and foster a lean, iterative development culture.. ~ Strong background in systems engineering, embedded software, and digital product development.. ~ Deep understanding of software development lifecycles (SDLC) and Agile frameworks.