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Other responsibilities include: production paperwork verification; production floor checks; performing GMP and housekeeping audits; responsible for Team Member food safety training.. Experience: 2 plus years in a food manufacturing environment production of soups sauces or toppings preferred.. HACCP certified preferred; must have broad knowledge of HACCP USDA GMP SSOP's.. Computer Skills: Basic computer skills for creating simple queries spreadsheets etc.. If you would like to learn more about your data privacy rights and how you may use that information, please read our Job Applicant Privacy Notice here.
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.
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.
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
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
On the F&B Operations team reporting to the SVP, F&B Operations Americas, you will evolve existing restaurant and bar operations, lead concept development for new restaurants and bars, support the on\-site implementation and openings process for both branded and bespoke F&B initiatives, and manage our in\-house growing portfolio of ready\-to\-use restaurant concept brands under STiR Collective\.. Lead the creation of original restaurant and bar concepts for new hotel developments, conversions, and renovations across Full\-Service, Lifestyle and Luxury Brands in the Americas\.. Oversee the development and evolution of a portfolio of six scalable turnkey restaurant concepts, from brainstorming through launch and performance evaluation\.. + Intermediate in Adobe Creative Suite \(InDesign, Illustrator, Photoshop\). + Academic background in Hospitality, Culinary Arts, Design, Marketing, or Business Administration
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.
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.
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
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.
Responsibilities Plans, directs and manages the activities of the Commodity Management Section, to include inventory management, supply management, receiving, purchasing, distribution, control of facility, pandemic, environmental supplies, office supplies, non-OIT consignment and prosthetics consumables, equipment instrumentation and applicable services.. Resolves any problem areas identified by the use of data and interpretation of such factors as value of items, volume purchase advantages, market conditions, storage facilities, holding characteristics, administrative costs, seasonal variations, cost of transportation, susceptibility of change and fluctuations, source of supply, and method of procurement, i.e., consignment agreements, blanket purchase agreements, etc.. Supervision: Supervises employees from separate but interrelated units comprised of the Inventory Management, Medical Supply Distribution and may include the Purchasing section.. In conjunction with the Patient Safety Coordinator and stakeholders, ensures compliance and immediate response to the VA National Center for Patient Safety Recall Office.. Work Schedule: Monday- Friday 7:30 - 4:00 pm Virtual: This is not a virtual position.
Today, our 82,000 associates serve more than 10 million customers a week across 10 Southeastern and Mid-Atlantic states.. Follow current Standard Practices regarding cleanup of Hazardous Waste product. Successfully complete Computer Based Training (CBT), Training Packet and Training Aid courses. Be able to handle a variety of substances associated with cleaning and packaging materials, fresh fruits, vegetables, house plants/flowers and household cleaners. Use hands to frequently/continuously handle currency (paper and coin) as well as operate a variety of equipment such as cash register, lottery machine (where applicable), scanner, computer, and calculator
With offices nationwide and abroad, NV5 helps clients plan, design, build, test, certify, and operate projects that improve the communities where we live and work. T his role is also open to those in Fayetteville, NC; Rocky Mount, NC; and Burlington, NC. Responsibilities include monitoring activities on construction sites and performing testing of soils, concrete, and asphalt pavement materials. Performs In-Place Density Tests using nuclear density gauge, drive sleeve, or sand cone method. Concrete/Grout/Masonry sampling (including: air content; slump testing; visual observations; casting samples of concrete cylinders, mortar cubes, and grout prisms; and obtaining core samples).
SummaryThis position serves as a Supervisory Inventory Management Specialist for expendable (EX) assets/materials for the Logistics Service supervising multiple supply series of consumable medical supply/inventory used in the healthcare system as well as the micro-purchase program and recognized as the Commodity Management Division's subject matter expert serving as an advisor and consultant to the Chief Supply Chain Officer on inventory management matters and control of consumable inventory.. Effective CommunicationLeadershipPlanning and EvaluatingProblem SolvingReasoningTechnology ApplicationExperience refers to paid and unpaid experience, including volunteer work done through National Service programs (e.g., Peace Corps, AmeriCorps) and other organizations (e.g., professional; philanthropic; religions; spiritual; community; student; social).. Physical Requirements: The work is primarily sedentary and is usually accomplished while seated at a desk or table, typically in an adequately lighted and climate controlled office.. Information about ICTAP and CTAP eligibility is on OPM's Career Transition Resources website at Policy: The posting of this announcement does not obligate management to fill a vacancy or vacancies by promotion.. It is the policy of the VA to not deny employment to those that have faced financial hardships or periods of unemployment.
Embracing increased ambiguity, you are comfortable when the path forward isn't clear, you ask questions, and you use these moments as opportunities to grow.. Uphold and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements.. Demonstrates thorough abilities providing solution strategy and Application Evolution Services (AES, formerly AMS) delivery as a SAP Solution Architect;. Demonstrates thorough abilities developing a scalable and robust SAP Solution Strategy in a hybrid IT landscape;. With a focus on AES, demonstrates thorough abilities assisting clients in the support of SAP application packaged solutions and improving business processes; and taking a proactive approach to quality as opposed to a reactive one;
Collaborate with stakeholders to understand their needs and translate them into clear, actionable requirements for SAP Ariba solutions.. Translate user requirements to Configure and customize SAP Ariba modules to meet specific business requirements. Strong understanding of SAP Ariba modules, particularly in areas like sourcing, procurement, and invoice management (SAP Ariba Sourcing, SAP Ariba Contracts and SAP Ariba SLP). SAP MM Functional Consultant Certification. Certifications in SAP Ariba procure to pay modules
Hybrid role – this is not fully remote. Deep expertise in the electronics manufacturing services (EMS) industry, including knowledge of markets, business operations, and all functional areas. Leadership experience in manufacturing operations across both large and small organizations, with exposure to best-in-class practices in areas such as process flows, Manufacturing Execution Systems, Lean methodologies, Theory of Constraints, OEE, TPM, Cellular Manufacturing, and tools like SMED, 5S, QFD, FMEA, 8D, and CAPA. Equipment: Familiarity with a broad range of manufacturing and prototyping equipment, including CNC machines, sheet metal equipment, molds, 3D printers, SMT machines, and other industrial tools. Software Knowledge: Proficient in ERP systems, PLM tools (ARAS experience is a plus), and EDA/CAD tools such as SolidWorks, PTC, or AutoCAD. Strong command of MS Office (Word, Excel, Access, PowerPoint) and other relevant software for data analysis and communication.
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.
Engineering background (Electrical, Mechanical, Chemical, or Embedded Software).. Familiarity with software-driven safety systems and electromechanical components (diodes, capacitors, PCBA).. We are seeking a highly technical and quality-driven leader to oversee global product safety and quality engineering across a diverse portfolio of commercial fire safety products.. Oversee investigations into electromechanical and chemical suppression systems (e.g., foam, pressurized water, PCBA, embedded software).. Support internal software and firmware development teams (homegrown systems, backend logic, UI for fire professionals).