Collecting information
Organizing data
Toyota Manufacturing is looking to develop new innovative solutions to support the future of mobility, and values being a member of a local and global community.. Along with great pay, amazing benefits, and a stable work environment – Toyota Manufacturing has it all.. Technical skills and knowledge in any of the following areas: PLC's, Computers & Information Technology, Hydraulic/Pneumatic, Motion/Motor Control, Welding and Machining.. Experience within industrial processing (example: PLC programming, controls, IoT data collection / storage / analysis, mechanical precision, vision system, robot maintenance, etc. Experience with predictive maintenance through condition monitoring (for example: vibration analysis, oil analysis, thermography, current analysis, etc
Performs various process improvements of machines and equipment, including molding/extrusion through packaging.. Troubleshoots equipment breakdowns and performs mechanical, pneumatic, and electrical maintenance whenever required to ensure uninterrupted customer supply.. Orders and obtains replacement parts in storeroom in support of preventive maintenance or proactive replacement efforts.. Adherence to plant safety requirements, OSHA and QSR/GMP/ISO guidelines as applicable.. Specific work experience required in use of Vision systems, electrical troubleshooting of circuits from low level signals up to 480 VAC, Allen-Bradley Programmable Logic Controllers (PLCs), and making modifications to Ladder Logic.
Our client, a world-leading Pharmaceutical Company in Wilson, NC is currently looking for an Process Engineer to join their expanding team.. Job Title: Process Engineer (Upstream, Downstream) / Pharma Manufacturing. Must have Upstream and/or Downstream experience. A minimum of eight (8) years of process/plant engineering experience in GMP MFG large molecule biologics facilities.. Experience in green or brown field GMP MFG facility start-up including process systems, automation, utilities, facilities and operations.
To develop and manage a preventative and predictive maintenance program and inventory tracking procedures.. Organize and implement TPM (Total Predictive Maintenance) at the site if applicable.. Manage the work assignments of all mechanical, mobile shop and maintenance planner.. Ability to troubleshoot and repair machinery using blueprints, P&ID (piping and instrumental diagram) schematics and root/cause failure analysis.. Participate in the planning and implementation of all capital projects for the mill.
We seek a strategic and experienced Senior EDI Analyst (or EDI Manager) with 5+ years of hands-on EDI experience to drive and optimize our Electronic Data Interchange (EDI) operations.. This role will lead the management, enhancement, and expansion of EDI processes on an OpenText EDI platform running on IBM i, with a Windows-based mapping platform.. Own and manage the OpenText EDI platform on IBM i, ensuring seamless daily operations.. Experience managing OpenText EDI on IBM i or a comparable enterprise-level EDI platform.. General command knowledge of IBM i systems and experience working with SQL or querying tools for data analysis.
The DAP (Device, Assembly, Packaging) QA Floor Representative will provide direct quality oversight of floor operations for combination product device manufacturing.. This role ensures compliance with regulatory requirements and quality standards while supporting operational efficiency in a fast-paced, high-growth environment.. Provide real-time quality assurance (QA) oversight of device, assembly, and packaging operations on the production floor.. Collaborate cross-functionally with engineering, operations, supply chain, and technical services teams.. Experience in quality assurance within a pharmaceutical or medical device manufacturing setting.
Role Title: SAP MM/PP Functional Consultant. This role involves leading the implementation, configuration, and support of SAP Materials Management (MM) and Production Planning (PP) modules to enhance supply chain and manufacturing processes.. The ideal candidate will have proven experience with SAP MM and PP modules, strong analytical and problem-solving skills, and the ability to translate business needs into effective system solutions.. S/4 HANA experience required. Experience within any other modules such as P2P, QM, OTC/SD, FICO to support other SAP leads as needed cross-functionally
Installing, configuring, calibrating, and maintaining control, measurement,t and indicating instrumentation (pneumatic, analog & digital);. Configuring and programming Programmable Logic Controls (PLC) and Programmable Automation Controllers (PAC);. Organize and order PLC control components to maintain plant process control systems.. Must have proven experience in PLC logic and programming with Allen Bradley PLC’s and other types of controllers.. Must be able to create and read logic and flow diagrams for program design, programming, simulation and testing, and start-up
We have a variety of Automation Engineer positions open - check out the link below. The Automation Engineer, DSM Downstream will provide support to the Drug Substance Manufacturing (DSM) facility.. This role focuses on leading the full Automation scope for delivery of DeltaV logic for Downstream process areas including Buffer Preparation/Hold, Purification – Chromatography (LPC), Viral Filtration (VF), Ultrafiltration (UF), Diafiltration (DF), and Dispensing.. The Automation Engineer, DSM Upstream will provide support to the Drug Substance Manufacturing (DSM) facility.. This role focuses on leading the full Automation scope for delivery of DeltaV logic for Upstream process areas including Inoculum Lab, Media Preparation, Seed Culture, Large Scale Bioreactors, and Harvest.
This is a fully remote role but occasionally, on an as-needed basis, you may be asked to travel for conferences, client visits, or training.. From Manufacturing, Packaging, and Labeling, to Distribution and Technology Vendors, Clinical Supply Consulting partners with teams to optimize efforts, better anticipate resource and expenditure needs and provide in-depth IRT and Clinical Supplies training, support, and planning services.. Interpret relevant protocol information to develop packaging/labeling design and/or global distribution strategy. Work collaboratively with other departments for the creation and approval of product labeling and import/export logistics. Prior experience working with IRT or other software systems related to Clinical Supplies
We’re thrilled to be partnering with a growing, industry-leading metal fabrication and machining company in Central NC to hire a Quality Manager who’s ready to lead with impact.. Are you a detail-oriented, proactive professional with a passion for quality, process improvement, and team leadership?. Partner with production and engineering teams to streamline operations and boost efficiency. Interpret blueprints, train others in blueprint reading, and manage measurement and tolerance checks. Strong skills in blueprint reading, measurement analysis, and problem-solving
Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.. A Japan-based company, our goal is to translate science into smiles by delivering therapies where no adequate treatments currently exist, working from drug discovery to product development and commercialization.. You will work with all functional groups and our Tech Transfer Team to drive the program.. You will also be heavily involved with facility startup activities including digital systems, equipment and process validations as well as DS tech transfer activities.. Proficiency with Document Management and Investigation generation (e.g. in Veeva) as well as Change Control.
Job Description At IPS, you will apply your knowledge, skills, and passion to make a difference in the lives of people by solving complex challenges related to pharmaceutical, biotech, and animal health research and manufacturing facilities.. We are looking for a dedicated Senior Process Automation Engineer to join our talented team at our office located in Cary, NC. In this role, you will provide the project team with technical leadership, automation expertise, and instrumentation support for the design, engineering, construction, and qualification of Pharmaceutical and Biotech related projects.. Develop the design and specifications for DCS, PLC, and SCADbased process control systems for IPS clients and projects.. About Us IPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries.. With the addition of Linesight, IPS has over 3,000 professionals in over 45 offices across 17 countries in the Americas, Europe, Asia Pacific, Southeast Asia, Australia, and the Middle East. Specialties Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.
The Maintenance Planner is responsible for managing the planning and scheduling of all maintenance work to include developing, scheduling, optimizing, analyzing, and closure of work orders of all types.. Maintaining and responsibility for the Computerized Maintenance Management System (CMMS).. Collaborate with Spare Parts Coordinator to develop, implement and optimize kitting process.. Plan and schedule 3rd party maintenance and ensure activities are accurately reflected in CMMS.. Required to follow all Good Manufacturing Practices (GMPs), Safe Quality Food (SQF) and Personal Protective Equipment (PPE) policies.
Kellanova is seeking an experienced Operations Supervisor to lead our night shift (7pm -7am) production team in our Cary, NC plant.. Continuous Improvement Have an owners mindset, and all acronyms that come with continuous improvement, 5S, RCA, and LEAN. Were Looking for Someone With Demonstrate knowledge of managing safety and/or quality programs and processes High school diploma or GED with substantial related proven leadership and supervisory experience in a manufacturing Ability to work evenings.. Get to Know Us At Kellanova, we are driven by our vision to be the worlds best-performing snacks-led powerhouse, unleashing the full potential of our differentiated brands and our passionate people.. Our portfolio of iconic, world-class brands include Pringles, Cheez-It, Pop-Tarts, MorningStar Farms, Special K, Krave, Zucaritas, Crunchy Nut, among others.. Kellanovas Culture of Best means we bring our best to all that we do in pursuit of our vision to be the worlds best performing snacks-led powerhouse.
- Provide product team support including, Material Review Board (MRB), customer complaint activities, statistical analysis, validation support, inspection plans, metrology, quality metrics and report functions.. - Apply quality engineering practices and guidance to support project teams and manufacturing operations using Six Sigma tools, FMEA, CE Diagram, DOE, MSA, Validation Protocol development, review and approval and Control Plans.. - Good understanding of Continuous Improvement Methodologies, including lean, six sigma, statistical applications and validation. - Good understanding of Continuous Improvement Methodologies, including lean, six sigma, statistical applications and validation.. - Proficiency in Minitab, Microsoft Project, word processing, database, and spreadsheet applications.
With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year.. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations.. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.. In this vital role you will report to the Sr. F&E Manager and be responsible for providing technical and administrative leadership to a group responsible for planning/scheduling adherence, troubleshooting, repairing, maintaining and improving the reliability of GMP and non-GMP equipment at Amgen, North Carolina.. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
Beam is seeking a highly energetic Facilities & Maintenance Sr Manager/Associate Director for the further development and on-going operation of the maintenance, calibration, and facilities site programs.. Collaborate with the property manager/landlord on matters related to the building lease and services as required. Support CAPA, Change Control, Deviation, Risk Analysis, Root Cause Analysis, and other Quality Systems. Business Owner for site CMMS system for both NC and MA. Manage, develop and maintain all space planning requirements, including internal employee moves, new hires and floor plans
The Research Triangle Park (RTP) facility is home to Catalent's Inhalation franchise including product development, clinical and commercial manufacturing for pMDI, DPI and Nasal Sprays.. Catalent Pharma Solutions is Morrisville, NC is hiring a Supervisor, Line Maintenance who is responsible for training and overseeing maintenance personnel in the performance of all critical manufacturing process equipment available at the Catalent Morrisville site.. High School or GED required with seven (7) or more years of mechanical experience in pharmaceutical manufacturing/processing.. Associate's degree with five (5) or more years of maintenance experience in filling and processing required; OR Bachelors with four (4) years or more years of mechanical experience in pharmaceutical manufacturing/processing required;. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting.