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The Medical Device Assembler would be working for a Fortune 500 company and has career growth potential.. State-of-the-art pharmaceutical manufacturing facility, not a typical warehouse. Benefits are available to full-time employees after 90 days of employment and include health, optical, dental, life, and short-term disability insurance. · Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices as well as setting up, operating, performing maintenance on and troubleshooting equipment.. Ability to work in compliance with all local, federal, and USDA regulations.
With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year.. Working closely with multiple subject areas, including manufacturing, process engineering, process development, utility operations, maintenance, quality assurance, and validation to implement operational improvements. Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility utility equipment/systems such as Pharmaceutical Water, Clean Steam, Clean Air generation and distribution, and CIP; and as well as other Plant Utility equipment needed to support these processes such as Chilled Water chillers, cooling towers, steam boilers, air compressors, etc.. and familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and qualifications/validation. Understanding of the execution process of capital projects in a GMP Biopharmaceutical Production facility including procurement, construction, startup, and validation
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;
ABOUT USArc3 Gases is a family-owned, independent distributor of industrial gases, welding supplies, safety products, and hardgoods used in metal fabrication industries.. JOB SUMMARYThe primary function of the Quality Control (QC) Technician is to support the gas plant, branches and Advanced Cylinder Management (ACM) team in the oversight and management of all ACM barcode tracking operations.. Manage all aspects of our ACM cylinder barcode tracking process at the plant level.. Assist QC Technician in any required training for gas plant employees.. Provide end-of-day administrative support to the gas plant's Distribution Manager in the office.
Job Description SummaryThe Reliability Engineer will work closely with Sibelco plant maintenance, production and leadership teams to develop and utilize effective tools and systems for measuring reliability of our production process.. Lead in maintenance improvement tools (PM Optimization, RCM, RCA, RCFA, FMEA, etc.). Technical SkillsExperience w/ predictive maintenance technologies including, but not limited to, vibration analysis, oil analysis, infrared Thermography, ultra sound and motor current analysis.. Minimum 5 years utility systems/management and/or facilities/plant management and maintenance.. Certified Plant Engineer or Certified Maintenance Reliability Professional is preferred.
Educational support, extensive R&D investment and strong customer partnerships ensure the development of machining technologies that change, lead, and drive the future of manufacturing.. Setting up, operating, and maintaining 5-axis CNC milling equipment to perform machining to meet key performance indicators.. LEVEL “A” Must make major adjustments to CNC programs and set-ups as required and work with Engineering to develop best machining programming techniques and tooling selection as required, document and report any and all adjustments/corrections.. You possess minimum of a High School Diploma or GED. Associate Degree or Diploma from a Technical College or Trade School preferred.. Minimum of 2 years of CNC milling experience.
Read customer orders, work orders, shipping orders and/or requisitions to determine items to be moved, gathered, distributed, or shipped.. Ensure grounds and warehouse are kept neat, orderly, and safe for employees and customer traffic.. Objective: Looking for a Cool Job in a fast-paced environment with a dynamic team representing the industry leader in HVAC equipment?. The Warehouse Associate is responsible for the day-to-day warehouse upkeep, including picking and verifying orders, loading, and unloading of products, and inventory control using warehouse equipment state of the art technology.. The ultimate goal of this role is to procure, process, and dispatch products to customers and vendors for one of our established wholesale HVAC distributorships.
Discover a more connected QC Tech career At Lambert's Cable , as a QC Tech, you’ll work in the field reviewing active construction projects Connecting you to great benefits Weekly Paychecks Paid Time Off, Parental Leave, and Holidays Insurance (including medical, prescription drug, dental, vision, disability, life insurance) 401(k) w/ Company Match Stock Purchase Plan Education Reimbursement Legal Insurance Discounts on gym memberships, pet insurance, and much more!. What you’ll do as a QC Tech You will work in the field reviewing active construction projects, walk and review completed construction projects ensuring for site clean up, close out documentation is fulfilled.. You will ensure active construction work is completed to Lambert's requirements and Customer satisfaction and requirements You will ensure internal CORE documentation matches the completed LCS and Customer requirements, verify and report to market leadership of issues or lack of documentation or compliance issues.. You will make minor field corrections to installation should issues be identified You will handle small materials, run small materials to field crews You will operate, work, and report via general computer applications.. Building stronger solutions together Diversity and inclusion are an essential part of our culture and success.
Our legacy is rooted in innovation and excellence, earning us a spot on Fast Company’s esteemed annual list of the World’s Most Innovative Companies for 2024.. As a Service Supervisor - Multifamily with Hines, you will be responsible for overseeing and coordinating all mechanical and technical support for the property with limited direct supervision.. Adjust and operate the fire alarm and life safety systems. Two or more years of property maintenance management or leadership experience in a related industry. ¹Includes both the global Hines organization and RIA AUM as of December 31, 2023.
This includes knowledge and stewardship of the following: First Principles, unit operations, Equipment Flow Diagrams, Capability Calculations, Material & Energy Balances, Facilities (fitness for use), Root Cause applications, Equipment and Unit Operation Changes/Improvements including new technologies, Scale-ups, Periodic Reviews, Process Safety, Maintenance/Reliability, etc.. This Aseptic Process Engineering position serves as a technical resource in Aseptic Processing and Parenteral Technologies such as Equipment Preparation, Formulation, Filling, Freeze Drying, and Isolation systems, providing expert process engineering support globally.. Parenteral sites supported include Indy Parenteral (IPM), Fegersheim, Sesto, Suzhou, Research Triangle Park (RTP), Concord and Alzey.. Responsibilities will be range from due diligence, tech transfer, engineering batches to deviation investigation support.. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities).
Title: Non-Aseptic Production Operator. Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat opioid use disorder (OUD).. The Non-Aseptic Production Operator position is working in the roles of Syringe Inspector, Parts Washer, Component Prep, & Compounding/Formulation.. This includes but is not limited to manual visual inspection booths, steam sterilizer(s), parts washer(s), pouching equipment, formulation tanks, and associated equipment, weight scales, pumps, filter testing equipment and other associated equipment.. Communicates with Production Management, Quality Assurance, Quality Control, Maintenance and Engineering staff pertaining to status of manufacturing operations, including but not limited to: equipment reliability, environmental problems, and potential quality and compliance concerns.
Maintain current Good Manufacturing Practices (cGMP). Alert the Shift Lead and/or the Business Unit Leader immediately if there are any safety concerns or equipment downtime issues.. Recommend proactive action to remedy problems with equipment, componentry, raw materials or product. Two (2) years of machining experience with set-up, change-over, shut-down capabilities in a manufacturing environment.. Physically capable of lifting 50 pounds and Pushing or pulling weight in excess of 1000 pounds with a manual hand truck.
Perform environmental monitoring of the cleanrooms, biosafety cabinets (BSC), isolators, and other support areas.. Support laboratory and environmental monitoring investigations.. Ability to work safely and conscientiously in manufacturing and laboratory environments.. Ability to identify and addresses compliance, environmental, safety, and process deviations as required, with ability to escalate to appropriate personnel.. High School Diploma or AA with + years of Environmental monitoring or microbiology experience S. in Microbiology, biological or pharmaceutical sciences, or related discipline with - years of related experience.
About LevitonAt Leviton, we build what's next to light, power, and connect everyday spaces, from electrical to lighting, to data networks, and energy management.. About the roleLeviton, is looking for an experienced production supervisor to join our fiber network cable manufacturing operations in Fuquay Varina, NC!. The Production Supervisor is responsible for coordinating resources and supervising the manufacturing of scheduled production.. Responsibilities *This is not a remote positionOperates the department in a manner that supports established budgets for volume, scrap and labor.. Performs supervisory duties including, but not limited to: hiring, training, scheduling, assigning work, evaluating and rewarding performancePerforms audits on Preventive Maintenance (PM), in-process checks, changeover log, line organization (5S), line scrap and production boardsDrives process improvement, sees that all projects have accountability, and that promise dates are metAssists with root cause analyses and 8D where applicableOversees established bill of material and WIP inventory.
Takerepresentative samples of and test raw materials and fresh concrete.. Take representative samples of and test raw materials and fresh concrete.. Must adhere to all Lindsay Precast and OSHA safety rulesInspect welds.. File and maintain the following records:Suppliers' test reports for cementitious materials, aggregates and admixturesPlant and field tensioning reportsConcrete recordsPre-and-post-pour inspection reportsCalibration records for equipmentQualifications:At least two years of experience in precast concrete production.. Able to read and interpret precast concrete production drawings.
Split week schedule will be as follows: Sunday-Wed or Wed-Sat, 10 hours per day/ 40 hour work week.. EW's will have at least 1 day of the weekend date off (either Sat or Sunday will be off).. Job Details: Under general supervision, this position will perform routine sampling and testing in a GMP Manufacturing facility in support of the Microbiology and Environmental Monitoring group.. Knowledge of Aseptic technique.. Proficient in good documentation practices (GMP experience not required but basic laboratory writing skills/GDP/GLP knowledge preferred) Pay Rate between $29 - $33/Hr on W2 based on experience."
Company DescriptionRRD is a leading global provider of marketing, packaging, print, and supply chain solutions that elevate engagement across the complete customer journey.. The company offers the industry's most trusted portfolio of creative execution and world-wide business process consulting, with services designed to lower environmental impact.. Makes necessary color corrections and/or press adjustments prior to production run to meet and maintain the quality specifications of the workClean, lubricate, and maintain the press, making minor repairs and replacing worn or broken parts as requiredPerforms periodic maintenance recommended by the manufacturer.. In addition to base salary, depending on the role, the total compensation package may also include participation in a bonus, commission or incentive program.. RRD offers benefits including medical, dental, and vision coverage, paid time off, disability insurance, 401(k) with match, life insurance and other voluntary supplemental insurance coverages, plus tuition assistance, parental leave, adoption assistance, and employer/partner discounts.
Discounts on gym memberships, pet insurance, and much more!. You will work in the field reviewing active construction projects, walk and review completed construction projects ensuring for site clean up, close out documentation is fulfilled.. You will ensure internal CORE documentation matches the completed LCS and Customer requirements, verify and report to market leadership of issues or lack of documentation or compliance issues.. You will make minor field corrections to installation should issues be identified. You have have 1-3 year's minimum experience within the Underground Utility Construction Industry but will train right applicant
This site is a long-standing pillar of the community and is growing and expanding.. Nutro and Greenies (Dry Pet Food)Required Shifts: 12-hour Weekly Rotating Shifts: Day Shift: 6 am - 6:30 pm, Night Shift: 6 pm - 6:30 am, M - Th8-hour Weekly Rotating Shifts: 1st Shift: 6 am - 2:30 pm, 2nd Shift: 2 pm - 10:30 pm, 3rd Shift: 10 pm - 6:30 am, M - FOvertime required as needed to meet business needs.. Workplace transport equipment (forklift, yard dog, train) assignments require training and getting on and off frequently.. Performs QC tasks such as metal checks, inspection of date codes, item numbers, CCP and OPRP checks as required.. Best-in-class learning and development support from day one, including access to our in-house Mars University.
AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives.. AskBio's gene therapy platform includes Pro10™, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters.. The rAAV vectors tested/characterized by the team will support capsid technology development, intellectual property portfolio, and internal progression of early-stage gene therapy programs.. Job ResponsibilitiesPerform routine and complex execution of molecular biology and biochemistry analytical methods such as qPCR, d/ddPCR, ELISA, HPLC, endotoxin etc.. Preferred Education, Experience and SkillsRelevant work experience (0-2 years) in areas such as, analytical testing, development, and technology transfer; in rAAV/gene therapy, recombinant protein/biomolecules, and/or other advanced therapeutic modalities.