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We offer innovative technologies, service and parts, and years of global experience in corrugating, finishing; slitting and packaging; stationery; bookbinding and security documents.. Customers rely on our machines to produce and convert items such as corrugated boxes, folding cartons, passports, notebooks, copy paper, board, and coated and other specialty papers.. For more information, visit bwpapersystems.com. Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries.. X-matrix alignment Kaizen facilitation. Be adept in continuous improvement toolsets (Lean, Six Sigma, etc
as Lean, Six Sigma, Kaizen and etc, this role will lead initiatives that improve study start-up, data integrity, cycle times, and overall performance.. Deep understanding of Phase I clinical trial operations, including study start-up, subject safety, GCP compliance, and data collection.. Certification in Lean, Six Sigma, Kaizen, or equivalent process improvement methodologies (Black Belt or higher preferred).. Familiarity with FDA regulations, ICH-GCP guidelines, CAPA systems, and audit readiness best practices.. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products.
We offer innovative technologies, service and parts, and years of global experience in corrugating, finishing; slitting and packaging; stationery; bookbinding and security documents.. Customers rely on our machines to produce and convert items such as corrugated boxes, folding cartons, passports, notebooks, copy paper, board, and coated and other specialty papers.. For more information, visit bwpapersystems.com. Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries.. X-matrix alignment Kaizen facilitation. Be adept in continuous improvement toolsets (Lean, Six Sigma, etc.)
as Lean, Six Sigma, Kaizen and etc, this role will lead initiatives that improve study start-up, data integrity, cycle times, and overall performance.. Deep understanding of Phase I clinical trial operations, including study start-up, subject safety, GCP compliance, and data collection.. Certification in Lean, Six Sigma, Kaizen, or equivalent process improvement methodologies (Black Belt or higher preferred).. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products.. Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products.
Ensures compliance to Terumo’s quality policy, rapid response to shop floor process flow issues, and assist/lead continuous improvement kaizen event activities.. Maintain and follow TMC Quality System requirements, including but not limited to understanding of change control, validation, documentation practices, and design control requirements.. Initiate, lead and champion lean projects, i.e., Lean Production, Lean Support, with the Production, Process Development, Manufacturing Engineering and support functions.. Drive the ongoing introduction and advancement of lean manufacturing culture, principles and practices across the plant; work with local management to create the Lean Vision for the plant.. Support production in the creation of visual staffing plans, lean deployment, and standard work sequencing and production task time adherence.
Drive values stream optimization through the application of proven methodologies such as Six Sigma, LEAN, Kaizen events etc.. Ensure process control plans (SPC, sampling, inspection methods) are appropriate and effective.. Partner with internal support functions (i.e., laboratory operations, calibration & metrology, supplier control, distribution etc.). Prior experience in medical device manufacturing environment coupled with certifications from ASQ preferred.. Demonstrate a strong understanding and working knowledge of the Quality Sciences (Acceptance Sampling, SPC, continual improvement, Six Sigma, LEAN, Design of Experiments, COQ, Cause & Effect analysis etc.)
We are looking for a Quality Assurance Manager for the JPM CBRN Task Order 2 contract. The contractor shall develop resource-effective quality engineering plans and solutions, as well as innovative approaches to quality process implementation, from the Engineering and Manufacturing Development (EMD) phase to transition into Low-Rate Initial Production (LRIP) and Full-Rate Production (FRP), and within Industry-accepted standards and best public and private sector practices. The contractor shall use approved quality metrics (e.g., process control limits, thresholds, root cause analysis) to evaluate vendor compliance with the requirements and specifications defined in acquisition contracts. Knowledge in Industry-accepted quality standards (i.e., International Standards Organization (ISO) 9001 philosophy, regulations, and Industry technical data convention). Shall possess, at minimum, a Lean Six Sigma green belt certification, or its equivalent.
SUMMARY: The Plant Manager is responsible for overseeing all daily operations of a fluid dairy manufacturing facility, including in-house bottle production.. Lead and manage all aspects of plant operations including milk processing, filling, packaging, bottle manufacturing (blow mold), maintenance, sanitation, warehousing, and shipping.. Develop and implement continuous improvement initiatives, including Lean Manufacturing and Six Sigma practices.. Experience managing operations in a plant with in-house blow molding/bottle manufacturing is highly preferred.. Strong knowledge of GMPs, HACCP, SQF, or other food safety programs.
These individuals analyse client needs, develop operational strategies, and offer guidance and support to help clients streamline processes, improve productivity, and drive business performance.. Working in this area, you will also provide guidance on implementing lean manufacturing principles, optimising supply chain integration, and leveraging digital technologies.. You embrace technology and innovation to enhance your delivery and encourage others to do the same.. Address conflicts or issues, engaging in difficult conversations with clients, team members and other stakeholders, escalating where 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.. Our Product Development & Manufacturing (PD&M) Team helps our clients leverage advanced strategies, operational approaches and technologies to innovate, develop and manufacture products and services in a manner that significantly increases operational efficiency and drives new levels of enterprise-wide growth in a connected world.
Our business reach spans satellite television service, live-streaming and on-demand programming, smart home installation services, mobile plans and products.. Today, our brands include Boost Mobile, DISH TV, Gen Mobile, Hughes and Sling TV.. EchoStar has an exciting opportunity for an Aviation Supplier Partner Manager in our Hughes Network Systems division supporting our AERO Mobility business unit.. Certification in supply chain management (e.g., APICS, CSCP, CPM) is a plus.. Familiarity with industry standards (e.g., AS9100, FAA regulations) and quality control methodologies (e.g., Six Sigma, FMEA, Root Cause Analysis).
Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organisation providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and speciality chemical industries around the world. Syngene' s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, and Merck KGaA. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Experience: 10-15 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically for large molecule products. Experience in chromatography, bioanalytical, and bioassay methods for monoclonal antibodies and other biologic molecules. Overall responsible for Quality Control operations, including product support, microbiology lab, stability studies, and testing of raw and packaging materials; ensure compliance with Good Laboratory Practices (GLP) and other regulatory requirements.
The Sr. Corporate Packaging Engineer is a technical resource for the various packaging locations across the ASR Enterprise.. He/she will work with dry food packaging operations to include, but not limited to the following packaging equipment: Vertical form fill & seal machines, baggers, horizontal sealers, cartoners, scales, labelers, case formers/loaders, conveying, palletizing, stretch wrapping and robotics.. Provide key technical support in capital projects and new product and packaging material testing/start-ups.. Strong background and proven results in Leading Continuous Improvement efforts through the application of Lean Manufacturing and 6 Sigma Activities.. Recognized technical abilities and practical experience with strong capabilities in the following areas: Theory/functionality of manufacturing systems and unit operations; Continuous improvement; Food science/chemistry or packaging science; Statistics and analytical methods; Process measurement and control; Mechanical aptitude; Troubleshooting; Ability to understand and apply general engineering principles
MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies.. The Sr. Director/Executive Director, Quality Control is responsible for activities including internal QC testing, testing at contract testing labs, contract drug substance, drug product manufacturing organizations (CMOs), commercial and developmental stability (Stability).. This individual will work closely with other areas such as Biopharmaceutical Development, Manufacturing, Supply Chain Operations, Quality Assurance and CMC Regulatory Affairs to manage method transfers, method qualification and validation, data oversight and ensure timelines coincide with product development and production schedules.. Ensures internal and external quality control testing is performed in compliance with cGMP and maintains data integrity, within a system of quality assurance. Technical understanding of antibody structure, activity and related process impurities
A growing medical manufacturing client is adding a Manufacturing Manager to their team onsite in Gaithersburg, MD. This position is a key member of the leadership team and is responsible for the management of departmental activities in all aspects of the tissue manufacturing process in accordance with local, state, and federal statutes and regulations. Provides leadership for all aspects of tissue processing, packaging, policy and procedures, team development and regulatory compliance. Ensures all quality control and quality assurance guidelines associated with tissue processing are in place and met. Must have experience working in a tissue-based manufacturing facility (allograft) Knowledge of tissue donor consent, screening, and recovery.. A working knowledge of lean manufacturing and continuous improvement processes Ability to conceive, plan, provide training for, and implement major new processes and procedures.
Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organisation providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and speciality chemical industries around the world.. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, and Merck KGaA. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.. Experience: 10-15 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically for large molecule products.. Experience in chromatography, bioanalytical, and bioassay methods for monoclonal antibodies and other biologic molecules.. Overall responsible for Quality Control operations, including product support, microbiology lab, stability studies, and testing of raw and packaging materials; ensure compliance with Good Laboratory Practices (GLP) and other regulatory requirements.
Review manufacturing, supply chain, and procurement processes and costs (e.g., make vs buy analysis, spend analysis, strategic sourcing, operational due diligence). Apply Six Sigma and Lean principles to provide operational recommendations and detailed implementation plans to enhance efficiency, effectiveness, or sustainability of operations. Conduct commercial and operational due diligence to advise clients on the potential benefits, costs, risks, and value drivers of a transaction. Experience in advanced analytics tools (e.g. Alteryx, Tableau, PowerBI) and Six Sigma Proficiency with PC environment and related software, including Microsoft Office applications (e.g., PowerPoint, Excel). Must have 3 years of prior experience in procurement and sourcing such as spend analysis, make vs buy analyses, strategic sourcing, outsourcing, supplier management, negotiations, etc.
Direct end-to-end Manufacturing Department activities including material preparation & cell culture, through bulking of drug substance.. Broad knowledge and perspective of upstream/downstream/central services operations. Minimum BS/BA degree required in chemical/biochemical engineering or biological sciences/life sciences in pilot or commercial biologics manufacturing. Understanding of Lean Six Sigma or Lean Manufacturing is an asset.. When we put unexpected teams in the same room, we ignite bold thinking with the power to inspire life-changing medicines.
We leverage our capabilities to meet and exceed the requirements of our customers and empower them to remain ahead of evolving threats and complexities in a dynamic security landscape.. Lead initiatives focused on Lean Manufacturing, Six Sigma, and other best practices to reduce waste, improve efficiency, analyzing production processes and workflows to identify bottlenecks and recommend solutions.. Collaborate with quality, engineering, and production and supply chain teams to address quality issues and implement corrective actions promoting alignment and shared goals.. Proven experience in leading operational excellence initiatives, with certifications in Lean, Six Sigma, or equivalent methodologies.. Director of Operations (Physician Practices)Director, Customer Success and Service TransformationDirector of Operations, Healthcare Advisory PracticeDirector, Customer Success and Service TransformationExecutive Director - Hopkins Student Center OperationsBusiness Unit Director - Medical Waste Management
Join to apply for the Director, Global Logistics role at MESO SCALE DIAGNOSTICS, LLC. This role will report to the Vice President, Operations and partner with leadership in Sales, Finance, Operations, and Quality/Regulatory to lead integrated planning for strategic supply chain planning of products.. Sign in to set job alerts for "Director Global Logistics" roles.. Senior Director of Global Supplier OperationsDirector, Hilton Supply Management (HSM) Business PerformancePEPI: Director, Supply Chain: Procurement & Sourcing (OPEN TO ALL U.S. LOCATIONS). Global Procurement Associate Director Manufacturing Site LeadEY-Parthenon - Strategy and Execution - Supply Chain - Director - Multiple Locations
Set standards for highly engineered, complex rocket motors and their manufacturing processes, including Lean Manufacturing, Delivery Performance and Talent Management. Foster and maintain a safety-focused operating environment of continuous improvement, on-time delivery and superb quality. Develop strategies for optimizing manufacturing workflows, implementing Lean, Six Sigma, and other methodologies to enhance productivity and operational efficiency. Ensure strict adherence to industry regulations, including DOD4145, ITAR, DFARS, etc. This position falls under a Federal Explosives License issued by the Bureau of Alcohol, Tobacco, Firearms and Explosives (ATF) for this location.