Plant Continuous Improvement Specialist Job at Ardagh Group (Huron)

Continuous Improvement Specialist

We are looking for an experienced Continuous Improvement Specialist to support o...

Location

United States , Cincinnati

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Proven experience in quality control within a manufacturing environment
Strong proficiency in Excel and familiarity with Minitab
Understanding of lean manufacturing principles and their application
Knowledge of safety and ergonomics standards in industrial settings
Six Sigma Green Belt certification and practical project experience
Ability to perform detailed time studies and process analysis
Skilled in developing standard work documentation and balance charts
Excellent analytical and problem-solving skills

Job Responsibility

Validate job instructions by ensuring processes align with prescribed guidelines
Conduct time studies to analyze value-added tasks, foreign elements, and non-cyclic work
Develop standard work combination sheets to optimize workflows
Break down jobs into distinct elements, supporting balanced work charts
Utilize Excel extensively and leverage tools like Minitab for data analysis
Collaborate on plant layout improvements to enhance efficiency
Promote safety and ergonomics within manufacturing processes
Implement lean manufacturing practices to streamline operations
Apply Six Sigma principles to address quality challenges and drive improvement
Ensure consistent quality control measures are applied throughout production

What we offer

medical
vision
dental
life and disability insurance
company 401(k) plan

Continuous Improvement & Process Engineer

Under the supervision of the Director of Innovation, the Continuous Improvement ...

Location

United States , Concord

Salary:

Not provided

ROCK OF AGES CANADA INC.

Expiration Date

Until further notice

Requirements

Bachelor’s degree in industrial, Mechanical, Manufacturing Engineering, or related field
2–5 years of experience in industrial or manufacturing environments
Strong knowledge of Lean Manufacturing, Six Sigma, or other continuous improvement frameworks
Analytical skills and proficiency with tools such as Excel, BI tools, SCADA, or machine monitoring systems
Lean Six Sigma Green Belt certification
Experience using CAD for process or plant layout optimization
Hands-on experience with industrial machinery and ability to interpret technical documents, drawings, and manuals
Valid passport and driver’s license, with availability for frequent travel (~50%) within Quebec and the U.S.

Job Responsibility

Identify and implement improvements to increase machine productivity, efficiency, and uptime
Optimize block processing lines, slab production throughput, and performance of cutting, polishing, and finishing machines
Improve material flow and overall plant layout
Lead or support the installation, calibration, and commissioning of machines such as GMM, Simec, CNC, Eagle, or Graniroc
Ensure operator training and validate equipment performance
Document installation processes and contribute to machine optimization strategies
Manage continuous improvement projects end-to-end, applying Lean, Six Sigma, or similar methodologies
Prepare reports and recommendations for management
Develop long-term roadmaps for operational improvements
Work closely with maintenance teams, operators, and the Electromechanical Optimization Specialist

What we offer

Competitive salary
401(k) and Roth 401(k) with company match
Comprehensive Health/Dental/Vision insurance
Life/Disability/AD&D Insurance
Employee Assistance Program
Paid Time off (Vacation/Holidays)

Fulltime

New

Drug Product Quality Assurance Specialist

In this vital role within the Plant Quality Assurance organization the Drug Prod...

Location

United States , Thousand Oaks

Salary:

104287.35 - 141094.65 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master's degree and 2 years of quality experience OR Bachelor's degree and 4 years of quality experience OR Associate's degree and 8 years of quality experience OR High school diploma / GED and 10 years of quality experience

Job Responsibility

Partners with Manufacturing, Facilities & Engineering, Quality Control, and other cross-functional stakeholders to facilitate root cause analyses, risk assessments, CAPAs, and effectiveness verification activities
Participates in and provides quality oversight for quality records including Deviations, Change Controls, and CAPAs, assuring adherence to procedural requirements and regulatory expectations
Partners with our colleagues in Manufacturing, Supply Chain, Facilities and Engineering and Automation to maintain our strong culture of Quality and Safety and ensure we continue to meet Amgen standards
Provides Quality Oversight of the manufacturing facility including manufacturing operations, inspection and utilities, as well as nonroutine activities such as process and product validation
Provides quality expertise and guidance to operational staff and within cross functional Amgen teams
Reviews and approves controlled documents, including but not limited to Standard Operating Procedures, Protocols and Reports
Ensures that operations align with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and Controls
Participates in Amgen internal/external audits and inspections
Directly interacts with regulatory agencies during on-site inspections
Contributes to and drives continuous improvement projects in cross-functional collaboration

What we offer

Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans

Fulltime

New

Specialist Quality Assurance

Responsible for providing oversight and leadership for quality systems execution...

Location

Singapore , Singapore

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master's degree and 2 years of directly related experience OR Bachelor's degree and 4 years of directly related experience OR Diploma and 8 years of directly related experience
8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems.
Direct experience with bulk manufacturing of biopharmaceuticals/API preferred.
Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff.
Experience with regulatory audits and inspections
Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.

Job Responsibility

Provide Quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning, process qualification, regulatory approval and market supply
Support routine GMP documentation review activities (e.g. electronic batch records, SOPs, logbooks, work orders, batch production reports and validation protocols etc.) and ensure key performance indicator met targeted metrics
Co-lead and support the deployment of Amgen quality systems, including management review, validation, change control and CAPA and ensure that the systems are managed in compliance with cGMP expectations
Participate in complex root cause investigations for deviations
Review and approve deviation investigations, change controls, and other quality records (with focus on highly complex records)
Provides Quality Assurance support in New Product Introduction (NPI) team
Coach site Quality Assurance professionals on resolution of complex problems
Participate in regulatory inspections, and interact directly with regulatory inspectors
Supporting other Quality Assurance initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation.

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Project Manager - MES (Medical Devices / Life Sciences)

We are currently seeking a Project Manager - MES (Medical Devices / Life Science...

Location

Puerto Rico , San Juan

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

10+ years of strong proficiency in: C#, ASP.NET, .NET Core, SQL Server, WPF or Blazor (for HMI/Dashboard development)
5+ years of experience with MES architecture and shop floor system integration (PLCs, SCADA)
Proven experience managing MES implementations in: Life Sciences, Medical Devices (Class II/III preferred)
PMP (Project Management Professional) OR Certified Scrum Master (CSM)
Strong understanding of Quality Management Systems (QMS)
Familiarity with: FDA 21 CFR Part 11, GAMP standards, ISO 13485, FDA Design Controls
Hands-on experience with Computer System Validation (CSV)
Strong documentation and audit readiness experience
Strong leadership and stakeholder management
Excellent communication and reporting skills

Job Responsibility

Define project scope, objectives, and deliverables in collaboration with senior management and key stakeholders
Develop comprehensive project plans including timelines, milestones, and resource allocation
Drive end-to-end execution of MES implementation projects, ensuring alignment with organizational goals
Forecast project requirements and manage budgets effectively
Track project expenses and identify/mitigate variances proactively
Optimize resource utilization across teams and project phases
Lead cross-functional teams including software engineers, automation specialists, and QA teams
Delegate tasks effectively, ensuring accountability and high performance
Drive delivery using Agile or hybrid SDLC methodologies
Identify and mitigate project risks, issues, and bottlenecks

Fulltime

Inventory Control Specialist

The Inventory Control Specialist ensures accurate inventory records by performin...

Location

United States , Stokesdale

Salary:

20.60 USD / Hour

Owens Corning

Expiration Date

Until further notice

Requirements

Experience in inventory control within a manufacturing or production environment
Proficiency with ERP systems (QAD or other manufacturing focused systems preferred)
Strong "detective" mindset with the ability to troubleshoot and resolve complex inventory issues
High attention to detail and the ability to retain and apply technical information
Effective communication, collaboration skills, and a track record of reliability and consistent performance
Do repetitive movements (hand, wrist, and arm)
Normal and/or corrected hearing and vision with good hand eye coordination
Walking, bending, twisting, stooping, climbing stairs, and lifting objects
Lift up to 35 lbs.
Withstand heat in excess of 95 degrees

Job Responsibility

Maintain comprehensive knowledge of the plant’s material flow, product lines, and inventory control processes
Conduct thorough cycle counts and physical audits of raw materials, WIP, and finished goods to ensure system integrity
Validate WIP locations and monitor high-priority areas and items to maintain variances within acceptable limits
Lead preparation and execution for annual physical inventories, including inventory control document management and reconciliation activities
Investigate inventory discrepancies, negative balances, and shortages using transaction histories, PO verifications, component variance reports and other supporting documents
Identify and correct discrepancies related to production errors, scanning mistakes, shipping/receiving variances, or incorrect substitutions
Expertly navigate ERP system, RF scanners, and MS Office (Outlook, Teams, Excel) to manage and communicate inventory status changes, transfers, and to resolve system inaccuracies
Review and interpret complex Bills of Materials (BOMs) to identify inaccuracies, decipher multi-level items, and execute necessary system corrections
Process and reconcile production documentation to ensure accurate movement of materials from raw components to finished goods
Effectively communicate inventory issues and resolutions to supervisors and production teams

What we offer

insurance (medical/dental/vision/life/disability/supplemental offerings)
401k
liberal paid time off (vacation, personal floating and standard holidays)
Employee Assistance Services
Stock Purchase Program

Fulltime

Industrial Engineer

As a successful family-owned company on a path to global growth, the Brose Group...

Location

Serbia , Pančevo

Salary:

Not provided

Brose Fahrzeugteile

Expiration Date

Until further notice

Requirements

Bachelor's degree in Engineering or other Technical Sciences
Minimum 3 years of experience in a similar role within a manufacturing environment (automotive industry preferred)
Solid knowledge of automotive industry standards and tools (IATF 16949, VDA, OEE, FMEA, structured problem solving)
Good technical understanding of mechanical systems, pneumatics, and industrial sensors
Strong analytical and communication skills with the ability to work in cross-functional teams
Fluent English (written and spoken)

Job Responsibility

Ensure production equipment meets required cycle times and quality standards to satisfy customer expectations
Analyze production performance and implement improvements to continuously enhance KPIs, productivity, and cost efficiency
Maintain technical availability of production machines by coordinating with maintenance teams, specialists, and suppliers
Keep all production documentation updated (work instructions, setup instructions, autonomous maintenance, poka-yoke, and process parameters)
Maintain production data in SAP (Bill of Materials, routings, production versions, work centers, Kanban cycles)
Design and maintain production layouts (AutoCAD and on-site) to improve material flow, inventory management, safety, and workplace organization
Support new product launches by participating in the Product Development Process (equipment procurement, FMEA, MTM, ergonomics)
Coordinate engineering changes between customer teams and internal production teams
Participate in continuous improvement initiatives and plant standardization projects such as VSM, 6S, TPM

What we offer

Flexible office concept
Variable working hours
Results-oriented compensation
Personalized benefits
Private health insurance
Company sports activities
Family support programs
Company canteen

Project Manager

Sowga, part of the Pareto FM Group, is looking for an experienced Project Manage...

Location

United Kingdom , London

Salary:

45000.00 - 65000.00 GBP / Year

paretofm

Expiration Date

Until further notice

Requirements

Proven experience delivering M&E and/or HVAC projects as a Project Manager
Strong background within Building Services, MEP, or Facilities Management projects
Experience managing projects from pre-construction through to commissioning and handover
Strong understanding of mechanical, electrical, and HVAC systems
Experience managing subcontractors, suppliers, and site teams
Proven budget management, cost control, and commercial awareness
Experience working on live operational sites
Strong understanding of building services drawings, specifications, and technical documentation
Knowledge of UK Building Regulations and CDM requirements
Experience preparing and reviewing RAMS

Job Responsibility

Taking full ownership of assigned M&E and HVAC projects from inception through to completion
Planning and managing project programmes, budgets, resources, and timelines
Coordinating installation, testing, commissioning, and handover activities
Managing subcontractors, suppliers, specialist contractors, and site teams
Preparing and reviewing RAMS, construction documentation, and project plans
Monitoring project costs, expenditure, forecasts, and financial performance
Managing project variations, valuations, change control, and commercial correspondence
Liaising with clients, consultants, main contractors, and internal stakeholders
Chairing project meetings and providing clear progress updates
Procuring materials, plant, and subcontract services

What we offer

Competitive salary dependent on experience
Company car
Company iPhone
Pension scheme
25 days annual leave plus bank holidays
Opportunity to work on varied and technically interesting projects
Autonomy and ownership within a growing projects division
Career progression opportunities within the wider Pareto FM Group
Ongoing professional development and training support

Fulltime

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Plant Continuous Improvement Specialist

Job Description

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