CrawlJobs Logo

Manufacturing Manager

https://www.baxter.com/ Logo

Baxter

Location Icon

Ubicación:
United States , Batesville

Category Icon
Categoría:

Job Type Icon

Tipo de contrato:
No proporcionado

Salary Icon

Salario:

104000.00 - 143000.00 USD / Año
Guardar empleo
Save Icon
Aplicar al puesto

Descripción del trabajo:

Lead inventory operations and global logistics for Batesville’s multi-shift operations. Oversee a 200,000 sq. ft. multi-site warehouse, manage $33M in inventory, and coordinate 20–30 daily inbound truckloads. This role is accountable for meeting budget, quality, and operational goals while ensuring compliance and driving continuous improvement.

Responsabilidades:

  • Drive operational excellence in cost, productivity, inventory turnover, transportation, and safety
  • Implement standardized processes and continuous improvement initiatives using Lean, BOS, and DMAIC principles
  • Monitor KPIs for order fulfillment, supplier performance, and inventory accuracy
  • develop plans to meet objectives
  • Manage staffing, talent development, and engagement programs to build a high-performing team
  • Ensure compliance with corporate, federal, and regulatory requirements (cGDP, cGMP, trade/export)
  • Promote alignment with customer needs and foster innovation to improve efficiency and service
  • Standardize processes internally and with external suppliers to improve efficiency
  • Oversee cycle count process and ensure inventory accuracy
  • Champion workplace engagement programs and foster a positive, values-driven culture
  • Partner with HR on employee relations, disciplinary actions, and training programs
  • Promote safety and quality commitments
  • lead initiatives for zero-harm workplaces
  • Use Baxter Operating System (BOS) to measure productivity, optimize processes, and encourage innovation

Requisitos:

  • Bachelor’s Degree in Operations, Logistics, Supply Chain, Industrial Engineering, or related field
  • 3–5 years of experience in manufacturing, logistics, or warehousing
  • Strong leadership and communication skills with ability to influence across all levels
  • Deep understanding of supply chain operations, financial impacts, inventory management, and service levels
  • Proven ability to lead cross-functional projects and develop top talent
  • Strategic thinker with analytical and problem-solving skills
  • adaptable to change
  • Expertise in warehouse and distribution management
  • experience with JDE and Agile systems
  • Knowledge of Lean Six Sigma, Operational Excellence, EHS, GMP, FDA guidelines, and process validation
  • Applicants must be authorized to work for any employer in the U.S.
Lo que ofrecemos:
  • Medical and dental coverage
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • Educational assistance programs
  • Paid holidays
  • Paid time off ranging from 20 to 35 days based on length of service
  • Family and medical leaves of absence
  • Paid parental leave
  • Commuting benefits
  • Employee Discount Program
  • Employee Assistance Program (EAP)
  • Childcare benefits

Información adicional:

Oferta publicada:
06 de enero de 2026

Tipo de empleo:
Tiempo completo
Tipo de trabajo:
Trabajo presencial
Compartir enlace de empleo:

¿Buscas más oportunidades? Busca otras ofertas de trabajo que coincidan con tus habilidades e intereses.

Briefcase Icon

Empleos similares para Manufacturing Manager

Nuevo

Supply Planner

Align supply and demand, manages constraints, and ensures product flow from glob...
Ubicación
Ubicación
United States , Irvine
Salario
Salario:
45.19 - 62.21 USD / Hora
bio-rad.com Logo
Bio-Rad Laboratories
Fecha de expiración
Hasta nuevo aviso
Flip Icon
Requisitos
Requisitos
  • Bachelor’s degree in Supply Chain, Business, Management or other related field
  • 5+ years’ experience in supply planning, inventory management or manufacturing operations within an ERP/DRP environment
  • Expert analytical, numerical and problem solving skills
  • Proven ability to think strategically, execute tactically and be detail oriented
  • Strong working knowledge of planning systems – SAP APO (preferred), Kinaxis, or i2, JDA/Manugistics
  • Expert computer skills with advance working knowledge in Windows Office environment
  • Proven ability to plan and coordinate workflow and outputs efficiently across multiple functional groups and geographies to align group objectives, timeframes and deliverables, as well as to provide actionable feedback to keep processes and deliverables on track
  • 4-5 years’ experience in supply
  • ERP Experience ideally: SAP, Kinaxis and TMS
Responsabilidades
Responsabilidades
  • Align supply and demand, manages constraints, and ensures product flow from global manufacturing and OEM partners into Bio-Rad’s distribution network
  • Manage and optimize our inventory investment and cycle time to meet our customer’s expectations for product delivery
  • Tiempo completo
Leer más
Arrow Right

Manufacturing supervisor

This is where your work makes a difference. At Baxter, we believe every person—r...
Ubicación
Ubicación
United States , Saint Paul
Salario
Salario:
64000.00 - 88000.00 USD / Año
https://www.baxter.com/ Logo
Baxter
Fecha de expiración
Hasta nuevo aviso
Flip Icon
Requisitos
Requisitos
  • BS degree in a business, scientific, or engineering discipline with 1 year of manufacturing experience or high school diploma or equivalent with 3 years related manufacturing experience
  • Demonstrated interpersonal and leadership skills with ability to interface well with other departments and lead effectively and efficiently in a team environment
  • Ability to manage multiple priorities in a manufacturing plant setting
  • Strong professional writing skills and ability to prepare technical reports
  • Ability to understand GMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry
  • Strong assessment and troubleshooting skills
  • Computer proficiency in Microsoft Office and ability to use enterprise software
  • Interact with all levels of personnel to analyze and solve problems related to manufacturing, Quality, documentation, and personnel issues
  • Work in and facilitate a team-oriented environment
  • Ability to collect and analyze data and information to determine paths for process improvement and potential root cause
Responsabilidades
Responsabilidades
  • Communicates guidance, support, direction and leadership through effective interactions with all personnel during daily operations
  • Supervises the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities
  • Identifies/prioritizes/provides resources as appropriate
  • Interviews, hires, coaches, motivates, develops, recognizes and manages performance of direct reports
  • Reviews, approves, and manages documentation for batch and system records
  • Assists in release of product for distribution and meeting product release time goals
  • Identifies, initiates and facilitates continuous improvements, lean manufacturing activities and initiatives, such as 5S, visual management, kaizens
  • Insures resources and raw materials are utilized in the most efficient and productive manner possible
  • Supervise daily activities in a specific production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (cGMPs), SOPs, environmental health and safety (EHS) guidelines and any other regulations that may apply
  • Monitor and insure efficiency and effectiveness in various areas and train employees
Lo que ofrecemos
Lo que ofrecemos
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
  • 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
  • Flexible Spending Accounts
  • Educational assistance programs
  • Paid holidays
  • Paid time off ranging from 20 to 35 days based on length of service
  • Family and medical leaves of absence
  • Paid parental leave
  • Tiempo completo
Leer más
Arrow Right

Project Manager II

We are seeking a highly skilled Project Manager II to oversee the financial mana...
Ubicación
Ubicación
United States , Richardson
Salario
Salario:
No proporcionado
ilerwork.com Logo
Ilerwork
Fecha de expiración
Hasta nuevo aviso
Flip Icon
Requisitos
Requisitos
  • Minimum of 5 years of project management experience in the commercial MEP (Mechanical, Electrical, and Plumbing) space
  • Experience managing projects within industries such as life sciences, semiconductor manufacturing, food and beverage production, and research labs is essential and must be clearly demonstrated on the resume and in notes
Responsabilidades
Responsabilidades
  • Manage the financial aspects of commercial HVAC projects within the Process Solutions space, with a focus on high purity/process piping
  • Oversee project budgets, costs, and financial forecasts to ensure successful project delivery
  • Work closely with internal teams and clients to ensure project goals are met
Lo que ofrecemos
Lo que ofrecemos
  • Professional development opportunities to support your career growth
  • Work-life balance programs and flexibility option
  • Relocation assistance available for the right candidate
  • Tiempo completo
Leer más
Arrow Right
Nuevo

Manufacturing Scientist

Bio-Rad in Cressier is currently looking for a Manufacturing Scientist (m/f/d) -...
Ubicación
Ubicación
Switzerland , Cressier
Salario
Salario:
No proporcionado
bio-rad.com Logo
Bio-Rad Laboratories
Fecha de expiración
Hasta nuevo aviso
Flip Icon
Requisitos
Requisitos
  • Degree (Bachelor, Masters or HES) in Life Sciences (Biology, Chemistry or similar.), Dipl. Ing. or M.Sc. or B.Sc. or equivalent
  • Min. 3 years of experience working in the diagnostics field, which has enabled to acquire the lates techniques in biology, biochemistry and /or immunology and the automation
  • Proven scientific and technical expertise in Diagnostic/Pharmaceutical industry
  • Structured and methodical
  • Communication skill
  • French or German as mother tongue, with at least basic knowledge of the other language, and fluent in English
Responsabilidades
Responsabilidades
  • Contribute to technical transfer projects for establishing robust and compliant manufacturing processes and associated control strategy
  • Own and maintain the knowledge of manufacturing processes throughout the product lifecycle
  • Author, review, and approve technical documents such as batch records, sampling plans, SOPs, risk assessments, study protocols, technical reports
  • Provide first line technical support to manufacturing in compliance with relevant instructions and quality requirements
  • Contribute to enhancing process understanding and identifying key sources of variability and root causes of product and process failures
  • Manage change review and implementation, risk assessments, quality investigations, impact assessment, and CAPAs in cross-functional teams
  • Plan and organize training for manufacturing personnel
Lo que ofrecemos
Lo que ofrecemos
  • a competitive salary
  • annual bonus and salary review
  • training and development programs, with access to LinkedIn Learning
  • Tiempo completo
Leer más
Arrow Right
Nuevo

Associate Director, Operations

You'll coordinate manufacturing operations and all related processes. It covers ...
Ubicación
Ubicación
Dominican Republic , Bajos de Haina
Salario
Salario:
No proporcionado
https://www.baxter.com/ Logo
Baxter
Fecha de expiración
Hasta nuevo aviso
Flip Icon
Requisitos
Requisitos
  • Bachelor’s degree in engineering (Automation / Electrical / Electronic / Mechatronic / BSEE BSME) or related field and 20+ years related experience
  • BS, BBA, BSIE or MMA or equivalent experience preferable
  • More than 15 years of leadership experience covering all facets of the manufacturing process in medical devices production, pharmaceutical, biotechnology, or a related setting
  • Excellent interpersonal relations skills
  • Knowledge of GMP-QSR’s, OSHA, BHEST, SPEC, SOP, and HR policies
  • Significant knowledge and practical experience with Business Excellence models and lean enterprise principles
  • Availability to travel as required
  • Bilingual (English and Spanish)
Responsabilidades
Responsabilidades
  • Ensure the improvement of production systems, methods, and processes to reduce costs operations and generate added customer value to the product
  • Ensure that builds run under control and constant process improvement are pursued by assuring through accurate structure, constant data collection, and analysis
  • Manage product and process engineers while they identify, develop, and apply preventive and corrective measures
  • Maintain a good level of performance indicators in accordance with established goals
  • Perform standard cost revision, quotation process, as required and support launch of new products
  • Supervise and coordinate activities related to extrusion, sub-assemblies, and finished goods, ensuring efficient use of resources across all shifts
  • Advance situations impacting personnel, products, or processes in a timely manner
  • Coordinate the Maintenance Area, ensuring accurate prioritization for daily operation and keeping critical metrics in line with Plant Goals
  • Implement and maintain effective preventive and corrective maintenance procedures
  • Ensure conformance to regulatory, financial, security, and other relevant standards in manufacturing and maintenance processes
  • Tiempo completo
Leer más
Arrow Right
Nuevo

Quality Engineer I - Temporary

Join Bio-Rad as our Quality Engineer and work in our Woodinville, WA site! Work...
Ubicación
Ubicación
United States , Woodinville
Salario
Salario:
38.54 - 43.73 USD / Hora
bio-rad.com Logo
Bio-Rad Laboratories
Fecha de expiración
Hasta nuevo aviso
Flip Icon
Requisitos
Requisitos
  • Bachelor’s degree or equivalent in a related scientific discipline
  • 0-2+ years experience or equivalent combination of education and experience
  • Ability to apply GMP / ISO regulations and validation principles in a regulated manufacturing environment preferred
  • Basic understanding of risk management best practices and regulations for the medical device industry
  • Quality Engineering, Six Sigma Green Belt Certifications desirable
  • Skilled in statistical methods, statistical process control and experimental design preferred
  • Ability to work well in fast paced and cross-functional teams
Responsabilidades
Responsabilidades
  • Attend cross functional Daily Management meetings and represent Quality Assurance following up on blocking issues and implementing counter measures
  • Manage the Material Review Board and ensure thorough data-driven documentation of non-conformities and risk based determination of CAPA
  • Review data for trends, manage corrections and corrective action and support Global Supply Chain and business partners as requested
  • Support release of high-quality product by managing the Material Review Board and making risk-based and compliant decisions
  • Maintain the integrity of the Quality Management System by ensuring investigations are well designed, executed and documented
  • Provide confidence to internal and external customers by following through on actions, continually improving processes, and promoting quality culture
  • Demonstrate focus and accountability by attending Daily Management and consistently meeting commitments with timeliness and reliability
  • Facilitate risk management practices and ensure all quality requirements are satisfied
  • Tiempo completo
Leer más
Arrow Right

Innovation Project Engineer

The Senior IVS Project Engineer is responsible for ensuring the completion of IV...
Ubicación
Ubicación
Costa Rica , Cartago
Salario
Salario:
No proporcionado
coloplast.com Logo
Coloplast
Fecha de expiración
Hasta nuevo aviso
Flip Icon
Requisitos
Requisitos
  • University degree in Industrial Engineering, Quality, Production, Supply Chain, or equivalent
  • Minimum 3 years of experience in medical device manufacturing with a deep knowledge of project management methodologies and standards
  • Able to work at a high level with minimal supervision
  • Experience leading multidisciplinary teams
  • Proven ability to solve problems creatively
  • Strong familiarity with project management software tools, methodologies, and best practices
  • Proven ability to successfully complete projects according to defined scope, budget, and schedule
  • Excellent numerical skills and understanding of data analysis
  • Minimum English level B2+ in reading, writing, and conversation
  • Able to travel approximately 20-25 days per year
Responsabilidades
Responsabilidades
  • Responsible for analyzing and defining the scope of projects within IVS Project Management, Global Quality
  • Ensure the successful completion of the project within the scope, schedule, and budget
  • Establish and maintain project governance, standards, methodologies
  • Ensure project status and relevant decisions within the project are communicated to all team members and stakeholders
  • Ensure standardized templates, tools, and systems, that are effective and continuously maintained together with the PM & PMO community in CP
  • Coordinate and manage local projects
  • Monitor and manage resources and budgets across portfolio
  • Responsible for reporting status, KPIs, risks, and issues to the Head of Project Office and the Steering Committee
  • Provide regular reporting to senior leadership on portfolio performance, risks, and benefits realization
  • Regular engagement of key stakeholders to align on expectations and needs
Leer más
Arrow Right
Nuevo

Salvavidas de Piscina

El Salvavidas de Piscina es responsable de garantizar la seguridad de los huéspe...
Ubicación
Ubicación
Colombia , Cartagena
Salario
Salario:
No proporcionado
fourseasons.com Logo
Four Seasons
Fecha de expiración
Hasta nuevo aviso
Flip Icon
Requisitos
Requisitos
  • Certificación vigente de Salvavidas emitida por un organismo reconocido
  • Certificación en RCP y primeros auxilios y entrenamiento en rescate acuático
  • Experiencia previa 3 años como salvavidas, preferiblemente en hoteles, resorts o clubes
  • Nivel de inglés básico-intermedio
  • Conocimiento en: Rescate en piscinas
  • Rescate con técnicas de remolque
  • RCP
  • Manejo de ahogamientos
  • Uso de equipos de rescate (flotadores, desfibrilador)
Responsabilidades
Responsabilidades
  • Monitorear continuamente la piscina y áreas aledañas, previniendo accidentes y detectando comportamientos inseguros o situaciones de riesgo
  • Responder de forma inmediata ante emergencias acuáticas, aplicando técnicas de rescate y maniobras de reanimación cardiopulmonar (RCP) cuando sea necesario
  • Velar por el cumplimiento de las normas de seguridad y control de aforo, garantizando que los huéspedes usen las instalaciones de manera segura
  • Brindar atención y asistencia a los huéspedes, informando sobre las reglas de seguridad y resolviendo dudas con cortesía y profesionalismo
  • Mantener en óptimas condiciones el área de la piscina, asegurando la limpieza, el orden y la disponibilidad de equipos de seguridad (salvavidas, botiquines, etc.)
  • Verificar periódicamente la calidad del agua y el funcionamiento del equipo, reportando cualquier falla o anomalía al personal de mantenimiento
  • Coordinar con otros departamentos (Seguridad, Mantenimiento, Housekeeping y Gerencia) para garantizar una operación segura y eficiente del área de piscina
Lo que ofrecemos
Lo que ofrecemos
  • Salario competitivo
  • Excelente formación y oportunidades de desarrollo
  • Alojamiento gratuito en otros hoteles y resorts de Four Seasons
  • Servicio de lavandería gratuito para los uniformes de los empleados
  • Comidas gratuitas para los empleados
  • Tiempo completo
Leer más
Arrow Right