Manufacturing Systems Specialist Job at ESSITY ITALY S.P.A. (Ecatepec)

Manufacturing Execution Systems Specialist

This role is focused on design, development, validation, and continuous improvem...

Location

United States , Thousand Oaks

Salary:

107545.40 - 145502.60 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

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

Job Responsibility

Design, develop, and maintain DP Manufacturing Electronic Batch Records (EBRs) using Körber PAS-X
Translate DP manufacturing processes / user requirement specifications into compliant MES templates, recipes, and workflows
Ensure EBRs and data reporting out of MES are robust, efficient, and aligned with GMP requirements
Support validation activities for MES / EBRs including testing and defect resolution
Provide day-to-day MES support to manufacturing operations, including troubleshooting and on-call support
Partner with NPI leads to enable MES readiness for New Product Introductions
Support deployment of new MES capabilities and system integrations (SAP, PI, DeltaV, Rockwell, Kepware)
Identify and implement improvements to MES design, usability, and performance
Contribute to MES standardization and best practices across the site and network
Support change control activities ensuring compliance with GMP procedures

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Specialist Manufacturing Drug Substance

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Or Master's degree and 2 years of Manufacturing/Quality Support experience
Or Bachelor's degree and 4 years of Manufacturing/Quality Support experience
Or Associate's degree and 8 years of Manufacturing/Quality Support experience
Or High school diploma / GED and 10 years of Manufacturing/Quality Support experience

Job Responsibility

Serve as the subject matter expert for specific manufacturing processes, equipment, systems or deviations & CAPAs management, providing technical leadership across the site
Own and maintain SOPs, batch records, deviations, CAPAs, CAPAs EVs and technical documentation to ensure compliance with cGMP and regulatory standards
Lead troubleshooting efforts for complex process or equipment issues, conducting root cause analyses and implementing preventive measures
Monitor manufacturing data and key performance indicators metrics to identify trends, risks, and opportunities for improvement
Drive continuous improvement by exploring new technologies, digital tools, and best practices to enhance process efficiency and reliability
Provide formal training and mentorship to team members on new or complex manufacturing processes, systems, deviations, and CAPAs/EVs management
Represent Manufacturing in cross-functional meetings, audits, and investigations, translating technical insights into actionable recommendations
Lead or support change controls, deviations, and CAPAs to ensure consistent product quality and regulatory compliance
Plan and manage projects related to process optimization, ensuring timely execution and alignment with quality standards
Support a culture of accountability, safety, and performance by modeling high standards and reinforcing compliance expectations

What we offer

Health and welfare plans for staff and eligible dependents
Financial plans with opportunities to save towards retirement or other goals
Work/life balance
Career development opportunities
Retirement and Savings Plan with generous company contributions
Group medical, dental & vision coverage
Life & disability insurance
Discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans and an annual site shutdown

Fulltime

Hseq Specialist - Systems

LANXESS UK is now recruiting a HSEQ Specialist – Systems to work at our Trafford...

Location

United Kingdom , Manchester

Salary:

Not provided

LANXESS

Expiration Date

Until further notice

Requirements

Experienced HSEQ Specialist from a manufacturing background with a relevant degree qualification
Strong knowledge of HSEQ systems, regulatory compliance, and ISO standards
Skills in data analysis, training, and cross-functional teamwork
Happy being site based and enjoy building relationships and encouraging a culture focused on safety and sustainability

Job Responsibility

Maintain and update HSEQ systems, policies, and procedures
Ensure compliance with environmental permits, ISO standards, and waste management
Coordinate internal audits and lead incident investigations
Manage environmental data, performance reporting, and regulatory requirements
Collaborate on safety training and HSEQ improvement initiatives

What we offer

Competitive compensation packages inclusive of a global bonus program and an individual performance bonus program
Comprehensive benefits including retirement plans, health programs, life insurance and medical care
Flexible working arrangements with the global Xwork program
Training and development
Diversity and inclusion

Fulltime

Sr Business Systems Specialist (Quality Management)

As a Sr Business Systems Specialist on the Super User Network (SUN) Quality Assu...

Location

United States , St. Louis

Salary:

80000.00 - 120000.00 USD / Year

Nestlé Purina

Expiration Date

Until further notice

Requirements

High school diploma or GED equivalent
5+ years of experience working with SAP's Quality Management (QM) module or equivalent enterprise quality management systems, including configuration, troubleshooting, and supporting end users across factory operations
3+ years of experience in factory-related processes such as production scheduling, quality checks, and manufacturing operations

Job Responsibility

Research, troubleshoot, and resolve SAP QM issues across multiple functional areas, performing root cause analysis and providing sustainable solutions
Support and manage inspection lot processes, including triggers, status management, test plans, and execution of usage decisions
Maintain and troubleshoot material batch structures, including shelf-life calculations, salvage dates, and batch status
Evaluate QA processes and assess compliance with Nestlé and Nestlé Purina standards, identifying gaps and driving continuous improvement
Leverage working knowledge of SAP technical concepts (including IDOCs, batch jobs, configurations, and data tables) to support issue resolution and system performance
Partner with QA, IT, and business teams to drive resolution, communicate updates, and support ongoing QA operational effectiveness
Lead and support system implementations and business initiatives, including gap analysis, user acceptance testing, and validation across functional areas
Participate in a rotating on-call schedule, supporting critical incidents that impact factory production and ensuring timely escalation, communication, and resolution

What we offer

Performance-based incentives
401k with Company match
Healthcare coverage
Broad range of other benefits

Fulltime

Senior Specification Author and Data Systems Specialist

Join the TAG Center of Excellence in a senior technical role connecting product ...

Location

United States , Solon

Salary:

Not provided

Nestlé Purina

Expiration Date

Until further notice

Requirements

Bachelor's degree is required (technical or related field advantageous)
Technical or vocational certifications in digital, data, or automation platforms (e.g., Power Automate, SharePoint, Salesforce, Power Apps, SAP, TraceGains) are a plus
Proven ability to work independently in complex, regulated environments, exercising sound judgment and partnering effectively across functions
5+ years of hands-on experience working with enterprise specification, recipe, BOM, and manufacturing master data systems (e.g., SAP Product Life Cycle, SAP S4HANA, TraceGains or similar)
Familiarity with Specification Author activities, including creation, maintenance, and approval of Raw Material, Purchasing, Market Requirement, and Packaging specifications within regulated environments
Experience working in cross-functional environments (Product Development, Packaging, Quality, Manufacturing, IT), preferably within manufacturing or technical operations
Exposure to data management, reporting, automation, or digital improvement initiatives that support efficiency, data quality, and continuous improvement

Job Responsibility

Author and maintain Raw Material, Purchasing Specifications, and Market Requirement, ensuring timely creation, updates, and approvals
Ensure alignment between recipes, BOMs, specifications, and manufacturing master data
Maintain high-quality, compliant data in SAP, TraceGains, and related systems
Apply specification and master data standards consistently, flagging inputs or decisions that introduce compliance, audit, or factory readiness risk
Provide day-to-day administration and user support for key TAG platforms (SAP, TraceGains, SharePoint, Power Apps, Power Automate, and Salesforce)
Translate technical, regulatory, and compliance requirements into clear, usable system workflows and documentation
Support system testing, upgrades, access management, issue resolution, and user enablement
Identify and propose system enhancements and automation opportunities, evaluating them through a risk, value, and sustainability lens
Proactively identify opportunities to simplify, standardize, and optimize specification, recipe, and BOM processes in line with TAG Digital Strategy and efficiency objectives
Strengthen Specification Author consistency and data quality through clear documentation, standardized ways of working, and best-practice sharing

Fulltime

Specialist Manufacturing - Production Process Owner

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States of America , Thousand Oaks

Salary:

107545.40 - 145502.60 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

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

Job Responsibility

Support change control activities to ensure GMP, regulatory, and operational compliance
Evaluate and justify process or equipment changes and assist with project execution
Participate in continuous improvement and operational excellence initiatives to enhance safety, quality, and efficiency within DP operations
Support implementation of new processes, equipment, and major initiatives within Drug Product operations
Collaborate with Capital, Engineering, Process Development, Quality, and other functions to define requirements and achieve operational readiness
Assist in developing and implementing SOPs, batch records, training, validation, and automation configurations
Analyze manufacturing data and performance metrics to identify trends, deviations, and opportunities for improvement
Develop and implement data-driven solutions to improve yield, reliability, and compliance
Support data monitoring using analytical tools such as Enterprise Data Lake and Spotfire, ensuring configuration alignment with process design and GMP requirements
Support timely investigation and resolution of manufacturing deviations

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Accounts Payable Specialist (Manufacturing / Distribution)

We’re seeking an Accounts Payable Specialist to support high-volume invoice proc...

Location

United States , Vista

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

3+ years of accounts payable experience
Experience in manufacturing, distribution, or similar environment preferred
Familiarity with high-volume invoice processing
ERP Systems: SAP, NetSuite, or similar (required)
Microsoft Excel: intermediate (required)

Job Responsibility

Process high-volume vendor invoices and ensure proper approvals
Match purchase orders, receipts, and invoices (3-way matching)
Prepare and process check runs and electronic payments
Reconcile vendor statements and resolve discrepancies
Maintain accurate records of all accounts payable transactions
Communicate with vendors regarding billing and payment inquiries
Support month-end close and AP reporting
Assist with process improvements and workflow efficiencies

What we offer

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

Quality Assurance Specialist - Manufacturing Support

Serve as Quality Assurance Specialist responsible for Plant Quality Assurance (P...

Location

United States of America , Holly Springs

Salary:

104287.35 - 141094.65 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED and 10 years of Quality, Manufacturing, Process Development or Process Engineering experience OR Associate’s degree and 8 years of Quality, Manufacturing, Process Development or Process Engineering experience OR Bachelor’s degree and 4 years of Quality, Manufacturing, Process Development or Process Engineering experience OR Master’s degree and 2 years of Quality, Manufacturing, Process Development or Process Engineering experience OR Doctorate degree

Job Responsibility

Provide Quality oversight to ensure that Operations’ products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations
Ensure that facilities, equipment, materials, organization, processes, and procedures comply with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and other controls
Perform review and approval of cGMP processes, procedures, documents and records, including but not limited to Batch Production Records, Deviations, work-orders, Change Controls and Corrective Action/Preventative Actions (CAPA)
Author/review/approve quality documents, such as SOPs, user requirements, risk assessments, training materials, engineering documents, automation documents, environmental qualification protocols/reports, validation protocols/reports
Oversee and provide guidance during on-the-floor analytical testing
Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements
Ensure that changes that could potentially impact product quality are assessed according to procedures
Ensure that deviations from established procedures are investigated and documented per procedures
Alert senior management of quality, compliance, supply and safety risks
Provide project management support, leading efforts to drive timely achievement of tasks and develop strategies for system implementation

Fulltime

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Manufacturing Systems Specialist

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