Corporate Quality Chemical Engineer Job at Polynt Group (Carpentersville)

Metallurgist Engineer

The Metallurgist Engineer supervise and manage processes related to the producti...

Location

Mexico , Chihuahua, Ciudad de Mexico

Salary:

Not provided

Victaulic

Expiration Date

Until further notice

Requirements

Metallurgical Engineering or similar
English
8 years of experience in a similar position
Nodular iron manufacturing
In-process molding
Induction of furnace refractory maintenance
Sand molding processes
Statistical tools
Continuous improvement methodology, Lean Manufacturing, Six Sigma
Data and trend analysis

Job Responsibility

Daily process walkthroughs, monitoring metal transformation to ensure quality standards are met
Perform metallurgical analysis, laboratory testing, and material evaluations to ensure products meet technical and regulatory specifications
Production optimization, identifying areas for improvement in existing processes and proposing solutions to increase productivity and reduce waste
Regulatory compliance and safety, ensuring all activities are carried out in accordance with safety and environmental regulations and meeting quality standards and industry regulations
Interdepartmental collaboration, working as a team with other departments such as engineering, maintenance, quality, and production to resolve technical issues and optimize overall operations
Ensure all activities are carried out in accordance with applicable safety, occupational health, and environmental regulations and standards to achieve regulatory compliance in your area
Mentor production, process engineering, quality, and maintenance personnel
Assertive communication with Corporate
Assist in the primary contact for issues related to the metal composition of the casting product
Manage and train their resources

Sr Manager, Quality Engineer

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Costa Rica , Cartago

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Quality, Industrial, Chemical, Biomedical or related Engineering
10+ years in Quality roles, with at least 5 in leadership positions
Validated experience in quality management systems in the medical, biotechnology or pharmaceutical industry
In-depth knowledge of international laws and standards (ISO 13485, FDA, GMP, MDSAP, among others)
Process engineering, validations and quality controls
Risk analysis and problem-solving tools (FMEA, Six Sigma, CAPA)
Audit and regulatory compliance management
Proficiency in oral and written English
Inspiring and focused leadership
Effective communication and partner management

Job Responsibility

Ensure the establishment, maintenance and improvement of a quality system that aligns with regulatory, normative and corporate requirements
Approve local specifications and procedures as a Quality representative
Represent the Quality function during audits and with regulatory bodies
Implement strategies to identify, assess, and mitigate quality risks in processes, equipment, and materials
Control the accurate administration of the material and human resources required
Provide guide support to internal and external customers to ensure compliance with plant goals and company standards
Promote improvement, simplification, innovation, and initiatives passionate about meeting regulatory requirements
Represent the Director of Quality in their absence and in strategic committees
Build and complete development and training plans for the members working in the Quality sector
Ensure the continuous training and development of the Engineering teams

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Manager, Compliance Quality Systems

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Costa Rica , Cartago

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Quality, Industrial, Chemical, Biomedical or related Engineering
10+ years in Quality roles, with at least 5 in leadership positions
Validated experience in quality management systems in the medical, biotechnology or pharmaceutical industry
In-depth knowledge of international laws and standards (ISO 13485, FDA, GMP, MDSAP, among others)
Process engineering, validations and quality controls
Risk analysis and problem-solving tools (FMEA, Six Sigma, CAPA)
Audit and regulatory compliance management
Proficiency in oral and written English
Inspiring and focused leadership
Effective communication and collaborator management

Job Responsibility

Quality System Management: Ensure the establishment, maintenance and improvement of a quality system that meets regulatory, normative and corporate requirements
Approve local specifications and procedures as a Quality Representative
Act as the Quality function’s liaison during internal and external audits and interactions with regulatory bodies
Risk Management and Compliance: Implement strategies to identify, assess, and mitigate quality risks in processes, equipment and materials
To control the accurate administration of the material and human resources required for compliance with processes
Technical and Business Leadership: Provide authority support to both on-site and off-site customers to ensure compliance with plant goals and company standards
Promote improvement, simplification, innovation and consistency to regulatory standards projects
Represent the Director of Quality in their absence and in strategic committees
People Management and Talent Development: Build and complete development and training plans for the members of the department passionate about Quality
Ensure the continuous training and development of the teams responsible for Quality Engineering

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Manager, Compliance Quality Systems

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Costa Rica , Cartago

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Quality, Industrial, Chemical, Biomedical or related Engineering
10+ years in Quality roles, with at least 5 in leadership positions
Validated experience in quality management systems in the medical, biotechnology or pharmaceutical industry
In-depth knowledge of international laws and standards (ISO 13485, FDA, GMP, MDSAP, among others)
Process engineering, validations and quality controls
Risk analysis and problem-solving tools (FMEA, Six Sigma, CAPA)
Audit and regulatory compliance management
Proficiency in oral and written English
Inspiring and focused leadership
Effective communication and collaborator management

Job Responsibility

Quality System Management: Ensure the establishment, maintenance and improvement of a quality system that meets regulatory, normative and corporate requirements
Approve local specifications and procedures as a Quality Representative
Act as the Quality function’s liaison during internal and external audits and interactions with regulatory bodies
Risk Management and Compliance: Implement strategies to identify, assess, and mitigate quality risks in processes, equipment and materials
To control the accurate administration of the material and human resources required for compliance with processes
Technical and Business Leadership: Provide authority support to both on-site and off-site customers to ensure compliance with plant goals and company standards
Promote improvement, simplification, innovation and consistency to regulatory standards projects
Represent the Director of Quality in their absence and in strategic committees
People Management and Talent Development: Build and complete development and training plans for the members of the department
Ensure the continuous training and development of the teams responsible for Quality Engineering

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Manager, Compliance Quality Systems

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Costa Rica , Cartago

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Academic background: Quality, Industrial, Chemical, Biomedical or related Engineering
10+ years in Quality roles, with at least 5 in leadership positions
Validated experience in quality management systems in the medical, biotechnology or pharmaceutical industry
In-depth knowledge of international laws and standards (ISO 13485, FDA, GMP, MDSAP, among others)
Technical skills: Process engineering, validations and quality controls
Risk analysis and problem-solving tools (FMEA, Six Sigma, CAPA)
Audit and regulatory compliance management
Proficiency in oral and written English
Leadership proficiencies: Inspiring and focused leadership
Effective communication and collaborator management

Job Responsibility

Quality System Management: Ensure the establishment, maintenance and improvement of a quality system that meets regulatory, normative and corporate requirements
Approve local specifications and procedures as a Quality Representative of the Areas under their responsibility
Act as the Quality function’s liaison during internal and external audits and interactions with regulatory bodies
Risk Management and Compliance: Implement strategies to identify, assess, and mitigate quality risks in processes, Equipment and materials
To control the accurate administration of the material and human resources required for Compliance with processes
Technical and Business Leadership: Provide authority support to both on-site and off-site customers to ensure compliance with plant goals and company standards
Promote improvement, simplification, innovation and consistency to regulatory standards projects
Represent the Director of Quality in their absence and in strategic committees
People Management and Talent Development: Build and complete development and training plans for the members of the department passionate about Quality
Ensure the continuous training and development of the teams responsible for Quality Engineering

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Manager, Compliance Quality Systems

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Costa Rica , Cartago

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Academic background: Quality, Industrial, Chemical, Biomedical or related Engineering
Experience: 10+ years in Quality roles, with at least 5 in leadership positions
Validated experience in quality management systems in the medical, biotechnology or pharmaceutical industry
In-depth knowledge of international laws and standards (ISO 13485, FDA, GMP, MDSAP, among others)
Technical skills: Process engineering, validations and quality controls
Risk analysis and problem-solving tools (FMEA, Six Sigma, CAPA)
Audit and regulatory compliance management
Proficiency in oral and written English
Leadership proficiencies: Inspiring and focused leadership
Effective communication and collaborator management

Job Responsibility

Quality System Management: Ensure the establishment, maintenance and improvement of a quality system that meets regulatory, normative and corporate requirements
Approve local specifications and procedures as a Quality Representative
Act as the Quality function’s liaison during internal and external audits and interactions with regulatory bodies
Risk Management and Compliance: Implement strategies to identify, assess, and mitigate quality risks in processes, equipment and materials
To control the accurate administration of the material and human resources required for compliance with processes
Technical and Business Leadership: Provide authority support to both on-site and off-site customers to ensure compliance with plant goals and company standards
Promote improvement, simplification, innovation and consistency to regulatory standards projects
Represent the Director of Quality in their absence and in strategic committees
People Management and Talent Development: Build and complete development and training plans for the members of the department passionate about Quality
Ensure the continuous training and development of the teams responsible for Quality Engineering

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Chief Process Engineer

The Chief Process Engineer leads the Process Engineering group at the Woodward C...

Location

United States , Woodward

Salary:

Not provided

CF Industries

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering from an ABET-accredited university (Chemical Engineering preferred)
Minimum 7 years of engineering experience in oil, gas, or chemical manufacturing
Preferred: 3+ years of experience with ammonia, urea, nitric acid, or UAN facilities
Strong written and verbal communication skills
ability to interact across all organizational levels and clearly document technical work
Demonstrated commitment to safety and experience working within a strong process safety management framework
Familiarity with relevant codes, regulations, and industry standards
Must be legally authorized to work in the United States

Job Responsibility

Lead and manage the Process Engineering team, overseeing daily activities, staff development, and support for operating units, storage, loading, and off-sites
Promote a culture of safety, inclusion, and sustainability, supporting corporate goals for workforce safety, greenhouse gas reduction, diversity, and community engagement
Ensure routine monitoring of operating KPIs, working with Operations and Maintenance to identify and resolve performance deficiencies
Oversee technical evaluations of catalyst and equipment performance, ensuring timely, sound, and economically justified recommendations—especially ahead of turnarounds
Allocate engineering resources to resolve technical issues, collaborating across Operations, Maintenance, and other disciplines with a safety-first approach
Provide technical oversight on capital projects, ensuring safe, high-quality, and cost-effective execution aligned with design standards and timelines
Ensure timely resolution of action items from PHAs, audits, and Operating Standards, maintaining safety and regulatory compliance
Identify and develop improvement projects that enhance process safety, environmental performance, efficiency, and production capacity
Maintain open communication with site leadership, aligning engineering priorities with operational goals and proactively addressing risks and threats
Develop engineering talent, enhancing technical competency and work quality through mentoring, training, and strategic development

Fulltime

Evonik Rotation Program - Early Career Engineers

Explore a world of opportunities with us. Look ahead with us and help shape inno...

Location

United States , Richmond; Birmingham; Little Rock; Blair; Pasadena

Salary:

Not provided

Evonik Industries

Expiration Date

Until further notice

Requirements

Receive Bachelor of Science degree in Chemical Engineering or Mechanical Engineering Curriculum between December 2025 and June 2026
Begin employment with Evonik Corporation in July 2026 as part of the Evonik Rotation Program cohort
Must be mobile and willing to relocate to another region (NA and/or internationally) for the duration of the program (2 years)
Be knowledgeable of engineering fundamentals, standard industry practices, and regulatory requirements and/or operations management through previous work experiences (Co-Op or internships) in the chemical industry preferred
Excellent written, verbal, and organizational skills
Ability to interact and communicate effectively with all levels of the organization
Excel in a project team environment with high adaptiveness to variable situations
Demonstrated ability to think critically and solve problems
Proficiency in Microsoft Office applications
Highly organized and efficient in time management

Job Responsibility

Provide technical and methodological assistance to defined production and operations areas to increase productivity or reliability of processes and/or equipment
Support the evaluation of concepts for expansions including small and mid-sized Capital Investment Projects, quality increase, production availability and/or operations management
Provide technical support in basic engineering, detail engineering, process development and scale-up of customer projects or production processes
Support preparation of basic engineering and design documentation on capital projects and customer projects in compliance with all applicable standards where required
Support preparation of project scope and financial feasibility studies to gain project approval
Act in assigned roles within site assignments which may include process, project, maintenance & reliability engineering or roles within a subject matter expert team such as Energy & Utilities or RD&I support roles
Analyze, monitor and document data using pre-set tools, methods and formats to improve processes and increase reliability or quality process and products
Collaborate with other departments from procurement, plant engineering, supply chain, EHSQ and HR as well as controlling and regulatory to support project or task execution
Supports business processes by understanding and effectively using standard office equipment and standard software packages, while providing technical guidance as needed to operators or support staff
Develop appropriate plans or perform necessary actions based on recommendations and requirements to improve performance of processes, product or equipment

What we offer

hybrid and flexible working environments with #SmartWork
performance-based remuneration
occupational health benefits
attractive career paths
high-quality development programs

Fulltime

Corporate Quality Chemical Engineer

Polynt Group

Location:
United States , Carpentersville

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 21, 2026

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