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Your Job
Molex's Copper Solutions Business Unit is expanding its Enterprise Solutions team and seeking a System Applications engineer who can bridge customer concepts with manufacturable, high performance interconnect solutions.
In this position, you will engage directly with major hyperscale and networking customers to translate early stage system concepts into practical mechanical and interconnect architectures.
You'll work from the system level viewpoint, creating solutions that integrate cable based, rack level, and chassis level architectures aligned with emerging industry trends.
Our Team
Molex brings together innovation and technology to deliver electronic solutions to customers worldwide.
With a presence in more than 40 countries, Molex offers a full suite of solutions and services for many markets, including data communications, consumer electronics, industrial, automotive, commercial vehicle and medical.
What You Will Do
* Act as the technical bridge between R&D and customers by designing and prototyping application-specific, innovative solutions; leading hands-on implementation and pilot deployments; delivering training and enablement; and capturing real-world application feedback to inform new product development from concept through production.
* Communication and alignment with the other functional groups internal to Molex including Global Sales and Marketing, Product Development Engineering, Project Management, and manufacturing to ensure successful design transfers and lessons learned capture.
* Work with customers to interpret early architectural concepts, white board sketches, and block diagrams, and translate them into feasible Molex system level solutions.
* Develop system architectures that integrate Molex components across rack level, chassis level, and emerging cable based systems.
* Account for electrical, thermal, and signal integrity constraints when proposing mechanical concepts.
* Participate in customer meetings, internal reviews, and site visits requiring both in person and virtual collaboration.
* Provide mechanical design concepts using CAD.
Who You Are (Basic Qualifications)
* Bachelor's degree in Mechanical Engineering degree or related technical discipline.
* Relevant engineering experience in system level, applications, product architecture, or hardware development in networking industry.
* Experience directly interfacing with customers.
* Basic understanding of electrical, signal integrity, and thermal design constraints.
* Ability to visualize and design concepts from abstract customer inputs.
* Experience in 2D/3D CAD design tools.
What Will Put You Ahead
* Experience in NX.
* Experience in networking industry within hyperscalers, CMS, ODM, OEMs, or similar environments in electronics manufacturing.
* Experience with rack level and chassis level design and system integration.
* Background with cable midplanes, backp...
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Type: Permanent Location: Lisle, US-IL
Salary / Rate: Not Specified
Posted: 2026-04-25 08:13:31
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Your Job
Molex is seeking a Principal High-Speed Optoelectronic Design Lead to join our Optical Solutions Business Unit (OSBU).
In this role, the successful candidate will be part of a world-class engineering team, contributing to the development of next-generation Photonic Integrated Circuits (PICs).
The successful candidate will be responsible for designing, implementing, and validating advanced high-speed optoelectronic components for PICs, transceivers, and optical engines.
The Principal High-Speed Optoelectronic Design Lead will provide design support for existing and advanced photonic technology and collaborate with global, cross-functional teams and supplier partners to develop next-generation photonic solutions.
Our Team
The PIC Components and Technology Development team are responsible for the research and development of advanced technology platforms and solutions for the next generation of optical connectivity in AI fabrics, data centers, and datacom applications.
Reporting to the Director of Photonics Technology, you will be a key member of the team and will serve as the technical lead for developing advanced integrated RF interconnect technologies such as TSV and EPIC for 400G/L PAM4, CPO, and 1.6T/3.2T coherent products and will closely collaborate with the PIC component design, signal integrity, layout, test & reliability, and transceiver design teams as well as with external partners like semiconductor foundries, OSATs, CMs, and vendors.
This role can be based anywhere in the Unites States or Canada.
What You Will Do
* Lead the R&D, design, and EVT/DVT activities with regards to developing advanced integrated high-speed optoelectronic components for 400G/L PAM4, CPO, and 1.6T/3.2T coherent products.
* Closely collaborate with the SI/PI, opto-mechanics & packaging, and test & reliability teams to provide appropriate test vehicles for EVT/DVT of high-speed components.
* Work with external partners, foundries, CMs, and OSATs to develop required processes and demonstrate production level performance, reliability, and quality.
* Intimately collaborate with the SI/PI and transceiver design teams to build and validate predictive RF models for pluggables and transponders including external ASICs components such as DRV, TIA, DSP (LPO, LRO).
* Collaborate with the PIC component design & PDK teams in developing advanced modulator devices for the next generation of PIC products.
* Mentor other SI/PI engineers and cross functional groups on advanced EM simulation and design techniques based on commercial software tools and custom codes.
Who You Are (Basic Qualifications)
* PhD - or equivalent - typically in Electrical Engineering, Microwave Photonics, Physics or related technical fields
* At least 12 years of relevant industry experience in designing advanced RF interconnects and/or signal/power integrity for optical connectivity applications
* Strong knowledge of Si and/or III-V photonic i...
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Type: Permanent Location: Fremont, US-CA
Salary / Rate: Not Specified
Posted: 2026-04-25 08:13:26
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ABOUT THE ROLE
Join our team at Amsted Automotive Group as a Journeyman Tool & Die Maker! In this key role, you will apply your skills and expertise to design, manufacture, and maintain high-quality tooling for our production processes.
This is a second-shift position with normal hours being Monday through Friday from 2:30pm - 10:30pm.
WHAT YOU'LL DO
* Interpret blueprints and use precision measuring devices to create or modify tooling based on job specifications.
* Set up and operate tool room machines, selecting appropriate materials and tools while adhering to safety protocols.
* Ensure all tools are sharpened and maintained in optimal condition before storage or release to production.
* Utilize knowledge of jigs, fixtures, and dies to set up and run test dies, troubleshooting and correcting any issues to meet specifications.
* Operate hand tools and, as needed, perform heat treating or welding on components.
* Comply with all safety regulations, including lockout procedures, while maintaining a clean and organized workspace.
* Complete necessary documentation, including tool logs and condition reports for tracking and data collection.
* Collaborate effectively with skilled trades and production staff, offering insights into manufacturing capabilities.
* Undertake additional tasks as directed by supervisors.
WHAT YOU'LL NEED TO SUCCEED
* Completion of a formal apprenticeship program or an equivalent eight-year training program recognized by the skilled trades committee or equivalent verifiable tool and die maker experience.
* Proficiency in troubleshooting and repairing dies, tools, fixtures, and jigs, both in-press and at the bench.
* Strong understanding of precision measuring and gauging tools.
* Experience operating lathes, mills, and grinding machinery.
* Exceptional attention to detail and precision, with the ability to minimize risk of damage during operations.
* Commitment to safety and quality in all aspects of work.
WHAT’S IN IT FOR YOU
* Quarterly Profit-Sharing
* Medical, Vision, Dental
* Prescription Drug Plan
* 401K
* Paid Vacation & Holidays
* Short Term Disability
* Tuition Reimbursement
* Employee Recognition
* Discount Programs
WORK ENVIRONMENT & PHYSICAL REQUIREMENTS
* Required Personal Protective Equipment (PPE):
* Safety glasses with side shields
* Earplugs
* Additional PPE for specific tasks
* Constant Activities (75-100% of the time):
* Reaching forward or to the sides
* Frequent Activities (50-75% of the time):
* Standing, bending, twisting, walking
* Lifting or carrying items up to 15 lbs
* Operating power tools and motorized equipment such as forklift, overhead crane
* Working quickly
* Visually inspecting items and clearly communicating with others
* Occasional Activities (25-50% of the time):
* Kneeling, squa...
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Type: Permanent Location: Saginaw, US-MI
Salary / Rate: Not Specified
Posted: 2026-04-25 07:55:54
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Your Job
We are seeking a talented and experienced Vibration Test Specialist to join our dynamic team.
The successful candidate will play a critical role in ensuring the quality and reliability of our products through testing and data analysis.
Our Team
Molex brings together innovation and technology to deliver electronic solutions to customers worldwide.
With a presence in more than 40 countries, Molex offers a full suite of solutions and services for many markets, including data communications, consumer electronics, industrial, automotive, commercial vehicle and medical.
What You Will Do
* Advise lab leadership on current capabilities and assist in driving improvements to keep pace with industry demands.
* Collaborate with internal partners to solve complex vibration challenges and drive product improvements.
* Technical specialist related to all aspects of vibration testing.
* Conducting vibration testing and analysis.
* Provide input for the design and review of vibration fixtures.
* Implementation of effective control strategies.
* Developing and implementing vibration testing and analysis procedures.
* Providing technical expertise and guidance on vibration testing, control issues, and fixture design.
* Collaborating with cross-functional teams to solve complex vibration problems.
* Staying current on industry trends and advancements to continuously improve processes and procedures.
* Documenting and presenting vibration testing results and recommendations to internal and external stakeholders.
* Develop engineering calculations, documentation, and technical reports.
* Design and conduct engineering experiments to find workable solutions.
* Communicate analyses and test solutions.
* Coordinate vibration control, testing and analysis across all Molex reliability labs.
Who You Are (Basic Qualifications)
* Master's degree in engineering
* Three (3) years or more experience in vibration testing and analysis in an aerospace, defense, or automotive industry
* Knowledge of vibration control principles and techniques.
* Experience utilizing test equipment such as electrodynamic shakers, milliohm meters, digital power supplies, DAQ systems, and environmental chambers.
* Experience performing root cause analysis on test failures and providing technical insight to internal partners.
* Experience with vibration analysis techniques to assist in failure analysis.
* Experience validating new test setups, equipment, and software through Measurement System Analysis (MSA) studies, correlation studies, and comparison (round robin) testing efforts.
* Three (3) years or more experience in the setup and utilization of electrodynamic shakers, 0-2500Hz frequency range.
* Three (3) years or more experience the design and characterization of fixtures for use on electrodynamic shakers.
* Experience with lean six sigma concepts and too...
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Type: Permanent Location: Rochester Hills, US-MI
Salary / Rate: Not Specified
Posted: 2026-04-25 07:48:36
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Your Job
Georgia-Pacific is seeking an experienced Robotics Engineer to join our Manufacturing IT Automation team.
This role is a hands-on technical position focused on the planning, design, implementation, integration and support of material handling and warehouse automation systems across manufacturing sites and remote distribution centers.
The Automation Systems Engineer will be an integration expert for platforms that tie shop-floor PLCs and devices to MES, WM, ERP and automation orchestration systems (including AGV/robotic systems), and will enable reliable, maintainable, and scalable automation solutions for 24/7 operations.
What You Will Do
* Serve as a technical leader and subject-matter expert for material handling and warehouse automation platforms and integration frameworks.
* Design, develop, implement and support automation integrations between PLCs, MES, WM, AGV/robotic controllers, orchestration systems and ERP.
* Partner with Process Control, Engineering, Operations, manufacturing IT, architects and vendors to create and optimize common automation platforms and deployment patterns.
* Develop and maintain automation system and platform architectures, diagrams, runbooks and support documentation for triage and sustainment.
* Analyze manufacturing and system data flows to identify reliability, performance and optimization opportunities.
* Participate in QA/testing of automation functionality and drive defect resolution.
* Develop training materials and enablement content so site operations and local IT can act as first-level support.
* Build and contribute to monitoring, alarming and troubleshooting tools and dashboards to accelerate incident resolution by on-site and remote staff.
* Provide 1st and 2nd level automation support; participate in an on-call rotation to support 24/7 operations.
* Facilitate issue resolution with vendors, site operations, and manufacturing IT teams.
* Drive continual improvement initiatives for AGV and other automation platforms from ideation through implementation.
* Travel to manufacturing and distribution sites for fieldwork and projects (see travel expectations below).
Who You Are (Basic Qualifications)
* Bachelor's degree in Information Technology, Computer Science, Engineering or other STEM field, OR at least 4 years of equivalent technical experience.
* Demonstrated professional experience in industrial automation, manufacturing IT, or production operations (supporting industrial or warehouse automation).
* Hands-on experience with industrial automation systems or manufacturing application software.
* General familiarity with MES and WM systems and a clear understanding of data flows between MES, PLCs, AGV/automation systems and ERP.
* Basic PLC knowledge or experience (development, troubleshooting or integration).
* Experience learning new technologies, managing multiple projects/tasks, and working with...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2026-04-25 07:48:33
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Your Job
Molex is seeking a Process Development Engineer to join our team in Naperville, IL.
This role is responsible for conceptualizing, designing, and implementing robust manufacturing processes that allow Molex to capture new and challenging business.
A core aspect of this role is developing and proving feasibility of novel manufacturing strategies to ensure the process can be successfully scaled up.
The engineer should possess a working knowledge of automation principles to ensure effective communication, and smooth adoption of volume manufacturing solutions.
This position emphasizes early-stage development of process concepts, ensuring scalability and manufacturability, and requires close cooperation across multidisciplinary teams from concept through to full-scale deployment.
Our Team
The Process Development Engineer reports to the Manufacturing Integration Engineering (MIE) Manager, and is embedded in the MIE team.
They will engage in regular collaboration with a diverse team including business development managers, applications engineers, design engineers, process engineers, and automation teams.
Work is split between office and production floor settings.
Occasional travel may be required for process transfer activities or coordination with external partners.
What You Will Do
* Generate innovative process concepts that address integration challenges and support the introduction of new products, technologies, and automation solutions.
* Lead feasibility studies, proof-of-concept trials, and pilot-scale experiments to evaluate and refine proposed process solutions, with a focus on improving manufacturing readiness.
* Drive early risk mitigation and design-for-manufacturing discussions to ensure flawless scale-up.
* Design detailed process flows, layouts, and specifications in collaboration with design, automation, and production teams.
* Collaborate with design engineering and production teams to execute on prototype and pre-production builds.
* Guide the seamless transfer of process concepts to automation specialists, and ensure process automation is effectively implemented.
* Support troubleshooting and provide technical expertise, especially during pilot and scale-up phases.
* Contribute to training materials and coach manufacturing staff on the adoption of new process concepts and best practices.
Who You Are (Basic Qualifications)
* Bachelor's degree in an engineering field
* Three (3) years or more experience in manufacturing process development or process engineering
* Experience developing and scaling up novel process solutions within a manufacturing context
What Will Put You Ahead
* Five (5) years or more experience with electronics manufacturing, especially flexible and hybrid electronics
* Experience with software tools such as NX, Solidworks, AutoCAD, Excel, Minitab, or other design and data analysis software
* Experience with automation principles...
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Type: Permanent Location: Naperville, US-IL
Salary / Rate: Not Specified
Posted: 2026-04-25 07:48:25
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Your Job
Molex is rapidly growing and seeking a new Reliability Test Engineer to join our team in Lisle, IL.
In this position you will evaluate mechanical test requirements to ensure cable designs and manufacturing processes produce high speed data cables that meet or exceed the customer's expectations.
This position will focus on our BiPass Cable Technology and products.
Our Team
The Datacom & Specialty Solutions Division is dedicated to designing and delivering high-quality, high-speed data cable products for a variety of applications.
Our team collaborates across multiple departments, including product development, manufacturing, and quality assurance, to ensure we exceed customer expectations and uphold Molex's commitment to excellence.
What You Will Do
* Evaluate, plan, and conduct mechanical testing to prove the quality of our data cable products.
Coordinate lab activities with multiple departments, including product development, manufacturing, signal integrity, and quality.
* Perform mechanical testing of High-Speed cable assemblies.
Support data analysis, identification of critical to quality aspects of product design and manufacturing process and author reports to summarize findings.
* Collaborate closely with multifunctional teams to determine quality and suitability of cable assembly products.
Maintain records for test execution, schedule, and reporting.
* Create and execute test plans, conduct requirements reviews, perform test verification and validation, analyze results and document results.
* Create test process documentation, specifications, and work instructions.
* Understand, support, and contribute to Molex TQM and Quality / Environmental Management Systems by following approved policies and procedures.
Who You Are (Basic Qualifications)
* Bachelor's degree in Mechanical Engineering or a related technical discipline.
* Experience in product testing and measurement.
* Working knowledge of standard mechanical test equipment.
* Proficiency with Microsoft Word, Excel, and PowerPoint.
* Strong verbal and written communication skills, demonstrating the ability to convey complex technical concepts clearly and concisely with global teams.
* Analytical ability to apply logical reasoning, test assumptions, observe results, and make informed corrections.
* Willing and able to travel up to 10%
What Will Put You Ahead
* Master's degree in Mechanical Engineering.
* Experience with Python.
* Experience with mechanical test and measurement equipment such as force measurement equipment and flex test equipment.
* Working knowledge of TDR modules, 4-port network analyzers, and bit error rate testers.
* Experience using relational databases with software such as Microsoft SQL or MySQL.
* RF/microwave circuit design and PCB layout with software such as Mentor Graphics PADS or Cadence Allegro.
* Exposure to advanced PCB fabrication methods...
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Type: Permanent Location: Lisle, US-IL
Salary / Rate: Not Specified
Posted: 2026-04-25 07:48:18
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Classification: Exempt
Job Summary:
The Assistant Production Manager is responsible for assisting the Production Manager in organizing and supervising work in the Production Department.
Performs other duties as required and reports to the Production Manager or Operations Manager.
About Us:
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with an ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay, benefits, and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Our full-time employees enjoy:
* 401K Plan with Company Match
* Medical, Dental, Vision, FSA/HSA
* Life Insurance, Disability Insurance
* Vacation, Sick Time, Holidays
* Choice of Global Cash Card or Direct Deposit
* Career Advancement
* Learning & Development Opportunities
* Inclusive and Diverse Team Environment
Benefits may vary for positions covered by a collective bargaining agreement.
Essential Functions:
* May hire and train new staff or assist management with this process.
* As requested by the Manager, conducts, or assists with performance evaluations.
* Assists the Manager with employment actions, including discipline and termination of employees by company policy.
* Monitors and recommends changes in work methods and/or equipment usage to improve labor utilization, production efficiency, and department expenses.
* Conducts new hire and ongoing training in all production departments.
* Consults with engineering, sales, and service management to ensure the smooth operation of the plant.
* Responsible for the execution of company production policies, procedures, and standards.
* Responsible for monitoring and ensuring that standards for production, quality, housekeeping, and safety are met.
* Responsible for adherence to department budgets, as well as hiring, discipline, and employee relations.
* Follow written and verbal instructions, attend meetings, and perform other tasks as directed by supervision.
Additional Functions:
* May work with and support other branch personnel as required by supervisor.
Qualifications:
* Organizational skills.
* Ability to lead, motivate, and develop staff.
* Recognize colors, sizes, and types of products.
...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2026-04-24 08:51:53
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Classification:
Non-Exempt
*
*Up to $15/Hr.
- Paid Weekly
*
* Benefits
*
*
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The Soil Counter/Sorter handles, counts, sorts and records incoming soiled textiles from the customer.
Identifies damaged or abused textiles.
Prepares and transfers textiles to other departments.
Performs other tasks as needed.
Our full-time employees enjoy:
401K Plan with Company Match
Medical, Dental, Vision, FSA/HSA
Life Insurance, Disability Insurance
Vacation, Sick Time, Holidays
Choice of Global Cash Card or Direct Deposit
Career Advancement
Learning & Development Opportunities
Inclusive and Diverse Team Environment
Essential Functions:
- Open bag of soiled textiles, then sort them by type, size and color.
- Count textiles manually or electronically, and transfer them into sorting systems.
- Identify damaged or abused textiles and record into sorting systems.
- Meet efficiency and safety standards for the position.
- Follow instructions as directed by supervision.
Additional Functions:
- Work in other production positions as needed.
Qualifications:
- Recognize colors and sizes, count accurately.
- Comprehend and follow direction.
Typical Physical Activity:
- Physical Demands consist of standing, walking, reaching overhead, pushing, pulling, grasping, lifting up to 50 lbs.
and stooping.
- Physical Requirements consist of being able to meet the physical demands for the entire shift.
Typical Environmental Conditions:
- Production areas of a typical industrial laundry facility, which includes variations in temperature, odors, humidity, lint and dust.
Soiled linens come from a variety of customers such as restaurants, hotels, medical facilities and shops.
Travel Requirements:
- none.
Education:
- none.
For a general description of benefits that are being offered for this position, please visit alsco.com/benefits.
Alsco is an Affirmative Action/Equal Employment Opportunity Employer.
Revised: 04/29/2022
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants ...
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Type: Permanent Location: Miami, US-FL
Salary / Rate: Not Specified
Posted: 2026-04-24 08:51:40
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Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world's most in demand and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life's essentials - and creates lasting value for its colleagues, customers, and other stakeholders.
Learn more about the company's Customized Polymer, Sustainable Fiber, Durable Metal, and Integrated Solutions at www.greif.com and follow Greif on Instagram and LinkedIn.
OUR VISION:
Being the customer service company in the world.
OUR PURPOSE:
Creating packaging solutions for life’s essentials.
Job Requisition #:
034054 General Labor (Evergreen) (Open)
Job Description:
ROLE OVERVIEW:
Under direct supervision, performs a variety of routine activities including, but not limited to preparing job sites, ensuring safety conditions, transporting materials, using power tools and other equipment, building temporary structures, and collaborating with other plant workers.
GREAT BENEFITS INCLUDE:
* Health, dental, vision insurance effective day one!
* Greif pays 75% of health premiums.
* Company paid life/AD&D insurance, STD/LTD insurance, EAP.
* Many other company paid benefits!
* Enjoy up to 80 hours of vacation to rest, recharge, and do what matters most.
* Greif is recognized with the 2025 Gallup Exceptional Workplace Award for our commitment to our colleagues.
Key Responsibilities
* Routinely clean and lubricate equipment, maintain a manufacturing area free from debris and dirt, ready or put away tools as assigned.
* Closely follows directions to operate machinery, hold or supply routine materials and tools, and load or unload items on machinery and assembly lines.
* Performs routine property care activities.
* Performs any non-technical routine tasks at the plant.
* Routine quality checks on finished products.
* Reports any issues to supervisor or higher-level colleague.
* Follow safety regulations.
* Performs other duties as assigned.
Education and Experience
* Typically possesses a high school diploma (or equivalent).
Knowledge and Skills
* Basic verbal and written communication skills.
* Ability to listen, understand, and follow directions.
* Ability to work in a variety of roles.
Required Rotating Shift Schedule
* 1st Shift: Work 7 days from 6:30 AM – 2:30 PM, followed by 4 days off.
* 2nd Shift: Work 7 days from 2:30 PM – 10:30 PM, followed by 1 day off.
* 3rd Shift: Work 7 days from 10:30 PM – 6:30 AM, followed by 2 days off.
* This cycle then repeats.
Wage
* Starting $23.26 per hour, after successful completion of 90 days pay rate is $26.71 per hour.
#LI-NG1
At Greif, we believe that our colleagues are the center of our success.
Our Total ...
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Type: Permanent Location: Milwaukee, US-WI
Salary / Rate: Not Specified
Posted: 2026-04-24 08:49:05
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Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world's most in demand and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life's essentials - and creates lasting value for its colleagues, customers, and other stakeholders.
Learn more about the company's Customized Polymer, Sustainable Fiber, Durable Metal, and Integrated Solutions at www.greif.com and follow Greif on Instagram and LinkedIn.
OUR VISION:
Being the customer service company in the world.
OUR PURPOSE:
Creating packaging solutions for life’s essentials.
Job Requisition #:
034052 1st Shift: Utility/General Labor Neenah Plant (Open)
Job Description:
ROLE OVERVIEW:
Employee will be responsible for assisting machine operators in producing products safely and efficiently, ensuring product quality and packaging requirements meet customer specification, running with minimal process issues, assist in achieving OEE goals, and helping to maintain the integrity of process equipment.
1st Shift
6:00am to 2:00pm Monday through Friday
Key Responsibilities
* Operate machinery in a safe and efficient manner
* Responsible for keeping production areas and other defined areas clean and organized
* Must be able to push/pull/lift up to 50lbs repetitively
* Must be able to use and read a tape measure and caliper
* Must be able to work at least 8+ hour work days
* Following all plant safety rules, wearing proper PPE at all times
* Attend Line Board Meetings
* Must be able to solve problems under pressure
* Continue to look for ways to reduce downtime
* Work overtime as needed
* Perform other duties as assigned
* Ensure all products meet the customer and product requirements.
* Ensure packaging of finished goods per customer specification.
* Accurately fill out production reports on a daily basis.
* Be able to read engineering sheets, and make suggestions for improvement.
* Fill in on other machines such as but not limited to one area.
Education and Experience
* Must have High School Diploma or GED Equivalent
Knowledge and Skills
* Must have analytical skills to solve problems
* Basic tape measure reading skills
* Customer focused; positive attitude
* Attention to detail and numbers oriented to ensure quality
* Well-organized and exercise sound judgment in decision making
* Ability to work independently with minimal supervision
* Ability to communicate to cross functional team effectively, both verbally and in writing
At Greif, your work has purpose, colleagues care about your well-being, and you have the opportunity to grow and thrive.
Service and leadership are the core of everything we do.
Our global presence provides us a ...
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Type: Permanent Location: Oshkosh, US-WI
Salary / Rate: Not Specified
Posted: 2026-04-24 08:48:55
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The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Reporting to the Director of Electron Beam Engineering, the E-beam Engineer will be responsible for growth, engineering projects, and support of break down maintenance globally. In support of the Sterigenics business unit’s strategic plan the E-beam Engineer will focus on the electron beam irradiation plants.
Routine support of approximately 8 plants will be required on an as needed basis.
This position provides a unique opportunity to directly execute, and project manage Capex growth or maintenance-type projects or support other assigned project managers in their remote coordination of activities.
With Total productive maintenance as a strategic priority, a strong interest and involvement with plant engineering maintenance initiatives and support will be key.
Development, tracking and communication of project and maintenance performance indicators will be essential with safety and quality being central tenets of all efforts. A solid engineering education with electrical and mechanical experience will be fundamental requirements. Experience and general knowledge of control system architecture, functionality and operations is considered desirable.
The E-beam Engineer will be expected to autonomously execute on responsibilities with course directions set by the Director of Engineering.
The E-beam Engineer will liaise routinely with Operations, Maintenance, Quality, EHS, OpEx, Purchasing, Legal and Finance as required throughout the project life cycle to ensure stakeholder alignment.
Active travel to facilities internally will be necessary.
Must be willing to travel up to 50%.
Duties and Responsibilities
Expand Capacity to Support Growth
* Support, develop, coordinate, report and manage scope, schedule, budget development on projects/initiatives at Electron beam plants.
+ Utilize structured reporting and project management methodologies.
+ Advise on address/resolve technical challenges.
+ Provide routine communication to Senior Executive Team on KPIs
Maximize Investment Returns
* Total Productive Maintenance (TPM)
+ Assist Operatio...
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Type: Permanent Location: Haw River, US-NC
Salary / Rate: Not Specified
Posted: 2026-04-24 08:40:55
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The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Principal Technical Consultant
The Principal Consultant is an expert and lead in technical consults.
They will oversee, write, and research client projects to safeguard global health.
This will also include the review of all necessary written information (e.g., Product Adoptions, Test Plans, FDA Responses) from peers and any additional research or other considerations.
Location:
Salt Lake City, Utah, USA
Essential Duties for Principal Consultant:
Consulting
* Review and write assessments and other related documents (i.e.
Product Adoptions, Test Plans, FDA Responses)
* In preparation for assessment deliverable, work cross-functionally with other departments to guide where expertise is necessary
* Communicate with the client to obtain additional information for projects or related testing
* Perform literature research
* Build and implement process improvements
* Know and follow the Nelson Service Standard and Code of Ethics
* Act as a mentor to develop peer experts and as an expert to lead the scientific direction of at Nelson Labs
* Understanding of global capabilities and competencies (including networking with other facilities)
* Known as an expert in specific areas of consultation
* Expected to present at Nelson Labs seminars and other areas of presentation
* Possesses a greater diversity in the areas of consultation
Regulatory Compliance
* Know and follow applicable regulatory requirements (GMP, GLP, ISO, AAMI, ASTM, etc.).
* Participate in Committee meetings as appropriate including US ISO Delegate as appropriate.
* Present at Nelson and other seminars as appropriate
* Know and follow company policies and procedures.
* Complete required training on time.
* Leads the industry as an expert.
Professionalism
* Attend work regularly and reliably.
* Adhere to all policies and procedures.
* Perform other duties as assigned
Competencies of this position
* Excellent project management skills
* Excellent verbal and written communication skills
* Excellent technical writing skills an...
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Type: Permanent Location: Taylorsville, US-UT
Salary / Rate: Not Specified
Posted: 2026-04-24 08:40:54
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The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Associate Validation Engineer
Reporting to the Quality Assurance (QA) Manager or equivalent manager/supervisor, Associate Validation Engineer will provide management with information and data on all key aspects of each customer’s validation project, which is used by both the plant and the customer to determine the course of routine processing.
Must effectively interface with Sales, Operations, Corporate EO Technology, Laboratory (if any), EHS, Quality, Engineering and other Sterigenics’ facilities, as well as customers and regulatory personnel.
Duties and Responsibilities
* Plans, organizes, and coordinates customer validation activities at the facility.
* Writes validation protocols and final reports supplied by the facility.
* Reviews and approves customer or consultant supplied validation or test protocols for execution within the limitation of the facility’s equipment and Sterigenics operating procedures and compliance with current regulatory standards.
* Responsible for the execution of validation protocols and technically driven customer projects, which include but are not limited to the following:
+ Scheduling the project runs, ancillary resources, lab testing and sample handling.
+ Cycle programming and preparation of necessary process documents and safety assessments.
+ Microbiological samples
+ Data collection and analysis of temperature and humidity probe data
+ Assuring proper handling, storage and shipping of bioburden, LALs, biological indicators, or residual samples to the appropriate laboratory
* Assures that all validation calibration activities are performed according to Sterigenics procedures and traceable to NIST.
* Provides support to Maintenance or Engineering in the performance of IQ/OQ/PQ activities of new or existing facility equipment.
* Responsible for annual equipment re-commissioning (sterilization and laboratory).
* Update validation status in the relevant systems.
* May be required to assist with corrective action and validation process improvement activit...
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Type: Permanent Location: Salt Lake City, US-UT
Salary / Rate: Not Specified
Posted: 2026-04-24 08:40:54
-
The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Plant Engineer
Reporting to the Director of Engineering, the Plant Engineer is a “hands on” position that supports local maintenance and operations and will lead small to medium growth and maintenance engineering projects for assigned facilities of Sterigenics in support of the business unit’s strategic plan.
Responsibilities will be on the East Coast Ethylene Oxide (EO) sterilization plants. Routine support of approximately 3 EO plants will be required on an as needed basis.
This position provides a unique opportunity to directly execute, and project manage Capex growth or maintenance-type projects or support other assigned project managers in their remote coordination of activities.
With Total productive maintenance as a strategic priority, a strong interest and involvement with plant maintenance initiatives and projects will be key.
A solid engineering education with mechanical and electrical experience will be fundamental requirements.
Familiarity with Building and NFPA codes is considered highly beneficial as is a business insight. Experience and general knowledge of control system architecture, functionality and operations is considered desirable. The Plant Engineer will be expected to autonomously execute on responsibilities with course directions set by the Director of Engineering.
The Plant Engineer will liaise routinely with Operations, Maintenance, Quality, EHS, OpEx, Purchasing, Legal and Finance as required.
Active travel to facilities within the geographical area will be necessary.
Important: Must recognize and be willing to travel up to 25% within geographical region.
Duties and Responsibilities
* Identify and correct any unsafe work conditions or practices.
* Project design, installation, and commissioning.
* Execute delivery for small complexity projects (maintenance, continuous improvement, or regionally coordinated projects)
* Ensure safety and compliance requirements and expectations are met for facility, equipment, and emission control systems.
* Evaluate and monitor status of critical facility equipment performance (e.g., emissio...
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Type: Permanent Location: Oak Brook, US-IL
Salary / Rate: Not Specified
Posted: 2026-04-24 08:40:51
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The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Sr.
Process Engineer
The Process Engineer analyzes process data to identify inefficiencies in the sterilization process and implements appropriate improvements.
The Engineer also leads development and documentation of new sterilization processes.
In collaboration with EHSS, the Engineer field verifies, updates, revises, and modifies process and plant drawings and diagrams to comply with Sterigenics PSM program.
This position will primarily support the EO technology.
DUTIES AND RESPONSIBILITIES:
* Perform all responsibilities in a safe manner.
Follow Sterigenics Health and Safety procedures and requirements
* Lead cross-functional process improvement initiatives, applying advanced statistical analysis and simulation tools to optimize performance
* Designs robust processes that meet quality, safety, and regulatory standards, with scalability across multiple sites or systems
* Support Project Managers with development of new process designs, process flows, and Piping and Instrumentation diagrams (P&ID) for large scale projects
* Conduct root cause investigations for complex process failures utilizing recognized RCA tools (e.g.
5-Why, Fishbone diagrams, etc.) and implement sustainable corrective actions
* Develop and optimize SOPs and process-related technical standards
* Support General Facility Enhancement designs and commissioning; perform field inspections and verifications as needed
* Update and maintain repository for facility installed equipment summary files
* Work in close collaboration with Environmental, Health, and Safety to ensure process safety information is compliant with Process Safety Management (PSM) procedures and requirements
* Lead a committee to develop and document best practices for sterilization processes
* Coordinate drawing updates resulting from field-verified redlines
* Review, verify, and update existing controls drawings to the latest vendor revisions
Equipment activities:
* Perform site visits to assist in troubleshooting process related deviations
* Analyze process data and utilize RCA tools to i...
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Type: Permanent Location: Oak Brook, US-IL
Salary / Rate: Not Specified
Posted: 2026-04-24 08:40:49
-
The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Expert Biocompatibility Consultant
The Expert Biocompatibility Consultant is a senior scientific contributor responsible for leading biocompatibility assessments and biological evaluations for medical device products in global, highly regulated environments.
This role operates at the assessment, strategy, and advisory level and is ideal for professionals who have already built depth in biocompatibility and now influence decisions through technical judgment, documentation, and communication.
You will partner closely with clients, internal technical teams, and leadership to develop defensible, regulator-ready assessments that safeguard patient health and support product approval worldwide.
Key Responsibilities
Biocompatibility & Scientific Leadership
* Lead development and authorship of biocompatibility assessments, biological evaluations, and risk assessments
* Perform and synthesize literature-based evaluations of materials, compounds, and device use
* Apply ISO 10993 principles and FDA expectations to support regulatory submissions and decision-making
* Provide peer review and technical guidance on complex or high-risk projects
* Author opinion memos and other patient safety–focused technical documentation
Client & Consulting Engagement
* Serve as a subject-matter expert during client discussions and project initiation
* Clearly communicate scientific and regulatory rationale to technical teams, clients, and senior stakeholders
* Collaborate cross-functionally to deliver integrated, high-quality project outcomes
* Support proposal development and scope review in partnership with project leadership
Thought Leadership & Standards
* Participate in international standards development
* Deliver technical presentations at conferences, seminars, webinars, and industry forums
* Contribute to continuous improvement of internal processes, templates, and best practices
Required Qualifications (Must-Have)
* Significant experience in biocompatibility assessment within a medical device environment
* Demonstrated expertise authoring a...
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Type: Permanent Location: Taylorsville, US-UT
Salary / Rate: Not Specified
Posted: 2026-04-24 08:40:49
-
The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Controls Engineer
Reporting to the Controls Engineering Manager, the Controls Engineer is responsible for supporting industrial control system endeavors throughout the Sterigenics network.
The Controls Engineer can work independently and collaboratively, assist with developing the scope, schedule, and budget associated with system programming and controls projects, as well as effectively execute and complete projects safely, within budget, and on schedule.
This role is fully remote and requires domestic and periodic international travel per business needs (approximately 40-60% travel).
Collaboration with external and internal customers (Sales, Operations, EHS), requiring the ability to have diplomacy to work through differing priorities, project scope, and schedules.
Ability to manage contractors in the capacity of supplying parts and services.
A strong engineering background, with electrical competency is required for the successful candidate.
Duties and Responsibilities
* Evaluate and implement technology improvements/advances inclusive of controls.
* Work with project management and other engineering disciplines, managing the deployment of control systems for new processes and upgrades for existing systems as required.
* Assist facility Maintenance Supervisors, General Managers and Regional Maintenance Managers in troubleshooting facilities problems related to control systems and help develop solutions using data driven decision making.
* Improve facility reliability by managing and monitoring system controls and managing system lifecycles.
* Work with Contractors, Project Managers, Technology Engineers, and Regional Maintenance Managers in a team approach to improve facility operations and systems.
* Manage installation projects, to include budgeting, tracking, and providing purchase orders, and execute testing as needed to support objectives.
* Understand, read, create, and debug code programming logic into PLCs, SCADA and HMI.
* Develop, review, approve, and execute IQ and OQ documentation as related to software validation practice...
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Type: Permanent Location: Oak Brook, US-IL
Salary / Rate: Not Specified
Posted: 2026-04-24 08:40:48
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Job Description
Under the supervision of the Mechanical Engineering (ME) Manager for Student Success and ME Associate Department Chair for Graduate Studies, the Graduate Academic Advisor position will provide academic advising for graduate students majoring in mechanical engineering programs and assist with related academic administrative matters.
Essential Duties and Responsibilities
• Advise prospective and current graduate students in the Department of Mechanical Engineering about academic program requirements and provide timely guidance on choosing and completing a program or concentration.
• Assist students with formulating program-specific study plans, verifying progress towards degree requirements and discuss course options based on focus area.
• Maintain records of student advising sessions and interactions including appointments held and appropriate notes/records on academic progress to ensure advising continuity.
• Maintain accurate database of graduate student records.
• Enter, evaluate, and audit student data in Workday Student to ensure students are progressing through their academic programs in a timely manner and to certify completion of course and non-course requirements for graduation.
• Work with students on academic probation to identify and address factors affecting their academic performance.
• Organize new and current graduate student information sessions, new graduate student orientation events, along with social and professional events for Mechanical Engineering graduate students.
• Advise current graduate students on on-campus course, web, international and non-course opportunities to enhance professional skills, competencies and career readiness.
• Serve as primary point of contact to the department chair, associate department chair, faculty advisors, department staff and current students in mechanical engineering regarding graduate school policies and procedures from admission to graduation.
• Collect and analyze student census data from registrar’s office and Workday for evaluation and assessment of the graduate program, including creating dashboards of key student metrics.
• Manage responses to inquiries from prospective students about mechanical engineering graduate programs and Stevens, in general.
• Coordinate communications to graduate students regarding departmental, school, and Institute policies and procedures as it relates to program requirements and the graduation process and coordinate mandatory advisement sessions.
• Interface with ISSS for consultation to ensure that international students maintain full-time student status at the Institute in order to comply with rules and regulations of the US Immigration and Naturalization Service.
• Attend Mechanical Engineering Graduate Committee meetings and follow through with the action items.
Qualifications
• Required Education: Bachelor’s degree
• Required Experience: Minimum of 2 years of experience in aca...
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Type: Permanent Location: Hoboken, US-NJ
Salary / Rate: Not Specified
Posted: 2026-04-24 08:40:21
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Technical Consultant, Poultry
The Technical Consultant’s (TC) primary role is to provide technical support to customers and building technical competencies of Elanco sales and its channel partners.
The TC is responsible for the successful development and implementation of technical platforms and programs, making sure that those are aligned to the company’s objectives.
Furthermore, the TC is in charge in the execution/monitoring company-sponsored clinical trials.
Your Responsibilities:
a) Technical Support: Capability Build up and Deployment
* Provides technical support to customers thru farm visits, virtual consultations, necropsy support and training programs.
* Develop and implement current and relevant technical programs and materials to internal sales and channel partners as aligned with the building capabilities program and channel partner development.
* Responsible for the review and/or approval of promotional materials (e.g., technical presentations).
* Continuously updates the team on the current diseases, management tools and competitors’ products in the market.
* Contribute actively to differentiate Elanco technical capabilities and products from competitors.
* Conduct field trial: proper design of trial protocols, monitoring of implementation to results interpretation and conclusion, as required by and aligned with regulatory, sales and marketing
* Actively participate and contribute to local and international technical fora and events highlighting Elanco’s commitment to the industry.
* Adhere to company policies and procedures when interacting and promoting products and customers, to protect the Elanco brand and business.
* Implementation of EKS initiatives, regional and global projects collaboration.
b) Customer Centricity:
* Analyzes needs and requirements by interacting with customers and sales teams, determining appropriate needs and aspirations to match and develop technical capabilities and support.
* Support Sales teams thru meeting customers and gathering feedback on a first-hand basis.
* Develop a deep un...
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Type: Permanent Location: Mandaluyong, PH-00
Salary / Rate: 1160000
Posted: 2026-04-24 08:31:41
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Global Quality Auditor Lead
As a Global Quality Auditor Lead, you will be part of the Elanco Global Quality Compliance and Auditing (EGQCA) organization, supporting Elanco Animal Health through internal and external audits focused on aseptic pharmaceutical manufacturing.
In this role, you’ll be responsible for ensuring that operations across commercial supply chains, including contract manufacturers and internal sites, comply with global regulatory expectations, Elanco’s quality standards, and industry best practices, particularly in sterile/aseptic environments.
Your Responsibilities:
* Conduct end-to-end audits of aseptic pharmaceutical manufacturing operations, including internal sites and external partners, to evaluate compliance with current Good Manufacturing Practices (cGMP), Elanco quality standards, and applicable global regulations
* Develop detailed audit plans, lead pre-audit risk assessments, and produce comprehensive audit reports that highlight findings, assess risk level, and provide clear recommendations to stakeholders at all levels
* Mentor and train new auditors, supporting their qualification process and contributing to the continuous improvement of audit processes and audit team capabilities
* Lead risk assessments across commercial supply chains—integrating audit findings and operational risks to influence compliance strategy, quality oversight, and mitigation plans
* Support business continuity and product supply by auditing critical aseptic suppliers, participating in mock inspections, and conducting due diligence evaluations for new partnerships and acquisitions
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree (or equivalent work experience) in physical or biological sciences, engineering, or other technical area, or combination of education and experience
* Required Experience: Minimum of 5 years of auditing experience in aseptic pharmaceutical manufacturing, with a deep understanding of sterile product processes and global compliance requirements
* Top 2 skills: Ability to identify and com...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: 150000
Posted: 2026-04-24 08:31:39
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your role:
The Shift Leader ensures that all aspects of front-line operations are completed to schedule, and in compliance with EHS and Quality requirements.
In addition, the Shift Leader will identify opportunities for, and implement actions to achieve, continuous improvement in their area of responsibility.
They will also act as a coach to the operations team and provide support to ensure the operators can carry out their role effectively.
The Shift Leader will have a full understanding of the high-level manufacturing processes including applicable EHS and Quality aspects.
Your Responsibilities:
* Lead shift operations to ensure safe, compliant, and on-time production in line with EHS and Quality standards
* Monitor daily activities (logs, BPRs, training, work orders) to ensure accuracy and compliance
* Plan and coordinate shift activities, including maintenance, changeovers, and resource allocation
* Collaborate with cross-functional teams (Maintenance, QA, QCL) to support production schedules
* Drive continuous improvement through problem-solving, Gemba walks, and team engagement
* Lead troubleshooting of plant issues and escalate when required
* Ensure effective communication across shifts and with site leadership
* Manage deviations, incidents, and support initial investigations
* Coach, develop, and performance-manage the operations team, including training and development plans
* Support workforce planning, including shift cover, absence management, and contractor oversight
What You Need to Succeed (minimum qualifications):
* Minimum of 5 GCSE’s or equivalent
* Experience/knowledge of production areas
* Effective time management and co-ordination skills
* Previous demonstration of desired behaviours
Additional Information:
* Rotating shift: 4 consecutive working days followed by 6 days off
* Banked hours: Extra hours may be accumulated and used for additional time off or schedule adjustments
* Location: Speke, UK
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely t...
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Type: Permanent Location: Liverpool, GB-LIV
Salary / Rate: 45000
Posted: 2026-04-24 08:29:36
-
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
* Aufbereitung virushaltiger Vorstufen, Formulierung und aseptische Abfüllung von Impfstoffen
* Gefriertrocknung von Impfstoffen und Verbördeln von Impfstoffflaschen
* Vorbereiten und Bedienen von Produktionsanlagen im Produktionsbereich Abfüllung
* Aseptisches Arbeiten im Reinraum
* Durchführung von Reinigungs-, Vor- und Nachbereitungsarbeiten
* GMP-gerechte Dokumentation
* Einsatz zur Aufrechterhaltung der Produktion im Schicht-/Wechseldienst, auch nach Dienstschluss und am Wochenende
* Umgang mit MS-Office-Programmen
* Buchung von Prozessaufträgen im SAP-System
* Flexibler Einsatz auch in anderen Unternehmens-/Produktionsbereichen u.a.
in der bakteriellen und viralen Produktion, Central Service, L&P, Hygiene Monitoring, wenn dies aus betrieblichen Gründen notwendig ist
Fachliche Qualifikationen und persönliche Voraussetzungen:
* Abgeschlossene Ausbildung im pharmazeutisch-, biologisch- oder chemisch-technischen Bereich oder vergleichbare Qualifikation
* Produktionserfahrung im GMP Umfeld wünschenswert
* Sehr hohes Hygienebewusstsein
* Arbeiten im Team
* Bereitschaft zum flexiblen Arbeitseinsatz sowie Einsatzbereitschaft an Wochenenden
* Gute Deutsch- und Englischkenntnisse in Wort und Schrift
* Strukturierte und flexible Arbeitsweise, Zeit- und Selbstorganisation
Was wir anbieten:
* Interessantes und abwechslungsreiches Arbeitsumfeld in einem modernen und wachsenden globalen Unternehmen der Pharmaindustrie
* Raum für Initiative und Flexibilität
* Spannende Entwicklungsmöglichkeiten
* Firmenfitnessprogramm
* Verpflegungsgeld
* Vorteile für Unternehmen
* Teamevents
* Bis zu 30 Tage Urlaub
* Sonderurlaubstage (Hochzeit, Arbeitsjubiläen etc.)
* Attraktive Vergütung gemäß Betriebstarifvertrag inklusive Weihnachts- und Urlaubsgeld
* 38 Stunden/Woche
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veter...
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Type: Permanent Location: Cuxhaven, DE-NI
Salary / Rate: Not Specified
Posted: 2026-04-24 08:29:28
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Your Job
The jobsite located in Mont Belvieu, TX is hiring a Field Safety Coordinator.
Our Team
Optimized Process Designs, LLC (OPD) is an engineering/construction company headquartered in Katy, TX with an expertise in the natural gas, natural gas liquids, and petrochemical industries.
OPD is part of the larger Koch Engineered Solutions (KES) organization which provides a variety of capabilities across many industries.
Originally incorporated in 1980, OPD has developed a strong reputation for honesty, integrity, and ability to successfully execute projects.
OPD has a key advantage in being able to supply construction services as well as engineering/procurement.
This enables clients to have a ''one stop shop'' for the overall project, providing increased efficiency and avoiding potential interface problems.
OPD's industry experience, flexibility, and personal attention have made us a preferred partner to our customers and our tight knit, highly productive, team atmosphere makes OPD a great place to work.
What You Will Do
Some core responsibilities for a Field Safety Coordinator include:
• Conduct walk-through inspections of field job sites to identify and eliminate hazardous conditions and unsafe acts performed by employees.
• Organizes and prepares the delivery of safety meetings and training.
• Ensure employees are following safe work procedures as specified in OPD's New Hire Orientation, tool-box meetings, and OSHA required training.
• Anticipate, identify and evaluate hazardous safety conditions and environmental risks.
• Make recommendations for correcting unsafe conditions and actions.
• Responds to and conducts accident investigations and injury/accident case management.
• Apply the Company's Substance Abuse Testing policy to maintain compliance, including but not limited to drug screen collections and records management while adhering to HIPAA standards.
• Responsible for partnering with HR & site leaders on employee issues and/or concerns (e.g., on-boarding questions, code of conduct, etc.)
• Responsible for conducting mandatory new hire safety orientation training as needed.
• Administer the safe permitting process (Lock Out Tag Out, etc.).
Some physical demands of being a Field Safety Coordinator include:
• Capable of working in outdoor weather and environmental conditions including extreme heat and humidity, extreme cold, and high elevations.
• Lifting and carrying awkward objects up to 60 lbs.
• Standing for extended periods of time up to 12 hours per day.
Working through breaks as necessary.
• Moving the entire body.
Considerable use of arms, legs, climbing, lifting, balancing, walking, stooping, crawling, twisting, reaching, and bending on a regular basis.
• Use hands to handle, control, and feel objects and/or tools.
We expect all field employees to:
• Actively participate in a strong safety culture.
• Recognize safety hazards and risks.
• Participate in onsite safety ...
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Type: Permanent Location: Baytown, US-TX
Salary / Rate: Not Specified
Posted: 2026-04-24 08:18:46
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Your Job
We're seeking an experienced Systems Integration Engineer (SIE) to lead hardware validation and interoperability efforts for Active Copper Cable (ACC) and Active Electrical Cable (AEC) assemblies used in high-speed networking systems.
This role is focused on systems containing embedded PCAs with DSPs, retimers, equalizers, power management, and control interfaces, integrated directly within the cable module.
In this role, you will serve as a technical authority for PCA-based cable module bring-up, debug, and system-level interoperability, working across hardware, firmware, signal integrity, and networking teams.
You will drive root-cause investigations, evaluate design robustness, and help define validation best practices for electronically complex interconnects.
This position is ideal for an experienced engineer who thrives at the intersection of PCA hardware, embedded electronics, and networking system interoperability.
Our Team
Molex's Copper Solutions Business Unit (CSBU) is a global team that works together to deliver exceptional products to worldwide telecommunication and data center customers.
CSBU is one of the most highly technically advanced business units within Molex.
Our engineering teams design cutting edge solutions for high-speed, high-density products that maximize speed, signal integrity, and efficiency.
Why Join Us
You will be getting in on the ground floor of a booming sector inside Molex as part of a team building the infrastructure and processes that enable world-class interoperability testing.
This role offers deep technical ownership, visibility into product readiness, and the opportunity to influence how embedded cable electronics interoperate at scale.
You will work hands-on with advanced interconnect technology and play a key role in ensuring robust, repeatable interoperability across lab and customer environments.
What You Will Do
ACC / AEC Hardware & PCA Validation
* Lead bring-up and validation of ACC/AEC cable assemblies with embedded PCAs
* Validate DSP-, retimer-, and equalizer-based designs against electrical, functional, and interoperability requirements
* Assess PCA behavior within the cable module including power, resets, control interfaces, and signal integrity impacts
* Validate system-level interactions between cable PCAs and switches, NICs, and host platforms
Interop Debug & Root-Cause Analysis
* Lead investigation of interoperability issues involving active cable PCAs
* Perform deep lab debug across PBCA hardware, embedded firmware, signal integrity, and link training layers
* Drive root-cause analysis for link failures, marginal performance, power-up issues, and qualification escapes
Design Review & Validation Strategy
* Review PBCA schematics, layouts, and design tradeoffs impacting signal integrity, power, thermals, and reliability
* Evaluate how PBCA design decisions affect interoperability across vendor platforms
* Define valida...
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Type: Permanent Location: Conway, US-AR
Salary / Rate: Not Specified
Posted: 2026-04-24 08:18:40
