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Essential Functions -
* Operate cranes and hoists effectively and safely, transporting castings to and from machines using an air hoist and/or cranes.
* Remove excess metal from castings using pneumatic hand grinding or stand grinding equipment.
* Inspect the castings to ensure quality.
* Perform preventive maintenance inspections on the tools and production equipment daily to ensure safe operating condition.
* Communicate with other grinders, forklift drivers and machinists to increase the flow of product to the Finish Department.
* Complete production requirements on a daily and weekly basis.
* Become trained in Lock-out/Tag-out and other applicable safety programs if required.
* Lift and move parts and objects weighing up to 100 lbs.; frequently moves and positions parts and objects weighing up to 100 lbs.
in difficult work positions.
* Use hand tools such as hammers, pry-bars, wrenches etc.
safety and properly.
* Stack parts properly and safely on floor or skids as directed.
* Inspect hooks, slings, chains, cranes and hoists to make sure they are in safe operating condition and lifting devices are not used in excess of weight limits.
* Inspect grinders and other tools to ensure they are in safe operating condition.
* Perform and assist with general housekeeping and cleaning of area, department and plant on a daily basis.
* Keep work area clean, organized and in safe condition.
* Other activities as may be assigned in order to maintain production requirements of the department or plant.
Work assignments will be made at the discretion of management.
Qualifications –
* Must be able to read, communicate and understand instructions in the English language
* Must be physically able to stand for long periods of time
* Must actively engage in safe working practices
* Must be able to tolerate hot working conditions and a loud environment
* Must be comfortable working in small spaces
* Previous experience utilizing basic hand tools, hoists, and tape measure preferred
* Ability to lift up to 50 lbs
* Must be at least 18 years old to apply
* Previous foundry experience a plus
#DNMRO
Behaviors
Preferred
* Team Player: Works well as a member of a group
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
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Type: Permanent Location: Lincoln, US-NE
Salary / Rate: Not Specified
Posted: 2025-07-25 08:37:45
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Your Job
Georgia-Pacific Dixie® Consumer Products Operation is seeking qualified professionals for the Environmental Health & Safety Leader role at our Bowling Green, Kentucky facility.
This role is crucial in building a partnership with front-line leadership and collaborating with business partners to develop and mentor the production team relating to EH&S.
In this role, the EH&S Leader establishes and optimizes systems and processes to effectively address the facility EHS risk profile.
The EH&S Leader role consists of an estimate of 80% Safety and 20% Environmental.
Our culture is defined by the Principle Based Management™ philosophy which guides everyday decision making and provides employees with opportunities to contribute and personally benefit from the value they create.
Our Team
The Bowling Green Plant is part of the Dixie® brand plates and bowls paper products manufacturing operations.
We are proud to safely manufacture quality products that have a competitive advantage and solid growth within the marketplace.
The EH&S Leader will work closely with management to promote a culture of safety and environmental stewardship, supported by the Dixie divisional EHS leadership.
What You Will Do
* Embrace influential leadership to support the organization while advancing our Principle-Based Management (PBM) culture.
* Partner with site leadership to influence team members to achieve our Path to Zero Safety Strategy in line with Koch's Safety Vision.
* Partners with site leadership to ensure facility risk profile is reduced through development and implementation of key objectives, strategies targets and measures.
* Responsible for all systems and processes that manage EHS risk at the facility (Compliance standards, compliance standard ownership model, Risk Management System, Hazard Identification and Risks Assessment (HIRA), Safety Improvement Planning, Safety Training, etc.).
* Effectively communicates facility safety vision, strategies, and performance to internal and external stakeholders.
* Foster an environment where employees exercise their decision rights regarding EH&S ensuring the vision is developed and integrated.
* Facilitate EH&S ownership by the line organization through integration of the EH&S Management System.
* Drive continuous improvement using tools and activities, including self-assessments and audit processes; incident/near miss investigations; metrics and targets (leading and lagging indicators); and periodic reviews of performance, culture, and talent.
* Coach, mentor and develop members of the safety team(s).
* Own and effectively manage the injury management and workers compensation process.
* Design and deliver EHS training programs for employees at all levels.
Who You Are (Basic Qualifications)
* Experience in Environmental, Health, and Safety in a manufacturing or industrial setting.
* Experience using and applying effective safety management...
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Type: Permanent Location: Bowling Green, US-KY
Salary / Rate: Not Specified
Posted: 2025-07-25 08:36:42
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Your Job
Molex is seeking a Process Engineer to join our team at our Temp-Flex facility in South Grafton, MA to s upport the Design Engineers, Manufacturing Engineers and manager on all new projects through process development and optimization, troubleshooting, and quality issues.
The Process Engineer will participate in the development of new and existing equipment that meets needs for next generation cable products and technology.
Our Team
This role will be working in our Process Engineering team reporting to the Process Engineering Manager.
The Process team is part of our RF and Microwave Solutions team reporting into the Copper Solutions Business Unit.
What You Will Do
* Lead process development efforts to support product development for next generation cable products and technology.
* Set-up and run new processes for products in development, aid in running initial prototypes, and provide feedback to Design Engineering team for iterative improvement.
* Utilize knowledge of product design, raw materials and equipment capabilities to develop optimal process settings for products in development as well as improvements for products in volume production.
* Provide input to machine development engineering team for new equipment.
* Organize documentation for processes to be in accordance with standards.
* Work with manufacturing engineers to improve work flow and machinery on production lines.
* Provide input to technical personnel to design machine control systems for future and existing equipment.
* Aid appropriate technical personnel in programming PLCs and motor drives to control all types of production machines.
Who You Are (Basic Qualifications)
* Bachelor's degree in an Engineering Field
* Two (2) years or more of process OR manufacturing engineer experience
* Wire and cable manufacturing experience
* Knowledge of control systems/PLCs/control drives
What Will Put You Ahead
* Extrusion experience with small diameter cables and high temperature plastics.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company, Molex is a leading supplier of connectors and interconnect components, driving innovation in electronics and supporting industries from automotive to...
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Type: Permanent Location: South Grafton, US-MA
Salary / Rate: Not Specified
Posted: 2025-07-25 08:36:29
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*
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*Please Note: This position will be posted through Friday, July 25th, 2025
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Please Note: Excellent customer service skills are a must! Part-time positions are available.
Please tell us about your availability!
Our Retail Centers are open 9:00 a.m.
to 9:00 p.m.
Mondays through Saturdays and 9:00 a.m. to 7:00 p.m.
Sundays.
Pay: $16.15 Hr.
Your pay could increase based on the amount of textiles you can produce each hour.
This position is eligible for Daily Pay! Work today, get paid today! We’ve partnered with DailyPay, a voluntary benefit to offer employees access to their pay on their own schedule.
Part Time employees in our Retail and Sales/Operations Division are eligible for paid holidays, sick leave, jury duty and bereavement leave. All employees may also make pre-tax or post-tax (Roth) contributions to our retirement plan – must be 18 years of age to participate.
Goodwill of Colorado is a Public Service Loan Forgiveness Program (PSLF) eligible employer.
JOB SUMMARY:
The Associate I, Textiles Production will primarily work in a production environment sorting, hanging, pricing, and tagging donated textiles while following company quality standards and guidelines to determine which items will be placed on the sales floor to be sold.
The Associate may occasionally be in contact with customers and expected to be responsive in communication and provide excellent customer service.
ESSENTIAL FUNCTIONS:
* Sort donated textiles by season, color, and quality of product.
* Inspect textiles to ensure the product is in good saleable condition (buttons, zippers, etc.)
* Hang, size, and price, tag, and prepare textile items to be sold by loading them on Z-racks.
* Make decisions to price according to Goodwill standards of quality and value of the product which may include researching the item’s value on the internet or utilizing other company tools and standards.
* Provide excellent customer service to fellow staff and customers; answer product questions as needed.
* Follow all retail center policies and procedures.
* Follow all safety processes and procedures to help provide a safe working environment for employees and customers.
* Crosstrain as needed in other departments and areas when required.
* Maintains a clean and organized work area to provide a safe and efficient workflow for employees and customers.
* Your job duties may extend beyond the tasks listed and may include additional responsibilities as required.
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed below are representative of the knowledge, skill, and/or ability required.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education:
* A High school diploma or equivalent preferred.
Experience:
* One (1) year of retail experience...
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Type: Permanent Location: Fort Collins, US-CO
Salary / Rate: 16.15
Posted: 2025-07-25 08:36:23
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*
*Please Note: This position will be posted through Friday, July 25th, 2025
*
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*
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*
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Goodwill of Colorado is seeking candidates with production (for example retail, restaurant, hospitality, production or similar industries) as well as cash handling experience to become our Retail Generalist Associates.
Career growth opportunities are prevalent within Goodwill of Colorado.
Grow your experience while serving your community!
This position will be full-time and will require open availability (including evenings and weekends).
Our Retail Centers are open 9:00 a.m.
to 9:00 p.m.
Mondays through Saturdays and 9:00 a.m. to 7:00 p.m.
Sundays.
Pay: $17.15 Hr. This position is eligible for Daily Pay! Work today, get paid today! We’ve partnered with DailyPay, a voluntary benefit to offer employees access to their pay on their own schedule.
Full Time employees in our Retail, Sales/Operations, Commercial Contracts are eligible for Medical, Dental, Vision, Retirement, Long Term Disability, Short Term Disability, Life and Accidental Death and Dismemberment, Flexible Spending Accounts and several voluntary supplemental benefit offerings. In addition, these positions are eligible for paid time off in the form of vacation, sick, holiday, floating holiday, jury duty and bereavement leave. Goodwill of Colorado is a Public Service Loan Forgiveness Program (PSLF) eligible employer.
JOB SUMMARY:
The Associate II, Retail Generalist will have existing knowledge in retail products, merchandising, pricing, and quality inspection.
Acting as a back-up for all areas within the Retail Store, the Retail Generalist could be performing multiple tasks in different departments on any given day.
These tasks include but are not limited to: donation receiving, material handling, processing both hardline and softline goods, working the sales floor, and operating the cash registers.
The Retail Generalist will work both in a production environment as well as being active on the sales floor.
The Retail Generalist will have contact with customers and will need to provide excellent customer service displaying an “Attitude of Gratitude” in order to support the mission of the organization.
ESSENTIAL FUNCTIONS:
* Crosstrain in other departments/areas and act as back-up for other areas as required.
* Work closely with department supervisors to determine which areas are short-handed with staff or in meeting Retail Store goals.
* Accept donations from customers, to include loading/unloading of product ensuring that every item is handled with care to show respect to the donor and for the item.
* Sort and inspect donated items making decisions on quality and value of product, pricing it accordingly, and researching value as necessary.
* Uses and becomes certified on pallet jack, walkie stacker, forklift, hand dolly, or other equipment or tools to effectively move and store donated product.
* Ensure that the sales floor is well s...
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Type: Permanent Location: Fort Collins, US-CO
Salary / Rate: 17.15
Posted: 2025-07-25 08:36:22
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Kyfora Bio, the bioprocessing brand of Polysciences, advances cell and gene therapy innovation through specialized transfection reagents and excipients designed for viral vector and mRNA delivery systems.
Leveraging over six decades of chemical R&D and manufacturing experience, Kyfora offers scalable, cGMP-compliant solutions that support the entire development lifecycle—from bench to clinic—enabling next-generation therapies to reach patients efficiently and safely.
Kyfora Bio is an innovative, science-driven company specializing in next-generation transfection reagents and enabling technologies for gene and cell therapy research and development.
As a growing biotech organization, we are committed to supporting therapeutic breakthroughs through advanced delivery tools that simplify and accelerate upstream bioprocessing workflows.
We are seeking a Product Manager to lead strategic expansion of our product portfolio—including our novel transfection technologies—for research and therapeutic applications as well as commercial manufacturing.
This role is ideal for a scientifically grounded, market-savvy professional passionate about delivering high-impact solutions to the biopharma and biotech sectors.
Key Responsibilities
* Product Strategy & Portfolio Expansion
Identify unmet needs, evaluate technology trends, and analyze competitor offerings to drive product roadmap development.
Define and execute long-term strategies to enhance our transfection reagent portfolio and associated product lines.
* New Product Development & Commercialization
Guide new product initiatives from concept to market, including requirements gathering, value proposition development, pricing, and technical positioning.
Lead cross-functional launch execution and post-launch performance tracking.
* Market Intelligence & Voice of Customer (VOC)
Conduct market research and VOC initiatives to validate concepts, prioritize opportunities, and refine go-to-market strategy.
Stay abreast of trends in gene delivery, upstream bioprocessing, and emerging therapeutic applications.
* Lifecycle & Performance Management
Optimize existing product offerings through proactive performance monitoring, inventory planning, cost/margin analysis, and content updates.
Partner with operations, supply chain, and quality to ensure product excellence.
* Scientific Communication & Enablement
Develop technical content, marketing assets, application notes, and product web pages.
Support internal sales training, customer engagement, and distributor onboarding with compelling and scientifically accurate materials.
* Customer and Partner Engagement
Collaborate with key academic, biotech, and CDMO partners to support product evaluation and adoption.
Provide technical support and assist with the execution of targeted campaigns, webinars, and tradeshows.
Required Qualifications
* Bachelor’s degree in Molecular Biology, Bioc...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: 125000
Posted: 2025-07-25 08:36:10
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Polysciences technical operations and scientific laboratories offer custom synthesis, contract manufacturing and packaging, and laboratory products.
We are proud to offer a broad range of products and tailored solutions for the life sciences, bioprocessing, microparticles, medical device, specialty chemical and eChem industries.
We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA’s ChemStewards® Management System.
We believe the best scientific innovations are built through collaborations.
Polysciences is looking for a synthetic organic chemist to conduct research and process development of organic monomers, polymers, and small molecules in the R&D group.
The ideal candidate will work closely with the principal or senior R&D scientists to conduct experiments, reactions, and purifications to advance product and process development projects.
The position requires skill and knowledge in synthetic organic chemistry, and experience in polymer chemistry.
As an R&D Scientist, you will work closely with a dynamic team of researchers, engineers, and other professionals to contribute to the advancement of our specialty chemical products and solutions.
Essential Functions:
* Conduct synthesis and purification of organic small molecules, reactive monomers, and polymers leading to high purity compounds that meet required specifications
* Set up and carry out processes using organic chemistry glassware, reactors, and purification equipment.
* Identify improvements and options for current and planned synthesis and purification procedures and equipment based on observations, experience, literature, patents, and chemical database searches.
* Follow reaction progress and characterize materials using standard analytical methods and instruments.
* Deliver procedures and materials meeting timelines and specifications to advance projects on schedule
* Communicate results in reports and presentations
* Write well-organized chemistry portions of the process development reports and batch records suitable for validation and production.
* Maintain a safe, clean, and organized environment (5S) in the R&D synthesis laboratory.
* Provide information for analytical and QC teams to develop analytical methods and characterize products
* Work closely with cross-functional teams, including engineers, product managers, and quality control personnel, to drive existing projects forward and to assess the feasibility and scalability of new projects.
Qualifications
• BS or MS in Chemistry with an organic synthesis focus preferred with 2-3 years of relevant industrial experience.
• Current knowledge of synthetic organic reactions, mechanisms, polymerization methods, and purification techniques.
• Knowledge and hands-on experience of standard analytical equipment, techniques and data interpretation to determine the structure and properties of organic molecules and polymers (e.g.
NMR, LCMS, GCM...
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Type: Permanent Location: Warrington, US-PA
Salary / Rate: 100000
Posted: 2025-07-25 08:35:35
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At InterContinental London Park Lane, we are currently looking to for a Laundry Attendant to join the team.
Welcome to InterContinental London Park Lane
Located at one of the capital's most prestigious addresses, where the late Queen Elizabeth II once resided.
Our hotel redefines traditional luxury, offering a blend of modernity and flexible sophistication in the heart of Mayfair.
Inspired by its scenic views overlooking two Royal Parks, our establishment boasts elegant natural interiors and award-winning seasonal cuisine.
Our Laundry Attendants are:
* Passionate about delivering great service.
* Experienced in Hotel Cleaning, as a Room Attendant or Public Areas Attendant.
* Experienced with handling guests queries and concerns.
* Able to work a variety of shifts including nights
* Willing to learn new things and work as part of a wide hotel team.
We are committed to offer and provide our Laundry Attendants with a competitive salary and a large range of benefits:
* £32,843.20 annual salary (£15.79 per hour) plus service charge, paid overtime and great IHG perks!
* 28 days holiday each year, including bank holidays, this increases up to a maximum of 33 days (Pro Rated)
* Wagestream - a financial wellbeing app giving you the opportunity to save, track and withdraw your pay as you earn it.
* Free meals on duty
* Professional career development with our IHG Leadership programs plus access to our digital online learning platform and numerous other learning and development opportunities.
* We provide every employee company sick pay and life insurance.
* Amazing discounts for our hotels and restaurants around the world
* Discounts from over 15,000 stores – all the way from retail to cinema
* Most importantly, we’ll help you grow, and develop you as an individual and inspire incredible.
At InterContinental London Park Lane, our ambition is to define our unique culture.
* The kind of culture that inspires you to be all you can be.
* An invitation to tap into your unique personality to deliver and achieve incredible things.
* An expectation to play your part in empowering and inspiring others.
* An opportunity to learn, grow and push what’s possible.
* The promise of a personal and professional journey
* A place where everyone can belong and feel part of something bigger.
We are open 7 days a week 365 days a year and need people to work a range of shifts and days.
Please click ‘apply’ now!
You must meet the legal requirements to work in the UK.
At IHG Hotels & Resorts, we are proud to be an equal opportunity employer.
We firmly believe that all our colleagues deserve to be treated equally and have the same opportunities to develop and grow their skills within our business and provide equal employment opportunities to all applicants and colleagues without regard to an individual's, race, colour, ethnicity, national orig...
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Type: Permanent Location: London, GB-ENG
Salary / Rate: Not Specified
Posted: 2025-07-25 08:31:31
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Position Summary
This position will design tooling and equipment to be used in the manufacturing of composite parts, assemblies for aerospace manufacturing using Solid Works and other software systems.
Target Responsibilities
* Accept, embrace, and promote the following Core Values of Core Natural Resources: Safety, Sustainability & Continuous Improvement
* Provide complete tooling concepts from basic engineering surfaces and customer Statement of Work.
* Provide complete tool models and designs for manufacturing of a finish product.
* Be a well-rounded professional who thoroughly understands the manufacturing processes and end uses of our products.
* Be willing to assist wherever needed
* The ideal candidate will possess the skills above and be willing to work on off hours and weekends on occasions as workloads vary.
* Responsibilities:
* Create tool designs from customer supplied part models and specifications.
* Internally interface with Project Manager, Manufacturing, and Inspection.
* Import and analyze customer’s engineered surface and create needed tooling following the statement of work
* Create and release designs / models with a concurrent design build philosophy
* Generate and supply data / drawings for off-site fabrication
* Track, prioritize, and estimate progress on tasks
* Work seamlessly with all team members as well as other teams within the organization
Required Skills and Experience
* Proven knowledge and hands on experience with modeling software, specifically SolidWorks and NX is required
* Knowledge and experience of different types of tooling including, but not limited to assembly fixtures, vacuum trim fixtures, mechanical clamping trim fixtures, traditional composite and metal mold tools, high temperature mold tools, room temperature mold tools
* Ability to work from blueprints, 3D-model, and customer specifications to produce a completed design to release to manufacturing
* Ability to collaborate effectively with colleagues, communicate openly, and contribute to achieving shared goals
Required Skills and Experience
* A bachelor’s degree in engineering
* Working knowledge of SolidWorks NX or other modeling system
* Familiarity with standard composite molding and fixturing
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Type: Permanent Location: Triadelphia, US-WV
Salary / Rate: Not Specified
Posted: 2025-07-25 08:31:16
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program.
The Quality Tech has the responsibility for performing analytical procedures on raw materials, in-process samples and finished products as well as assisting with investigation and resolution of operational product issues.
Shift: Night Shift- 6:00PM to 6:00AM
Pay: $22.00 and up based on experience
ESSENTIAL DUTIES and RESPONSIBILITIES:
* Conduct and interpret lab tests.
* Package and prepare samples for shipment to third party testing locations.
* Respond to internal calls to answer technical product questions.
* Perform laboratory computations leading to accurate data reporting.
* Troubleshoot lab issues.
* Conduct routine maintenance on all lab equipment.
* Contact lab supply vendors.
* Assist inventory control process.
* Ensure all laboratory chemical MSDSs are reviewed and filed.
* Read and properly interpret documents such as lab results, GMP manuals, HACCP programs and procedure manuals.
* Solve practical problems and comfortably deal in high pressure situations.
* Possess the ability to interpret a variety of instructions furnished in written and oral forms.
* Complete routine clerical work such as filing, checking and entering required information into the computer system.
* Follow plant and laboratory GMPs to maintain a clean work area.
* Advise operations associates to assure GMPs are followed in the plant.
* Perform environmental and product testing and communicate results to the plant and corporate management groups as needed.
* Send timely “Out of Specification” (OOS) notices as needed to internal and appropriate corporate management
QUALIFICATIONS:
* Previous laboratory experience, preferably in a food grade manufacturing facility
* Strong knowledge of laboratory testing procedures and computer software applications
* Exceptional analytical and organizational skills
* Strong interpersonal and communication skills
Actus Nutrition is an equal opportunity employer.
We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected characteristic as defined by federal, state, or local laws.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
NONE
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Type: Permanent Location: Fond Du Lac, US-WI
Salary / Rate: Not Specified
Posted: 2025-07-25 08:31:15
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TEXT ‘GoodwillJobs’ to 314-665-1767 to apply
Apply at: www.esgw.org/jobs
The Production Associate performs duties according to the established Best Practices of ESGW. Meets daily production goals.
Duties will include processing donations; sorting and preparing merchandise for sale, replenishing stock and/or removing merchandise from the sales floor. Greets and assists guests and/or donors.
Assists with accepting donations at the donation door as needed and/or assigned.
Must be cross-trained and assist in all aspects of production, as directed.
* Ability to work with people having different abilities.
* Able to perform repetitive tasks independently.
* Knowledge of current trends helpful.
* Requires standing, stooping, bending, and carrying for entire shift (excluding break times).
* Requires the use of hands for simple grasping, pushing and pulling, and fine manipulation.
* Requires tolerance to extreme changes in temperature and humidity.
* Ability to move independently or with reasonable accommodation within the facility and community.
* Applicant must be physically and mentally able to perform all job requirements.
* All positions require the completion of a background check.
Acknowledging or having criminal convictions does not constitute an automatic bar to employment.
Easterseals-Goodwill offers a comprehensive & competitive benefits package including:
* Medical, Vision, Dental, and Voluntary Products
* Paid Time Off (PTO)
* 401(k) Retirement Plan + up to 4% contribution
* Tuition Assistance
* Flexible Spending + Health Savings Accounts
* 10% Discount on ESGW Services
* Employee Wellness Program
* 30% Discount at Goodwill Stores
Easterseals-Goodwill is a 501(c)(3) nonprofit organization and is a qualifying employer for the Public Service Loan Forgiveness (“PSLF”) program.
Under the PSLF, you may be eligible for student loan forgiveness on qualifying loans under specific terms. Contact your loan provider for more information.
Easterseals-Goodwill (ESGW) is an equal-opportunity employer and encourages all qualified applicants to apply.
We are committed to maintaining a recruitment process that is fair and accessible to everyone.
Our goal is to foster a workplace that values diverse perspectives and creates an environment where individuals from various backgrounds feel respected and supported.
We do not discriminate based on race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, genetics, or veteran status, in accordance with applicable laws.
If you need assistance or accommodation during the application process, please inform us, and we will do our best to provide appropriate support.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Yo...
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Type: Permanent Location: Sandy, US-UT
Salary / Rate: Not Specified
Posted: 2025-07-25 08:31:11
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Libbey is seeking a highly technical and visionary Electrical Controls Engineer IV to lead the design, development, and deployment of innovative automation systems.
This role requires deep expertise in Allen-Bradley Kinetix servo platforms, advanced motion control, and computer systems integration.
The ideal candidate is not only proficient in programming and commissioning servo-driven machines, but also understands the broader architecture—networking, industrial PC integration, SCADA, and data systems—that drive modern automation platforms.
RESPONSIBILITIES
* Design and implement complex automation systems featuring Allen-Bradley Kinetix servo motion (coordinated motion, camming, and registration systems).
* Develop modular, scalable control logic in Studio 5000 Logix Designer, using best practices with UDTs, AOIs, and structured code organization.
* Engineer and troubleshoot high-speed deterministic motion systems and synchronized multi-axis platforms.
* Integrate control systems with industrial PCs, edge devices, databases, and enterprise software.
* Configure and maintain EtherNet/IP networks, switches, and secure communication between PLCs, HMIs, and SCADA systems.
* Create and manage HMI/SCADA interfaces in FactoryTalk View and/or Ignition, including advanced data handling and alarm strategies.
* Work cross-functionally with software, IT, and operations teams to ensure seamless machine-to-system integration.
* Lead controls-related R&D initiatives, prototyping, and technology scouting.
* Mentor junior engineers and provide architectural input for long-term automation strategy.
* Maintain documentation including I/O lists, electrical schematics, system topologies, and support manuals.
REQUIREMENTS & QUALIFICATIONS
* Bachelor’s degree in Electrical Engineering, Computer Engineering, Mechatronics, or a related field is required
* 10+ years of hands-on experience in controls engineering
* Proven expertise in:
* Allen-Bradley Kinetix servo systems (5500/5700)and motion tuning
* Studio 5000 / Logix5000programming and project organization
* FactoryTalk View ME/SEHMI systems
* EtherNet/IP, CIP Motion, and device communication
Strong understanding of computer systems architecture including:
* Industrial networking (switch configuration, VLANs, NATs)
* Integration with Windows-based HMIs, OPC servers, and data logging systems
* Working knowledge of PC-based control, SQL databases, and virtualization
Competency in AutoCAD Electrical or equivalent for panel design and documentation
Deep familiarity with machine safety design, standards (e.g., ISO 13849, NFPA 79), and risk assessment
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Type: Permanent Location: Toledo, US-OH
Salary / Rate: Not Specified
Posted: 2025-07-25 08:29:16
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About the role
Join Amsted Automotive – Cold Form & Finishing as a Header Operator, where you’ll set up and operate advanced multi-operation machinery, perform precision inspections using optical and measurement tools, and work hands-on with developmental and prototype setups.
If you’re experienced in reading blueprints, adjusting machine controls, and ensuring tooling and formed parts meet exact specs, we want to hear from you.
Train on 1st shift and grow with us on 2nd – in a role that challenges your skills and supports your growth.
What you'll do
* Set up and operates machine that automatically performs multi-operations.
* Performs first piece inspection of part with optical inspection equipment, or equivalent measurement equipment.
* Adjust controls to synchronize machine actions for various operations on each customized job.
* Read and understand tool layouts and part progressions.
* Will perform developmental set-ups and prototyping on new parts.
* Confer with other workers about machine setups and operational specifications.
* Shall observe operations to detect machine malfunctions and to verify that machine setups conform to specifications.
* Measure and inspect formed parts to ensure conformance to product specifications.
* Read blueprints to determine specified tolerances and sequences of operations for machine setup.
* Position and move work pieces through a series of dies that compress and shape stock to form die impressions.
* Adjust wedges & brass settings to set pressures and depths of ram strokes and to synchronize machine operations.
* Repair, maintain, and/or replace tooling when worn, broken or out of print.
* Remove tooling from machines when production runs are finished.
* Use overhead crane, forklift, and hand truck to bring and remove supplies as needed.
* Use measuring instruments to ensure and record quality information.
* Will train on first shift and then move to 2nd shift after training has been completed.
What else you need to know
* Work may require extended periods of sitting, standing, lifting, bending, stooping and performing repetitive motion tasks
* Excellent manual dexterity, ability to lift and carry up to 80 pounds frequently
* Work is performed in a manufacturing environment with continuous exposure to noise
* Must be able to work necessary overtime if required
What’s In It For You
We create a supportive environment where employees thrive! With a range of benefits designed to enhance your health, well-being, and financial security, we’re here to support you every step of the way.
Join us and experience the exceptional perks that make Amsted Automotive a great place to work!
Health And Wellness
* Medical Insurance
* Dental and Vision Insurance
* Prescription Drug Benefits
* Wellness Reimbursement
* Telehealth
* Onsite health screenings
* Mental health r...
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Type: Permanent Location: munith, US-MI
Salary / Rate: Not Specified
Posted: 2025-07-25 08:28:32
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine.
Johnson & Johnson is hiring for an Associate Director, Lean Development to be located in either Springhouse, PA; Titusville, NJ; Raritan, NJ; Beerse, Belgium; High Wycombe, UK; Allschwil, Switzerland and may require up to 15 % domestic & international travel.
The Associate Director, Lean Clinical Development will be responsible for driving Strategy and Strategic Alignment within and across Global Development (GD) in order to lead the Effective Planning, Implementation, and Change Management for complex, key prioritized projects.
They will design and develop the strategy for a Continuous Improvement Culture and will work cross functionally to develop a Value Stream Roadmap using Lean strategies and concepts, translate this roadmap into tactical plan and measure the business benefit.
You will be responsible for:
* Lead and drive the improvement elements of key projects to deliver value to the organization and to ensure process and system elements are efficient and cost effective.
* Coach and mentor Green Belt candidate and others implementing improvement projects.
* Development of self and others through training and compliance requirements.
* Interact with multiple levels of management, influence/partner across business functions, and have responsibility for critical business deliverables.
* Address challenges with respect to applying Lean concepts to the clinical development environment and the change management inherent in this.
* Provide lean/six sigma expertise to project teams in Global Development, as well as lean process mapping and facilitation during project setup and execution.
Qualifications
Education:
* A minimum of a Bachelor’s degree or equivalent in Business, Engineering, Science or a related field is required.
Master’s Degree is preferred.
Required...
....Read more...
Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-07-25 08:28:12
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Mechelen, Antwerp, Belgium
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine.
Johnson & Johnson is hiring for an Associate Director, Lean Development to be located in either Springhouse, PA; Titusville, NJ; Raritan, NJ; Beerse, Belgium; High Wycombe, UK; Allschwil, Switzerland and may require up to 15 % domestic & international travel.
The Associate Director, Lean Clinical Development will be responsible for driving Strategy and Strategic Alignment within and across Global Development (GD) in order to lead the Effective Planning, Implementation, and Change Management for complex, key prioritized projects.
They will design and develop the strategy for a Continuous Improvement Culture and will work cross functionally to develop a Value Stream Roadmap using Lean strategies and concepts, translate this roadmap into tactical plan and measure the business benefit.
You will be responsible for:
* Lead and drive the improvement elements of key projects to deliver value to the organization and to ensure process and system elements are efficient and cost effective.
* Coach and mentor Green Belt candidate and others implementing improvement projects.
* Development of self and others through training and compliance requirements.
* Interact with multiple levels of management, influence/partner across business functions, and have responsibility for critical business deliverables.
* Address challenges with respect to applying Lean concepts to the clinical development environment and the change management inherent in this.
* Provide lean/six sigma expertise to project teams in Global Development, as well as lean process mapping and facilitation during project setup and execution.
Qualifications
Education:
* A minimum of a Bachelor’s degree or equivalent in Business, Engineering, Science or a related field is required.
Master’s Degree is preferred.
Required/Preferred Experien...
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Type: Permanent Location: Mechelen, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-07-25 08:28:12
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Allschwil, Basel-Country, Switzerland
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine.
Johnson & Johnson is hiring for an Associate Director, Lean Development to be located in either Springhouse, PA; Titusville, NJ; Raritan, NJ; Beerse, Belgium; High Wycombe, UK; Allschwil, Switzerland and may require up to 15 % domestic & international travel.
The Associate Director, Lean Clinical Development will be responsible for driving Strategy and Strategic Alignment within and across Global Development (GD) in order to lead the Effective Planning, Implementation, and Change Management for complex, key prioritized projects.
They will design and develop the strategy for a Continuous Improvement Culture and will work cross functionally to develop a Value Stream Roadmap using Lean strategies and concepts, translate this roadmap into tactical plan and measure the business benefit.
You will be responsible for:
* Lead and drive the improvement elements of key projects to deliver value to the organization and to ensure process and system elements are efficient and cost effective.
* Coach and mentor Green Belt candidate and others implementing improvement projects.
* Development of self and others through training and compliance requirements.
* Interact with multiple levels of management, influence/partner across business functions, and have responsibility for critical business deliverables.
* Address challenges with respect to applying Lean concepts to the clinical development environment and the change management inherent in this.
* Provide lean/six sigma expertise to project teams in Global Development, as well as lean process mapping and facilitation during project setup and execution.
Qualifications
Education:
* A minimum of a Bachelor’s degree or equivalent in Business, Engineering, Science or a related field is required.
Master’s Degree is preferred.
Required/Preferr...
....Read more...
Type: Permanent Location: Allschwil, CH-BL
Salary / Rate: Not Specified
Posted: 2025-07-25 08:28:11
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Manufacturing Pharmaceutical Process Operations
Job Category:
People Leader
All Job Posting Locations:
Hangzhou, Zhejiang, China
Job Description:
配料和灌装团队按照公司规定的流程，持续稳定高效的生产出符合cGMP/ISO，以及强生政策要求。 This position is responsible to supervising compounding and filling team to strict follow company established process, ensure the product are effectively manufactured, and continuously comply with cGMP/ISO and Johnson & Johnson policy requirement.
• 确保员工按照公司程序完成生产任务，并确保员工工作环境安全（包含提供适当的个人防护用品） This position is responsible for ensure operator complete production by stickily follow site established process and procedure, ensure safety of working environment (including provide proper PPE) • 及时向公司管理层汇报任何GMP以及EHS相关的偏差，未遂偏差 Rectifying or reporting on any deviation and near miss from GMP or EHS, • 持续改进生产流程、积极参与质量系统改进活动，持续减少生产过程废料支持公司商业目标的达成 Continuously focusing on production process improvement, actively support quality system improvement, continuous reduces waste from production process, to support of achieving business objectives.
• 关注员工个人发展，持续帮助员工达成其业绩目标 Focusing on employee development, provide coach and mentor to operators in support of achieving their goals
Main responsibilities:
1.
Produce the Quality Products a) Manages and directs the compounding and filling team to achieve production objectives, including site KPIs, Functional KPIs b) Be responsible for the product quality by ensuring the high standard manufacturing environment is maintained for the clean rooms, ensuring the products are manufactured complying with the approved procedures and regulatory requirements, continuing to develop the operator’s aseptic skills, keeping improving the existing filling and compounding process c) Continuously improve manufacturing process, and environment through proper use quality tools, SPC, CAPA, etc.
2.
Leadership a) Develop complete individual ownership of Quality by the Production workforce b) Develop operators’ skills in the aseptic, machines, GMP compliance and continuous pr...
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Type: Permanent Location: Hangzhou, CN-33
Salary / Rate: Not Specified
Posted: 2025-07-25 08:28:05
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Deliver
Job Sub Function:
Warehouse & Distribution
Job Category:
People Leader
All Job Posting Locations:
Grecia, Costa Rica
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Ortho Warehouse Team Lead to be in Grecia, Costa Rica.
Purpose:
Reporting to the Plan Logistics Manager, the Team Lead will lead the materials handling team to support DePuy Synthes Operations in receiving, storing, shipping, and repacking materials, while focusing on team leadership, training, development, and operational excellence.
This role is crucial for collaborating with Global PP&L Planning Teams to assess and consolidate direct materials supply demand, manage supply risks with external suppliers and business partners, and escalate significant issues to senior stakeholders to mitigate short- and medium-term supply challenges.
This role ensures the safe, complaint, and efficient storage, movement of Raw Materials, Work in Progress (WIP), and Finished Goods in accordance with Free Trade Zone (FTZ) regulatory requirements and Johnson & Johnson internal standards.
As we set up our new site, it will be crucial for the Warehouse Team Lead to work closely with our IT project teams as we set up our new ERP system.
This will involve testing and ensuring all necessary transactions are available for warehouse movements, along with training of new hires as they come on board.
This Leader will work closely with our in-house business excellence team to ensure all site standards are met in the warehouse
You will be responsible for:
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Work closely with a team of MRP planners and oversee warehouse personnel for both inbound and outbound duties.
* Oversee management of inbound and outbound docks for transportation from our 3PL external warehouse and our global transportation partners.
* Oversee third party integrators that will be in a shared space in the warehouse to ensure there is no disruption and sign off inbound inventory from these suppliers where r...
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Type: Permanent Location: Grecia, CR-A
Salary / Rate: Not Specified
Posted: 2025-07-25 08:27:57
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
US331 CA Irvine - 31 Technology Dr
Job Description:
Johnson and Johnson MedTech is recruiting for a NPD ENGINEER II located fully on site in Irvine, CA.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
The engineer will use their technical and leadership skills to advance the development and manufacturing of innovative products.
As an engaging leader and problem solver, he/she will be involved with the daily production work activities and proactively identify and solve technical, logistical, and people challenges.
DUTIES & RESPONSIBILITIES
* Identifies, designs and develops the necessary equipment related to new product development.
* Performs material tests.
* Studies the existing processes to implement improvements on new products.
* Responsible for preparing and managing specifications.
* Assists technicians and engineers about unusual problems.
Responsible for purchasing and designing equipment that meets safety and environment requirements.
* Performs activities of process/product validation.
RESPONSIBILITIES OF NPD ENGINEERS II
* Can supervise, coordinate and technically revise the work of a limited group of technicians.
Responsible for communicating business related issues or opportunities to next management level
* Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and
* Environmental practices and that all resources needed to do so are available and in good condition
* Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
* Performs other duties assigned as needed
QUALIFICATIONS:
* Bachelors Degree in Engineering (Mechanical, Bio, Electrical)
* Masters in Science is preferred.
* P...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-25 08:27:54
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Automation Engineering
Job Category:
People Leader
All Job Posting Locations:
Raynham, Massachusetts, United States of America
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
----------------
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
----------------
We are searching for the best talent for a Manufacturing Systems Lead to be in Raynham, MA.
The Manufacturing Systems Lead will report to the MAM Site Lead and will be responsible for the development and lifecycle management of Manufacturing Systems and data (Manufacturing Execution Systems (MES), DNC, OEE, Automation Network, OSI PI, Cybersecurity, etc) within Raynham & Bridgewater.
This role leads the local Manufacturing Systems site team, and partners with the Manufacturing Systems global standards team, IT/JJT, Operations, Tech Ops and Quality to define, implement, and sustain the site Manufacturing Systems and data roadmap, aligned to global strategy & standards.
Key Responsibilities
· Handles all aspects of supervising personnel, including hiring and terminations, and is accountable for conducting effective performance management and meaningful career development conversations.
· Encourage a diverse, equitable & inclusive environment where leadership and talent development is top priority.
Take ownership for talent acquisition, performance and development of self and others.
· Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives and ‘One Team’ culture in day-to-day interactions with teams.
· Responsible for managing operational aspects of their team & systems, (e.g.
goals, budget, workflow, performance, system uptime and compliance), ensuring key performance indicators are being met or exceeded, as well as ensuring achievement of team goals within expected standards.
· Work with various partners to understand customer problems, business processes and value to build the sites manufacturing system’s and data roadmap & investment plan along with...
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Type: Permanent Location: Raynham, US-MA
Salary / Rate: Not Specified
Posted: 2025-07-25 08:27:50
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
People Leader
All Job Posting Locations:
Danvers, Massachusetts, United States of America
Job Description:
Employer: Abiomed, Inc.
Job Title: Manager, Supplier Engineering
Job Code: A011.8774
Job Location: Danvers, MA
Job Type: Full-Time
Job Duties: Lead the Supplier Engineering Department on supply chain engineering projects to meet strategic objectives.
Work cross-functionally with Manufacturing Engineering, Quality, Planning & Procurement, Logistic, Lifecycle Engineering and Product Development to facilitate joint supplier projects and programs.
Facilitate continuous improvement/Kaizen projects at suppliers and in-house, to drive quality increases, lead time, capacity gains, and cost reduction.
Drive second source program to mitigate business risk.
Manage “Quality at Source’’ programs to fully enable Kanban implementation and acceptance of good parts, including process capability and MSA data analysis at the supplier.
Serve as technical lead for supplier qualification and first article inspection.
Participate in supplier evaluation program.
Provide supplier/component risks and mitigation plans for each new product entry.
Lead incoming inspection Material Review Board (MRB) and issue resolution.
Work closely with process engineering to ensure thorough and robust design, development, and implementation of manufacturing processes.
Provide guidance and technical consultation to other engineers and product-development teams on requirements, specifications, design and verification, and validation with respect to supplier related topics.
Drive part obsolescence replacement and qualification.
Manage department staff and budget to meet business and corporate needs.
Participate in continuous improvement initiatives (Six Sigma, Lean Manufacturing) and process optimizations.
Identify and resolve both technical and personnel issues.
Up to 25% travel required (domestic & international).
Requirements: Employer will accept a Master's degree in Mechanical Engineering, Industrial Engineering or related field and 2 years of experience in the job offered or in a Manager, Supplier Engineering-related occupation.
This job posting is anticipated to close on 7/29/2025.
Johnson & Johnson is an Equal Opportunity Employer.
All qualified applica...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-07-25 08:27:45
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine.
Johnson & Johnson is hiring for an Associate Director, Lean Development to be located in either Springhouse, PA; Titusville, NJ; Raritan, NJ; Beerse, Belgium; High Wycombe, UK; Allschwil, Switzerland and may require up to 15 % domestic & international travel.
The Associate Director, Lean Clinical Development will be responsible for driving Strategy and Strategic Alignment within and across Global Development (GD) in order to lead the Effective Planning, Implementation, and Change Management for complex, key prioritized projects.
They will design and develop the strategy for a Continuous Improvement Culture and will work cross functionally to develop a Value Stream Roadmap using Lean strategies and concepts, translate this roadmap into tactical plan and measure the business benefit.
You will be responsible for:
* Lead and drive the improvement elements of key projects to deliver value to the organization and to ensure process and system elements are efficient and cost effective.
* Coach and mentor Green Belt candidate and others implementing improvement projects.
* Development of self and others through training and compliance requirements.
* Interact with multiple levels of management, influence/partner across business functions, and have responsibility for critical business deliverables.
* Address challenges with respect to applying Lean concepts to the clinical development environment and the change management inherent in this.
* Provide lean/six sigma expertise to project teams in Global Development, as well as lean process mapping and facilitation during project setup and execution.
Qualifications
Education:
* A minimum of a Bachelor’s degree or equivalent in ...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-25 08:27:24
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Affairs
Job Category:
Scientific/Technology
All Job Posting Locations:
Toronto, Ontario, Canada
Job Description:
We are searching for the best talent for our Associate Director, Medical Affairs, Lung Cancer position, located in Toronto, Ontario, Canada.
ABOUT ONCOLOGY
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
The Associate Director, Medical Affairs, Lung Cancer is responsible for providing Medical and scientific leadership to a cross-functional team.
This role is responsible and accountable for providing leadership as well as high level, evidenced-based, clinical and scientific expertise to internal and external partners, support cross-functional teams identifying barriers and opportunities and implementing medical affairs tactics and initiatives.
The successful candidate will lead Evidence Generation Processes in collaboration with the therapeutic area team and in direct communication with the global organization.
This person will provide leadership and support for evidence generation activities including local Phase IV clinical studies and Investigator Initiated Studies.
The Medical Science Director will also work closely with external sites to ensure flawless integration of the new assets into the health care system.
YOU WILL BE RESPONSIBLE TO:
- Lead the development and execution of the medical strategy for lung cancer aligned to the brand strategy
- Serve as the internal medical authority on lung cancer, providing disease area knowledge across the organization
- Contribute to the development of TA plans, including drug launches, lifecycle management and indication expansions
- Build and maintain strong relationships with external partners including; key opinion leaders (KOLs), medical societies and academic and community institutions
- ...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-07-25 08:26:46
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Surgeons (Commission)
Job Category:
Professional
All Job Posting Locations:
Boston, Massachusetts, United States of America, Danvers, Massachusetts, United States of America, Manchester, New Hampshire, United States, Portland, Maine, United States, Portsmouth, New Hampshire, United States
Job Description:
We are searching for the best talent for an Associate Surgical Account Manager or Surgical Account Manager to be in Boston North or Boston West, Massachusetts, United States.
This is a field-based role available in Boston North/ West.
While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
Purpose: We are growing both our focus and device line-up in order to support Cardiac Surgeons and Heart Failure Cardiologists across the US.
With our continued success, we are looking to expand our commercial team.
You will work closely with our cardiology sales and clinical team who will be responsible for driving growth across the designated territory.
Through our Impella® product portfolio you will enable physicians and staff to recover hearts and save patients’ lives.
Job Responsibilities:
* Gain distribution and utilization of the Impella 5.5 (left sided treatment)
* Gain distribution and utilization of the Impella RP (right sided treatment)
* Manage EXCEL sites and clinicals on new Surgery, Heart Failure, ECMO technologies
* Work collaboratively within the area to achieve quarter over quarter growth
* Drive excitement and vision of heart recovery solutions with existing devices and future technologies
* Call point(s): Cardiac Surgeons, Heart Failure Cardiologists, “Heart Team” (to include Interventional Cardiologists, Intensivists, & Perfusionists)
* Staff major conferences: HFSA, AHA, STS, AATS, and ISHLT
* Staff local heart failure symposiums
* Build surgical vertical in established Impella programs – Full product portfolio
Qualifications
* Bachelor’s degree required
* A minimum of 10+ years experience of cardiac surgery and/ or combined cardiology medical device sales required for the Surgical Account Manager level
Or
* A minimum of 5+ years experience of cardiac surgery and/ or combined cardiology medical device clinical or sales required for the Associate Account Manager level
...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-07-25 08:26:30
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Your Job
Georgia-Pacific's Consumer Manufacturing Group is hiring a Reliability Engineer to support our Consumer Products operations at the Pennington Mill.
In this on-site role, you will collaborate with operations, maintenance teams, and equipment manufacturers to develop and implement strategies that enhance equipment reliability across diverse manufacturing processes.
By aligning with our Principle-Based Management® philosophy, you will drive continuous improvement in safety, performance, and operational efficiency while creating value for the business.
This role is integral to fostering a culture of innovation, accountability, and long-term success at the mill.
Our Team
Georgia-Pacific's Naheola Mill in Pennington, Alabama, employs over 900 people to produce key consumer products, including Angel Soft® bath tissue, Sparkle® paper towels, and bleached paperboard for Dixie® cups and plates.
As the largest employer in the community, the mill actively supports outreach, workforce development, and education initiatives.
Located in a region known for excellent hunting, fishing, and outdoor recreation near the Tombigbee River, the area offers a mild climate, low cost of living, and easy access to Gulf Coast beaches, making it an attractive place to live and work.
What You Will Do
* Participate and support in all areas to achieve Environmental, Health & Safety excellence.
Possesses a passion for identifying and mitigating critical hazards.
* Root Cause Analysis Champion: Leads department Root Cause Analysis to the latent root cause of complex and/or repetitive failures and put in place executable corrective actions, tracking to completion.
* The Reliability Engineer develops and supports asset strategy execution for Power / Recovery / Recaust assets and reports to the Utilities Manager.
* Validates and builds as necessary asset strategies (OBC, PMs, Lubrication, Outage planning, etc) and systems based on RCAs.
Works closely with equipment owners, remote monitoring teams as well as local maintenance and reliability teams.
* Analyze operational KPIs to identify gaps and areas of potential improvement.
Utilize work processes to effectively improve equipment and process reliability.
* Transfer technical knowledge to operators and supervisors and promote continuing development of a reliability culture.
* Supports Boiler and Turbine Outage Planning and Execution.
* Provide technical support on both capital and non-capital projects.
* Work both individually with little supervision and together with a team to achieve improved reliability results.
Who You Are (Basic Qualifications)
* Two-year degree in Engineering or other technical field, or equivalent experience in manufacturing or military.
* Four (4) or more years of experience working within a continuous manufacturing / industrial environment with an operation, maintenance, reliability focus, or equivalent military environment.
What W...
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Type: Permanent Location: Pennington, US-AL
Salary / Rate: Not Specified
Posted: 2025-07-24 09:43:25
