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Join PACS: Elevate Healthcare with Us!
PACS is elevating healthcare by revolutionizing our approach to leadership and quality care.
Guided by our core values of love, excellence, trust, accountability, mutual respect, and commitment , we strive to foster a culture of compassionate care within our teams and the communities we serve.
As we grow rapidly, exciting opportunities await you to engage in impactful projects and contribute valuable insights to stakeholders nationwide.
If you're ready to make a difference and embrace our mission of creating real change, we invite you to join us at PACS.
Together, let's shape the future of healthcare!
Join Our Team and Thrive!
At PACS, we believe our employees are our greatest asset.
That's why we offer an exceptional benefits package designed to enhance your well-being and support your lifestyle.
Our Comprehensive Benefits Include
* Health Coverage: Enjoy medical, dental, and vision plans to keep you and your family healthy.
* PTO and Vacation: Benefit from generous paid time off and holidays to relax and recharge.
* Financial Wellness: Take advantage of Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA) to manage your healthcare expenses effectively.
* Retirement Planning: Secure your future with our 401(k) plan, complete with company contributions to help you build your retirement savings.
* Support When You Need It: Our Employee Assistance Plan (EAP) provides confidential support for personal and professional challenges.
Join us at PACS and take advantage of a workplace that truly values you!
Position Focus: This RN Delegator role will primarily support communities located in Oregon and Washington.
Location Preference: Candidates who reside in Oregon or Washington are strongly preferred.
Licensure Requirement: Must already be licensed in Oregon and Washington
General Purpose
The Nurse Delegator plays a pivotal role in ensuring residents receive exceptional care by expertly delegating nursing tasks, providing comprehensive staff training, and meticulously overseeing medication management services.
This position also assists in coordinating and completing resident assessments to ensure all individualized service plans are accurate and up-to-date.
ESSENTIAL DUTIES AND RESPONSIBILITIES
* Delegates Nursing Tasks: Delegates nursing tasks in accordance with applicable state nursing laws and practice acts, maintaining consistent communication with residents, their families, and their healthcare practitioners.
* Provides Staff Training: Develops and delivers training to staff on health-related services, including but not limited to personal care and medication administration best practices.
* Conducts Resident Assessments & Planning: Assesses the health, functional, and psychosocial status of residents.
Actively participates in the development of individualized service plans, assisting in the comprehensive management of care and services to ma...
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Type: Permanent Location: Farmington, US-UT
Salary / Rate: Not Specified
Posted: 2025-07-13 08:26:32
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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 Senior Corporate Quality Assurance Manager – Animal Nutrition has the responsibility for implementing and maintaining the Quality Assurance and Regulatory Program at Actus Nutrition Animal facilities.
This includes managing the quality aspects quality audits for ACTUS facilities and ACTUS vendors.
Establishing Quality Assurance specifications for raw materials and finished products and ensuring that these specifications are met; liaise with plant quality personnel on analytical methods and product out of specification issues.
The ideal candidate would be based out of our Corporate Office in Eden Prairie, MN and be willing to travel 50-75% of the time to our Animal Nutrition facilities in Wisconsin and Illinois.
ESSENTIAL DUTIES and RESPONSIBILITIES:
* Implement and monitor the company’s Quality Assurance and Regulatory Program at Actus Nutrition Animal facilities according to established policies and procedures.
* Establish quality assurance specifications for finished products and ingredients and ensure that these specifications are met and adhered to.
* Serve as a contributing member of Animal Feed organizations such as AAFCO to influence and understand changes in the industry.
* With the Purchasing Department, establish quality specifications for incoming raw materials, monitoring these raw materials to ensure that specifications are met.
* Assist with international and domestic registrations for animal feed products.
* Liaise with plant quality personnel on analytical methods assuring consistency across ACTUS facilities and toll manufacturers.
* Liaise with Product Information Manager to organize and update all history files and standard books finished products, including formulation, tags/labels, product standard and product change requests.
* Remain current on matters relating to production methods, formulations, analytical techniques and federal regulations as they relate to the Company’s products.
Make recommendations for improvement as necessary.
* Work with the animal nutrition facilities to investigate, document and respond to retail and B2B customer complaints with effective corrective and preventive actions.
* Assist other corporate quality function personnel with enterprise projects and initiatives as needed.
* Expert on State and Federal regulations around Animal Feed and labeling compliance.
* Develop and assist in training quality assurance and production personnel for ACTUS employees.
* Develop quality...
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Type: Permanent Location: Eden Prairie, US-MN
Salary / Rate: Not Specified
Posted: 2025-07-13 08:22:46
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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
031469 Utility Quality Control Inspector 1st Shift (Open)
Job Description:
Key Responsibilities
* Conducts visual and measurement inspections on incoming and in-process materials.
Confirms quality and specifications, communicates required adjustments, and rejects and returns unacceptable materials as necessary.
* Reads blueprints, plans, and specifications to understand the requirements of products and services.
* Measures product dimensions, examines functionality, and compares the final product to the specifications.
* Approves finished products by confirming specifications and conducting required tests.
Returns products for re-work if needed and completes documentation to confirm re-work.
* Documents and updates inspection results by completing reports and logs.
* Ensures measurement equipment is operating correctly by adhering to all operating instructions and performing preventive maintenance and repairs.
* Looks for opportunities to adjust and improve production processes and procedures.
* Informs supervisor when quality issues and concerns arise.
* Assists the supervisor, as needed, with various audits and compliance projects.
* Performs other duties as assigned.
Education and Experience
* Typically requires basic knowledge of job procedures and tools obtained through work experience and may require vocational or technical education.
Knowledge and Skills
* Possesses working knowledge of and ability to use multiple types of measuring equipment (e.g., scales, measuring tapes, micrometers, calipers, etc.)
* Demonstrates good written and oral communication skills.
* Demonstrates good interpersonal skills.
* Possesses strong analytical and problem-solving skills.
* Ability to analyze and present findings in a clear, concise, and logical manner.
* Possesses good organization, prioritization, and time management skills.
* Ability to meet critical deadlines and work in a fast-paced environment.
Compensation Range:
The pay range for this position is $17.31 - $25.96.
Typically, a competitive wage for new hires will fall between $19.13 to $19.13.
Offers for this position may vary based on market data and other factors such as job-related knowledge, skills, experience, and geographic location.
If the competitive wage is equal in both fields, the starting rate is the same for all applicants that apply for this role.
The starting rate is not representative of future compensation increases.
The position may also be eligible for a short-term incentive.
Benefits Statement:
Greif offers a comprehensive benefits package, including medical, dental, paid time off, and other competitive benefits which are available for eligible colleagues effective day one.
Protect Yourself From Sca...
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Type: Permanent Location: Homerville, US-GA
Salary / Rate: Not Specified
Posted: 2025-07-13 08:20:07
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Global Compliance Specialist
Location: Houston, Texas (Onsite, 5 days a week)
Position Summary:
The Global Compliance Specialist will report directly to the BII Director of Risk and Compliance.
This key role in the Risk Management and Compliance department focuses on ensuring compliance with regulations (both for legal and trade compliance), completing organizational filings and questionnaires, and supporting compliance research and policy writing.
The position is vital for maintaining operational efficiency while adhering to global laws and regulations.
Essential Job Functions and Responsibilities:
Global Compliance:
* Coordinate import and export activities, including audits, record-keeping, and ensuring compliance with U.S.
Customs Regulations, Export Administration Regulations, Foreign Asset Control Regulations, and Anti-boycott Regulations.
* Assign, document, and maintain Harmonized Tariff Codes (HTSUS) and Export Classification Numbers (ECCN) for all products.
* Conduct interviews and compile information for compliance with anti-corruption and other laws and regulations pertinent to the organization’s business activities.
* Develop, implement, and improve internal processes and written work instructions to maintain compliance with regulations.
* Provide training to internal users and gatekeepers on import/export requirements.
* Serve as the primary liaison with Shared Services, customs brokers, and freight forwarders for import/export documentation, licensing, and transaction screenings.
* Stay updated on regulatory changes and update internal policies as needed.
* Coordinate the valuation of imported merchandise, ensuring proper reporting of payments and customs valuation requirements.
* Work with IT to ensure system compatibility with trade compliance requirements.
Patent Administration:
* Maintain a database of patents and trademarks and their respective locations.
* Coordinate communications with intellectual property counsel and advisors.
* Log and track intellectual property registration activity as required.
Compliance Regulations & Research:
* Conduct legal and policy research, interpreting legislation and compliance standards.
* Investigate regulatory requirements, jurisdictional regulations, and government agency guidelines.
* Provide consultation on compliance matters.
* Develop and maintain a global research network.
* Prepare research findings and assist with action planning.
Compliance Policy Writing:
* Develop and draft compliance policies and procedures to support regulatory requirements.
* Assist with the distribution and implementation of compliance policies as directed by the RM&C department.
RM&C Department Support:
* Provide research or project support as assigned by the RM&C Manager.
Position Requirements:
* Highly organized, detail-oriented, and able to manage multiple competing priorities.
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-07-12 08:56:39
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? À propos de CTI Santé
CTI Santé est une entreprise innovante spécialisée dans le développement et la mise en œuvre de solutions technologiques au service des professionnels de santé.
Basée à Hossegor, elle accompagne ses clients sur tout le territoire avec une approche humaine, sécurisée et performante de la donnée médicale.
La société a rejoint le Groupe HARRIS Computer en avril 2025, renforçant ainsi son positionnement et son rayonnement à l’échelle internationale.
? Vos missions
Rattaché(e) au directeur du développement, vous interviendrez sur trois grands axes :
? 1.
Gestion du parc matériel interne
* Suivi des postes en collaboration avec l'équipe Harris (ordinateurs, téléphones, accessoires)
* Accompagnement des utilisateurs internes
?️ 2.
Infrastructure et sécurité interne
* Supervision et maintenance des serveurs physiques et virtuels
* Gestion des comptes et authentification centralisée (Keycloak)
* Mise à jour des outils internes (Docker, Debian, Windows)
* Suivi des sauvegardes, journaux et sécurité
? 3.
Environnements clients
* Installation, maintenance et suppression de la solution CTI
* Communication avec les équipes techniques clients
* Mise en place des connexions aux sources de données clients
* Gestion des accès distants, licences, certificats de sécurité
?️ Environnement technique
* Jira, Jenkins, Docker, ElasticSearch (Kibana, Fleet)
* Infomaniak (DNS, e-mails, newsletters)
* Windows / Windows Server (clients), Debian / Windows (interne)
* Bitwarden, Keycloak, RabbitMQ
? Profil recherché
* Formation Bac+2/+3 en informatique ou équivalent
* Expérience d'1 à 3 ans souhaitée en gestion d’infrastructure et support technique
* Autonomie, rigueur et bonne communication
* Sensibilité à la sécurité
? Avantages proposés
* Mutuelle prise en charge à 100%
* Tickets restaurant
* Un cadeau offert pour votre anniversaire ?
* Prime vacances
* Télétravail partiel sur conditions
✅ Pourquoi rejoindre CTI Santé ?
* Une entreprise à taille humaine et en pleine croissance
* Une ambiance de travail conviviale à deux pas de l’océan
* Des valeurs fortes : engagement, innovation, proximité
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Type: Permanent Location: Paris, FR-75
Salary / Rate: Not Specified
Posted: 2025-07-12 08:34:41
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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.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
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: Quality Control Associate, Biochemistry
This role will be a laboratory-based position with the QC Biochemistry group responsible for a wide variety of biochemical assays.
This role will rely heavily on an ability to perform regular functions within a GMP environment and perform flawless lab work on high value projects.
Regular projects include release and stability testing, assay development, validation, training, technical writing, and regular use of specialized equipment/software.
Your Responsibilities
* Conducts a range of biochemical assays, encompassing both routine and non-routine testing, on various sample types including raw materials, in-process materials, finished goods, environmental monitoring samples, and stability samples.
This includes method development, execution, and troubleshooting.
* Prepares, reviews, and approves a variety of essential QC documentation, including test protocols, validation protocols, special outlines, reports, Certificates of Analysis (CoAs), out-of-specification/out-of-trend (OOS/OOT) investigation reports, and deviation reports.
* Ensures the QC laboratory operates in full compliance with current Good Manufacturing Practices (cGxP) guidelines, encompassing laboratory safety, performance standards, meticulous documentation practices, regular equipment maintenance, and adherence to environmental regulations.
* Generates, reviews, and approves analytical data to ensure accuracy, completeness, and regulatory compliance.
Investigates and documents any OOS/OOT results and deviations encountered during testing.
Validates new and revised testing methods and qualifies existing methodologies as needed.
* Serves as a subject matter expert (SME) and liaison between the QC department and other internal departments, external vendors, and contractors.
Provides training to other analysts on laboratory procedures and assays, and stays current with the latest analytical techniques and best practices through continuing education and software proficiency.
Participates in internal assessments and ...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 31.93
Posted: 2025-07-12 08:34:36
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Business Intelligence Solution Architect
Overview:
We seek a skilled Business Intelligence Solution Architect to join our Research & Development (R&D) department, reporting to the Development Manager of our BI and Database Administration (DBA) teams at Ingenious Med.
This role involves hands-on architecture, designing and implementing new features, and optimizing existing BI solutions.
Responsibilities include data modeling, developing data ingestion and integration strategies, implementing best practices, and evaluating new BI platforms.
The Technical Lead will collaborate closely with developers and DBAs within a small Agile SCRUM team, providing technical leadership and mentorship.
Key Responsibilities:
- Gain a thorough understanding of existing Ingenious Med solutions.
- Take ownership as a technical lead, guiding existing solutions toward target architectures.
- Participate in team design discussions to address new BI requirements.
- Deliver quality code to meet assigned requirements and user stories.
- Thoroughly test functional units of code before committing to source control.
- Assist with system integration, regression, and performance testing as needed.
- Identify opportunities for new tools to improve integration processes.
- Troubleshoot production issues and provide third-tier support when necessary.
- Engage in continuous learning to stay current with new technologies.
Key Competencies:
- Strong work ethic and commitment to quality results.
- Excellent analytical and problem-solving skills.
- Outstanding written and oral communication abilities.
- Ability to manage multiple projects simultaneously in an organized manner.
- Capacity to explain complex technical concepts in simple terms when needed.
- Adaptability to shifting priorities and effectiveness in a fast-paced environment.
- Team-oriented and highly collaborative.
- Provide technical leadership and mentorship to BI developers.
- Ensure security, scalability, and performance optimization of BI solutions.
Required Qualifications:
- Bachelor’s Degree in Computer Science or a related field.
- 7+ years of experience in BI, data engineering, or analytics roles.
- 5-7 years of experience with SQL Server and T-SQL.
- 3-5 years of experience with ETL data ingestion pipelines.
- 2-4 years of experience with Power BI.
- 2-4 years of experience with SSRS.
- 2-4 years of experience with SSIS.
Preferred Qualifications:
- Experience with source control systems.
- Proficiency with Visual Studio and Azure DevOps (ADO).
- Experience with Azure or other cloud platforms.
- Familiarity with MicroStrategy.
- Coding experience in object-oriented languages such as Java or C#.
- Scripting experience with PowerShell or Python.
- Knowledge of HIPAA and healthcare industry standards.
This position offers an opportunity to lead and innovate within our BI initiatives, contributing significantly to our organization's success.
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: 138000
Posted: 2025-07-12 08:34:35
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
People Leader
All Job Posting Locations:
Chicago, Illinois, United States, Des Moines, Iowa, United States, Madison, Wisconsin, United States of America, Milwaukee, Wisconsin, United States, Santa Clara, California, United States of America
Job Description:
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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Shockwave Medical, Johnson & Johnson is hiring for a Regional Sales Director in Iowa/Wisconsin.
The position is fully remote, and you must be located in the territory.
This position requires up to 50% if needed.
This position does not provide relocation.
Position Overview
The Regional Sales Director will build and develop a regional sales team to deliver best in class performance for revenue and growth.
Responsible for building and managing the regional sales force and generating revenue and creating a successful strategy.
Work closely with Marketing, R&D and Area VP of Sales to identify market needs and execute on the sale/commercialization of new products.
Essential Job Functions
· Build, oversee and help drive a team of regional field sales representatives that maximize sales revenues, attain corporate objectives and exceed sales goals
· Forecast annual, quarterly, and monthly sales revenue streams accurately
· Identify, devel...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-12 08:16:34
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
People Leader
All Job Posting Locations:
Birmingham, Alabama, United States, Huntsville, Alabama, United States, Mobile, Alabama, United States, Pensacola, Florida, United States, Santa Clara, California, United States of America
Job Description:
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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Shockwave Medical, Johnson & Johnson is hiring for a Regional Sales Director in Alabama.
The position is fully remote, and you must be located in the territory.
This position requires up to 50% if needed.
This position does not provide relocation.
Position Overview
The Regional Sales Director will build and develop a regional sales team to deliver best in class performance for revenue and growth.
Responsible for building and managing the regional sales force and generating revenue and creating a successful strategy.
Work closely with Marketing, R&D and Area VP of Sales to identify market needs and execute on the sale/commercialization of new products.
Essential Job Functions
· Build, oversee and help drive a team of regional field sales representatives that maximize sales revenues, attain corporate objectives and exceed sales goals
· Forecast annual, quarterly, and monthly sales revenue streams accurately
· Identify, develop, and implement ...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-12 08:16:34
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science Portfolio Management
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
We are searching for the best talent for Associate Director, Global Data, Platforms & Partnerships - GCSO to be in Raritan, NJ.
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
Purpose:
The Associate Director, Global Data, Platforms & Partnerships is a hands-on, hybrid role of data steward & data feasibility analyst.
The Associate Director will have data stewardship responsibilities that include governance and support for several datasets, to ensure data quality, integrity, security and compliance.
He / She will partner with the technology team to maintain and update metadata repositories, ensuring that data definitions, data dictionaries, lineage, and relationships are well documented and accessible to users.
He / She will develop deep familiarity with the various real-world datasets such as Optum, IBM Merative MarketScan, Flatiron, etc, that exist within the global data lake.
The Associate Director will partner with data users across the company, to understand data requirements, evaluate real world data sources, and conduct analyses to determine the feasibility of the various data sets and recommend the best data source to answer a key business question or a key research question.
You will be responsible for:
Major responsibilities of this role are data stewardship, data intelligence and data feasibility.
This position entails a significant amount of hands-on analytics responsibility.
Key partnership will be with the internal global commercial data science and real-world evidence teams for key commercial and research activities.
In addition, there will be close partnership with J&J Technology (JJT) data sciences.
This position will report to the Senior Director, Global Data, Platforms & Partnerships.
This includes the following:
Data Feasibility
* Collaboration: Work with data users across the company to underst...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-12 08:16:17
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At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯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.â¯Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
* Business Improvements ä¸å¡æ¹è¿
* Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
* æ¯æè´¨éæ¹è¿æ´»å¨ï¼å¯¹äº§å/è¿ç¨è¿è¡æç»æ¹è¿åææ¬æ¹åã
* Review/analyze the effectiveness of PDCA, Six Sigma, Kaizen, Lean Techniques and/or other improvement tools and programs.
* è¯ä¼°ååæè´¨éå·¥å
·å项ç®çæææ§ï¼æ¯å¦PDCAï¼å
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* Conduct benchmarking to develop more effective methods for improving quality.
* éè¿æ æ管çå¼åæ´ææçè´¨é管çæ¹æ³æåè´¨éã
* Supports the development of quality engineering and quality compliance with the right skill sets for new product introductions, and product life cycle management.
* å¼ååéçè´¨é管çæ¹æ³åºç¨äºè´¨éå·¥ç¨åè´¨éåè§çåå±ï¼è¿ç¨å¨æ°äº§å导å
¥å产åçå½å¨æ管çã
* Compliance/Regulatory åè§ç®¡ç
* Review/analyze whether current product and processes (including actions or decisions conducted) are in compliance to standards such as the QSRs, ISO 13485, etc.
* è¯ä¼°ååæç°æ产ååå¶ç¨æ¯å¦åè§ï¼æ¯å¦QSRsï¼ISO13485çæ³è§è¦æ±
* Champions compliance to applicable Global Regulations and standards (e.g.
QSRs, ISO, EN and Medical Device Directive (MDD) requirements) including providing support during internal and external audits.
* æ¯æå·¥åçå
å¤é¨å®¡æ ¸ï¼éµå®éç¨çæ³è§åæ å(ä¾å¦QSRs, ISO, ENåMDD)è¦æ±ã
* Conduct periodic line audits to assess for production controls such as lot segregation. Review results of area audits to ensure that corrective and preventive actions are adequate.
* æ§è¡å¨æå®¡æ ¸è¯ä¼°ç产ç°åºæ¯å¦åè§ã审é
åºåå®¡æ ¸çç»æç¡®ä¿çº æ£åé¢é²æªæ½ææã
* New Product/Process Introduction æ°äº§å/å¶ç¨å¯¼å
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* Partners with R&D and other cross functional partners to ensure the proper application of design controls, risk management and the investigation/correction of design failures/challenges.
* åè°ç ååå
¶ä»çè·¨é¨é¨åä½ç¡®ä¿ç¸å
³é¢åè´¨é管çå¯æ§ãæ¯å¦è®¾è®¡ç®¡çï...
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-07-12 08:16:15
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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:
Product Development Testing
Job Category:
Business Enablement/Support
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a R&D Technician II to join our team located in Santa Clara, 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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
The R&D Technician II will use technical skills in the development of innovative products to treat peripheral, coronary, and heart valve diseases.
The R&D Technician II will participate on multiple cross-functional development teams that manage projects from concept through commercialization.
Perform and support a variety of development and engineering activities, which mainly focus on disposable devices prototyping, fabrication and testing.
Will work directly with other R&D technicians and R&D engineers to complete duties described below.
Essential Job Functions
* Generate functional prototype from design concepts and assist the transfer of R&D product build to manufacturing
* Support product builds through all R&D project phases, providing feedback on assembly process
* Assist other technicians, assemblers and engineers on procedures and product assembly
* Assist engineers with product and process development and improvement
* Perform testing to support design, process, and ...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-12 08:15:32
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Primary Functions:
* Develop a solid understanding of existing Ingenious Med solutions.
* Develop a sense of ownership as a developer moving existing solutions toward target architectures.
* Participate in team design discussions addressing new reporting requirements.
* Deliver quality code to satisfy all requirements/user stories as assigned.
* Fully test functional units of code before committing to source control.
* Assist with system integration, regression, and performance testing as needed.
* Identify opportunities for new tools to improve integration processes.
* Troubleshoot production issues and serve as third tier support when needed.
* Conduct regular self-guided study to stay current on new technologies.
Job Qualifications:
The qualifications we are looking for are mixture of work experience and educational background.
They are split into Minimum Qualifications (must have) and Additional Qualifications (nice to have) along with soft skills (competencies) needed for the role:
Minimum Qualifications:
* Bachelor’s Degree, preferably in Computer Science or related field or equivalent experience.
* 1+ years of experience working with SQL Server, TSQL
* 1+ years of experience working with SSRS
* 1+ years of experience working with SSIS
Additional Qualifications:
* Source Control Experience
* Visual Studio and ADO
* MicroStrategy
* Power BI
* Coding in OO language Java/C#
* Scripting PowerShell/Python
Soft Skills:
* Strong work ethic and dedication to quality results
* Outstanding analytical and problem-solving skills
* Excellent written and oral communication skills
* Ability to work several projects in parallel in an organized manner
* Ability to explain complex technical concepts in layman’s terms when needed
* Adaptable to shifting priorities and works effectively in a fast-paced environment
* Team oriented and very collaborative
The above statements are intended to describe the general nature and level of work being performed
by people assigned to this job.
It is not designed to be utilized as a comprehensive list of all duties,
responsibilities, and qualifications required of employees assigned to this job.
Working Environment:
This job operates in a professional office environment or remote home office location.
This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Periods of stress may occur.
This role may occasionally encounter Protected Health Information, Personal Identifiable Information or Privacy Records, and it is essential that all employees adhere to confidentiality requirements as outlined in the Employee Handbook and Harris’ Security and Privacy policies, as well as apply the concepts learned in the annual Security Awareness training.
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Type: Permanent Location: San Pedro, CR-SJ
Salary / Rate: 20400
Posted: 2025-07-11 10:49:04
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About the Company
Vantage Group Holdings Ltd.
(Vantage) was established in late 2020 as a re/insurance partner designed for the future.
Driven by relentless curiosity, our team of trusted experts provides a fresh perspective on our clients’ risks.
We add creativity to tech-enabled efficiency and robust analytics to address risks others avoid.
Vantage provides specialty re/insurance through its operating subsidiaries in Bermuda and the U.S.
Vantage has approximately 350 colleagues in both the United States and Bermuda. We have offices in Chicago, IL, Norwalk, CT, Arlington, VA, Boston, MA, New York, NY and Hamilton, Bermuda.
Additionally, we are a highly geographically diverse workforce with colleagues based in 35 states and counting.
We fully support work flexibility including remote and hybrid work arrangements.
About the role:
At Vantage, the Actuarial Analyst, Reserving will provide reserving support to a variety of insurance lines.
This position will be integral in performing the quarterly reserving process, expanding the depth of analysis, and building additional monitoring tools.
This role reports to our Head of Reserving, U.S.
and is a remote or hybrid opportunity based in one of Vantage’s office locations.
Vantage’s US colleagues have the flexibility to work anywhere in the United States (excluding US territories and possessions).
The base salary expectation for this role is between $75,000 and $95,000.
Actual base salary for the selected candidate may be higher commensurate with candidate experience and expectations.
Additionally, Vantage offers its colleagues performance-based bonus potential, strong health & welfare benefits, retirement plans with company match, competitive time off plans, a highly flexible work environment, and much more.
Responsibilities & Accountabilities:
* Perform reserve analysis, leveraging internal and external data and intelligence.
* Collaborate closely with pricing, claims, finance, risk management, and data/analytics to ensure well-informed assumptions.
* Assist with maintaining reserving methods and monitoring tools to support the reserving function and the business.
* Assist in creating reports, presentations, and other materials for various audiences.
* Contribute to adherence to actuarial best practices within reserving analysis.
* Find innovative and creative ways to leverage data and analytics to support the reserving function.
Ideal Candidate Profile:
* 1-3 years of Actuarial experience.
* Bachelor’s degree in actuarial science, mathematics, finance, statistics, economics, or related field; or the equivalent in work experience.
* Two or more exams passed preferred and desire to pursue CAS credentials (which would be supported by Vantage).
* Prior experience within the Property & Casualty insurance industry; reserving experience is a plus.
* Skilled with Excel and reporting tools such as Power BI.
* Some experience in...
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Type: Permanent Location: Chicago, US-IL
Salary / Rate: 85000
Posted: 2025-07-11 10:42:01
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Your Job
The Principle Materials Engineer serves as one of Molex's key contributors in the filed of polymer materials.
In a manner and direction consistent with the overall group vision and strategy, this individual is responsible for managing aspects of complex technical projects or programs related to materials or process technology innovation, selection, specification, evaluation, deployment, failure analysis, and / or testing.
The Principle Materials Engineer is also expected to support technology transfer and knowledge sharing with suppliers, external collaborators, and customers.
Our Team
Molex is a global leader in electronic components and solutions, with a strong focus on innovation, quality, and customer service.
The company has been in operation for over 80 years and has a strong presence in various industries, including automotive, telecommunications, consumer electronics, aerospace, defense, medical, and industrial automation.
Candidates can expect to work in a dynamic and fast-paced environment that values creativity, collaboration, and excellence.
Molex is committed to investing in its employees and providing opportunities for growth and development .
What You Will Do
* Deliver on various strategic project commitments configured to address the technical needs / opportunities identified through:
* direct engagement with internal stakeholders from product development and manufacturing
* group technology track roadmaps
* identified technical needs of the enterprise
Support the product development and manufacturing teams with materials application engineering support, support on design reviews and new product development challenges, materials and manufacturing process related problem solving and failure analysis, and technical engagement with the raw material supply base.
Monitor relevant research and development activities in universities and industry through literature searches, seminars, conferences, supplier visits, and external courses.
Create, identify, and help secure intellectual property through patents, publications, and / or trade secrets.
Conduct problem solving and failure analysis consultations, including sample management, coordination of work activities with internal and external analysis / testing facilities, and reporting of results, conclusions, and recommendations.
Review and update existing Molex Engineering Specifications related to raw materials.
Create new Engineering specifications and best practices as required to ensure strong and robust engineering practices related to raw materials and their processing enterprise-wide.
Operate and maintain the pertinent experimental, analytical, and testing equipment (not required to operate equipment on a regular basis.
Only occasionally).
Support management in the coordination and preparation of knowledge shares, technical seminars, and meetings.
Understand, support, and contribute to current Molex Total Quality Manage...
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Type: Permanent Location: Lisle, US-IL
Salary / Rate: Not Specified
Posted: 2025-07-11 10:36:36
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Your Job
The Principle Materials Engineer serves as one of Molex's key contributors in the filed of polymer materials.
In a manner and direction consistent with the overall group vision and strategy, this individual is responsible for managing aspects of complex technical projects or programs related to materials or process technology innovation, selection, specification, evaluation, deployment, failure analysis, and / or testing.
The Principle Materials Engineer is also expected to support technology transfer and knowledge sharing with suppliers, external collaborators, and customers.
Our Team
Molex is a global leader in electronic components and solutions, with a strong focus on innovation, quality, and customer service.
The company has been in operation for over 80 years and has a strong presence in various industries, including automotive, telecommunications, consumer electronics, aerospace, defense, medical, and industrial automation.
Candidates can expect to work in a dynamic and fast-paced environment that values creativity, collaboration, and excellence.
Molex is committed to investing in its employees and providing opportunities for growth and development .
What You Will Do
* Deliver on various strategic project commitments configured to address the technical needs / opportunities identified through:
* direct engagement with internal stakeholders from product development and manufacturing
* group technology track roadmaps
* identified technical needs of the enterprise
Support the product development and manufacturing teams with materials application engineering support, support on design reviews and new product development challenges, materials and manufacturing process related problem solving and failure analysis, and technical engagement with the raw material supply base.
Monitor relevant research and development activities in universities and industry through literature searches, seminars, conferences, supplier visits, and external courses.
Create, identify, and help secure intellectual property through patents, publications, and / or trade secrets.
Conduct problem solving and failure analysis consultations, including sample management, coordination of work activities with internal and external analysis / testing facilities, and reporting of results, conclusions, and recommendations.
Review and update existing Molex Engineering Specifications related to raw materials.
Create new Engineering specifications and best practices as required to ensure strong and robust engineering practices related to raw materials and their processing enterprise-wide.
Operate and maintain the pertinent experimental, analytical, and testing equipment (not required to operate equipment on a regular basis.
Only occasionally).
Support management in the coordination and preparation of knowledge shares, technical seminars, and meetings.
Understand, support, and contribute to current Molex Total Quality Manage...
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Type: Permanent Location: Rochester Hills, US-MI
Salary / Rate: Not Specified
Posted: 2025-07-11 10:36:34
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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:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
Key Responsibilities:
Be compliant with applicable laws and regulations, and follow guidelines in the J&J Credo Maintain Operational Excellence
* Responsible for executing accounting and daily operations for Intercompany Accounting process area.
* Timely closing & execution of financial periods as per closing calendar and in accordance with SLA commitments, fully observing Compliance, Internal Audit & SOX requirements.
* Accountable for completeness, accuracy and validity of the actuals reported within process/entity scope.
* Deep expertise, fully knowledgeable of the Worldwide Procedures and compliance requirements for respective areas.
* Regular focus on Balance Sheet reconciliations to minimize open items.
* On the job training for new team members / BPO partners.
* Support auditors and legal authorities with the execution of required activities.
* Understand, adhere, and execute per worldwide policies and procedures.
Identify compliance risks and recommend solutions.
* Ensure strong internal controls are in place, in order to achieve “adequate” internal and external audit ratings.
Talent Management
* Recruit, Onboard and Training of new joiners.
Be a Trusted Business Partner
* Execute global Strategy & Solutions in line with taxonomy.
* Support Process Subject Matter Experts (SME's) and Operational Key Contacts (OKC's) to ensure cross sector, cross region, and cross process alignment, ensuring good documentation is maintained and consistency of a global approach.
Create Game-Changing Innovation
* Generate ideas, fosters, and implements continuous improvement mindset, identifying and pursuing process efficiency opportunities.
* Execute process improvements, generating ideas and implementing in line with global standards.
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-07-11 09:07:46
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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:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
Professional
All Job Posting Locations:
Alexandria, Virginia, United States, Alexandria, Virginia, United States, Atlanta, Georgia, United States, Baltimore, Maryland, United States, Birmingham, Alabama, United States, Boise, Idaho, United States, Boulder, Colorado, United States, Charleston, South Carolina, United States, Charleston, West Virginia, United States, Charlotte, North Carolina, United States, Chicago, Illinois, United States, Daytona Beach, Florida, United States, Fargo, North Dakota, United States, Indianapolis, Indiana, United States, Jackson, Mississippi, United States, Kansas City, Kansas, United States, Kansas City, Missouri, United States, Lansing, Michigan, United States, Las Vegas, Nevada, United States, Lincoln, Nebraska, United States, Little Rock, Arkansas, United States, Louisville, Kentucky, United States, Milwaukee, Wisconsin, United States, Nashville, Tennessee, United States, New Brunswick, New Jersey, United States of America {+ 8 more}
Job Description:
Job Description
Johnson & Johnson is currently seeking a Sr.
Product Manager within Shockwave Medical. This is a remote role available in all regions within the Continental United States. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
We invite candidates from any location across the country to apply.
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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of ath...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-11 09:07:29
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ERM is hiring a Desert Tortoise Authorized Field Biologist to serve as a field contact representative during operations for project efforts in Beatty, NV.
This is a Full-time (40+ hours per week) limited term role for a duration of 6 months, extendable.
RESPONSIBILITIES:
* Implement Environmental Protection Measures in project-specific Environmental Assessment as related to desert tortoise, special status plants, and migratory birds.
* Provide on-site training for all personnel on avoidance of take of desert tortoise.
* Conduct pre-construction bio-clearance surveys for desert tortoise, special status plants, and migratory birds.
* Move desert tortoises from work areas as needed under NDOW Special Purpose Permit.
* Conduct protocol level pre-project surveys for desert tortoise.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Coordinating with construction contractors, project managers, and resource specialists.
* Other duties as assigned or required.
REQUIREMENTS:
* Must have appropriate certified training, field survey experience, and handling experience to be approved by USFWS as a Desert Tortoise Authorized Biologist (DTAB) for the project or have been approved as a DTAB previously.
* Must have sufficient desert tortoise handling experience to be approved to move desert tortoise out of harm’s way under NDOW Special Purpose Permit.
* BS degree in a natural science field of study preferred.
* Minimum of two field seasons with biological field work.
* Minimum 3 years’ experience required.
* Desert Tortoise experience is required.
* MSHA Part 48 Certification strongly preferred.
* Ability to work safely outdoors in variable weather conditions and in challenging terrain.
* Must be amenable to working during night shift as occasionally required.
* Must have a strong attentional to detail in documentation of work.
* Must have strong organizational and communication skills and work effectively as part of a large team.
* Work schedule may include weekends and/or over-time.
* Desire to work in the field for extended periods of time and maintain a positive attitude.
* Willingness and ability to travel as needed.
* Demonstrated independent and effective problem solving and decision-making skills.
For the Desert Tortoise Authorized Field Biologist position, we anticipate the annual base pay of $73,132.80 – $82,284.80, $35.16/hr – $39.56/hr (USD), limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s ...
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Type: Permanent Location: Las Vegas, US-NV
Salary / Rate: Not Specified
Posted: 2025-07-11 09:05:52
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ERM is hiring an EH&S Advisor in San Rafael, CA, supporting a key client. In this position, you will provide project management and senior technical assistance.
The ideal candidate will have extensive knowledge of environmental compliance, including management systems, storm water, SPCC, water/wastewater, and hazardous materials and waste programs, with specific knowledge of California regulatory requirements.
This is a part-time (8 hours a week), limited-term role with a duration of 6 months, extendable.
RESPONSIBILITIES:
* Provide technical expertise, oversight, and quality control on environmental permitting and compliance projects and related activities in support of ERM client’s project and facilities.
* Participate in or lead process improvement initiatives and strategies, and conduct inspections with regulatory agencies.
* Oversee development of plans, permits, and reports for hazardous waste, SPCC, storm water, NPDES, and wastewater programs.
* Support water stewardship/sustainability development programs
* Execute task and project management requirements to assist in the implementation of environmental compliance and management system programs and processes.
Specific duties may include: project and task budget tracking, invoice review, staff coordination and mentoring, regulatory assessments, conducting programmatic management of change (MOC) tasks, quality assurance and quality control (QA/QC) evaluations, and documentation of best practices and lessons learned.
* Conduct regulatory and/or management system audits or assessments.
* Provide expertise in applicable environmental regulations including NPDES, SPCC, water, and waste and industry applications as a member of a technology team with the support of other ERM subject matter experts.
* Be an active team member on project and maintain client’s scope/budget/schedule expectations.
* Ensure quality standards on project deliverables.
* Build strong collaborative relationships with our client and other ERM employees.
REQUIREMENTS:
* BA/BS and/or MS degree in environmental studies, planning, environmental engineering, chemistry, or related field; PE, CHMM, or similar registration in California required, or ability to obtain within 1 year preferred.
* Minimum of 6 years of experience in permitting, agency coordination, and EHS compliance projects.
* Perform environmental compliance assessments and audits, and implement follow-up corrective actions to ensure compliance with federal, state, and local regulations.
* Support the development and implementation of EHS compliance and management system programs.
* Provide general environmental compliance support to clients, including on site services, as needed.
* Excellent written and verbal communication skills; experience writing comprehensive technical re...
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Type: Contract Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-11 09:05:50
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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
031471 Quality Control Lab Technician (Open)
Job Description:
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
* Adheres to all mill safety policies.
Participates in mill-wide safety, housekeeping and all continuous improvement programs including Operational Excellence (OPEX), Lean Manufacturing, 5S, etc.
* Has a thorough understanding of QC Lab practices, using Quality Control testing equipment to conduct periodic checks on paperboard -- weight, caliper, moisture, dimensions, strength, water absorption, appearance of paperboard
* Assist on machine turnovers and product trials, inventories, uses SBP, MES, PARCView and Valmet systems, and various other tasks as needed.
* Conducts QC checks on all reel turn-ups
* Operates and troubleshoots chemical make-down and delivery systems
* Operates powered industrial vehicles safely to handle chemicals, move parts, etc.
as needed
* Works closely and coordinates with the production team to produce quality paperboard.
* Responsible for making quality control recommendations to production to save, oddlot, or reject paperboard and communicate decision with Shift Supervisor.
* Safely participate in outage activities including maintenance and upkeep of steam and condensate equipment.
QUALIFICATIONS
* Must have a good understanding of paper properties and the testing associated with these properties
* Must have a good understanding of the paper making process
* Must be willing to work rotating shifts and work overtime as needed.
* Requires 8.25 hours/day-6 to7 days/week and periodic splitting 12-hour shifts.
* Must be computer literate and have the ability to learn SBP, MES, PARCView, Valmet, and some basic Microsoft applications.
* Must be willing to safely work with all chemicals
* Must be able to safely and efficiently work with paper testing equipment.
* Perform the safe and efficient use of basic hand tools.
* Cut 7 square feet samples across the sheet every reel change and ensure:
Proper weight, caliper, moisture – ply-bond, ring crush, water, cobb/water immersion test, drop test, assist crew on breaks, prepare steam / hot air for weight and grade changes Proper operation of the calendar stack system water box system.
Know How To:
Use a calculator
Read a micrometer
Read a tape measure
Perform simple math calculations
Perform general computers skills; SBP and MES skills a plus
Chemical system rounds every four (4) hours
Attendance required in all safety meetings Reporting for work on time required.
Other
Follow all standard work practices and understand how varying will affect our final product quality.
Understand and support all Continuous Improvement initiatives.
This list is not all inclusive. Additional expectations may be issued throughout the n...
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Type: Permanent Location: Austell, US-GA
Salary / Rate: Not Specified
Posted: 2025-07-11 09:02:35
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Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principle Duties and Responsibilities
1. Implements and sustains positive health, safety and environmental culture throughout assigned site(s). Establishes short- and long-term strategic plans to foster adoption of health, safety and environmental programs in collaboration with site and corporate leadership.
2. Facilitates with local sites incident investigation and reporting procedures from follow up to closure including root cause analysis, corrective actions, loss sources and trending.
3. Utilizes safety management software to create metric and KPI dashboards and utilize data to create reports for site leadership showing leading and lagging trends, statuses and other relevant report out metrics.
4. Performs certification review ensuring staff with certifications for activities including but not limited to forklift operation and lock out tag out are current based upon organizational policies and external regulatory bodies.
5. Applying continuous improvement practices, identifies waste in current processes and programs and recommends and implements new standards.
6. Utilizing corporate standards and templates, implements local and facility specific compliance programs.
7. In partnership with Corporate Risk Management, leads property risk improvement opportunities to identify gaps in life safety and facility protection obligations. Manages planning actions to set targets and objectives for the site and oversees actions through completion.
8. In coordination with Corporate Risk Management, local site leadership, local authorities and governing bodies, develops site specific security, emergency action and crisis management plans.
9. Performs periodic safety and security audits in collaboration with Safety Specialists and plant leadership. Partners with local site leadership and Safety Specialists for the Corporate Internal Safety & Security Audits.
10. Develops training programs specific to Safety including but not limited to proper use of personal protective equipment (PPE), mat...
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Type: Permanent Location: Beaverton, US-OR
Salary / Rate: Not Specified
Posted: 2025-07-10 08:49:59
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
Como funcionária(o) na Alcoa, você pode nos ajudar a cumprir nosso propósito e realizar nossa visão de reinventar a indústria do alumínio.
Faça parte da equipe que está ajudando a moldar um local de trabalho melhor, com um melhor equilíbrio entre a vida pessoal e profissional e com oportunidades iguais que ajudam todos (as) a prosperar.
Você tem o poder de moldar as coisas para torná-las melhores.
Sobre a função:
* Fiscalização e suporte aos empregados referentes aos serviços de infraestrutura, alimentação e restaurante, transporte fretado e frota de veículos leves;
* Acompanhar a mobilização/desmobilização de todos os recursos (equipamentos, ferramentas, materiais, suprimentos etc.);
* Realizar apontamento diário dos recursos (pessoas, equipamentos, materiais);
* Roteirização diária de itinerários conforme agendamento para atender empregados que utilizam o Transporte.
O que você pode oferecer para a função:
* Formação: Ensino Médio Completo;
* Familiaridade com normas de segurança do trabalho (NR’s) e práticas de HS;
* Disponibilidade para residir em São Luis/MA
* Habilidade básica em ferramentas tecnológica como Excel e sistema de acompanhamento de obras.
O que está sendo oferecido:
* Reconhecida como uma das melhores empresas para se trabalhar pelo programa Great Place to Work;
* Reconhecida pelo Guia Exame de Diversidade como uma das empresas com as melhores práticas relacionadas à inclusão, equidade, gênero, etnia, raça, pessoas com deficiências (PCDs) e pessoas LGBTQIA+;
* Destaque no Índice de Igualdade Corporativa de 2022 da Campanha de Direitos Humanos como uma das melhores empresas do Brasil para profissionais LGBTQIA+ com uma pontuação perfeita;
* Academia Alcoa com planos de desenvolvimento robustos;
* Telemedicina e telenutrição;
* Programa Conte Comigo – assistência financeira, jurídica e psicológica.
Data de encerramento das aplicações: 15/07/2025
Informação adicional
* Você será contatado(a) apenas se for selecionado(a) para uma entrevista; esse processo pode levar até quatro semanas a partir da data de encerramento da divulgação.
About the Location
The Alumar Consortium, managed by Alcoa, located 25 kilometers from the center of São Luís - MA, began its operations in 1984.
It is made up of companies with a tradition in the areas of alumina and aluminum production, with different participations in the two factories that make up the Complex.
At Alcoa, we are committed to generating value in our relationships with all stakeholders in our business, communities and environment.
We build inclusive and secure environments so that our people can live and expr...
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Type: Permanent Location: Sao Luis, BR-MA
Salary / Rate: Not Specified
Posted: 2025-07-10 08:31:03
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Cost Analysis Lead - Taiwan (IFP SCF)
Job Description
Position Overview:
Finance Business Partner with lead responsibilities to support Taiwan Mill Operations teams.
Reporting directly to Head of Supply Chain Finance (APAC) this position is a pivotal role in connecting operational, commercial, and finance teams through managing the cost-of-goods financial function of various manufacturing environments within Taiwan.
Key Responsibilities:
* Provide timely and accurate cost analysis, sound financial advice, and counsel to mill management teams to assist in managing manufacturing costs, optimizing processes, and meeting overall business objectives.
* Lead the annual budget, quarterly forecast, and monthly of cost outlook cycles and associated communication and analytical activities.
* Collaborate with cross-functional teams to provide timely and accurate product cost forecasts, change analysis, key cost drivers, productivity initiatives, and capital projects.
* Drive process improvement and standardization activities to ensure a well-connected and value-added finance team.
* Identify and recommend to internal customers opportunities for improving cost performance of the mill to ensure competitive manufacturing facilities.
* Apply various analysis techniques (eg benchmarking, sensitivity analysis, breakeven analysis) to inform better business decisions.
* Ensure application of corporate financial controls within the mill finance area.
* Design and delivery of training programs to improve financial awareness of mill teams to better understand financial consequences of operational activities.
* Lead Product Cost Analyst ensuring distribution of workload, effective Mill Management support, and achievement of core business objectives, and financial deadlines.
Primary Location
Taipei Office
Additional Locations
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
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Type: Permanent Location: Hsin-Yi, TW-TPE
Salary / Rate: Not Specified
Posted: 2025-07-10 08:29:31
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Your Job
The Mechanical Designer will add value by performing Computer Aided Design work to assist in the development of new or existing device and dispenser products.
This position will require the ideal candidate to possess knowledge of mechanical drafting and design principles, practices, and procedures to assist the design and development of new or improved products.
Under the direction of Engineers, they will design and commercialize new products using SolidWorks 3D design software along with SAP/Engineering Control Center PLM software.
This candidate will be required to design parts produced from various manufacturing processes including plastic Injection molding.
What You Will Do
* Using 3D CAD to transform concepts, sketches, or designs from the lead engineer into designs suitable for a specific manufacturing process.
* Actively design and detail products through various stages of the development cycle.
* Integrate electrical and mechanical components including wire harnesses, wire routing, PCB footprint.
* Interact regularly and collaboratively with Electrical, Mechanical, and Project Engineering.
* Manage and create BoMs.
Organize, and maintain engineering change information within SAP.
* Willingness to take ownership, learn from your peers, be personally accountable, and offer opinions.
* Other duties in support of Product Development may be assigned as recourse needs require, such as prototype and testing.
Who You Are (Basic Qualifications)
* A.S.
in Mechanical Design, or 5 years of Design Work Experience.
* 3+ years of 3D CAD experience
* Solid Works experience desired, however experience with similar 3D modeling software considered.
What Will Put You Ahead
* Expert knowledge of SolidWorks
* Knowledge of plastic part design and injection plastic molding
* Experience using SolidWorks Electrical/schematic
* Experience in wire harness design and wire routing
* Previous role as an CAD Admin
* SAP Engineering Control Center or other PDM
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
At Koch, employees are empowered to do what they do best to make life better.
Learn how our business philosophy helps employees unleash their potential while creating va...
....Read more...
Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-07-10 08:29:14
