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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.
R&D Technician – ELYSIS
A New Era for the Aluminum Industry
Carbon Free Aluminum
The ELYSIS™ technology is the greatest breakthrough in the aluminum industry since its beginnings in 1886.
Work is underway now to further develop this revolutionary new way to produce aluminum, eliminating carbon dioxide and all other greenhouse gas emissions from the traditional smelting process.
The ELYSIS process eliminates the use of carbon anodes, replacing those with proprietary materials.
It is the first industrial process that emits oxygen as its by-product and has the potential to transform an entire industry.
In 2018, two international aluminum producers, Alcoa and Rio Tinto, came together to form the ELYSIS joint venture with the provincial government of Quebec.
With support from the Canadian Government and Apple, the technology is progressing and is currently being designed to support the construction of new smelters or retrofits.
ELYSIS is headquartered in Montreal, with Technology Research & Development locations in Alma, Quebec, (Canada), in Jonquiere, Quebec, (Canada), in New Kensington, Pennsylvania, (United States), and in France.
Commercial quality metal produced by ELYSIS during the ongoing R&D process is already being used by Apple in a variety of products (The 16-inch MacBook Pro and the iPhone SE); Ab InBEV (cans); Audi (e-tron GT wheels produced by the RONAL Group), and Corona (cans).
Join the ELYSIS team in this exciting work!
About the location
The ELYSIS US Research & Development facility is located in the Alcoa Technical Center (ATC) in New Kensington, Pennsylvania. Located near Pittsburgh, the carbon-free smelting process was first developed at ATC, where a dedicated team is working to reinvent the aluminum industry for a sustainable future.
About the Role
As the R&D Technician I at Alcoa Technical Center (ATC) in New Kensington, PA, you will be an integral member of the research and development team, responsible for conducting experiments, installing and commissioning new equipment, and recording and documenting results and observations systematically and completely in laboratory notebooks and computer databases.
This role will be part of a pilot-scale development team, focusing on manufacturing and testing advanced proprietary materials for the development of innovative technology.
Key Activities / Responsibilities:
* Manufacture powders and components and prepare and test samples using laboratory analytical equipment and methods, consisting of LECO chemical analysis, physical measurements, Archimedes density, and various other analytical equipment
* Conduct a variety of laboratory experiments to support technological development
* Collect, organize, and report data to engineering/manag...
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Type: Permanent Location: Alcoa Center, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-31 07:25:14
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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.
As a leader within Alcoa, you can help fulfill our purpose and realize our vision to reinvent the aluminium industry.
Be part of the team that is helping shape a better workplace with a better work-life balance and the equal opportunities that help everyone thrive.
You have the power to shape things and individuals to make them better.
You’re a strategic thinker ready to make a big impact—and this is your opportunity.
Reporting to the VP of Strategy, Business Development, and Joint Ventures, you’ll take the lead on major growth initiatives that define the future of our business.
From identifying and valuing opportunities, to negotiating and executing deals, you’ll be at the forefront of transformative projects.
About the Role:
As the Global Director of Business Development, Acquisitions and Ventures, you will collaborate across teams and functions, driving high-impact partnerships, acquisitions, and new ventures that align with our corporate strategy.
Key responsibilities include:
* Lead and deliver large-scale business development projects—including acquisitions, joint ventures, new business lines, and expansions.
* Drive the full deal lifecycle: from opportunity ideation and strategic assessment to valuation, due diligence, negotiation, and execution of agreements.
* Manage internal and external stakeholders to ensure alignment and successful project delivery.
* Oversee financial modelling and market analysis to support valuations and maintain competitive intelligence.
* Mentor team members and enhance business development processes to build a high-performing team.
* Support executive decision-making through special projects and complex, non-standard analysis.
What’s on offer:
* Be part of a global operation where you can play a pivotal role in our ongoing success
* Global Career development opportunities to pursue your passion
* Car allowance
* Health insurance
* Long- and short-term incentive programs
What you can bring to the role:
* Ideally you will have at least 10 years’ experience in corporate, business, joint venture development, or investment banking.
* Postgraduate qualifications and experience in mining, minerals processing, or manufacturing would be highly beneficial.
* Proven experience leading complex transactions, including acquisitions and joint ventures, from valuation through to execution.
* Strategic thinking capability teamed with strong financial acumen and deep knowledge of valuation methodologies and financial statement analysis.
* Demonstrated success managing multiple high-priority projects under tight deadlines.
* Well-developed communication skills, with a proven track record in working with global cro...
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Type: Permanent Location: Rotterdam, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-10-31 07:25:09
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POSITION SUMMARY:
This is position that is responsible for the operation and supporting activities surrounding a particular coating process. The primary equipment will be operated through HMIs (Human-Machine Interfaces) and a series of switches, pushbuttons, and other interactive control points. Successful Operators will be capable to produce the required amount of product in a defined period while ensuring all (Environment, Health and Safety (EHS) and Quality requirements are continuously satisfied. The Operator will be required to work as part of a team with Operations Support, Engineering, Maintenance, and Management personnel. Some overtime will be required on occasion to meet production and project schedules. Limited travel may be required in support of training program. Operators will be provided the opportunity to progress within the role as defined below.
DUTIES AND RESPONSIBILITIES:
* Perform complex and multi-level tasks from procedures and work instructions defining the tasks.
* Maintain timely and accurate record keeping using provided tools including digital and handwritten data entry and notes.
* Maintain 100% compliance with personal protective equipment (PPE) requirements while operating equipment and/or performing supporting operations, includes ensuring your personal protective equipment is functioning properly prior to starting a task.
* Effectively identify and communicate non-standard situations including (EHS) and Product Integrity concerns.
* Operate support equipment (pre/post coating) and support Coater Operators
* Maintaining metal coating fixtures for use in coater which including visually verifying condition, removing residual coatings, and removing any contamination that may have affected the fixtures.
* Cross training in other coating process areas as needed to support production requirements. Will be required to complete the training program for each process prior to performed assignments in that area.
QUALIFICATIONS:
* High school diploma or general education degree (GED).
* At least 2 years’ experience working in a production manufacturing environment
* Additional Education, Training, Certifications, or Licenses that are applicable will be considered and may be used to supersede either of the other two requirements.
* Must be able to read, write, and communicate in English.
* Read and interpret documents such as safety rules, operating instructions, and procedure manuals.
* Write routine reports and correspondence either in digital or handwritten formats.
* Good mathematical skills, scientific principles and reasoning ability
* Mechanically inclined individual that thrives in a hands-on, demanding environment with little direct supervision once assignments are handed out.
* May be required to operate of forklift (training provided).
PHYSICAL DEMANDS: Reasonable accommodat...
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Type: Permanent Location: Oldsmar, US-FL
Salary / Rate: Not Specified
Posted: 2025-10-31 07:14:23
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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:
Sales Enablement
Job Sub Function:
Sales Training
Job Category:
Professional
All Job Posting Locations:
Bangkok, Bangkok, Thailand, Jakarta, Indonesia, Kuala Lumpur, Kuala Lumpur, Malaysia, Singapore, Singapore
Job Description:
Position Overview:
The role will lead the development and execution of education strategies across Southeast Asia, including shape the learning experience for both internal teams and external healthcare professionals in the rapidly evolving field of robotic and digital-assisted surgery.
The current scope includes on the VELYS™ Robotic-Assisted Solution and the broader complementary orthopaedic portfolio.
Secondly, as the clinical lead, this individual will support VELYS funnel development in presenting clinical and technical advantages of VELYS during product demos and clinical evaluation.
He or she will also provide hypercare support during critical evaluation period as well as starting up first few cases.
Where necessary, this lead will also help to address technical questions around VELYS and to escalate clinicians concerns to the global R&D team.
Strategically, this role will support the development of product business plans, ensuring product-market relevance that marketing plans are grounded in sound clinical imperatives.
Key Responsibilities:
1.
Professional & Commercial Education Development
* Design and implement VELYS Professional Education programs to support surgical excellence and improved clinical outcomes in knee and hip arthroplasty.
* Create Commercial Education Programs tailored to sales and marketing teams to enhance technical knowledge and value-based selling capabilities.
* Collaborate with regional and global stakeholders to ensure alignment with APAC education standards and compliance requirements.
2.
Market & Content Strategy
* Assess market dynamics, customer insights, and training gaps across SEA to inform educational priorities.
* Translate clinical and commercial needs into engaging, data-driven educational content and tools that address surgeon concerns and support decision-making.
* Monitor clinical trends, competitive landscape, and surgeon feedback to proactively evolve the education strategy.
3.
Clinical Insight & Portfolio Strategy
* Act as a clinical subject matter expert for VELYS Knee and Hip solutions—helping address key clinical concerns and guiding internal teams on evidence-based posi...
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Type: Permanent Location: Singapore, SG-01
Salary / Rate: Not Specified
Posted: 2025-10-31 07:07:46
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ERM is hiring a motivated hands-on Senior Environmental, Health and Safety (EHS) Consultant to join our growing Performance & Assurance technical team in Sunnyvale, California. This position is expected to involve working a minimum of 3 days on-site. This is a fixed-term, full-time role (40 hours a week) for a duration of 4 months, renewable.
The ideal candidate will have experience developing and supporting implementation of Cal/OSHA requirements, Standard Operating Procedures, Job Hazard Analysis/ Risk Assessments, Emergency Response Plans, Behavioral Safety Programs and Contractor Safety Management. Candidates should also have familiarity with research laboratory safety requirements, waste management (hazardous, non-hazardous, universal/ electronic), environmental reporting (HMBPs), and chemical safety requirements.
RESPONSIBILITIES:
* Oversee and direct team members to effectively manage tasks for on-time delivery and quality of their deliverables.
* Perform compliance audits to assess client compliance with applicable health and safety or environmental regulatory requirements, client standards, or management systems.
* Support our clients’ desire to improve safety performance by providing training, field coaching, and targeted EHS assessments.
* Identify follow-up corrective actions to close audit findings.
* Provide technical assistance on EHS compliance and EHS management system projects on a range of areas such as R&D laboratory safety, chemical safety, machine guarding, laser safety, robotics safety, hazardous materials use/storage/waste, EHS auditing.
* Develop and implement EHS compliance procedures, plans, permits, and reports.
* Manage tasks within assigned scope/budget/schedule and ensure quality standards on project deliverables.
* Build client relationships and nurture repeat business by continuously striving to exceed their expectations.
* Support ERM Partners and Project Managers to effectively manage and deliver projects.
* Build strong collaborative relationships with other ERM employees.
REQUIREMENTS:
* BS in engineering, environmental science, occupational health and safety, or related discipline preferred.
* A minimum of 7 years of applicable experience providing EHS support with an emphasis on health and safety.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Ability to succeed in a fast-paced consulting environment, handling multiple assignments, meeting strict deadlines, and being able to re-prioritize tasks as-needed.
* Valid driver’s license and good driving record.
Pay Transparency:
For the Environmental, Health and Safety (EHS) Consultant position, we anticipate the annual base pay of $76,000– $97,400, $36.54/hr - $46.82/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on ...
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Type: Permanent Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-31 07:06:36
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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 #:
032492 Safety Coordinator (Open)
Job Description:
Founded in 1877, Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world’s most demanding and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life’s essentials – and creates lasting value for its colleagues, customers, and other stakeholders.
OUR VISION:
Be the best performing customer service company in the world.
OUR PURPOSE:
We create packaging solutions for life’s essentials.
ROLE OVERVIEW: Under general supervision, performs generally non-routine risk assessments for processes and new equipment.
Submits corrective solutions to risks while also making fiscal and operational considerations.
Assists in safety and quality activities and improvement projects as directed by the manager.
Informs managers and supervisors of regulatory changes with which the company must comply.
Key Responsibilities
* Ensures that safety and environmental rules and regulations are followed.
* Advises managers regarding safety, compliance, and environmental issues.
* Implements compliance requirements and control procedures as prescribed by regulatory agencies.
* Performs safety orientation and conducts training updates for employees.
* Completes reports required by regulatory agencies and maintains environmental records.
* Implements safety and environmental programs in conjunction with corporate initiatives.
* May train employees on safety aspects of machine operations.
* Maintains system processes that support the safety and environmental function.
* May be responsible for quality processes.
* Incorporates and maintains safety observances, including but not limited to, use of all PPE by employees, ensuring guards and safety features are working, and promoting good safety practices and habits.
* May be responsible for regulatory water testing and reporting.
* May support site trails for process optimization and improvements.
* May conduct field sampling safely from various sampling points in and around Greif location(s).
* May perform customer service, purchasing, scheduling or other duties as required.
* Performs other duties as assigned.
Education and Experience
* High School Graduate or equivalent. Bachelor’s degree preferred.
* A minimum of 3 years of experience as a Safety or EHS Coordinator in an industrial manufacturing or plant facility is required. Over 4+ years of experience preferred.
Knowledge and Skills
* Solid knowledge of relevant safety regulations.
* Ability to identify unsafe work practices and/or able to recognize ...
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Type: Permanent Location: Tacoma, US-WA
Salary / Rate: Not Specified
Posted: 2025-10-30 08:21:52
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Diese Position ist bei TIB Molbiol (einer Tochtergesellschaft von Roche) in Berlin zu besetzen.
Im Team Quality & Regulatory spielst Du eine entscheidende Rolle bei der globalen Markteinführung unserer In-vitro-Diagnostika (IVD).
Als Regulatory Affairs Manager (m/w/d) bist Du der Dreh- und Angelpunkt für die Zulassungsstrategien in Schlüsselmärkten wie den USA und MDSAP-Regionen.
In dieser Position sicherst Du nicht nur die Compliance unserer technischen Dokumentationen , sondern arbeitest auch eng mit F&E und globalen Behörden zusammen, um innovative Diagnostiklösungen für Patient:innen weltweit verfügbar zu machen.
Deine zentralen Aufgabe
* Du erstellst und pflegst eigenständig Teile der Technischen Dokumentation, um die Konformität mit IVDR und internationalen Regularien sicherzustellen.
* Du wirkst aktiv an der Vorbereitung und Einreichung von Zulassungsunterlagen für die U.S.
FDA mit (z.B.
510(k), PMA, De-Novo) und betreust Registrierungsverfahren in MDSAP-Ländern (z.B.
Kanada, Australien).
* Du übernimmst die regulatorische Bewertung und Dokumentation von Produktänderungen (Change Control) und unterstützt bei der Aufrechterhaltung bestehender Zulassungen sowie bei Post-Market Surveillance (PMS) Aktivitäten.
* Als Fachexpert:in berätst Du interne Abteilungen wie F&E und Produktion bei regulatorischen Fragestellungen, einschließlich der strategischen Beratung von Entwicklungsteams.
* Du recherchierst, analysierst und bereitest relevante internationale Gesetze und Normen auf (z.B.
FDA-Regularien, MDSAP, ISO 13485) und wirkst an der Erstellung von SOPs (z.B.
FDA 21 CFR Part 820) mit.
* Du koordinierst die fristgerechte Beantwortung von Behörden- und Benannten-Stellen-Anfragen und nimmst aktiv an Audits (z.B.
durch Behörden, Benannte Stellen) teil.
Wer Du bist:
* Abgeschlossenes Studium (z.B.
Biologie, Chemie, Pharmazie, Medizintechnik, Regulatory) oder eine vergleichbare Qualifikation.
* Mindestens 3 Jahre Berufserfahrung im Bereich Regulatory Affairs für In-vitro-Diagnostika (IVD) oder Medizinprodukte.
* Nachgewiesene praktische Erfahrung oder sehr fundierte Kenntnisse in der Vorbereitung von FDA-Zulassungen (z.B.
510(k), PMA, De-Novo).
* Sehr gute Kenntnisse der IVDR sowie internationaler Zulassungsanforderungen, idealerweise bereits erste Erfahrungen mit MDSAP.
* Erfahrung in der regulatorischen Bewertung von Produktänderungen (Change Control) unter IVDR und MDSAP-Anforderungen s...
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Type: Permanent Location: Berlin, DE-BE
Salary / Rate: Not Specified
Posted: 2025-10-30 07:32:26
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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:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Zagreb, Grad Zagreb, Croatia
Job Description:
Territory to cover: Croatia
Based in Zagreb, Croatia
Full-time
The Medical Science Liaison (MSL) serves as a bridge between the pharmaceutical company and the healthcare community.
MSLs are responsible for building and maintaining relationships with key opinion leaders (KOLs), healthcare professionals, and clinical investigators.
Their primary role is to disseminate scientific information, provide clinical and scientific support for products, and gather insights from the field to inform the company's strategic direction.
MSLs engage in scientific discussions, attend medical conferences, and deliver presentations to ensure that stakeholders are well-informed about the latest research and product developments.
Strong scientific knowledge, communication skills, and the ability to translate complex data into practical insights are essential for success in this role.
We are currently looking for MSL in the field of oncology since we have a rich heritage and a strong pipeline in this TA.
The person will be responsible for different products (Rybrevant, Balversa, Akeega, Erleada) and customer as it will cover lung, bladder and prostate cancers.
Key Responsibilities
* To keep abreast of medical and scientific knowledge.
* Development and maintenance of a contact network with Leading Specialists.
* Proactive and reactive communication of medical scientific data to Leading Specialists.
* Organization and participation in Medical Education activities.
* Organization and participation in Advisory Boards in cooperation with Medical Advisor/Medical Director.
* Provision of scientific support to company Sales Representatives.
* Support Medical Affairs and GCO in study execution, including site identification and other data generation projects.
* Through scientific interactions, gain valuable insight into treatment patterns, including the discussion and measure of Scientific Alignment Score (where applicable, based on local conditions/regulations), and scientific activities in the therapeutic area and provide input to the company Medical Affairs Plan / business decision making.
* Through scientific interactions with Leading Specialists, champion medical benefits of products and contribute to ...
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Type: Permanent Location: Zagreb, HR-21
Salary / Rate: Not Specified
Posted: 2025-10-30 07:29:48
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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 – Surgeons (Commission)
Job Category:
Business Enablement/Support
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
Responsable Régional Chirurgie J&J Vision en CDI pour le secteur PACA (H/F)
Chez Johnson & Johnson, nous pensons que la santé est essentielle.
Notre force en termes d'innovation dans les soins de santé nous permet de construire un monde dans lequel nous contribuons à prévenir et à soigner les maladies complexes, où les traitements sont plus intelligents et moins invasifs, et où les solutions sont personnelles.
Grâce à notre expertise en matière de thérapies innovantes et de technologie médicale, nous avons une position unique pour innover aujourd'hui dans l'ensemble des solutions de santé afin de réaliser les progrès de demain et d'agir en profondeur pour la santé de l'humanité.
Pour en savoir plus, consultez le site https://www.jnj.fr
À propos de MedTech
Grâce à nos avancées biologiques et technologiques, nous créons des traitements de nouvelle génération, plus efficaces, moins invasifs et adaptés à chaque patient.
Votre expertise contribue à améliorer la santé des patients.
Pour en savoir plus, rendez-vous sur https://www.jnj.com/medtech
À propos de Vision Care
Grâce à nos avancées biologiques et technologiques, nous créons des traitements de nouvelle génération, plus efficaces, moins invasifs et adaptés à chaque patient.
Vous souhaitez améliorer les traitements de la vision ? Rejoignez une équipe qui repense les soins visuels ! Nos équipes s'attaquent aux défis les plus complexes en matière de santé oculaire.
Aidez-nous à combiner science, technologie et savoir-faire pour permettre aux professionnels de santé et aux patients de protéger, corriger et améliorer la vue pour tous.
Votre expertise contribuera à améliorer la santé des patients.
Pour en savoir plus, rendez-vous sur https://www.jnj.com/medtech
Nous recherchons les meilleurs talents pour Responsable Régional Chirurgie J&J Vision en CDI pour le secteur PACA (H/F).
Objectif: Le/la Responsable Régional assure la promotion et le développement des ventes du portefeuille de lentilles intra-oculaires JJV dans le domaine de la chirurgie de la cataracte, positionne J&J Vision comme un partenaire de choix, auprès d'une cible d'institutions privées et publiques, de chirurgiens ophtalmologistes.....
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-10-30 07:29:25
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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:
Career Programs
Job Sub Function:
Post Doc – Data Analytics & Computational Sciences
Job Category:
Career Program
All Job Posting Locations:
Remote (US), 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 Innovative Medicine (JJIM), a Johnson & Johnson company, is recruiting for a Postdoctoral Researcher which can be located remotely in the US.
The Data Science Analytics & Insights team within JJIM R&D develops innovative solutions using a variety of data sources across multiple different disease areas.
We are looking for an outstanding postdoc with a focus on Computer Vision (AI/ML Radiology).
Key Responsibilities:
* Conceive, develop, and implement analytics and AI/Machine learning radiology solutions to high-priority scientific problems
* Participate in cross-functional collaborations with external companies and internal scientific, clinical, and data science teams
* Shape internal/external collaborations and define the scope of research questions
* Extract insight from complex, unstructured radiology image or other imaging modalities data to improve drug discovery and healthcare (e.g., disease identification, patient stratification, disease insights)
* Clearly articulate highly technical methods and results to diverse audiences and partners to drive decision-making
Required Qualifications
* Ph.D.
degree in a quantitative discipline (e.g., artificial intelligence, computer science, applied mathematics, electrical engineering, or similar), or closely related field, completed within the past 3 years, or to be completed within the next 6 months.
* Demonstrated experience driving research in and applying Computer Vision techniques, such as Foundation models, Transformers, CNNs, Diffusion models, RNNs, GANs, and radiomics.
* Extensive experience with traditional Computer Vision applications, such as OpenCV, object detection, edge detection, image segmentation
* Extensive hands-on experience wi...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-30 07:28:45
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role:
As an Artificial Intelligence (AI) Engineer at Elanco, you will join a dynamic engineering team dedicated to designing, developing, and deploying cutting-edge AI solutions that drive innovation, efficiency, and value across the business.
This role is perfect for a creative problem-solver passionate about leveraging AI, specifically Generative AI and Agentic AI, to make a tangible impact.
This includes four strategic priorities:
* Pipeline Acceleration: Optimize the search and approval of high impact medicines with a focus on speed, cost and precision.
* Manufacturing Excellence: Improve the efficiency, quality and consistency of core manufacturing processes, specifically execution and equipment effectiveness.
* Sales Effectiveness: Simplify the process to find, trust and consume relevant customer insights that drive sales growth and improved engagement.
* Productivity: Expand operating margin through efficiency by systematically reducing our operating expenses across the company, improving profitability.
Your Responsibilities:
* Consume and Integrate AI Models: Design, build, integrate, and deploy AI powered solutions to solve complex business challenges.
* Collaborate Across Teams: Work closely with software/data engineers, data stewards/scientists, and business stakeholders to understand requirements and deliver scalable, integrated AI solutions.
* Build Production-Ready Solutions: Engineer and maintain robust solutions, with a focus scale, reliability and operational efficiency.
* Drive Innovation: Stay current with the latest advancements in AI and identify opportunities to apply new technologies to advance Elanco’s mission.
* Ensure Quality & Performance: Write clean, efficient, and well-documented code, and ensure all solutions are optimized for performance, security, and scalability.
* Translate Business Needs: Effectively translate business requirements into technical specifications for AI-driven products and features.
What You Need to Succeed (Minimum Qualifications):
* Educational Background: A Bachelor’s or Master’s degr...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-10-29 07:42:43
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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 – Specialty Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Norderstedt, Schleswig-Holstein, Germany
Job Description:
Über Johnson & Johnson MedTech
Bei Johnson & Johnson glauben wir, dass Gesundheit alles ist.
Unsere Stärke im Bereich der Gesundheitsinnovation befähigt uns, eine Welt zu schaffen, in der komplexe Krankheiten verhindert, behandelt und geheilt werden und Behandlungen intelligenter, weniger invasiv und Lösungen persönlich sind.
Durch unsere Expertise in innovativer Medizin und MedTech sind wir in der einzigartigen Position, innovative Lösungen in das gesamte Spektrum der Gesundheit zu injizieren, um die Durchbrüche von morgen zu erzielen.
Wir verbinden Wissenschaft, Technologie und Entschlossenheit, um die Gesundheit der Menschheit tiefgreifend zu verbessern.
Erfahre mehr unter https://www.jnj.com/
Johnson & Johnson Electrophysiology
Mit diesem Geschäftsbereich ist Johnson & Johnson führend im Bereich der kardiologischen Elektrophysiologie.
Die "Elektrophysiologie" ist ein Spezialgebiet zur Untersuchung und Behandlung von Herzrhythmusstörungen in der Kardiologie.
Die Aufgabe der Elektrophysiologie besteht darin, Herzrhythmusstörungen (insbesondere Herzrasen) bei einer Herzkatheteruntersuchung mit Hilfe von Elektrodenkathetern zu diagnostizieren und kurativ zu therapieren.
Was unser Team ausmacht
Johnson & Johnson Electrophysiology ist geprägt durch einen starken Innovationscharakter sowie eine moderne und schnell, aber gesund wachsende Organisation.
Teamgeist, das richtige Mindset und eine offene Kultur machen den Erfolg und die Zufriedenheit unseres Teams aus.
Wir leben das „WIR“: wir feiern nicht nur unsere Erfolge gemeinsam, sondern es herrscht eine positive Fehlerkultur, in der bemüht sind, Herausforderungen schnell und unkompliziert, gemeinsam zu lösen.
Wir kultivieren das Lachen und haben Freude an unserer Arbeit.
Wir schätzen Charakterköpfe mit Teamgeist, die Verantwortung übernehmen, sowie innovativ und lösungsorientiert voranschreiten. Möchtest Du auch mit Deinem Engagement mitgestalten sowie mit Leidenschaft große Ideen voranbringen? Dann werde Teil unseres Teams!
Zur Verstärkung unserer Teams in Deutschland suchen wir ab dem 01.10.2025 mehrere
Associate Clinical Consultant (d/m/w) im Außendienst
Trainee Sales Consultancy – Johnson & Joh...
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Type: Permanent Location: Norderstedt, DE-SH
Salary / Rate: Not Specified
Posted: 2025-10-29 07:19:33
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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 Product Development
Job Sub Function:
R&D Software/Systems Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Yokneam, Haifa District, Israel
Job Description:
About Cardiovascular
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
About the Role
Join the Core Technologies team at Johnson & Johnson MedTech EP, where you’ll be immersed in research and development of cutting-edge technology for cardiac rhythm diagnosis and treatment.
As a physicist in our team, you will help build technological infrastructures that underpin our world-leading systems.
Responsibilities
* Research and development of technological infrastructure for core medical systems.
* Develop intra-body tracking systems based on magnetic and electric fields.
* Signal processing of physiological signals.
* 3D reconstruction of physiological structures.
* Development and integration of various sensors (ECG, Ultrasound, Impedance, etc.).
Requirements
* Master’s degree (minimum) in Physics or Electrical Engineering (PhD preferred).
* At least 5 years’ experience in applied physics/electronics and system development.
* Proven experience in mathematical infrastructure/algorithm/simulation development.
* Neural network development experience – advantage.
* Outstanding PhD graduates in Physics or Electrical Engineering may be considered, even without professional experience.
* Strong ability to work independently and exceptional self-learning skills.
#LI-LM5 #LI-hybrid
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Type: Permanent Location: Yokneam, IL-HA
Salary / Rate: Not Specified
Posted: 2025-10-29 07:18:37
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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 Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Warsaw, Indiana, United States of America
Job Description:
Johnson & Johnson MedTech Orthopedics (a member of the Johnson & Johnson Family of Companies) is currently seeking a Quality Engineer II to join our outstanding team located in Warsaw, Indiana.
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
The Quality Engineer II position will apply leadership, interdependent partnering, and Quality Engineering expertise to ensure efficient and effective quality & compliance and continuous improvement in our end-to-end business with a focus in manufacturing operations.
They will also apply these principles and problem-solving skills to develop and optimize products & processes that are aligned with the overall business vision.
This individual will support process containment and bounding of nonconforming product.
They also apply appropriate risk management to prevent unanticipated failure modes and improve capability of processes. They pioneer methods and techniques to be used or adapt standard methods to meet needs.
They coordinate phases of work internally and externally and may direct activities of technical support staff.
This role supports new product introduction, continuous improvement initiatives, and base business products and processes.
Key Responsibilities:
* Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, GxP, and other applicable regulatory requirements
* Identifying and supporting resolution of Quality Issues. Owns and supports investigation, bounding, actions, reviews, and approval of non-conformances, CAPAs, and audit findings.
* Developing, tracking, and reporting quality metrics to improve Quality Systems.
* Conduct risk-based decision making and create and update risk documentation and manufacturing control plans.
* Use lean principles to make process improvements.
* Perform validation activities and support NPI projects as part of design transfer.
* Handle conflict resolution as it relates to technical situations.
* Coaching other...
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Type: Permanent Location: Warsaw, US-IN
Salary / Rate: Not Specified
Posted: 2025-10-29 07:18:36
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Classification:
Exempt
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The District Manager is responsible to meet or exceed Service goals in the management of a district of routes.
Reports to the Service Manager.
A DM may manage a service center and if the service center has more than 7 routes, the DM becomes classified as a Senior DM.
Our full-time employees enjoy:
* Medical, Dental, Vision, FSA/HSA
* Life Insurance, Disability Insurance
* Vacation, Sick Time, Holidays
* Choice of Global Cash Card or Direct Deposit
* Career Advancement
* Learning & Development Opportunities
* Inclusive and Diverse Team Environment
Benefits may vary for positions covered by a collective bargaining agreement.
Essential Functions:
- Develop and motivate a district to be a highly productive team through continual training, regular meetings, daily check-in, fostering a positive work environment, route rides, and building strong relationships with each RSR.
- Ensure customer loyalty and outstanding customer service through customer visits, audits, new installs, problem solving, open communication and negotiating with customers.
- Ensure all company policies and procedures are followed in their district, including safety and Service SOP.
- Manage retention and growth by motivating their district to solicit new customers, up-sell/cross-sell/sample all lines of service or product and ensure a profitable product mix.
Monitor and report competitive activity.
Oversee promotions, contests and continued excellent customer relationships.
- Leading their district to success, communicate changes and policies, oversee route organization, project a professional image and require of their district likewise, and cooperatively work with other departments in the branch.
- Complete general route responsibilities when necessary.
Safely operate a delivery vehicle, following all applicable laws and company policy.
- Follow written and verbal instructions and perform other tasks as directed by supervision.
- A Senior DM performs the above functions as well as oversees a ser...
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Type: Permanent Location: Phoenix, US-AZ
Salary / Rate: Not Specified
Posted: 2025-10-28 08:13:34
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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:
Professional
All Job Posting Locations:
Fort Worth, Texas, 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.
Johnson & Johnson is hiring for a Territory Manager – Shockwave Medical to join our team located in Forth Worth, Texas.
Position Overview
Territory Managers are responsible for cold calling, prospecting, and building relationships that will increase account revenue growth and customer satisfaction within specified product lines and geography.
Focus areas will include driving new business with responsibility for achieving sales expectations in an assigned territory while providing exceptional service and support to physicians to meet their patient’s needs.
The Territory Manager is responsible for case coverage in catheter labs while working with physicians and key decision makers.
Essential Job Functions
* Develop and implement sales strategies to effectively promote Shockwave products to appropriate hospital personnel and physicians.
* Meet with a variety of physicians and other hospital personnel to determine customers’ needs, goals, product usage, and types of cases handled.
* Educate customers on products and proper cli...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-27 07:05:13
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Driven by the quickening pace of innovation, Animal Health is on the verge of a revolution, powered by digital business models, technology and data.
Elanco IT is a catalyst for change, partnering to identify and deliver transformative solutions to solve our biggest business problems.
This includes four strategic priorities:
Pipeline Acceleration: Optimise the search and approval of high impact medicines with a focus on speed, cost and precision.
Manufacturing Excellence: Improve the efficiency, quality and consistency of core manufacturing processes, specifically execution and equipment effectiveness.
Sales Effectiveness: Simplify the process to find, trust and consume relevant customer insights that drive sales growth and improved engagement.
Productivity: Expand operating margin through efficiency by systematically reducing our operating expenses across the company, improving profitability.
Your role:
As a Machine Learning (ML) Engineer at Elanco, you will be a key member of our engineering team, specialising in the end-to-end lifecycle of custom and third-party (including open source) machine learning models.
You will translate complex business problems into scalable, production-ready AI solutions.
This role is focused on the practical application of machine learning, requiring a strong blend of software engineering discipline and deep ML expertise to design, build, and deploy models that deliver real-world value.
Your Responsibilities:
* Custom Model Development: Design, build, and train bespoke ML models tailored to specific business needs, from initial prototype to full implementation.
* Third-Party Model Utilisation: Identify, tune and deploy third-party ML models, covering proprietary and open-source models.
* Production Deployment: Manage the deployment of ML models into our production environments, ensuring they are scalable, reliable, and performant.
* MLOps and Automation: Build and maintain robust MLOps pipelines for Continuous Integration/Continuous Delivery (CI/CD), model monitoring, and automated retra...
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Type: Permanent Location: Hook, GB-HAM
Salary / Rate: 48700
Posted: 2025-10-26 07:16:43
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LCM Lead Asia Tissue
Job Description
Your Job
As a person, you’re a learner – a natural leader – someone who is always taking initiative to make things better and bring others along with you.
You live your life in alignment with the highest values of integrity and quality, always ensuring your responsibilities become a long-term success story.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
About Us
Kleenex®.
Huggies®.
Cottonelle®.
Scott®.
Scottex®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
As part of the R&D Tissue team, The LifeCycle Management (LCM) team oversees nurturing products in market for their area of responsibility:
* New product launches
* Product design cost savings (DTV – Design To Value)
* Technical support to ensure Business continuity and compliance, including material, quality or sourcing issues
As the LCM Leader for Intimate and Professional Care, your primary objective will be overseeing and managing our Dry Bath Tissue and Tissue Wipers product ranges in Western Europe.
You will work closely with our manufacturing mills to provide product and process expertise, as well as R&D leadership for the development and implementation of Design To Value and local renovation plans, ensures business continuity and compliance of materials and products.
Furthermore, you will be responsible for the launch of centrally led innovation projects and champion of consumer interests
You will report to the IFP Dry Tissue LCM Senior Team Leader and you will be an individual contributor (no direct reports).
Location: Mill based in Taiwan.
TaYuan Mill, ChungLi Mill and HsinYing Mill.
Travel: There will be up to 25% travel involved with this role, possibly more at the early stages to learn the process, assets and develop your network in our matrix organization.
YOUR KEY ACCOUNTABILITIES:
Design To Value:
* Accountable for DTV target delivery in their area of responsibility, influences and manages stakeholders End to End (E2E) through target setting, technical development and programme implementation to ensure R&D targets are met.
* Leads the management of DTV initiatives within their BU from idea to implementation, including any technical development and through change control and Innovation (IMF) processes as relevant.
Business continuity:
* Leads and coordinates wit...
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Type: Permanent Location: Ta-Yuan, TW-TAO
Salary / Rate: Not Specified
Posted: 2025-10-26 07:13:47
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Job Description
Position Summary
The Division of University Relations is hiring a Student Web Support and Content Migration Assistant.
We are looking for a student to join our Digital team in support of customer service, content updates, and key functionality enhancements for web pages including web page creation, maintenance, administration.
The role will help with the Stevens website relaunch and will have a majority focus on content migration, site updates, and quality assurance.
The role is temporary and ends on February 28th.
Position will be trained in use of enterprise systems and content updates including:
· Enterprise web content management system
· University help desk ticketing software
· Web governance and quality assurance system
· Task and project tracking systems
· CMS Content Migration
· Content editing and maintenance
Duties/Responsibilities
85% Update/Modify/Create web pages and web sites, support documentation
15% Provide customer support to university content editors
Required Qualifications
· Must be a current Stevens graduate student
· Basic Web site design experience
· Basic knowledge of web content management systems
· Experience updating and maintaining websites
Compensation Range
In compliance with the New Jersey Wage Transparency Act, the hourly range for this position is $15.49.
This range represents the University’s good faith estimate of possible compensation at the time of posting.
Stevens Institute of Technology determines compensation based on factors including the position’s scope and responsibilities, the candidate’s experience, education, skills, internal equity, market data, and organizational considerations.
The final salary will be set considering departmental budget, qualifications, and relevant credentials.
This pay range represents base pay only and excludes additional forms of compensation, such as incentives, stipends, or other applicable pay components.
For a full overview of our benefits offerings, please refer to the Stevens Institute of Technology Benefits Guidebook, available at:
Benefits Guidebook
Department
Web and Digital Strategy
General Submission Guidelines:
Please submit an online application to be considered a candidate for any job at Stevens.
Please attach a cover letter and resume with each application.
Other requirements for consideration may depend on the job.
Still Have Questions?
If you have any questions regarding your application, please contact Jobs@Stevens.edu.
EEO Statement:
Stevens Institute of Technology is an Equal Opportunity Employer.
Accordingly, Stevens adheres to an employment policy that prohibits discriminatory practices or harassment against candidates or employees based on legally impermissible factor(s) including, but not necessarily limited to, race, color, religion, creed, sex, national origin, nationality, citizenship status, age, ancestry, marital or domestic partnership or civil union status, familial status, ...
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Type: Contract Location: Hoboken, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-25 09:36:26
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Your Job
Phillips Medisize, a Molex company is seeking a Product Development Lead for Medical and Drug Delivery Devices to join our team at our Hudson, WI site.
In this role, you will spearhead the design, development and launch or cutting-edge medical device and drug delivery solutions.
This role offers the opportunity to guide technical direction, oversee system architecture and ensure compliance with industry standards, while working closely with customers and cross-functional teams.
Our Team
At Philips Medisize, we aspire to be the preferred partner of choice for leading global customers, to create innovative products that help people around the world live healthier, more productive lives.
We are an end-to-end provider of innovation, development, and manufacturing solutions to the medical, regulated products, automotive, consumer and defense markets.
Companies count on Phillips Medisize to bring their breakthrough ideas and innovative branded products to market - with confidence.
As a contract design and manufacturing organization (CDMO), we work closely with our customers to deliver proven, highly engineered products.
What You Will Do
* Lead the technical direction and execution of medical device and drug delivery projects from concept through launch.
* Collaborate with customers and cross-functional teams (R&D, Quality, Regulatory, Manufacturing,) to ensure seamless product development and compliance with FDA, ISO 13485, IEC 60601, and related standards.
* Oversee system architecture, design specifications, risk management, and verification/validation plans, while managing and mentoring engineering teams to foster innovation and technical excellence.
* Drive technical decision-making, risk mitigation, and documentation (DHF, DMR, technical files).
Lead root cause analysis and support CAPA for device issues.
* Stay current on emerging technologies and regulatory changes.
* Communicate project status and challenges to internal and external stakeholders.
* Guide system-level integration across technical domains (mechanics, electronics/software, molding/assembly, usability, etc.), and define development strategy with strong engineering and data traceability, especially in customer-driven programs.
Who You Are (Basic Qualifications)
* Bachelor's Degree or higher in Biomedical, Electrical, Mechanical, or Biological Engineering
* 7+ years' experience in medical device design/development, with 3+ years in technical leadership.
* Experience with FDA Class II/III devices, design controls, risk management (ISO 14971), and validation.
* Familiarity with FDA 21 CFR Part 820, ISO 13485, IEC 62304, IEC 60601
* Experience supporting development of regulatory submission documentation packages.
* Experience working with multiple quality management systems.
What Will Put You Ahead
* Experience leading development of Drug Delivery Devices, Wearables or Catheters.
* Worked ac...
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Type: Permanent Location: Hudson, US-WI
Salary / Rate: Not Specified
Posted: 2025-10-25 08:55:26
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Essential Duties and Responsibilities:
*
+ Coordinates and implements EHS programs designed to provide and maintain a sustainable work environment.
*
+ Establishes best practices and develops and implements training programs to maintain compliance with applicable Local, State, and Federal EHS regulations, as well as, internal policies and procedures.
*
+ Works with EHS Manager to oversee the development and advancement of the EHS management system, self-audit compliance program and internal inspections.
*
+ Evaluates and implements productivity improvements within the EHS discipline using TIPS and Lean tools.
*
+ Leads cross-functional efforts to continuously improve plant improvement processes.
*
+ Attends team meetings in support of the site’s compliance efforts.
*
+ Provides interpretation of existing and upcoming EHS issues/legislation affecting the plant.
*
+ Provides expert guidance to EHS and site leaders on environmental matters and compliance system design and implementation.
*
+ Proposes innovative strategies and programs for existing, emerging and new environmental concerns.
*
+ Serves as EHS focal point for designated plant product line(s).
*
+ Investigates incidents and compliance issues to determine and eliminate root causes.
*
+ Develops cost effective programs/procedures to minimize plant’s impact on the environment due to discharges, emissions, and releases.
*
+ Prepares and/or reviews routine reports for submission to agencies, trade associations, and company.
*
+ Supports site emergency response processes.
Education/ Skills/ Experience:
+ Bachelor’s degree (B.S.) or equivalent from four-year college or technical school and one to four years’ related experience and/or training in EHS with experience in regulatory structure in a manufacturing; or equivalent combination of education and experience.
+
o Proven track record of results; providing functional coaching in a manufacturing environment.
+
o Effective communicator with demonstrated ability to communicate effectively at all levels of the organization.
Able to interact comfortably with business and operations leaders to establish credibility and influence where necessary.
+
o Strong computer and data management skills desired.
Experience with web-based applications, Excel, PowerPoint, Word, is required.
+
o Must have the ability to prioritize in a challenging environment of competing needs and tactically implement and bring projects to closure in a timely manner.
o
# Embrace responsibility, initiative, capacity to work ind...
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Type: Permanent Location: Newton, US-IA
Salary / Rate: Not Specified
Posted: 2025-10-24 09:19:41
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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:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
Allschwil, Basel-Country, Switzerland, Beerse, Antwerp, Belgium
Job Description:
The Principal Statistician supports the design, execution, analysis, interpretation, and reporting or communication of data evidence for Pre/Early/Late Clinical Development, Research & Discovery, Medical Affairs, Real World Evidence, or Manufacturing Sciences programs for research, development, and/or marketed product needs in Janssen, with minimal supervision.
This position supports statistical aspects of business-critical and/or regulatory commitments, provides input to program plans with limited supervision, and represents Statistics & Decision Sciences (SDS) for cross-functional and intra-departmental teams or working groups.
He/She abides by the Credo and practices J&J Leadership Imperatives for Individuals: Lead, Shape, Connect, and Deliver.
Expertise: Demonstrates advanced data analytic expertise based on a foundation of statistical principles and a strong track record of applied experience leading to successful program support.
Is effective in the use of relevant computational tools for study, experiment, or trial research objectives.
Applies high quality statistical methodology in assigned projects with demonstrated understanding of the disease/scientific/functional area and health authority acceptability.
Quality and Compliance: Complies with organization and company standard operating procedures in timely fashion, such as training and project time accounting.
Understands and aligns with relevant regulatory guidances.
Contributes high quality and timely deliverables as assessed by stakeholders such as the project team, the clinical trial team, and the Statistics Area Head.
Ensures that documents, specifications, programs, and macros are consistent and comply with project and company standards.
Follows best practices for Data Integrity.
Drug Development: Demonstrates thorough knowledge of pharmaceutical research and development strategies and execution.
Takes a lead in providing SDS support to experimental design, modeling, analysis planning, analysis execution, interpretation, and statistical communications.
Is accountable for execution of individual project responsibilities, including: meetings with necessary project team members, reporting activities, exploratory analy...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-24 09:13:06
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Ardurra is seeking an Environmental Scientist/Wetland Scientist to join our team in one of our North or South Carolina offices!
As a trusted leader in providing reliable and innovative water resource solutions across the Southeast, we offer tailored and cost-effective approaches to protect public safety, improve watershed functions, and enhance quality of life.
As advisors to municipal and private sector clients, we help communities develop resilient and sustainable stormwater management programs.
Our work integrates watershed ecological assessments, hydrologic modeling, and water quality analysis to support NPDES compliance, green infrastructure planning, and long-term asset management.
We contribute scientific insight to capital improvement projects to meet regulatory and community goals.
Primary Function:
We are seeking a motivated and knowledgeable Wetland Scientist to play a key role in the planning, execution, and management of wetland and natural resource projects throughout the Southeast.
This is an exciting opportunity to work on diverse watershed projects in a collaborative and supportive work environment.
Primary Duties:
* Conduct wetland and stream delineations per USACE Manual and applicable Regional Supplements
* Prepare technical documents: delineation reports, jurisdictional determination packages, mitigation plans, and environmental permit applications
* Manage the environmental permitting process (404/401, NPDES, etc.) at the federal, state, and local levels
* Conduct site evaluations and assist in environmental assessments.
* Collaborate with senior engineers and multidisciplinary teams to develop innovative watershed planning and ecosystem restoration solutions.
* Lead field teams, data collection, and ecological assessments with a strong emphasis on collaboration and safety
* Coordinate directly with clients, regulatory agencies, and multidisciplinary project teams
* Mentor junior staff and contribute to the professional growth of our team
Education and Experience Requirements:
* Bachelor’s or Master’s degree in Environmental Science, Biology, Ecology, or a related field
* Approximately 7+ years of experience in wetland science and delineations
* Proficiency in ArcGIS, GPS data collection, and technical writing
* Understanding of the Clean Water Act, USACE protocols, and Section 404/401 permitting
* PWS (Professional Wetland Scientist) is preferred but not required
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers.
We nurture a family-like culture, striving to create a work environment that is enjoyable, challenging and rewarding but also fun.
We are acutely focused on developing our staff, whether through our internal Ardurra Academy or through our industry-leading Leadership program.
We have made a deliberate and focused commitment to nurture a p...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-10-23 08:45:17
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Bray Commercial is seeking an experienced and detail-oriented Quality Control Inspector to join our team in a fast-paced industrial manufacturing environment.
This role offers an exciting opportunity to contribute to a global leader in industrial valve and actuator solutions.
If you are passionate about quality assurance and have a strong background in inspection within a manufacturing setting, we encourage you to apply.
Job Summary
The Assembly Line – Quality Control Inspector is responsible for ensuring that assembled products meet all applicable quality standards, work instructions, checklists, and customer-specific requirements prior to final packaging and shipment.
This includes performing in-process inspections during assembly, final verification, proper labeling, and documentation.
The role is vital to maintaining product integrity, customer satisfaction, and reducing costly errors or rework.
Key Responsibilities
* Conduct in-process and final inspections of assembled products for conformance to engineering drawings, work instructions, and customer requirements.
* Review special instructions and order-specific checklists to ensure consistent compliance throughout the assembly process.
* Identify, document, and report defects or quality concerns to the Quality Manager.
* Provide feedback to production leadership regarding assembly personnel who may require retraining or process reinforcement.
* Maintain accurate inspection records and ensure traceability of inspected units.
* Support and participate in continuous improvement initiatives.
* Suggest and implement process or procedural enhancements as appropriate.
* Communicate clearly and professionally with team members across multiple departments.
Core Competencies
Knowledge
* Basic understanding of mechanical and electrical assembly principles.
* Familiarity with standard quality inspection practices (visual, dimensional, and functional).
* Ability to interpret engineering drawings, assembly procedures, and work instructions.
* Awareness of quality tools such as checklists, non-conformance logs, and corrective action reports.
Skills & Abilities
* Strong observational skills with high attention to detail.
* Effective interpersonal and communication skills.
* Proficient in Microsoft Excel; experience with ERP systems is a plus.
* Ability to multitask and prioritize in a fast-paced production environment.
* Self-motivated and capable of working independently with minimal supervision.
* Competent in basic math and measurement using inspection tools (e.g., calipers, rulers).
* Physically able to stand or walk for extended periods.
Qualifications & Experience
* High School Diploma or equivalent (required).
* Minimum of 2 years of experience in quality control or quality assurance in a manufacturing environment, preferably with both mechanical and electrical assemblies....
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-10-22 09:08:30
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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 #:
032287 QA Engineer (Open)
Job Description:
Founded in 1877, Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world’s most demanding and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life’s essentials – and creates lasting value for its colleagues, customers, and other stakeholders.
OUR VISION:
Being the best customer service company in the world.
OUR PURPOSE:
Create packaging solutions for life’s essentials.
ROLE OVERVIEW:
We are searching for a Quality Assurance Engineer to join our Petaling Jaya plant, where we manufacture steel drums.
Reporting to the QA Manager, you will oversee quality and inventory systems for the plant in support of established production standards, company objectives, and ISO requirements.
In this role, you are expected to devise, implement, and monitor plant quality
assurance and control programs, including food, safety, and environmental systems.
Our QA Engineers lead investigations into customer complaints and determine necessary corrective actions.
By performing root cause and laboratory analyses and conducting internal
and external quality audits, you support continuous improvement and lean manufacturing techniques.
Key Responsibilities
* Support and participate in the implementation and continuous improvement of the production system.
* Design, institute, and document quality assurance programs.
* Responsible for on-site coordination of the ISO and FSSC certification.
* Investigate and address customer complaints.
Perform root cause analysis, determine corrective actions and evaluate the effectiveness of corrective actions.
* Conduct internal audits for all departments and administer third party quality audits.
* Advise and consult with all departments on all continuous improvement and quality-related issues.
* Review monthly customer inventory reports for accuracy.
Reconcile variances between company's and customers' systems.
* Coordinate and administer physical inventories.
* May be responsible for completing laboratory analysis testing.
Requirements
* Typically possesses a Bachelor's degree or equivalent years of experience and 2-4 years of experience in a production environment.
* Experience with training and providing leadership to colleagues.
* Possesses in-depth experience with quality/assurance control in a high-volume production
* setting.
* Demonstrates excellent written and oral communication skills in Mandarin and English, Malay a plus.
* Possesses strong analytical, planning, and project management skills.
* Ability to work with testing...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: 54000
Posted: 2025-10-22 09:05:41
