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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
In Roche’s Pharmaceutical Research and Early Development organization (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
Within Roche’s Pharma Research and Early Development (pRED), Neuroscience & Rare Diseases (NRD) represents a major focus area where we are committed to realizing our long-term vision of changing lives of patients with severe brain disorders.
Our preclinical research and early clinical development activities center around large and rare indications within the four major pillars of dementias, multiple sclerosis, movement disorders, neurodevelopmental and neuromuscular disorders.
With unparalleled strengths across diverse disciplines, Roche is uniquely positioned to lead in transforming science into medicines for patients with disorders of the nervous system.
The Opportunity
We are seeking a motivated Research Associate to join the In Vivo Technologies Laboratory within the Systems Neuroscience Section of the Neuroscience and Rare Disease (NRD) Discovery team at Roche.
Our lab focuses on translational in vivo models, precise compound application, and development of sensitive endpoints to improve decision-making in drug development.
In this role, you will design, conduct, and report pharmacology studies in rodents, including drug administration, stereotaxic surgeries, behavioral testing, in-life sampling, and tissue collection.
You’ll collaborate closely with colleagues across NRD and pRED, gaining hands-on experience and a deeper understanding of neuroscience drug discovery.
You will work in an industry-leading Neuroscience department with a strong portfolio of preclinical and clinical CNS projects.
Our highly digital and automated workflows offer opportunities to adopt new technologies that enhance research quality and animal welfare.
We are looking for an enthusiastic team player with a passion for neuroscience, a growth mindset, and a commitment to excellence.
Who you are
* You hold a Bachelor's or Master's degree in Neuroscience or a closely-related area, or possess equivalent technical training and relevant experience, with a strong drive to advance research in central nervous system...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-11-29 07:12:44
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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:
Non-Standard
Job Sub Function:
Workday Associate D
Job Category:
Non-Standard
All Job Posting Locations:
Shanghai, China
Job Description:
* Support Site Record Coordinator to maintain the process of Document Control & Record Control under Ethicon Minhang Quality Management System.
支持工厂记录协调员进行爱惜康闵行质量管理系统下的文档控制和记录控制流程的维护。
* Support Site Record Manager for the execution of Record Management Program to ensure Record Management requirements and local procedures aligned to Franchise Record Management Policy and WWRIM Policy & associated standards.
协助工厂记录经理执行记录管理项目以确保记录管理要求和本地程序与事业部记录管理政策、WWRIM政策和相关标准保持一致。
* Maintain site document control and record control procedures to align with Franchise procedures, J&J Policy and regulation requirement.
维护工厂文档控制和记录控制程序以和事业部程序，强生政策和法规的要求保持一致。
* Update site internal document master list in a timely manner.及时更新工厂内部文档主清单
* Deliver the training of document Control & record control across whole plant.
对整个工厂进行文档控制和记录控制的培训
* Lead department record coordinators to implement site Record Management Program by executing the process of the archiving of Paper & Electronic records, control of Vital & Non-vital records, onsite record storage & offsite record storage.
组织部门记录协调员进行纸质和电子记录的归档、重要和非重要记录的控制、厂内和厂外记录保存流程以执行工厂记录管理项目。
* Take of Role of Quality Review Staff by following Product Release process for batch history record transfer and review activities.
依据产品放行程序负责质量审核人员的角色，以完成批生产历史记录的交接和审阅活动。
* Act as the backup of site training responsible and the site ComplianceWire Admin.
担任工厂培训人员的后援支持以及工厂ComplianceWire管理员。
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-11-29 07:12:40
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ERM is hiring an Environmental, Health & Safety (EHS) Consultant to support a key technology client facility in San Jose, CA.
In this role, you’ll assist with day-to-day safety operations, compliance assurance, and continuous improvement initiatives across laboratory and facility environments.
This is a part-time (24-40 hours per week) limited-term onsite consulting role with a duration of 1 month, extendable.
RESPONSIBILITIES
* Support Energy Isolation Plan development, implementation, and verification.
* Assist with laboratory compliance: hazard communication, SDS management, and inspections.
* Conduct ergonomic assessments for lab and office staff.
* Manage hazardous waste labeling, accumulation, and disposal in line with regulations.
* Perform routine inspections and recommend corrective actions.
* Participate in safety committee meetings and support site initiatives.
* Collaborate with Micron’s EHS team to ensure policy and regulatory compliance.
* Maintain accurate records and prepare summary reports.
REQUIREMENTS
* Bachelor’s degree in Environmental Science, Occupational Health & Safety, Industrial Hygiene, or related field preferred.
* Minimum 3 years of EHS experience in lab, semiconductor, or manufacturing environments preferred.
* Knowledge of OSHA and Cal/OSHA regulations, including LOTO, hazardous waste, and ergonomics.
* Strong communication and teamwork skills in a client-facing environment.
* Ability to manage multiple priorities and adapt to dynamic site conditions.
* Proficiency in Microsoft Office; experience with EHS systems like Enablon or Intelex is a plus.
Pay Transparency:
For the EHS Onsite Support position, we anticipate the annual base pay of $88,236 - $132,849, $42.42/hr – $63.86/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 fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/Flexforce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including Flexforce) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible.
See your recruiter for more details.
You can apply for this role through https://www.erm.com/careers/apply/ ...
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Type: Permanent Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2025-11-29 07:11:56
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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
In Roche’s Pharmaceutical Research and Early Development organization (pRED), we focus on the discovery and early clinical development of innovative treatments for some of the world’s toughest unmet healthcare needs.
To complement the immunology team in Cardiovascular, Metabolism, Immunology (CMI) Discovery and Translational Area (DTA), we are seeking a creative and collaborative scientist with deep knowledge and broad experience in building advanced in vitro models to develop, validate and apply more predictive human lung model systems to study mechanisms of respiratory diseases and accelerate drug discovery.
The Opportunity
In this hands-on lab-based position, you will be leading the development of advanced in vitro airway and alveolar models and the buildup of in vitro COPD models in a highly collaborative environment.
You will be the point of contact for scientists and research associates if projects require in vitro lung model support.
Your work will support our efforts to bring new targets into the portfolio and help advance them to the clinic.
Key responsibilities
* Develop, validate, and apply advanced in vitro lung models (air-liquid interface cultures & organoids in co-culture with primary immune cells)
* Further develop in vitro models from patient cells, maintaining and/or inducing a disease phenotype, including the automation of model generation
* Establish quantitative in vitro assays to evaluate epithelial and immune cell functions (e.g.
mucociliary clearance, structural remodelling, inflammation)
* Establish, execute and oversee genomic and drug screening in relevant in vitro lung models
* Analyze data using appropriate statistical methods and present data in a professional format suitable for external publication
* Work in cooperation with Research Associates and Scientists
Who you are
* You hold a PhD degree in Life Sciences (cellular/molecular biology, pharmacology, immunology) or a closely related discipline with 0-4 years post-PhD experience.
* You bring a strong technical and theoretical background/ expertise in (lung) epithelial biology.
* You have extensive hands-on experience with the development, validation and application of complex in vitro systems (organoids, air-liquid interface), preferably in the area of lung epithelial barriers or mucosal immunology.
* You come with scientific accomplishments and successful collaborations documented by publications in high-impac...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-11-29 07:11:45
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EVERWIN est une entreprise spécialisée et leader dans le développement des ERP de Gestion par Affaires.
Nous sommes à la recherche d'un Lead Développeur Delphi passionné pour rejoindre notre équipe dynamique et contribuer à des projets ambitieux.
Description du poste :
En tant que Leader technique / Développeur Delphi, vous assurez le pilotage technique de l'équipe de développement Delphi tout en participant activement à la conception et à la mise en œuvre des solutions globales.
Vous jouerez un rôle clé dans la définition des meilleures pratiques de développement et serez le point de contact principal pour les questions techniques au sein de l'équipe.
Vous assurerez la coordination du travail au sein de l’équipe et en liaison avec les autres équipes.
Missions :
* Concevoir et développer des applications robustes et performantes en utilisant Delphi.
* Assurer la qualité du code via des revues de code et le respect des normes de développement.
* Encadrer et former techniquement les développeurs junior et intermédiaires de l'équipe.
* Participer à la définition de l'architecture des projets et proposer des améliorations techniques.
* Collaborer avec les équipes produit et design pour comprendre les besoins des utilisateurs et traduire ces besoins en solutions techniques.
* Diagnostiquer et résoudre les problèmes techniques rencontrés lors du développement et de la mise en production.
* Rester à jour sur les évolutions technologiques et proposer des solutions innovantes.
Profil :
* Formation Bac+4/5 en informatique.
* Expérience significative en développement Delphi (au moins 5 ans).
* Solide connaissance des bases de données (idéalement Microsoft SQL Server)
* Expérience en gestion d'équipe et capacité à encadrer des développeurs.
* Compétences en architecture logicielle et en design patterns.
* Maîtrise des outils de gestion de version (Git, SVN…).
* Pratique de la méthodologie Agile (Scrum, Kanban)
* Bonnes capacités de communication.
Expérience en management.
* Sens de l'organisation et esprit d'équipe, capacité d’adaptation
* Autonomie et rigueur sont indispensables
* Anglais technique apprécié.
Ce que nous offrons :
* Un environnement de travail stimulant et collaboratif.
* Des projets variés et innovants.
* Des possibilités de formation et de développement professionnel.
* Un package salarial compétitif et des avantages intéressants (Aménagement de télétravail, mutuelle…)
* Environ 10 JRTT par an
* Titres restaurant
* Cadeau à l'occasion de votre anniversaire
Si vous êtes passionné par le développement et que vous souhaitez rejoindre une entreprise dynamique en pleine croissance, n'hésitez pas à postuler, nous étudierons avec attention votre candidature.
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Type: Permanent Location: Villeurbanne cedex, FR-69
Salary / Rate: 70000
Posted: 2025-11-28 07:48:14
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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.
About the Role:
Join us as an Occupational Hygienist in a part-time, fixed-term (12-month) position at our Pinjarra Refinery.
Reporting to the H&S Manager, you’ll work two days per week in a collaborative team environment with access to training, support, and career development opportunities.
This role offers exposure to a broad range of occupational hygiene responsibilities.
You’ll help ensure everyone on site understands potential hazards and control measures, applying the latest research to protect health and safety.
As a key contributor to all things Health and Safety, you will:
* Provide expert advice on occupational hygiene and lead monitoring programs, including data evaluation to maintain the Health Management Plan.
* Manage and improve hygiene programs addressing physical, biological, and chemical hazards, and support investigations and risk assessments to implement effective controls.
* Prepare and review reports to meet statutory obligations, while fostering continuous improvement in hygiene processes and stakeholder engagement.
* Oversee the site’s Fit Testing program, support the Occupational Health Technician, and hold statutory roles as Mine Air Quality Officer and Noise Officer.
What’s on offer:
* Career development opportunities to pursue your passion
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
* Tertiary qualification in occupational hygiene, health, science or an engineering related field.
* Eligible for provisional membership (as a minimum) of the AIOH.
* Experience in occupational hygiene (preferably in heavy industry).
* Mine Air Quality Technician/Officer and/or Noise Officer qualifications (preferred).
* Experience with laboratory quality management systems (highly regarded).
* Knowledge and effective application of relevant legislative requirements and codes of practice.
Additional information
* Interviews may progress prior to the closing date, although all applications will be considered.
* You will only be contacted if you are shortlisted for an interview, this process can take up to four weeks from the closing date.
About the Location
As one of the world’s largest alumina refineries, our Alcoa Pinjarra Refinery produces approximately 4.7 million metric tons each year. Located within the Shire of Murray in the Peel region of WA, just east of the Pinjarra town site, our workplace offers an inclusive and respectful environment, where we embrace change, new ideas and equal opportunity to succeed.
We are values led, vision driven and united by our purpose of ...
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Type: Permanent Location: Pinjarra, AU-WA
Salary / Rate: Not Specified
Posted: 2025-11-28 07:44:20
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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:
People Leader
All Job Posting Locations:
Hangzhou, Zhejiang, China
Job Description:
职位要求/录用条件：
1. 医学相关专业本科毕业，硕士优先
2. 有电生理行业背景优先
3. 良好的医学专业英文
4. 具有管理经验，能够带领团队创造价值
5. 能按时完成销售指标
6. 具有良好的口头和书面表达能力
7. 为人诚恳、正直、诚信
8. 能独立完成工作职责，并通过相关知识考试
工作职责:
1.区域管理和发展
· 根据所管辖区域的销售目标，制订并执行适合该区域的销售计划；
· 指导和监督区域内产品专员建立销售计划和达成销售指标；
· 发展和维持与重点客户的良好合作关系，以促进业务的持续增长；
· 安排和协调适合区域业务发展的各项市场及学术活动；
· 负责区域内招投标工作的完成。
2.区域销售渠道的建立和管理
· 在所管辖区域内，建立合理有效的代理商网络，确保目标医院的全面覆盖；
· 发展新的代理商，不断优化代理商网络的结构，督促代理商完成销售目标；
· 协助产品专员对代理商及其销售人员的培训和管理。
3.团队管理和发展
· 积极发展和培养人才，建立一支高凝聚力的队伍；
· 定期指导和提供反馈给下属，提升下属的工作绩效和能力；
· 在区域内树立积极正面的形象并定期跟踪下属的工作情况以确保下属的工作规范符合公司要求。
4.
专业性要求
· 掌握BW工作所需的基本的专业知识和产品知识；
· 区域学习的理论知识和简单跟台场景的知识和技能应用；
· 将基本的专业知识和产品知识应用到实际工作场景，提升学员在阵发性房颤、RVOT PVC和AFL的跟台实践和客户沟通能力；
· 精通阵发性房颤跟台、产品及客户沟通能力掌握室早和典型房扑的跟台。
Required Skills:
Preferred Skills:
Business Development, Business Savvy, Consulting, Developing Others, Inclusive Leadership, Innovation, Leadership, Market Savvy, Performance Measurement, Product Costing, Product Licensing, Product Lifecycle Management (PLM), Product Portfolio Management, Sales Enablement, Stakeholder Engagement, Strategic Sales Planning, Sustainability, Sustainable Procurement, Vendor Selection
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Type: Permanent Location: Hangzhou, CN-33
Salary / Rate: Not Specified
Posted: 2025-11-28 07:23:39
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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:
Singapore, Singapore
Job Description:
MedTech - Electrophysiology, the role of this Associate Clinical Sales Manager is responsible for overseeing and planning of the clinical support in EP (Electrophysiology) catheterization labs and designated hospitals or territories assigned, selling and promoting Electrophysiology products, technology & solutions amongst current and potential customers.
Close collaboration with Regional Marketing & Professional education on CME programs for end-users, possessing good & effective communication skillsets and strong capability building with team members.
Primarily focusing on Singapore and specific territories within Malaysia according to business goals ,objectives & sales targets.
* Manages a team of individual contributors and/or Supervisors, and is accountable for conducting effective performance management.
Develops tactical and operational plans for the Clinical Sales - Hospital/Hospital Systems team and supports organizational objectives and business goals.
Allocates resources to meet objectives and goals of the Clinical Sales - Hospital/Hospital Systems area.
Directs operations for strategic initiatives and serves as a primary point of contact for internal stakeholders.
* Manages a team of individual contributors and/or Supervisors, and is accountable for conducting effective performance management.
* Develops tactical and operational plans to achieve sales goals, and communicates plans to managers, supervisors, and individual contributors.
* Partners with sales leadership to identify quota credit or pay discrepancies.
* Ensures sales compliance to policy and programming and monitors business and compliance practices for all sales.
* Develops effective customer acquisition and retention processes from identifying potential customers to maintaining positive relationships with existing customers.
* Leads and participates in cross-functional groups to establish marketing campaigns, product direction, and productive solutions.
* Responsible for managing operational aspects of their team (e.g., workflow, performance, and compliance), as well as ensuring achievement of team goals within established timelines and budgets.
* Integrates Johnson & Johnson’s Credo and Leaders...
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Type: Permanent Location: Singapore, SG-01
Salary / Rate: Not Specified
Posted: 2025-11-28 07:23:12
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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:
Professional
All Job Posting Locations:
Oakland, California, United States, Walnut Creek, California, United States
Job Description:
We are searching for the best talent for Senior Plastic Surgery Sales Representative located in Oakland, Walnut Creek, or Marin County, CA covering the East Bay territory.
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 Sr.
Plastic Surgery Sales Rep.
position at Mentor Worldwide is an excellent opportunity to make an impact in the sales organization. The SPSR will support the Location geography by expanding the sales of Mentor products and to convert competitive products in a manner that is commensurate with company policy and sales direction. Specific responsibilities include:
Develop Customers/Account Management
* Demonstrates effective product differentiation selling skills and business development by providing a consultative sales approach to the customer’s business, developing effective pre-call plans, assessing customer needs, handling objections, presenting visual aids, closing, and following-up.
* Builds strong relationships and holds customers accountable to commitments; high level of customer interaction.
* Proficient in managing account growth; strong knowledge of business environment and products (educates the customer, seeks to understand customer circumstances, needs and concerns); motivates customers to become product advocates; builds strategic working relationships; ability to develop and service KOL's; allocate marketing programs.
* Ability to proficiently position the Mentor portfolio for both augmentation and reconstruction settings.
Productive and Efficient Territory Management
* Meets productivity goals across product portfolio.
* Manages and executes across multiple product call points including private practice, surgery centers, and hospitals. Demonstrates ability to assess territory metrics to develop and implement territory business plans.
* Implements and promotes marketing programs in private practice setting.
* Meets s...
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Type: Permanent Location: Oakland, US-CA
Salary / Rate: Not Specified
Posted: 2025-11-28 07:23:10
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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:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Groningen, Netherlands
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Quality Engineer to be based in Groningen!
As the Quality Assurance Engineer, you will play a crucial role in ensuring that our operations meet the highest standards of quality and compliance.
You will have the opportunity to work with a team of exceptional professionals and contribute to the success of our goals.
Your role will be to provide support for product and process development projects and the production process, as well as support in the implementation, improvement and development of the quality policy and the quality system in order to guarantee the quality of the goods produced by AMO Groningen.
As a Quality Engineer, you will:
* Ensure quality assurance within product and process development projects
* Perform and assess statistical analyses and support the implementation of statistical process control techniques, sampling schemes and other quality techniques.
* Assess and partly determine specifications for raw materials and consumables, processes, semi-finished products and end products in relation to internal and external quality standards.
* Drafting and reviewing protocols and reports.
* Review all changes to product specifications.
* Advising, reviewing and approving changes in products/processes or systems, in line with the applicable procedures.
Approving all QMS related procedures and work instructions.
Qualifications/Requirements:
* Bachelor’s degree in technical field or business administration
* 2–4 years of experience in a similar quality role
* Pro-active and analytical attitude with strong problem-solving skills
* Excellent writing skills and attention to detail
* Ability to work independently and in teams; flexible and accurate
* Fluent in Dutch (verbal and written) and proficient in English (reading well and speaking at a moderate level)
* Continuous improvement of the focus area in response to regulatory developments, trends, dev...
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Type: Permanent Location: Groningen, NL-GR
Salary / Rate: Not Specified
Posted: 2025-11-28 07:22:54
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ERM is hiring a motivated hands-on EHS Specialist to assist with the commissioning and start-up of a semiconductor manufacturing facility in Sunnyvale CA.
This is a full-time, limited-term role with a duration of 6 months, extendable.
Some weekend shifts available.
The ideal candidate will have experience with the EHS operations of semi-conductor manufacturing and will support the development implementation of OSHA requirements, Standard Operating Procedures, Health and Safety Plans, Job Hazard Analysis, Emergency Response Plans, Risk Assessment processes, Behavioral Safety programs and Contractor Safety Management.
Candidates should also have familiarity with manufacturing safety requirements, waste management (hazardous, non-hazardous, universal, electronic), environmental reporting (HMBPs), and chemical safety requirements.
RESPONSIBILITIES:
* Assist in the review of commissioning plans and related checklist.
* Provide field oversight of commissioning activities.
* Manage and update Daily logs.
Audit Log - monitor, correct and track issues until closed.
Identify follow-up corrective actions to close audit findings.
* Maintain accurate records and analyze data in excel, edit and present high quality presentations using Microsoft PowerPoint; Utilize Outlook and TEAMs for communication, calendar management and scheduling meetings.
* Provide weekly activity reports to EHS Managers and Senior Specialists.
Support and attend Safety Committee Meetings and Safety Walks monthly or as needed.
* Support Emergency Action Plan and Drill as scheduled.
* Perform compliance and system audits to assess project compliance with applicable health and safety or environmental regulatory requirements, client standards, or management systems.
* Upon request by Client EHS personnel, assist with near miss/incident investigation process.
* Be the voice of the engineer for safety needs.
Escalate issues and provide improvement ideas and feedback to Site Sr EHS Specialist on a weekly basis.
* Develop EHS compliance procedures, plans, permits, and reports.
* Support ERM Partners and Project Managers to effectively manage and deliver projects.
* Build strong collaborative relationships with other ERM employees.
REQUIREMENTS:
* High school diploma or equivalent required, bachelor’s degree is a plus.
* 5 to 10 years experience providing EHS support with an emphasis on health and safety in a semiconductor manufacturing environment.
* Proficient in various Microsoft Programs.
* Existing certification or working towards certification as Certified Industrial Hygiene (CIH) and/or Certified Safety Professional (CSP/ASP) certification a plus but not required.
* Demonstrated understanding of regulatory compliance and reporting processes.
* Requires the use of a Tyvek bunny suit as a part of the standard protective gear in controlled environments.
* Effective written/verbal communicat...
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Type: Permanent Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2025-11-28 07:21:20
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Chez PG Solutions, notre équipe de Croissance et Innovation relevant de la R&D regroupe plusieurs chefs de produits passionnés qui travaillent à transformer les solutions numériques destinées au secteur public.
Nous sommes actuellement à la recherche d’un Gestionnaire de produit (Product Owner) pour piloter l’évolution de notre gamme de produits en évaluation foncière et géomatique, dans un contexte de refonte vers une plateforme web moderne.
Le Gestionnaire de produit joue un rôle central dans notre démarche d’innovation.
Il agit comme lien stratégique entre les clients, la direction, l’équipe des ventes et l’équipe de développement, afin de faire évoluer le produit en réponse aux besoins du marché, aux tendances technologiques et aux exigences réglementaires.
Joueur clé au sein d’une équipe multidisciplinaire, la personne recherchée doit faire preuve de rigueur, d’autonomie et d’un excellent sens de la collaboration.
Elle est responsable de maintenir une vision claire du produit, de bâtir un plan d’évolution cohérent, et de mobiliser les parties prenantes autour de cette vision.
En collaboration avec l’équipe de développement, elle analyse les besoins des clients, propose des solutions concrètes, identifie les fonctionnalités clés et les communique de façon claire et structurée.
Profil recherché:
Nous sommes à la recherche d’une personne rigoureuse, curieuse et dotée d’un fort esprit de collaboration, possédant une bonne connaissance du domaine de l’évaluation foncière municipale au Québec, notamment en ce qui concerne le cadre réglementaire et les pratiques professionnelles en vigueur.
Une bonne compréhension des concepts et des outils en géomatique, tels que les systèmes d’information géographique (SIG), les données spatiales et la cartographie, constitue également un atout important.
Votre rôle:
* Actuellement, nous modernisons notre solution d’évaluation foncière en la faisant évoluer vers une plateforme web innovante, performante et conforme aux normes professionnelles du Québec.
Notre produit intègre également un important volet géomatique, essentiel à notre approche.
* En tant que Gestionnaire de produit, vous serez au cœur de la refonte de notre produit.
Vous piloterez la vision, la stratégie et l’évolution fonctionnelle de la solution, en collaboration avec les parties prenantes internes et externes.
Vous contribuerez à bâtir une plateforme web moderne, intuitive et conforme aux exigences réglementaires et aux meilleures pratiques du domaine.
Responsabilités:
* Compréhension du domaine et des utilisateurs
* Apprendre les systèmes, les processus de travail et les réalités opérationnelles de nos clients.
* Recueillir, analyser et documenter les besoins des utilisateurs, en clarifiant la portée des demandes.
* Représenter les utilisateurs et les parties prenantes auprès de l’équipe de développem...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 85000
Posted: 2025-11-27 07:48:08
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Join a community where people come first.
Systems & Software, a division of Harris, is hiring a Support Analyst to join our collaborative, community-driven team.
At Harris, you are not just a number: you are part of a culture that values continuous learning, mutual support, and personal growth.
As a Support Analyst, you will play a key role in delivering exceptional customer service.
You will engage directly with clients to resolve technical issues, manage support tickets, and identify when to escalate code-related challenges to our development team.
Your ability to communicate clearly, manage your time independently, and build trusted relationships will make you a valued part of our client success story.
This is more than just a support role.
It is an opportunity to grow within a community that invests in you, values your contributions, and fosters a strong sense of community across all levels.
Occasional travel may be required, offering even more opportunities to connect and learn.
If you are passionate about helping others, thrive in a people-first environment, and want to be part of a team that truly supports one another, we invite you to apply.
This role is looking for candidates based in Atlanta, Georgia, with required travel one week per month.
Each month requires one week of on-site work in the DeKalb utility area, one week in Atlanta, and the remainder of the month remote from home.
Additional travel may include annual group meetings in Vermont.
What your impact will be:
* Handle support calls or tickets.
* Install and update product line applications, integrated third party applications, and operating system and database applications.
* Exercise sound professional judgment in investigating technical problems.
* Collect detailed information to categorize requests and establish a method of resolution.
* Document all customer communication through tickets.
What we are looking for:
* Minimum one year of customer service experience in a technical environment or relevant experience.
* Proven problem-solving abilities.
* Strong verbal skills and exceptional written communication.
* Experience in technical documentation.
* Ability to multi-task effectively.
* Ability to work independently with minimal supervision.
* Provide onsite attention and support for specific clients.
Travel and onsite visits are required.
What we can offer:
* 3 weeks' vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Remote work and more!
About Harris:
Harris is a leading provider of mission critical software to the public sector in North America.
As a wholly owned subsidiary of Constellation Software Inc.
(“CSI”, symbol CSU on the TSX), Harris has become the cornerstone for CSI’s investment in utility, local govern...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: 70000
Posted: 2025-11-27 07:48:06
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Accounting Analyst II – Intercompany Accounting (12 Months Contract) (Global Business Services)
Job Description
Accounting Analyst II – Intercompany Accounting (12 months contract)
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In your Accounting Analyst II – Intercompany Accounting - (Global Business Services) role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Role Overview & Primary Accountabilities:
Project Management
* Support Intercompany related projects such as global initiative, system upgrades, automation initiatives, and process standardization.
* Collaborate with cross-functional teams (Finance, IT, Operations) to deliver project milestones.
* Document processes, develop SOPs, and provide training to stakeholders.
Intercompany Accounting & Reporting
* Ensure timely and accurate preparation and submission of intercompany billings requests in compliance with US GAAP accounting requirements.
* Prepare and reconcile intercompany accounts across multiple entities.
* Ensure timely and accurate month-end close activities related to intercompany transactions.
* Monitor compliance with internal controls and accounting policies
* Identify inefficiencies in intercompany processes and propose solutions.
* Assist team leader in preparation of reports or analyses or any ad hoc assignments.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
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 151 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
You’re driven to perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You’re also a Bachelor's degree in Accounting or Professional Accounting qualifications such as ACCA, CIMA or its equivalent with 2+ years relevant working experience and preferably in the same capacity, including practical experience in intercompany accounting.
You love what you do, ...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-11-27 07:45:34
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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 – Surgeons (Commission)
Job Category:
Business Enablement/Support
All Job Posting Locations:
Lublin, Lubelskie, Poland, Warsaw, Masovian, Poland
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Clinical Account Specialist (Biosense Webster)
Location: Warsaw or Lublin
Contract: full-time
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
Purpose:
The Clinical Account Specialist will be responsible for providing clinical support and promoting BW products among current and potential customers, developing professional education for end-users, collaborating effectively with sales team members, and driving business growth within the assigned territory.
You will be responsible for:
* Provide every day in Hospital /EP Lab/ professional clinical & technical support, troubleshooting, and training to Physicians, Electrophysiology Lab Staff, Technicians, Nurses, and administrators staff regarding all aspects of the company’s systems and catheter equipment.
* Understand and know clinical environment, competitor products – continuous development of the knowledge
* Serves as a troubleshooting resource during cases.
* Tailors’ product conversations to the audience to ensure proper understanding and optimal utilization.
* Demonstrates products features to meet customers’ unmet needs
* Become fluent in main types of arrhythmias
Qualifications / Requirements:
* University degree level or equivalent experience (Scientific/Business combinat...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-11-27 07:24:09
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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 01.02.2026 mehrere
Associate Clinical Consultant (d/m/w) im Außendienst
Trainee Sales Consultan...
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Type: Permanent Location: Norderstedt, DE-SH
Salary / Rate: Not Specified
Posted: 2025-11-27 07:24:09
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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
Job Category:
People Leader
All Job Posting Locations:
Danvers, Massachusetts, United States of America
Job Description:
Abiomed is recruiting for an Associate Director of Biostatistics, located in Danvers, MA.
Remote work options will be considered on case by case basis.
Associate Director will provide statistical expertise in the design, analysis, and interpretation of clinical trial programs, regulatory submission and filings; and the generation of evidence to support publication and product commercialization.
The Associate Director of Biostatistics will play a leadership role in multi-disciplinary project and study teams and will also interact closely with various steering committees for Abiomed sponsored prospective studies and registries.
Responsibilities:
* Participate in strategic planning in product development and study design
* Develop trial design options and provide guidance and leadership for on-going and planned clinical studies
* Participate in planning, design, development, and execution of clinical trial protocols
* Develop statistical sections of clinical study documents, including but not limited to clinical study report, statistical analysis plan (SAP), and study synopsis/protocol
* Produce and validate statistical analyses and outputs according to SAP
* Play a lead role in hypothesis generating process and contribute to statistical methodology in manuscript preparation
* Provide statistical expertise and guidance to internal and external stakeholders on ad hoc data analysis requests and publication/presentation efforts related to the project team
* Drive the development of internal repository in statistical methodology and statistical programming
* Lead and coordinate statistical methodology research in novel trial design
* Provide statistical oversight and quality control of deliverables from statistical department
* Prepare projects updates for weekly/monthly status meetings
* Maintain up to date knowledge of statistical methodology and relevant regulatory guidance
* Lead the development and implementation of SOP, work instruction and best practice for statistics department
* Play a lead role in development of internal guidelines and SOPs for clinical operation and data management
* Oversee and manage statistics and prog...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:55
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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 Planning
Job Sub Function:
Supply Network Planning
Job Category:
Professional
All Job Posting Locations:
Milpitas, California, United States of America
Job Description:
Johnson & Johnson Vision is recruiting for a Global Service Supply Planner, located onsite in Milpitas, CA.
About Vision
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 on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Service Planning’s purpose is to enable improved and/or sustained customer service satisfaction through meeting demand for a product over a period of time.
What to make, when to make it, how much to make, where to make it and what materials and resources are required are determined through the production planning process.
In addition to ensuring the desired customer service level is maintained, production planning seeks to maximize operating efficiency and optimize resource usage and inventory investment.
Key Responsibilities:
* Manage the regional spares deployment on weekly basis, and planning of spare parts in support of field engineers, distributors, and direct customers to maintain the target regional fill-rate.
* Determine supply and maintain target stocking inventory levels based upon usage and set targets at regional CSL (Central Stocking Location)/FSL (Forward Stocking Location).
Adjust targets per regional agreed and recommendation and planner approval
* Monitor service materials In-Transit, investigate and resolve in-trans materials that are beyond the desired number of days.
* Work closely with production planning and the repair depot to insure we are meeting customer expectations and desired customer service level.
* Establish effective communication with supporting functions to res...
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Type: Permanent Location: Milpitas, US-CA
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:51
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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:
Laboratory Operations
Job Category:
Professional
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
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
We are searching for the best talent for a Laboratory Operations Analyst II, Automation Engineer to be located in Spring House, PA.
Purpose: This position is part of the global Discovery, Product Development & Supply (DPDS) Operations Team responsible for operations within the Therapeutic Discovery (TD) and Preclinical Safety and Translational Sciences (PSTS) organizations.
The Lab Operations team in DPDS Operations looks after the lab workspace and equipment to enable the scientists to focus on their science using a knowledge of project management, drug discovery instrumentation and automation, and process excellence to evaluate, develop and deliver drug discovery laboratory processes and infrastructure.
The candidate will work effectively in multi-disciplinary teams and collaborate with internal and external partners - such as IT, Safety, Engineering, Facility Management - thus ensuring flawless execution of all projects and processes connected to the lab workspace and automation in particular.
The function requires a hands-on mentality and the ability to work autonomously for longer term activities independently adapting to project developments and proposing next steps.
This role focuses on the configuration of laboratory instruments and the implementation of automated scientific workflows.
You will support laboratory automation across discovery fields, reduce manual data entry and human intervention between instruments and software.
In addition, you will contribute to event-driven architectures and automated data quality control and validation with ubiquitous tracking of completeness, consistency, validity, and accuracy over time.
You will be responsible for:
* Designing and implementing automated lab instrumentation and workflows that span hardwar...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:32
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
People Leader
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
Johnson and Johnson Innovative Medicine (J&J IM), a pharmaceutical company of Johnson & Johnson is recruiting for a Director, R&D Data Science, Data Products – Global Development.
This position has a primary location of Titusville, NJ but is also open to Spring House, PA or Cambridge, MA. This position requires up to 25% travel.
About Innovative Medicine
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
Position Summary
The Director, Data Products – Global Development is responsible for leading the strategy, design, and delivery of user-centric, reusable data products that enable advanced analytics, data science, and AI/ML solutions across the Global Development organization.
This role ensures that high-value internal and external development data assets—including protocol, study design, operational, regulatory, disclosure, and real-world data (RWD/RWE)—are standardized, productized, and integrated into Janssen’s enterprise R&D data ecosystem.
Working closely with Global Development Data Science teams, Clinical Development, Operations, and Regulatory stakeholders, as well as the broader Data Strategy & Products organization, this leader ensures that Global Development data products are AI-ready, semantically consistent, and interoperable, enabling trial efficiency, regulatory readiness, and improved compliance outcomes.
Key Responsibilities:
Data Product Strategy & Execution
* Lead a team to define and deliver data products addressing critical Global Development use cases (e.g., study startup, TMF metadata, operational KPIs, submission readiness).
* Define and maintain a roadmap for Global Development data products, spanning protocol development through clinical trial disclosure.
* Develop data products through agile delivery and FAIR data principles, ensuring scalability, interoperability, an...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:07
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ERM is looking for a motivated, detail-oriented Consulting Associate, Environmental Geologist/Scientist/Engineer to join our growing team in Hartford.
The successful candidate will work on a variety of interesting site investigation, remediation, and hazardous waste management projects throughout our Great Lakes Northeast Business Unit service area; however, opportunities for travel throughout the United States and globally may also occur.
You may also have the opportunity to work on a variety of projects, covering the full spectrum of ERM’s services.
This is a great opportunity to work with ERM's technical experts to implement the latest investigation and remediation technologies, while building the required experience to obtain your professional registration.
RESPONSIBILITIES:
* Conduct field work, including soil, sediment, groundwater, building, waste, and surface water sampling, aquifer testing, drilling oversight and soil logging, soil boring and monitoring well installation, well development, purging and sampling, and construction oversight.
* Coordinate and direct drilling, surveying, and laboratory services.
* Provide support environmental remediation / demolition projects, and operations and maintenance of environmental remediation systems.
* Compile and evaluate soil, groundwater, air, sediment and other environmental data.
* Assist in preparation of reports for submittal to regulatory agencies.
* Review groundwater chemistry data and prepare figures/exhibits to support regulatory reporting.
* Perform Phase I and II environmental site assessments to support property transfer transactions.
* Assist in ensuring compliance with all federal, state and local regulations.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Communicate with subcontractors, regulatory agents, tenants, and clients during field activities.
REQUIREMENTS:
* Bachelor's of Science in geology, hydrogeology, environmental science, or environmental engineering required. Or equivalency of 8+ years related experience.
* Recent graduate to 2 years of experience, including willingness/interest in field assignments.
* Ability to work independently and as part of a team.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports required.
* Ability to succeed in a consulting pace, handling multiple project assignments and maintaining flexibility while meeting strict deadlines.
* Detail-oriented with mechanical aptitude and hands-on troubleshooting/problem-solving skills.
* Environmental field work experience and 40-hour OSHA HAZWOPER certification a plus.
* Up to 75% regional travel with possible multiple overnight stays; 25% office work
* Strong commitment to safety, including following established Health and Safety protocols.
* Driver's License ...
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Type: Permanent Location: Hartford, US-CT
Salary / Rate: Not Specified
Posted: 2025-11-27 07:21:58
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ERM is seeking Consulting Senior Associate, Archaeologist for an immediate opening to work on various projects throughout the United States with a focus on the Upper Midwest and Plains.
Working with an experienced Archaeologist, the successful candidate will conduct Phase I, II, and III archaeological fieldwork and office-based activities, including documenting and evaluating archaeological sites for eligibility for listing in the National Register of Historic Places (NRHP), and assessing project effects under the provisions of Section 106 of the National Historic Preservation Act (NHPA).
This individual will also participate in project planning and logistics and prepare appropriate report sections detailing the survey findings and assessment of resources.
Assignments will be field and office-based, with the expectation that up to 70 percent or more of the time will be in the field, especially during peak survey season.
This is an excellent opportunity for a junior professional looking to grow their career with global environmental consulting and sustainability leader.
ERM is seeking an individual to be based in Minneapolis, Minnesota.
RESPONSIBILITIES:
The Archaeologist will support cultural resource projects, which may include, but not limited to:
* Planning, developing, and performing surveys for project areas and archaeological sites.
* Conducting all levels of field survey, with the primary focus on Phase I survey.
* Walking long distances in challenging conditions (e.g.
weather, topography, environment).
* Preparing appropriate sections of cultural resources reports describing the survey and analysis of archaeological sites.
* Preparation of state specific forms.
* Complying with corporate Health and Safety.
* Performing other duties as assigned or required.
REQUIREMENTS:
* Master of Arts.
or Master of Science in archaeology, anthropology or related field.
* Meet Secretary of the Interior’s Standards for professional qualifications in archaeology.
* Completion of an archaeological field school.
* 1-5 years of experience in Phase I, Phase II, and/or Phase III archaeological fieldwork.
* Ability to lift up to 30 lbs.
* Experience as a crew chief or field director.
* Ability to work outdoors in variable weather conditions and on varied terrain, sometimes for extended periods of time.
* Ability to work weekends and over 40 hours per week when needed.
* Ability to travel frequently and on short notice.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Ability to follow instructions and work independently, and to take initiative to meet project deadlines.
* Demonstrated ability as a technical writer.
* Periodic drug and alcohol testing requir...
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Type: Permanent Location: Minneapolis, US-MN
Salary / Rate: Not Specified
Posted: 2025-11-27 07:21:54
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Company
Federal Reserve Bank of Atlanta
As an employee of the Atlanta Fed, you will help support our mission of promoting the stability and efficiency of the U.S.
economy and financial system.
Your work will affect the economy of the Southeast, the United States, and the world.
The work we do here is important, and how we do it is just as important as what we do.
We live our values of integrity, excellence, and respect every day.
We do the right thing, we do things right, and we treat people right.
A career at the Federal Reserve Bank of Atlanta gives you the chance to do work that touches lives and helps communities prosper.
OUR BANK - The Federal Reserve is the central bank of the United States and is one of the most influential, trusted, and prestigious financial organizations.
It consists of twelve Reserve Banks located around the country and the Board of Governors in Washington, D.C.
The Federal Reserve Bank of Atlanta territory covers the Sixth Federal Reserve District, which includes Alabama, Florida, and Georgia, and portions of Louisiana, Mississippi, and Tennessee.
The Atlanta Fed and the other Reserve Banks play an important part in all three of the Fed's functions: monetary policy, bank supervision and regulation, and the operation of a nationwide payment system.
PLEASE READ:
Internships are paid.
Summer housing will not be provided.
This is not necessarily an exhaustive list of all responsibilities, duties, performance standards or requirements, efforts, skills or working conditions associated with the job.
While this is intended to be an accurate reflection of the current job, management reserves the right to revise the job or to require that other or different tasks be performed when circumstances change (e.g.
emergencies, rush jobs, change in workload or technological developments).
Interns in Supervision & Regulation must be a United States Citizen and pass an enhanced background screening prior to hire.
SCOPE OF ASSIGNMENT:
* Help conduct Competitive Analysis and Bank Market Reviews
* Help complete the financial analysis of applications, conduct internal QA reviews for Apps/Enf, conduct IAP investigations
* Complete compliance/progress report reviews of financial institutions under enforcement action.
QUALIFICATIONS:
* Students must be currently enrolled at an accredited college or university in a Bachelor or Graduate degree program through the duration of the internship.
* Minimum cumulative GPA above 3.0 in academically rigorous curriculum.
* Must be committed to working a 40-hour work week for 10-12 weeks during the summer months.
PREFERRED MAJORS:
* Business Administration
* Finance
* Accounting
* Economics
* Data Analytics
CORE COMPETENCIES:
* Proficient in Microsoft Office Suite
* Excellent communication skills (verbal and written)
* Strong analytical skills
* Ability to work independently and take ownership of projects
* Gr...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-11-26 08:30:15
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About CORE
CORE Electric Cooperative is the largest member-owned electric distribution cooperative in Colorado dedicated to providing reliable, affordable, clean, and safe electric service to our communities.
With a commitment to innovation and member satisfaction, we strive to meet the evolving needs of our members while maintaining the highest standards of service excellence.
Job Summary
The Commercial Operations Program Manager oversees the Cooperative’s short term energy trading and scheduling activities to ensure reliable and cost-effective operations of CORE’s portfolio of owned and contracted generation resources.
This role is responsible for optimization of the energy portfolio, identifying near term resource and delivery needs, and compliance with operational resource adequacy program requirements.
Direct activities will include contract management, support for asset integration, pricing development, support for contract negotiations, and assisting with settlements.
Essential Duties and Responsibilities
* Oversee the short-term and long-term trading activities that are carried out by a contract real-time trading consultant/desk.
* Lead CORE’s efforts to procure and manage short-term power supply and portfolio optimization.
* Responsible for power trading activities for short-term power supply contracts.
* Ensure employees and consultants adhere to compliance requirements.
Ensure that risks are effectively evaluated and managed, and decisions appropriately and proactively presented.
* Works collaboratively with Control Center, Electric Resource Planning, Transmission Planning, Member Services, Accounting, Enterprise Risk and Regulatory Affairs.
* Sets clear expectations and holds consultants accountable for performance of energy portfolio goals and targets.
* Develops pricing models and recommends security requirements for large load development and off-system sales.
* Leads weekly trading meetings with consultant.
* Supports accounting and settlements, assists in preparation of reports concerning daily operation of generation resources, including owned and those under long-term contract.
* Responsible for origination activities for short-term power purchasing and sales.
* Responsible for overseeing the development and implementation of generation dispatch and portfolio optimization.
* Leads effective development and ongoing implementation of operational processes that deliver efficient, effective, and agile merchant activities.
* Supports analysis and development of an execution plan to manage transmission congestion, financial transmission rights and commercial aspects of COREs physical and contract transmission portfolio in an evolving structured power market.
* Leads development of advanced analytical techniques and tools that help the utility see and react to dynamic market conditions.
* Provides input on regu...
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Type: Permanent Location: Sedalia, US-CO
Salary / Rate: 122595.2
Posted: 2025-11-26 08:28:24
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Customer Support Analyst
About the Role
Join our team of technical experts and report to the Customer Support Manager.
In this role, you will be responsible for the installation, monitoring, maintenance, and troubleshooting of Creditron's payment management software, ensuring our clients receive exceptional technical support.
What You'll Do
* Diagnose, troubleshoot, and resolve technical issues related to Creditron products.
* Develop and maintain clear how-to guides and knowledge base articles.
* Install and manage software updates, patches, and new releases for clients.
* Provide friendly and effective customer support via phone and remote access tools (e.g., WebEx).
* Collaborate with third-party vendors to coordinate hardware support and repairs.
* Maintain detailed and accurate records in our incident tracking system.
* Support the physical payment processing hardware.
* Escalate customer billing and renewal inquiries to the appropriate internal teams.
What You'll Need
* A minimum of 5 years of experience in software customer service or technical support.
* A degree or diploma in a computer-related field (e.g., Computer Science, Computer Engineering).
* Proficiency in: Windows Servers, IT/Networking, SQL Server (2022+), IIS, SSRS, SSMS, Python scripting, SQL Server Profiler, and Microsoft Azure.
* A customer-centric mindset with excellent interpersonal skills to work effectively with diverse client roles.
* A proactive and resourceful approach to problem-solving.
* Strong attention to detail and a commitment to seeing tasks through to completion.
* The ability to manage multiple priorities and resolve issues efficiently in a fast-paced environment.
* Clear and professional communication skills, both written and verbal.
* Willingness to travel to customer sites in North America (up to 10%) during peak periods.
* Availability to work Monday to Friday (8:30 AM – 5:00 PM or 11:30 AM – 8:00 PM EST), with flexibility for occasional evening or weekend work for urgent issues.
Bonus Points If You Have
* Certifications in Microsoft Windows Server or MS SQL.
* ITIL certification.
* Experience with accounting or information systems.
* Experience with web application performance and scalability testing.
* Familiarity with computer hardware.
What We Offer You
* 3 weeks of vacation and 5 personal days.
* Comprehensive medical, dental, and vision benefits from day one.
* Company stock ownership and RRSP/401k matching programs.
* Lifestyle perks and wellness benefits.
* Remote work flexibility.
About Us
Creditron, established in 1994, is a leading provider of payment processing and receivables automation solutions for financial institutions, businesses, government entities, and non-profit organizations across North America.
With over 400 clients, including some of the world's most sophisticated companies, C...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 80000
Posted: 2025-11-26 08:13:21
