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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:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
San Angelo, Texas, United States of America
Job Description:
Johnson & Johnson is currently recruiting STEM2D interns for various functions at our site located in San Angelo, TX.
Candidates will be required to work onsite.
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
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 Summary:
Performs complex technical work including the design, manufacture and operation of structures, machines, and systems.
Responsibilities:
* Responsible for communicating business related issues or opportunities to next management level.
* Follow all Company guidelines related to Health, Safety and Environmental practices.
* Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
* Provides technical support for project planning, development, implementation, and modification; contributes extensively to engineering standards development, balancing corporate and customer needs.
* Exercises independent judgment on some details of work.
* Perform assignments that have complex objectives and require the investigation of multiple variables.
* Performs work which involves complex conventional types of plans, investigations, surveys, structures, or equipment with highly complex features for which there may be no precedents.
* Assignments usually include several of the following: equipment design and development, test of materials, preparation of specifications, process study, research investigations, and report preparation.
* Performs other duties assigned as needed.
Qualifications:
* Preferably currently enrolled in an undergraduate or graduate program in an engineering field.
* Lean...
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Type: Permanent Location: San Angelo, US-TX
Salary / Rate: Not Specified
Posted: 2025-03-27 07:12:30
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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:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Spring House, Pennsylvania, 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.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
OncoImmuno Internship Program Overview:
The OncoImmuno Summer Intern Program at Johnson & Johnson is a comprehensive learning and professional experience at one of the world’s leading health care companies.
This program is designed to build a future pool of talent/candidates with diverse backgrounds who may pursue and apply for other opportunities at Johnson & Johnson (https://www.careers.jnj.com/students) upon successfully completing their degree program.
The internship position is a full-time opportunity expecting to last 3 months (May 12 - August 15, 2025).
Based on business needs, internship positions may be available at various J&J locations throughout the US.
Including, but not limited to New Jersey, Pennsylvania, Massachusetts, and California.
We work on a “hybrid model” if you are NOT lab based. This means that you will be asked to report on site 3 times a week and can work remotely 2 times a week.
If you are selected for an internship position, you will work directly with your manager as your start date approaches to confirm your exact schedule.
Job Description
We offer an inclusive work culture that is open, innovative, and performance driven. As a summer intern in the OncoImmuno TR (Translational Research) Scientist role, you will be a member of a team dedicated to the research and development of new therapeutics and precision medicine strategies in various disease states in onco...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-27 07:12:28
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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 Documentation
Job Category:
Business Enablement/Support
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
Perform the principal duties of quality document clerk: 完成质量文件管理员的主要职责； ▪ Responsible for management, issuing and filing of internal and external documents; 负责管理、分发和保存内部及外来的文件； ▪ Responsible for control, retention and destruction of quality records; 负责质量记录的控制、保存和销毁； ▪ Responsible for purchasing and collection of external documents timely; 负责及时地采购和收集外来文件； ▪ Responsible of creating and modification of work instruction related to document control; 负责创建和修改与文件控制相关的工作指导书； ▪ Responsible for coordination of periodical review of documents.
负责协调文件的周期评审； ▪ Responsible for the trainings related with document management (if needed).
负责文件管理相关的培训（如需要）。 ▪ Other duties assigned by supervisor according to business requirement: 根据业务需要，由主管指派的其他职责：
Support the development and implementation of electronic systems related to document management or other duties.
支持与文件管理相关的电子系统开发和执行，或其他职责。 ▪ In accordance with DePuy Synthes Worldwide Quality strategy, participate in the development of the quality system and its day to day implementation: 按照 DePuy Synthes 全球质量战略，参与质量体系的发展及其日常实施： ▪ Participate in training to workshop employees and deploy on site the Quality philosophy based on FDA QSRs, ISO 13485 and NMPA requirements.
基于 FDA QSR, ISO 13485 和 NMPA 要求，参与车间员工的培训和现场质量管理； ▪ Ensure compliance to all GMPs requirements.
确保遵守所有的生产质量管理规范要求； ▪ Conduct internal quality audits as required.
按要求执行内部质量审核。 ▪ Perform all job duties in full accordance with: 执行所有工作职责完全按照： ▪ The J&J policies on Information, Assets protection, maintain password(s) confidential, protect critical Business Information.
信息、资产保护、维护密码、保护关键业务信息的强生公司政策； ▪ All J&J policies and local regulations.
强生公司所有的政策和地方性法规； ▪ The policies of the Health Care and Environmental programs.
卫生保健和环境规划的政策； ▪ The code of conduct policies.
行为守则政策。 ▪ Full responsibility and ownership (like all employees on site) for all audits support (including internal, Corporate, External, for Quality, H&S, Environment, etc.).
全权负责（和现场所有员工一样）所有的审核支持（包括质量相关的内审、总部审核、外审以 及环境、健康和安全相关的审核等）。
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-03-27 07:12:25
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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:
Supply Chain Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
Under and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Monitor all FGQA quality assurance functions.
* Establish and maintain appropriate documentation as required for Quality Assurance activities and the Quality Documentation Systems.
* Develop statistical sampling plans and perform process capability studies.
* Implement process control systems and provide technical support to process validations.
* Finish new test method protocol and report.
* Provide QS support in Product transfers and new products development.
* Assist in training new engineers, train technician and supervisors in process changes.
* Perform Complaint analysis investigation as needed.
* Participate in process/quality improvement projects.
* Support COGs initiatives.
* Responsible for following and administering safety.
* Compliance with safety policies and procedures.
* Follow J &J and Ethicon Records Management Policies for Convenience information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and the third-party vendor if applicable.
* Assist, review & approve non-conformances investigations & non-conforming product dispositions.
* Provide as needed, subject matter expert feedback on manufacturing process changes.
* Responsible for communicating business related issues or opportunities to next management level.
* Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
* Performs other duties assigned as needed.
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-03-27 07:12:20
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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:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
North Ryde, New South Wales, Australia
Job Description:
* Great Place to Work® Certified - 2024
* Competitive salary package, flexible work practices, award winning benefits
* Role based in Sydney
ABOUT THE COMPANY
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
Brief role intro…
THE OPPORTUNITY
We have an exciting opportunity for an Associate Clinical Specialist to join our NSW team supporting our dynamic Biosense Webster business.
As an Associate Clinical Specialist, you will provide expert clinical products and technical assistance to physicians and EP lab staff.
You will be assisting in the effective use of Biosense Webster’s systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during Cardiac Electrophysiology procedures.
RESPONSIBILITIES
* Attend all portions and successfully complete the ACS training program without exception, including co-travel case coverage.
* Collaborate and support team members and other internal and external partners.
* Understand the dynamics of an EP lab, including, but not limited to physicians, nurses, technicians, clinical, hospital administrators and staff.
* Prioritize and appropriately respond to requests in a high-stress environment.
* Additional duties include performing administrative work, including managing account documentation, compliance training requirements, expense reporting, and company system input.
ABOUT YOU
* Hold a Tertiary education within Medical Science, Biomedical Engineering or related fields.
* Possess a natural aptitude and passion for technology.
* Exhibit an ability to troubleshoot and remain calm under pressure.
* Be passionate about delivering exemplary patient outcomes.
* Love working as part of a c...
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Type: Permanent Location: North Ryde, AU-NSW
Salary / Rate: Not Specified
Posted: 2025-03-27 07:12:19
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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:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Adelaide, South Australia, Australia
Job Description:
* Great Place to Work® Certified - 2024
* Competitive salary package, flexible work practices, award winning benefits
* Role based in Adelaide
ABOUT THE COMPANY
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
Brief role intro…
THE OPPORTUNITY
We have an exciting opportunity for an Associate Clinical Specialist to join our SA team supporting our dynamic Biosense Webster business.
As an Associate Clinical Specialist, you will provide expert clinical products and technical assistance to physicians and EP lab staff.
You will be assisting in the effective use of Biosense Webster’s systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during Cardiac Electrophysiology procedures.
RESPONSIBILITIES
* Attend all portions and successfully complete the ACS training program without exception, including co-travel case coverage.
* Collaborate and support team members and other internal and external partners.
* Understand the dynamics of an EP lab, including, but not limited to physicians, nurses, technicians, clinical, hospital administrators and staff.
* Prioritize and appropriately respond to requests in a high-stress environment.
* Additional duties include performing administrative work, including managing account documentation, compliance training requirements, expense reporting, and company system input.
ABOUT YOU
* Hold a Tertiary education within Medical Science, Biomedical Engineering or related fields.
* Possess a natural aptitude and passion for technology.
* Exhibit an ability to troubleshoot and remain calm under pressure.
* Be passionate about delivering exemplary patient outcomes.
* Love working as part of a co...
....Read more...
Type: Permanent Location: Adelaide, AU-SA
Salary / Rate: Not Specified
Posted: 2025-03-27 07:12:17
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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:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Analyst II Clinical Data Manager to be in Raritan, NJ, Springhouse, PA, Horsham, PA or Titusville, NJ,
Purpose: The Analyst II Data Manager is a professional individual contributor role at junior level that provides oversight and accountability and/or executes data management activities and/or performs scientific data review for more than one trial of low to moderate complexity or for one high complexity trial.
The Analyst II Data Manager makes recommendations and influences decisions for specific trials or assignments.
This position analyzes and provides input into decisions with direction from manager or Data Management Leader (DML).
Work is received in broad terms.
Work is reviewed on an ongoing basis with Data Management Leader and the amount of instruction is limited
You will be responsible for:
* Take a leadership role with external suppliers, trial customers and other internal/external partners to establish, align and confirm data management and/or clinical data management expectations to the business for assigned trial(s) to include but not limited to:
+ Gather and/or review content and integration requirements for eCRF and other data collection tools.
o Establish conventions and quality expectations for clinical data.
+ Establish expectations for dataset content and structure.
+ Set timelines and follow-up regularly to monitor delivery of all data management milestones.
* Review clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
En...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-27 07:12:01
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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:
Inside Sales -- MedTech (No Commission)
Job Category:
Professional
All Job Posting Locations:
Anchorage, Alaska, United States, Belleville, Illinois, United States, Detroit, Michigan, United States, Fargo, North Dakota, United States, Idaho Falls, Idaho, United States, Indianapolis, Indiana, United States, Irvine, California, United States of America, Las Vegas, Nevada, United States, Madison, Wisconsin, United States of America, Portland, Oregon, United States, Riverside, California, United States, Salt Lake City, Utah, United States of America, Santa Clara, California, United States of America, Seattle, Washington, United States of America, Sioux Falls, South Dakota, United States, US019 MN Minneapolis - 800 Nicollet Ave
Job Description:
Johnson & Johnson MedTech Orthopaedics is recruiting for a VELYS Specialist, Clinical Experience in the U.S.
Capital and Digital Center of Excellence.
This is primarily based in the West – Alaska, WA, OR, ID, CA, NV, UT with consideration for North Central- IL, MI, MN, MT, ND, SD, WI
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
JNJ MedTech Companies offers an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials.
We are focused on our mission of developing innovative and comprehensive solutions that advance and inspire patient care and outcomes throughout the world.
The VELYS Clinical Specialists will focus on ensuring customer experience excellence for the digital surgery portfolio in the US. VELYS™ Digital Surgery is our platform of connected technologies leveraging data insights for our patients, surgeons and health care systems – pre-operatively, during surgical planning, and intra and post operatively. You can learn more information about VELYS Digital Surgery at www.velysdigital.com.
The VELYS Clinical Specialists will report directly to the Clinical Manager, Digital Surgery.
Main responsibilities
* Establish and maintain deep clinical knowledge of the VELYS suite of digital surgery products including: Orthopedic Robot, navi...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-27 07:11:52
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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:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, US054 PA Horsham - 200 Tournament Dr, US159 NJ Titusville - 1125 Trenton-Harbourton Rd
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 Analyst II, Clinical Data Manager to be located in Raritan, NJ, Titusville, NJ or Spring House, PA, Horsham, PA.
Purpose:
The Analyst II Clinical Data Manager is a professional individual contributor role at junior level that provides oversight and accountability and/or executes data management activities and/or performs scientific data review for more than one trial of low to moderate complexity or for one high complexity trial.
The Analyst II Clincial Data Manager makes recommendations and influences decisions for specific trials or assignments.
This position analyzes and provides input into decisions with direction from manager or Data Management Leader (DML).
Work is received in broad terms.
Work is reviewed on an ongoing basis with Data Management Leader and the amount of instruction is limited.
You will be responsible for:
* Take a leadership role with external suppliers, trial customers and other internal/external partners to establish, align and confirm data management and/or clinical data management expectations to the business for assigned trial(s) to include but not limited to:
+ Gather and/or review content and integration requirements for eCRF and other data collection tools.
+ Establish conventions and quality expectations for clinical data.
o Establish expectations for dataset content and structure.
+ Set timelines and follow-up regularly to monitor delivery of all data management milestones.
* Review clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization,...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-27 07:11:47
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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:
Cornellà de Llobregat, Barcelona, Spain
Job Description:
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
To maximize company product value through high scientific quality communication with Leading Specialists on a peer-to-peer basis.
Accordingly, to strategic lines of Medical Affairs Plan, the MSL is jointly responsible for achieving short-term and long-term company goals at local level.
To be a therapeutic area scientific expert, responsible for discussing our products, patients’ treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of Leading Specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders) and to be considered an internal and external trusted scientific counterpart.
MSLs should have their own Activity Plan and personal objectives.
The Individual Activity Plans must be based on the MSLs Country Activity Plan, which is aligned with the Medical Affairs Component of the relevant Brand Plans.
* To keep abreast of medical and scientific knowledge.
+ Continuous update on products, patient’s treatment trends, clinical activities and studies conducted within the therapeutic area in their region.
* Development and maintenance of a contact network with Leading Specialists.
+ Understand their needs, key value drivers, practical treatment patterns and scientific activities within therapeutic area
+ Communicate value of company products, incl.
clinical questionnaire discussions
+ Through scientific interactions, communicate medical benefits of products and contribute to foster innovative approaches
+ Represent the company within professional associations in the therapeutic area in cooperation with Medical Affairs/ Medical Education and other positions in the Medical Affairs Department
...
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Type: Permanent Location: Cornellà de Llobregat, ES-B
Salary / Rate: Not Specified
Posted: 2025-03-27 07:11:45
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Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Roche in 50 Worten:
Eine gesündere Zukunft.
Das treibt uns an, innovativ zu sein.
Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die benötigt wird.
Wir schaffen eine Welt, in der wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Das macht uns zu Roche.
Hauptverantwortlichkeiten:
Eine interessante Aufgabe im Bereich Diagnostics Operations – Particles Production.
Zu deinen Aufgaben gehört die Herstellung von essentiellen Einsatzstoffen auf Basis von verschiedenen Partikeln, die für diagnostische Testsysteme benötigt werden.
* Unter Einhaltung der Arbeits- und Umweltschutzbestimmungen sowie relevanten GMP-Regularien stellst du verschiedene Partikelprodukte nach bestehenden Herstellvorschriften.
* Hierbei bedienst/steuerst/überwächst du Equipment im Technikums- und großtechnischen Produktionsmaßstab.
* Du planst und koordinierst deine Arbeitsabläufe mit deinen KollegInnen, bestellst notwendige Einsatzstoffe, führst die Produktion durch und protokollierst deine Arbeit nach DIN EN ISO 13485.
* Inprozesskontrollen werden von dir anhand analytischer Verfahren (wie z.B.
Partikelgrößenbestimmungen, Konzentrationsanalytik, Bestimmung des isoelektrischen Punkts) durchgeführt und beurteilt.
* Darüber hinaus übernimmst du allgemeine Laborarbeiten wie z.B.
einfache Wartungsarbeiten, Spülen von Equipment, Dokumentation der Equipmentbelegung und des Equipmentstatus.
* Du arbeitest bei Troubleshootings, Validierungen und Qualifizierungen von Prozessen und Equipment mit.
Das Heben und Bewegen von Lasten bis zu 15 kg ist in seltenen Fällen erforderlich.
Wer Du bist:
Für diese Position bringst du die folgenden Qualifikationen mit:
* Du hast eine erfolgreich abgeschlossene Ausbildung zum Chemielaboranten (m/w/d), Chemikanten (m/w/d), CTA (m/w/d) oder eine vergleichbare Ausbildung oder bringst Berufserfahrung im angegebenen Umfeld mit.
* Du schätzt die Arbeit und Abstimmung im Team und unterstützt dieses in allen Belangen.
* Du besitzt Kenntnisse im Umgang mit SAP-Software.
* Du hast Erfahrung in der Durchführung von Batch Record Reviews und Stundenverbuchungen.
* Du bist vertraut mit der Zeiterfassung und verfügst über die notwendigen administrativen Fähigkeiten.
* Deine Freude an der praktischen Laborarbeit zeichnet dich ebenso aus wie dein handwerkliches Geschick.
* Du schätzt die Arbeit und Abstimmung im Team und unterstützt dieses in allen Belangen
Die Stelle ist auf 2 Jahre befristet.
(Bewerbung möglich...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-03-27 07:11:27
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Ardurrra is seeking a Land Use Planner to join our team in Nampa, ID or Meridian, ID!
Job Description:
We are seeking a highly motivated and experienced Land Use Planner to join our team.
In this role, you will be responsible for developing and implementing comprehensive land-use plans and strategies that support our client’s development goals.
You will also be responsible for coordinating the development of multiple projects from start to finish, ensuring that all projects are completed on time, within budget, and to the required quality standards.
The ideal candidate will have a strong understanding of local land use regulations, local planning principles, community engagement, and a passion for creating vibrant and sustainable communities.
Required Qualifications:
* Bachelor’s Degree in Land Use Planning or similar.
* 2+ years of experience in land use planning in the private or public sector.
* A minimum of 2 years of experience in a similar role, with a strong track record of successfully coordinating the development of land development projects.
* Excellent organizational skills, with the ability to manage multiple projects and priorities effectively.
* Strong understanding of local, state, and federal land use regulations and policies.
* Excellent communication, presentation, and interpersonal skills.
* Strong interpersonal and communication skills, with the ability to effectively communicate with a wide range of stakeholders, including engineers, contractors, cities, government agencies, surveyors, attorneys, and various departments within many municipalities.
* Ability to effectively manage multiple projects and meet deadlines.
* Strong problem-solving and decision-making skills, with the ability to identify and manage project risks and issues effectively.
* Ability to work as part of a team, with project managers, engineers, surveyors and other stake holders.
Key Responsibilities:
* Conduct site analyses and research to determine the feasibility of proposed land-use projects
* Prepare and present land use applications and development proposals to clients, government agencies, and community groups.
* Route plats and other necessary project documentation.
* Participate in public meetings and community engagement events to gather feedback and build support for development projects.
* Work to ensure projects meet zoning and other regulatory requirements.
* Collaborate with other departments to ensure projects are completed on time and within budget.
* Stay current on land use planning trends, laws, and regulations.
* Attend professional development opportunities to continue expanding your knowledge and skills.
We offer a competitive compensation and benefits package, as well as opportunities for professional growth and development.
If you are passionate about land use planning and have a track record of success, we encourage you to apply.
...
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Type: Permanent Location: Meridian, US-ID
Salary / Rate: Not Specified
Posted: 2025-03-27 07:08:16
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ERM’s Climate Risk and Opportunity Advisory (CROA) team, within our broader Corporate Sustainability & Climate Change (CS&CC) function, is growing quickly.
We are looking for consultants to support us in helping our clients shape and deliver on their climate strategies and disclosures.
There is a significant opportunity for individuals to progress within the organization, to take increasing responsibility for managing our work within the climate change space and developing market-leading offerings to meet our clients’ needs.
This role will focus on quantifying the financial implications of climate risk, but there are opportunities for the candidate to contribute to all of our team’s work across the climate change space (including relating to the low-carbon energy transition and net zero).
More details of the role, as well as the skills required to fulfil it, are detailed below.
Role Description & Key Responsibilities:
As a member of the Climate Risk and Opportunity Advisory Team, you will:
* Apply quantitative methodologies to climate risk and opportunity assessments, including financial statement analysis, discounted cash flow modelling, cost-benefit analysis, and uncertainty analysis such as Monte Carlo simulations.
* Engage directly with corporate clients, including senior leadership, to provide education on climate-related topics, and present your own analytical work and defend quantitative results.
* Build templated quantitative methodologies for climate risk estimation that can be leveraged on climate projects.
* Incorporate a wide range of data sources into your analyses including corporate financial data, geospatial climate data, academic research and industry-specific reports.
* Support the delivery of client deliverables by working with team members across the business.
* A key aspect of this will be to communicate the findings in a digestible way including developing client curiosity regarding how they start their journey to transitioning to a low carbon economy.
* Support business development and sales-related activities, including helping senior colleagues to draft client proposals and develop new offers.
* Contribute to ERM’s innovation and knowledge-sharing through ad-hoc involvement in thought leadership, internal newsletters, learning sessions, amongst other initiatives
PERSON SPECIFICATION
Well-placed candidates will match some or a significant part of the specification below:
Required:
* Background Academic and professional experience in climate change / sustainability as well as finance/economics. Understands the fundamentals of why climate change is happening, how it will start to affect business models/strategy/company revenue, Capex, Opex and familiar with the concepts of decarbonization & net zero pathways.
* Motivational Fit – Produce high-quality client-ready deliverables, can work independently, team player, demonstrates critical thinking and is comfo...
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Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2025-03-26 07:31:41
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General Summary
Maintains and distributes the sanitation chemicals and tools used in the production facility.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
1.
Mixes, samples, stages, and distributes all chemicals for usage according to company guidelines.
2.
Daily/weekly inventory of all chemicals.
3.
Maintains close relationship with chemical supplier to ensure the appropriate inventory of chemicals, dispensing equipment, parts and supplies.
4.
Assists with producing weekly chemical usage reports.
5.
Maintains the proper labeling of all chemical containers and point-of-use jugs, buckets, foamers, and door foamers according to company guidelines.
6.
Ensures proper storage of chemical containers, cleaning tools and brushes.
7.
Maintains the organization and cleanliness of the sanitation storage areas, chemical rooms, jugs, buckets and tanks.
8.
Maintains operable condition of all chemical dispensing equipment, foamers, door foamers, and pumps.
Troubleshoots any issues and repair leaks/malfunctions.
9.
Follows company safety guidelines and Good Manufacturing Practices.
10.
Regular attendance and punctuality are required due to working with people, items and equipment that are at the facility.
Job Specifications
1.
Sanitation experience is preferred.
2.
English/Spanish bilingual is a plus.
Working Conditions
1.
Refrigerated food manufacturing plant.
2.
The environment may be wet or dry and temperatures may range from 25°F to 110°F.
3.
Frequent exposure to hazardous material and waste.
4.
Repetitive lifting, kneeling, and bending with items in excess of 60 lbs.
is required.
5.
Repetitive hand, wrist, and finger activities.
6.
Production demands may require overtime and/or evening or weekend scheduling.
Compensation
$19.40 – $24.25 Hourly/Non-Exempt
Recipe for Success
Reser’s is the leading provider of fresh refrigerated deli salads, side dishes, and prepared foods for the supermarket, club store, and food service industries.
Family owned and operated, Reser’s has been a proud sponsor of good times at racetracks, picnics, B...
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Type: Permanent Location: Pasco, US-WA
Salary / Rate: Not Specified
Posted: 2025-03-26 07:28:43
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
$2,500 sign-on bonus eligible!
Why Work at Elwood?
The Elanco Elwood, Kansas facility was acquired from Kindred Biosciences in 2021 which offers a strong pipeline of innovative drugs for companion animals within the monoclonal antibody space.
Working at a monoclonal antibody start-up facility in Elwood, Kansas presents an exciting opportunity to contribute to cutting-edge research: Monoclonal antibodies are an innovative type of biologic drug that can target specific molecules in the body to treat a variety of diseases, including cancer and autoimmune disorders.
Working at a start-up facility that is developing these drugs is an opportunity to be on the forefront of medical research and contribute to developing treatments that can have a significant impact on pets' lives.
Your Role:
An operator is responsible for performing and documenting all tasks and activities associated with biologics manufacturing at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility.
* Execute and monitor critical processes for mAb manufacture such as media and buffer preparation, upstream expression, downstream purification, formulation, fill/finish, and/or secondary packaging.
* Operate in a USDA / FDA / EMA cGMP regulated environment, maintaining strict adherence to all applicable regulations.
* Accurately follow SOP’s and batch production records in operation of production equipment, performance of processing steps, and execution of daily tasks.
* Perform aseptic manipulations and demonstrate knowledge and experience of aseptic techniques.
* Interface with the Quality Control department to submit in-process samples and coordinate environmental monitoring during key process steps.
* Assemble, prepare, and maintain process equipment including, but not limited to biological safety cabinets, incubators, bioreactors, chromatography skids, columns, tangential flow filtration systems, pumps, fill/finish units, labelling/packaging units and ancillary equipment.
* Identify and support the implementation of process improvement ...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 24
Posted: 2025-03-26 07:25:43
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Production Operator - API
The Production Operator is responsible for preparing, executing, and cleaning/turnover of production processes in poultry vaccine production.
All tasks are performed in accordance with internal and external guidelines.
Your Responsibilities:
* Egg Handling (egg receipt, traying, disinfection processes, transferring eggs) and egg derived processes & tissue culture (candling, incubation, inoculation, harvest, inactivation)
* Centrifugation, concentration processes, and filling operations (product emulsification, liquid filling processes, lyophilization)
* Process and equipment preparation and process cleaning/disinfection activities including washing, wrapping, and sterilizing of glassware and equipment, loading/unloading autoclaves and disinfecting room surfaces and equipment.
* Ensuring appropriate number of materials (chemicals, consumables, etc.) are available
* Use of electronic systems (e.g.
SAP) to stage materials
What You Need to Succeed (Minimum Qualifications):
* High School Diploma or equivalent
* Ability to perform routine, repetitive tasks with moderate to limited degree of supervision.
* Ability to perform duties according to established SOP's, production records and company safety procedures.
* Complete training on time to maintain a current and up to date learning plan.
What Will Give You the Competitive Edge (Preferred Qualifications):
* Understands and practices proper aseptic technique and biosecurity measures
* Ability to concurrently completes documentation and follows established protocols
Additional Information:
* Shift: Monday-Friday, 7am-3:30pm
* Must maintain procedural conformance during all production hours including and not limited to weekday and weekend operations. This may include notifying supervisors/support staff via phone/email/teams to escalate findings of product non-compliances or equipment failures.
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, r...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: Not Specified
Posted: 2025-03-26 07:25:41
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Grow your career internally at Elanco, our best talent comes from within!
Your Role: Process Operator – Product Finishing
As a Process Operator for Product Finishing, you will play a key role in the granulating, blending, and bagging of animal health products.
In this role, you'll be responsible for meeting departmental goals, ensuring quality, quantity, and cost targets while maintaining safety, compliance, and industry standards.
This posting will offer a one-time sign on bonus of $2,500!
Your Responsibilities:
* Operate large-scale processing equipment and troubleshoot issues as they arise.
* Drive a fork truck and handle 60-pound bags as part of routine operations.
* Ensure all production operations align with cGMP and ISO 9000 standards.
* Follow proper documentation, verification guidelines, and safety procedures.
* Suggest and implement safety and process improvements to enhance efficiency.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma or equivalent.
* Required Experience: Experience operating industrial processing equipment and working in a manufacturing environment.
* Top 2 skills: Troubleshooting and problem-solving skills
What will give you a competitive edge (preferred qualifications):
* Familiarity with fork truck operation.
* Experience in the animal health or related industry.
* Previous experience with cGMP and ISO 9000 standards.
* Strong initiative and ability to work independently.
Additional Information:
* Location: Clinton, IN Manufacturing Site\
* 12-Hour Rotating Shift (Days/Nights)
This position is a fixed duration employee with a one-year contract, annually renewable for up to 4 years with a potential for a full-time position, based on individual performance and business needs.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work env...
....Read more...
Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-26 07:25:37
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Background:
At Elanco, we advance our vision of food and companionship enriching life by developing innovative solutions that protect and enhance animal health.
Since 1954, Elanco has been working to empower veterinarians, food producers, and all those concerned with animal health with the tools needed to help animals live healthy lives.
Job description:
There is an exciting opportunity to join a dynamic process development team responsible for development and scale up of new biopharmaceutical and vaccine products.
The Biopharma technical development team works collaboratively with an inclusive culture to deliver innovation for Elanco.
The Research Scientist is responsible for providing technical and scientific expertise for process development and commercialization activities of new drug substances/products with an emphasis on downstream purification processes.
The individual will be expected to lead downstream process development, scale up, technical transfers, process implementation, and material delivery activities for IVP or CT supply and registration.
Additionally the role will support process validation-related activities.
The role is focused on ensuring that a robust manufacturing process is developed according to quality by design and ‘end in mind’ principles.
The research scientist is expected to be hands on but will provide technical direction, coaching and mentoring to scientists.
The holder of the position is regarded as a technical expert for R&D Elanco globally and will work collaboratively with management and global project groups in line with site, functional and corporate business goals.
Key Responsibilities:
* Provide technical leadership for downstream development (protein purification) from early through late phase large molecule projects, ensuring phase appropriate technical development and collaborating closely with relevant functions.
* Provide technical leadership/expertise for delivery of process development projects based in the laboratories and pilot plant areas.
+ Ensure a sound laboratory/p...
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Type: Permanent Location: Liverpool, GB-LIV
Salary / Rate: 72000
Posted: 2025-03-26 07:25:35
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SBA Communications is a leading independent owner and operator of wireless communications infrastructure, including towers, buildings, rooftops, DAS and small cells.
We offer a competitive benefits and compensation package and are looking for team members who will thrive in our dynamic environment.
* We welcome your interest in SBA.
Let us know a little about you by checking all that apply:
* You are a self-starter.
* You are resourceful and thrive in a fast-paced environment.
* You have a strong work ethic.
* You are passionate and driven to achieve results.
* You are a team player who enjoys working in a collaborative environment.
* You continuously challenge yourself to find innovative ways to improve.
You may be a perfect fit.
At SBA, we operate with the highest sense of integrity and commitment to quality.
We focus on achievement and operate with responsiveness, timeliness and accountability.
Our culture of excellence incorporates working collegially, where every team member can contribute meaningfully and make a difference.
If you are ready to make an impact, join our team!
Your Next Career Opportunity – Business Intelligence Intern
Support the office in general.
Implement administrative policies alone or with other team members, performing the following duties.
What You Will Do – Primary Responsibilities
* Mobile app development.
* Create databases using vendor data.
* Query the SBA database using SQL/Excel to determine carrier frequencies.
* Interpret data of low to medium complexity in order for it to be entered into the research database.
* Assist with miscellaneous administrative duties within the department.
What You’ll Need – Qualifications & Requirements
* H.S.
Diploma/GED plus College Degree seeking student; or recent graduate and ....Read more...
Type: Permanent Location: Boca Raton, US-FL
Salary / Rate: 23
Posted: 2025-03-26 07:18:22
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IFP Marketing Manager (12 months contract)
Job Description
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 this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Role Overview & Primary Accountabilities:
* Responsible for planning, developing and implementing various offline/online marketing initiatives/campaigns, be it in the form of brand building, lead generation, nurturing and Key Account Management program/loyalty program or promotion program that can strengthen brand image, generate leads and loyalty to support sales achievement
* Establish good relationships and maximize cooperation with organizations/associations, KOLs, and other partners to get good support and coverage
* Collaborate with product management, sales, and other teams to define product positioning, messaging, and value propositions
* Develop an Annual Business Planning with sales team and lead execution of Marketing program to achieve business objectives
* Create integrated planning and materials to support communication and product promotion activities starting from distribution partners to customers
* Manage the product lifecycle from launch to end-of-life, ensuring continuous market relevance and customer satisfaction.
* Oversee the creation of marketing materials, including brochures, presentations, and case studies.
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 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 love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have pur...
....Read more...
Type: Permanent Location: Jakarta, ID-JK
Salary / Rate: Not Specified
Posted: 2025-03-26 07:17:45
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If you are an expert EHS /Facility Supervisor looking for an opportunity to grow, Emerson, has an exciting opportunity for you! Based in Olive Branch, MS, you will be responsible for leading the Warehouse Facility and powered equipment maintenance, along with Environmental Health & Safety functions to ensure compliance with all applicable environmental, health and safety regulations, policies, & procedures.
If you love working in a fast -paced environment and you have demonstrated mechanical and electrical aptitude, this is the job for you!
Ready to make your mark and embark on an exciting journey with us? We can't wait to hear from you!
In this Role, Your Responsibilities Will Be:
EHS Job Responsibilities:
* Implement, complete, and ensure adherence to Company's Environmental Health and Safety policies and procedures
* Ensure all required company and regulatory reporting requirements are submitted timely
* Develop non-EHS site personnel to support implementation of EHS programs
* Assist in the management of workers compensation
* Collaborate with regulatory agencies (OSHA, EPA, State/Local Regulators)
* Responsible to lead management personnel in the investigations of facility incidents and complaints regarding unsafe working conditions and practices. Help identify an immediate solution, the root cause, and supervise corrective actions to completion.
* Conduct routine safety observations to ensure compliance with regulatory agencies, company environmental, health, and safety policies, procedures and practices.
* Represent management during EHS Meetings along with the other facility personnel.
* Serve as a facilitator for hourly and supervisory employee EHS and New Hire training.
* Serve as an advisory Member of the Safety Committee and adhere to OSHA regulations.
* Performs other EHS duties as required by management.
Facilities Responsibilities:
* Schedule and lead preventative maintenance for all machining, assembly and other equipment located in the Olive Branch facility
* Provide maintenance support for the entire facility including management of utilities, HVAC, fire suppressant systems, etc.
* Plan and lead overall maintenance and special projects.
* Responsible for ensuring facility atmosphere,5S and hygiene compliance.
* Assist in upgrading existing equipment to safer efficient and productive alternatives.
* Establishes and maintains specific preventive maintenance schedules on equipment and facilities.
* Responsible for managing and coordinating outside vendors when onsite.
* Performs other facility duties as assigned.
WHO YOU ARE:
You build and implement plans that allocate resources precisely.
You analyze multiple and diverse sources of information to define problems accurately before moving to solutions.
You marshal resources (people, funding, material, support) to get things done.
FOR THIS ROLE, YOU WILL NEED:
* Bac...
....Read more...
Type: Permanent Location: Olive Branch, US-MS
Salary / Rate: Not Specified
Posted: 2025-03-26 07:17:40
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Associate Finance Manager - Sam's Club
Job Description
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 this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Position Summary:
In this fast paced, highly interactive role, you will contribute to the achievement of net sales, profit and share objectives by partnering with our Customer Development team in the development and execution of effective and efficient customer business plans while providing the team with timely financial analysis and insights to facilitate sound business decisions.
The Associate Finance Manager – Customer Development role provides you an opportunity to influence price and promotional activities with our major strategic customers, in essence, acting as CFO to the Customer Development team.
The position reports directly to the Sr.
Finance Manager – Walmart and is the senior financial advisor to the Director of Sales for the supported team.
Customer Development teams are typically located at remote office sites; therefore, the incumbent is generally the senior finance representative in the field.
Key customers include Customer Development Leaders and Team Members, Logistics Leaders, Headquarter Sales Leaders, Business Service Leaders, and Staff Business Analysis.
You will provide all the financial support for the customer team, supporting the achievement of business results by assisting in effective business and financial planning and by participating in the development and implementation of strategic and tactical operating plans.
A principal activity of this position is to ensure that business and financial planning processes meet business unit and corporate needs, and, through analysis, that plans, and programs are accurately presented and evaluated. It starts with YOU.
In this role, you will:
* Provide the Customer Development team with financial advice and counsel on all pertinent business matters by supplying ongoing, timely, and meaningful financial analysis, both routine and as needed, of business results, trade promotion, and other expenses.
Information provided should include both the impact to K-C and to the Customer.
* Provide external information to the Customer where required in support of joint annual planning, budgeting, and event analysis.
The level of support is dictated by the specific need of the customer.
* Coordinate the Integrated Customer Business Plan process to ensure timelines are met and plans are delivered.
Be the central point of contact for the forecasting of Volume, Sales and Trade Promotion for long range planning.
Identify opportunities for pr...
....Read more...
Type: Permanent Location: Rogers, US-AR
Salary / Rate: Not Specified
Posted: 2025-03-26 07:17:36
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Logistics Product Owner
Job Description
Kimberly-Clark is seeking a Product Owner to join our Digital Technology Solutions (DTS) department, a role critical to driving our digital transformation initiatives.
As a Product Owner, you are at the heart of maximizing product value, responsible for articulating and prioritizing the product backlog items for a Scrum team.
You will own the product backlog and ensure that the team builds the right product increments in the most efficient manner.
Your key responsibilities include executing the product vision, managing the backlog, and collaborating closely with multidisciplinary teams to develop innovative solutions that address customer needs and align with business goals.
You will work in an open, collaborative, and approachable manner with the product team (software engineers), inspiring optimal solutions that solve real customer problems and challenging the team to discover the smartest, most efficient solutions.
The ideal candidate should have a strong analytical mindset, excellent communication skills, and the ability to lead through influence.
You are expected to be proactive, enthusiastic about driving technological advancements, and adept at navigating complex challenges in a dynamic environment.
This position offers the opportunity to significantly impact product direction, ensuring operational efficiency and enhanced customer satisfaction.
As a Product Owner at Kimberly-Clark, you will play a crucial role in ensuring that our technology solutions are not only effective but also innovative and aligned with the strategic objectives of the company.
This is an excellent opportunity for a leader looking to make a meaningful impact in a global corporation while shaping the future of our digital operations.
Kimberly-Clark has an amazing opportunity to continue leading the market, and DTS is poised to deliver compelling and robust digital capabilities, products, and solutions to support it.
This role will have substantial influence in this endeavor.
If you are excited to make a difference applying cutting-edge technologies to solve real business challenges and add value to a global, market-leading organization, please come join us!
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 role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
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 prod...
....Read more...
Type: Permanent Location: Sao Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-03-26 07:17:28
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SUMMARY
The California Department of Public Health (CDPH) and Heluna Health invite applications for a full-time Senior Microbiologist in the CDPH Viral and Rickettsial Disease Laboratory (VRDL).
We are a team that works hard, appreciates each other, and strives to build a culture of equity, care, and participation in decisions that affect our work. The candidate will support efforts to enhance surveillance for viral vaccine preventable diseases and rickettsia by assisting with the development and optimization of real-time PCR detection methods and NGS sequencing protocols for measles, mpox, and hepatitis A viruses and Rickettsia.
The Senior Microbiologist will also support other NGS activities at CDPH related to sequence generation and data analysis for phylogenetics, genomic epidemiology, and other characterizations of vaccine preventable viruses and rickettsial pathogens.
The ideal candidate should have a solid laboratory background in molecular microbiology (virology preferred), laboratory experience in metagenomic and targeted sequencing methods, and molecular assay design (e.g., PCR, real-time PCR).
Knowledge of bioinformatics and pathogen genomics is desired.
The incumbent is also expected to stay up to date with scientific literature and contribute to the laboratory academically by assisting with abstracts and manuscripts.
The salary range for this position is $93,603.60 to $110,244.24 annually depending on experience/qualifications.
A cover letter and resume must be submitted with your application.
If hired for this position, applicant will be required to provide proof of full vaccination for COVID-19 prior to the start date or have a valid religious or medical reason qualifying the applicant for an exemption (that may or may not require accommodation).
ESSENTIAL FUNCTIONS
* Design, validate, and implement complex molecular methods for the detection and characterization of diseases of public health importance, including measles, mumps, mpox, and hepatitis A viruses and spotted fever group Rickettsia, with particular emphasis on implementation and use of whole genome sequencing technologies.
* Organize and perform scientific research on viral pathogens and rickettsia using real-time PCR, end-point PCR, and NGS methods in collaboration with other research scientists.
* Work as part of a research team to develop and implement new workflows, molecular assays, and analyses for genomic characterization of pathogens.
* Maintain organized and detailed laboratory records and assist with scientific writing such as SOPs, reports, posters, and manuscripts.
* Adhere and contribute to Quality Assurance protocols and standards.
* Follow safety and quality control procedures in the handling of hazardous biological and chemical materials.
* Participate in training of other technical staff and scientists.
* Perform other related duties as assigned.
JOB QUALIFICATIONS
* Proficiency in molecular bio...
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: 96603.6
Posted: 2025-03-26 07:16:48
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SUMMARY
The California Department of Public Health (CDPH) and Heluna Health invites applications for a full-time Research Associate in the CDPH Viral and Rickettsial Diseases Laboratory (VRDL).
In this role, the candidate will work collaboratively and cross-functionally with colleagues to develop molecular methods (PCR) and Next-Generation Sequencing (NGS) workflows that support the surveillance, diagnostics, and research efforts of the California Department of Public Health.
At the VRDL, this work directly supports laboratory testing for SARS-CoV-2, enteroviruses, adenoviruses, and other viral pathogens using molecular methods (PCR) and next-generation sequencing.
The incumbent should be experienced in working with microorganisms (specifically viruses) and using standard laboratory precautions.
Maintaining an organized, neat, and clean work environment, working well in a team environment, and being organized and detail-oriented are essential.
Additional duties include scanning submittal forms, filing patient records, and preparing shipping materials.
The position is in Richmond, CA.
The hourly range for this position is $23.00 to $29.37 per hour depending on experience/qualifications.
Must submit a resume with the application.
This position may be required to work flexible hours and weekends/holidays.
ESSENTIAL FUNCTIONS
* Assist with SOP development for PCR and NGS for viral pathogens.
* Accessioning samples into database (Access and LIMS), tracking specimens in storage, processing samples (nucleic acid extraction), and storing of laboratory specimens for testing and shipping.
* Check in and process samples for testing using pipetting devices.
* Organize and maintain archive repositories for different sample types.
* Autoclave and disinfect laboratory materials containing potentially infectious agents; dispose those materials following autoclaving/decontamination procedures.
* Maintain QA and QC records for the laboratory, when necessary.
* Prepare reagents and media for specimen processing and extraction.
* Perform data entry for patient information, routing samples for testing, and tracking.
* Use of Microsoft Word suite programs such as Microsoft Word, Excel, and Access.
* Other duties as necessary in the laboratory or office when deemed necessary.
* Reports laboratory test results using StarLIMS.
* Ensures adherence to Quality Assurance protocols and standards.
* Maintains laboratory records of specimens, virus stocks, and reagents.
* Performs, interprets, and reports surveillance and reference testing for viruses according to SOPs.
* Performs other related duties as assigned.
JOB QUALIFICATIONS
* Knowledge and experience with laboratory work environments (BSL-2 minimum), sterile technique, and molecular techniques are required.
* Experience with standard precautions for working with potentially infectious clinical specimens, particular...
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-26 07:16:48
