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Dakis permet aux détaillants et aux laboratoires d'impression d’opérer efficacement en magasin, en ligne et à peu près partout où ils peuvent vendre.
Entrez dans l’action en tant que gestionnaire de produit et jouez un rôle de leadership pour planifier et développer la nouvelle solution de Commerce Unifié pour la vente au détail.
Rejoignez une entreprise établie au cœur d'une Start-Up.
Mission principal:
Vous êtes responsable de la planification et de l'exécution du développement de produit tout au long du cycle de vie du produit, y compris: la définition de la vision du produit, la collecte et la priorisation des exigences des produits et des clients, et de travailler en étroite collaboration avec l'équipe de développement logiciel et de conception UI / UX pour assurer le développement du produit en temps opportun et de manière à ce que les objectifs de satisfaction client soient atteints.
En bref, stratégie, exécution et compréhension de l'utilisateur.
Description du poste et responsabilités:
* Travailler avec les principales parties prenantes pour affiner la vision du produit, définir les fonctionnalités et la feuille de route du produit, et pour gérer les priorités
* Être un expert en ce qui concerne le produit, la voix du client et de la concurrence, et incorporer l'apprentissage des utilisateurs dans l'entreprise pour améliorer davantage la stratégie et le produit
* Fournir une approche agile et une documentation contenant les fonctionnalités avec leur niveau de priorité et une justification correspondante
* Développer des histoires, des personas et des diagrammes de flux pour soutenir le développement de votre projet
* Bon jugement et capacité à présenter des options aux parties prenantes pour obtenir l'adhésion à vos solutions et plans proposés
* Jouer un rôle de leadership pour guider l'équipe de développement logiciel et de conception UI / UX et assurer une livraison rapide dans un processus de développement agile
* Traduire les exigences opérationnelles en exigences techniques bien définies
* Responsable de l'établissement et du respect des délais de développement définis avec le responsable du développement technique.
* Documenter, communiquer et former les équipes inter-fonctionnelles sur les nouvelles fonctionnalités et versions
* Documenter les nouvelles fonctionnalités
* Agir en tant que leader dynamique au sein de l'entreprise.
En tant que chef de produit senior, vous comblez l’écart entre la vision du fondateur et les produits de l’entreprise.
Vous facilitez une bonne communication entre vous, les dirigeants et l'équipe de développement de produits.
Principales qualifications et compétences souhaitées:
* 3+ années d'expérience en tant qu'analyste d'affaire ou chef de produit
* 3+ années d'expérience dans un emploi sur le marché SaaS
* Succès avéré dans la définition et le lanc...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 95000
Posted: 2025-03-24 07:04:46
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
Janssen Research & Development, L.L.C., a member of the Johnson & Johnson Family of Companies, is currently recruiting for a Drug Product Development & Delivery Co-Op (Summer 2025) for our site located in Malvern, PA for 6 months.
The candidate will be on site 5 days a week.
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/.
Here, your career breakthroughs will change the future of health, in all the best ways.
And you’ll change, too.
You’ll be inspired, and you’ll inspire people across the world to change how they care for themselves and those they love.
Amplify your impact.
Join us!
The Summer Intern will support activities related to the large molecule (therapeutic proteins, vaccine, CAR-T, or gene therapy) formulation development, process development in support of fill-finish activities, and/or related pharmacy studies (pharmacy manual studies including drug product design, development of Investigational Product Preparation Instructions)
Responsibilities include but are not limited to:
* Leading the execution of experiments related to drug product process development.
* Evaluate pumping and filtration technologies for pharmaceutical drug product processes.
* Develop and optimize unit operations such as mixing, filtration, and pumping for parenteral drug products.
* Collecting, recording, interpreting, and presenting experimental data appropriately
* Identifying and presenting relevant literature to the project team
* Coordinating testing schedules, presenting results, and authoring reports
* Communicating progress to supervisors
At the culmination of the internship, the intern will have gained:
* Exposure to the pharmaceutical industry
* General knowledge of drug product formulation and process ...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-24 06:57:45
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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 Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
San Lorenzo, Puerto Rico, United States of America
Job Description:
Job Summary
Reports to the Quality Team Leader or Designee, with the objective of maintaining high Quality Standards for Product Quality Control and operations compliance with regulatory requirements.
Conducts routine physical inspection procedure to in-process material, as well as finished goods, as needed.
Inspection involves the use of skilled specifications and established quality standards.
Performs audits to ensure product and processes comply with requirements.
Responsibilities
Under the direction of the Quality Team Leader or designee and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position will require someone who:
* Maintains high Quality Standards for Product Quality Control and operations compliance with regulatory requirements.
* Conducts routine physical inspection, testing, or evaluation to ensure quality of products according to current specifications/procedures.
* Performs product and process audits.
* Notify any product or process non-conformance and escalates as appropriate.
* Segregates and inspects Finished Goods samples and Retain Samples according to the requirements.
Delivers samples to Finished Goods QA Lab if needed.
* Performs data analysis and executes final disposition of the material as required.
* Performs batch records review accordingly with compliance requirements and complete record retention process.
* Maintain knowledge of all procedures, change to specifications and new regulations related to their areas of responsibility.
* Ensures on-time completion of assigned trainings.
* Support associates on defect awareness and specifications requirements.
* Support validation activities as required.
* Train new Technicians in Quality Assurance duties and responsibilities as required.
* Comply with all environmental, safety and occupational health policies (i.e., ISO14001 & OSHAS 18001).
* Perform environmental particulate monitoring as required.
* Comply with the OPCERT program for the certification of manufacturing associates.
* Evaluate and approve control and disposition of material to determine if it is accordi...
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Type: Permanent Location: San Lorenzo, US-PR
Salary / Rate: Not Specified
Posted: 2025-03-24 06:57:13
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
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: Manufacturing Manager
As a Manufacturing manager, you will lead production personnel, processes, and materials while ensuring compliance with internal and external regulations.
Success requires strong interpersonal, communication, and analytical skills to drive performance and achieve business objectives cross-functionally.
Your Responsibilities:
* Implements and sustains Operational Excellence initiatives and best practices throughout daily operations, fostering continuous improvement and efficiency.
* Leads area Process or Steering Teams, develops and monitors production schedules, ensuring compliance with schedules, manufacturing directions, Standard Operating Procedures (SOPs), Outlines of Production (OOPs), and all other relevant guidelines.
* Assigns accountability, addresses performance issues, and provides regular feedback.
Ensures team members possess the necessary training and expertise to perform their duties proficiently.
Acts as the first point of contact for grievances, administers disciplinary actions, and keeps Operations Management and HR informed.
* Manages the department budget, develops mid to long-term resource requirement plans, and makes recommendations to Operations Management regarding capital investments and equipment needs.
Monitors attendance, overtime usage, and approves timecards.
* Cultivates a safe work environment ensuring team members have adequate resources and comply with all safety standards.
Leads investigations into process deviations and non-conformances, ensuring appropriate documentation and resolution.
Oversees that all production records are completed correctly and in a timely manner.
What You Need to Succeed (minimum qualifications):
* BS Degree in Science (preferably Biology or Microbiology) or Engineering, or equivalent experience
* Demonstrate strong leadership and ability to work collaboratively across diverse teams.
What Will Give You the Competitive Edge (preferred qualifications):
* Some experience with SAP, JMP, Microsoft Visio and creation of pers...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: 122000
Posted: 2025-03-23 07:40:28
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Technician
The position will include routine testing of in process antigens and final product samples for the release of veterinary vaccines. The individual will be responsible for ensuring all methods are performed as written and filed with regulatory agencies and standard operating procedures.
Your Responsibilities:
* Perform required tests for bulk antigens, final products, and raw materials, as well as other procedures necessary to support company and laboratory objectives to meet specified timelines.
* Maintain aseptic laboratory technique at all times and ensure accuracy of test results through precision and attention to detail.
* Maintain accurate and concurrent testing records and ensure compliance with Company SOPs and specifications, USDA, and cGMP regulations. Assist with updating, writing, and maintaining SOP’s, bench records and data entry for the department.
* Environmental monitoring of clean rooms and personnel: assisting in and/or performing microbial and particulate tests (air sampling).
* Provide effective training as requested, confirming that individuals are trained on the procedure at hand and all required training documentation has been completed.
What you need to succeed (minimum qualifications):
* High School Diploma or equivalent required.
* Experience in working in a team environment and handling multiple tasks simultaneously.
* Proficient in Microsoft Word and Excel, capable of using a controlled informatics system.
What will give you the competitive edge (additional preferences):
* Bachelor of Science degree in Microbiology, Virology, Bacteriology, Biology, or related field
* Minimum of four (4) years of laboratory experience.
* Fundamental experience in cell culture, viral and/or bacterial propagation.
* Experience in biotechnology and aseptic technique.
Other Information:
* Location: Winslow, ME (Onsite)
* Shift: Monday-Friday, 7am-3:30pm (evening, weekend, and holiday hours may be required)
* Must b...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: 27.12
Posted: 2025-03-23 07:40:23
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General Summary: Under limited supervision, oversees the health and safety of Reser’s employee personnel and plant property.
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.
Principal Duties and Responsibilities
1.
Manages and Administers health and safety programs, including environmental policies in accordance with State and Federal OSHA compliance.
2.
Engages in promoting a Safety culture within the plant and the company.
3.
Manages and administers safety programs and policies throughout the plant.
4.
Develops and provides safety related resources and training.
Maintains related tracking documentation (LOTO, Powered Trucks, Confined Space, Machine Guarding etc.).
5.
Manages Accident Investigation and Root Cause Analysis – workplace injury/property damage.
6.
Advises and assists employees in adherence to company and governmental safety standards.
7.
Administers employee safety training (company LMS platform) and provides specific ‘Train-the-Trainer’ coaching.
8.
Manages plant safety committee activity and meetings.
9.
Conducts safety audits and observations both formal and informal.
10.
Partners with the PSM manager on environmental compliance and training (Anhydrous Ammonia)
11.
Ongoing communication with plant management teams.
12.
Works with Insurance companies, Loss Control representatives and local contractors to ensure EHS best practices.
Job Specifications
1.
3+ years’ experience of Occupational Health and Safety preferably in the food/ manufacturing industry is required.
2.
Bachelor’s Degree in Occupational (Environmental) Health and Safety or related field is preferred.
3.
Must have knowledge of Federal and State OSHA/EPA requirements.
4.
Excellent communication and advisory skills.
5.
Bilingual – English/Spanish, a plus.
Working Conditions
1.
Office and production environments – indoors and outdoors.
2.
Environment may be wet or dry and temperatures may range from 0°F to 100°F.
3.
Occasional exposure to possible hazardous materials and noise.
4.
May require long periods of standing and walking.
5.
Travel up to 10% of the time.
6.
Weekend work and off shift work is required.
7.
Occasional lifting with packages in excess of 35 lbs.
This position...
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Type: Permanent Location: Hillsboro, US-OR
Salary / Rate: Not Specified
Posted: 2025-03-22 07:49:59
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Company
Federal Reserve Bank of Dallas
PhD Dissertation Fellow – Federal Reserve Bank of Dallas Research Department
Advertiser: Research department, Federal Reserve Bank of Dallas
Field(s) of specialization: Any field
Position type(s): Other nonacademic
Location of job: 2200 N.
Pearl St., Dallas, TX, 75201, United States
Degree required: Doctorate
Job start date: Negotiable, but with a start date no later than August 1, 2025 and a termination date that should be no later than August 29, 2025
Job duration: Negotiable, with a minimum of 4 weeks and up to a maximum of 12 weeks
Letters of reference required: 1
Current search status: Position open
Posting end date: April 15, 2025
Call for candidates:
The Research Department of the Federal Reserve Bank of Dallas invites applications for two PhD Dissertation Fellow positions for the summer of 2025.
This program provides an excellent opportunity for PhD students in economics to engage in high-quality research and gain valuable exposure to scholarly work conducted at the Dallas Fed.
Fellows will have the opportunity to collaborate with the Bank’s research economists, visiting scholars, and other dissertation fellows, fostering a rich academic and research environment.
Qualifications/Skills:
* Open to PhD students from all PhD-granting institutions (both domestic and international).
* Applicants must have passed their qualifying exams and reached the dissertation stage of their program.
* Preference will be given to students expecting to complete their PhD in 2026.
* The program will be held in-person in Dallas, lasting from 4 to 12 weeks, during the summer of 2025.
* Fellows are expected to deliver a formal presentation at the Dallas Fed’s brownbag seminar series during the last two weeks of their fellowship.
To Apply:
We are currently accepting applications for 2 positions for the summer of 2025.
The deadline to apply is Tuesday, April 15, 2025.
Submit your application online.
Required documents include:
(1) Curriculum vitae
(2) Paper or writing sample
A letter from your principal academic advisor, commenting on your potential for producing high-quality research, the significance of your dissertation topic, and your progress to date, must also be uploaded with your submission.
For More Information:
Enrique Martínez García
Assistant Vice President and Head of the International Group
Email: enrique.martinez-garcia@dal.frb.org
Full Time / Part Time
Full time
Regular / Temporary
Temporary
Job Exempt (Yes / No)
No
Job Category
Internship Family Group
Work Shift
First (United States of America)
The Federal Reserve Banks are committed to equal employment opportunity for employees and job applicants in compliance with applicable law and to an environment where employees are valued for their differences.
Always verify and apply to jobs on Federal Reserve System Careers (https://rb.wd5.myworkdayjobs.com/FRS) or through verified Federal Reserve Bank soc...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: 29
Posted: 2025-03-22 07:45:30
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As a leading global animal health company, Elanco delivers innovative products and services to improve the health of pets and farm animals around the world because we believe making animals' lives better, makes life better.
Since 1954, we have provided solutions that support veterinarians, farmers and pet owners to advance our vision of Food and Companionship Enriching Life.
Elanco's promise to employees: Together, we foster an inclusive culture where everyone can make a difference, encouraging ownership, growth and well-being.
Elanco Animal Health ist eines der weltweit führenden Tiergesundheitsunternehmen.
Wir entwickeln und vertreiben innovative Produkte und Dienstleistungen, um Krankheiten bei Haus- und Nutztieren vorzubeugen und zu behandeln.
So schaffen wir einen Mehrwert für Landwirte, Haustierbesitzer, Tierärzte, Stakeholder und die gesamte Gesellschaft.
Mit unserer langjährigen Tradition im Bereich Tiergesundheit helfen wir unseren Kunden dabei, die Gesundheit ihrer Tiere zu erhalten und zu verbessern.
Die Lohmann Animal Health GmbH ist als Teil des Elanco Animal Health Unternehmens seit mehr als 50 Jahren ein weltweit führender Spezialist für die Herstellung von Geflügelimpfstoffen.
Unsere Impfstoffe werden dabei weltweit in über 70 Ländern exportiert.
Join our team!
Wir suchen Sie, zum nächstmöglichen Termin als neuen Produktionsmitarbeiter (m/w/d) für unsere Teams!
IHRE AUFGABEN UND VERANTWORTLICHKEITEN
* Mitarbeit bei der Herstellung von unseren viralen/bakteriellen Impfstoffen
* Selbständiges Bedienen, Einrichten und Überwachen von Produktionsanlagen im Schichtbetrieb und auch an den Wochenenden
* Gewährleistung eines reibungslosen Produktionsablaufs sowie Dokumentation nach GMP Richtlinien
* Durchführen von Reinigungsarbeiten, Vor- und Nachbereitungsarbeiten
* Aseptisches Arbeiten im Reinraum
* Einsatz auch in weiteren Produktionsbereichen am Standort in Cuxhaven möglich
* Umgang mit MS-Office-Programmen
* Buchung von Prozessaufträgen im System
* Durchführung des Hygienemonitorings
WAS SIE MITBRINGEN
* Abgeschlossene Berufsausbildung - pharmazeutische, biologische oder chemisch-technische Berufsausbildung ist von Vorteil, gerne auch aus der Lebensmitteltechnik.
* Produktionserfahrung im GMP Umfeld oder Erfahrung in der Bedienung komplexer Produktionsanlagen
* Sehr hohes Hygienebewusstsein
* Bereitschaft zum flexiblen Arbeitseinsatz, Schichtarbeit sowie Einsatzbereitschaft an Wochenenden
* Sorgfältige Arbeitsausführung, gute Kommunikationsfähigkeit und ausgeprägter Teamgeist
* Selbstständige und strukturierte Arbeitsweise
* Hohes Maß an Einsatzbereitschaft sowie Sicherheits- und Verantwortungsbewusstsein
* Erfahrung im Umgang mit MS-Office und SAP vorteilhaft
* Gute Deutschkenntnisse in Wort und Schrift, Englisch ist wünschenswert.
WAS WIR IHNEN BIETEN
* Attraktive Vergütung gemäß Tarifvertrag
...
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Type: Contract Location: Cuxhaven, DE-NI
Salary / Rate: Not Specified
Posted: 2025-03-22 07:42:01
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The Harris Public Sector Group's Schools' division is looking to hire a Financial Analyst accountable for providing financial assistance and examine for the division.
You will work with fellow Analysts, AR/AP Clerks, the Controller, and the business unit's Vice Presidents.
You will have a chance to join a fast-paced organization with a large, stable, and growing presence in the vertical market software industry!
We are looking for a candidate on the CPA path with accounting experience and proven data-based skills with attention to detail.
Reporting to the Controller, you will perform month, quarter, and year-end closing tasks, in addition to working with the Business Unit on various ad hoc projects.
WHAT WILL BE YOUR NEW ROLE
* Build relationships with and providing excellent customer service to the business unit(s)
* Completing the month-end and quarter-end close processes by breaking down results, preparing journal entries and detailed reconciliations, and reporting for senior management
* Tracking & breaking down deferred maintenance, hardware, software, and professional services revenue streams
* Forecast benefits, payroll taxes and depreciation and updating actual results for headcount, bookings, and backlog
* Calculate commissions owed based on invoicing/bookings
* Assisting with special projects & ad hoc reporting as needed by divisional Controller, EVP, and VP's
WHAT WE ARE LOOKING FOR
* 3+ years of progressive experience in Financial and accounting fields.
* CPA designation (or in pursuit of)
* Business or Finance degree
* Effective communicator that has the experience and the ability of working with all levels of management
* Solutions focused mindset with a desire to improve processes
* Exceptional data-based skills with an attention to detail
WHAT WILL MAKE YOU STAND OUT
* Experience with IFRS accounting standards and project accounting and software revenue recognition
* Positive attitude and a passion for continuous learning
* A dynamic personality with the ability to manage the expectations of many stakeholders
WHAT WE OFFER
* Three weeks' vacation and five personal days
* Comprehensive Medical, Dental, and Vision coverage from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Flexible work options
* And more!
About us:
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 government, school districts, public safety, and healthcare software verticals.
Our success has been realized through investments in our proprietary software and market expertise.
This focus, combined with acquiring businesses that build upon or complement our offerings, has h...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2025-03-22 07:40:52
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FA CM DO IPS PM HT PM HT CM
About this role: As a Clinical Manager with Fresenius Medical Care, you will ensure that quality patient care is delivered while maintaining clinical operations. As the facility leader, you will be part of a close-knit, collaborative team responsible for delivering unique care plans and providing dialysis treatment to patients facing end stage renal disease or chronic kidney disease.
Training and advancement: You will enter our Clinical Leadership Program that creates and supports a culture of continuous learning for our managers.
The curriculum will cover onboarding, essential functions, leading your business, and advanced leadership. As a Clinical Manager, you may advance your career into an Area Team Lead or Director of Operations role.
Our culture: We believe our employees are our most important asset — we value, care about, and support our people.
We are there when you may need us most, from tuition reimbursement to support your education goals, granting scholarships to family members, delivering relief when natural disasters strike, or providing financial support when personal hardship hits, we take care of our people.
Our focus on diversity: We have built a nurturing environment that welcomes every age, race, gender, sexual orientation, background, and cultural tradition.
We have a diverse range of employee resource groups (ERGs) to encourage employees with similar interests, goals, social and cultural backgrounds, or experiences to come together for professional and personal development, discussion, activities, and peer support.
Our diverse workforce and culture encourage opportunity, equity, and inclusion for all, which is a tremendous asset that sets us apart.
At Fresenius Medical Care, you will truly make a difference in the lives of people living with kidney disease.
If this sounds like the career and company you have been looking for, and you want to be a vital part of the future of healthcare, apply today.
PRINCIPAL RESPONSIBILITIES AND DUTIES
CLINIC OPERATIONS:
* Manages the operations of the clinic, including costs, processes, staffing, and quality standards.
* Provides leadership, coaching, and development plans for all direct reports.
* Partners with internal Human Resources, Quality, and Technical Services departments.
* Collaborates with or functions as the Home Therapies Program Manager to oversee the facility’s Home Therapies Program.
* Maintains integrity of medical and operations records and complies with all data collections and auditing activities.
* Accountable for completion of the Annual Standing Order Review and Internal Classification of Disease (ICD) coding.
* Manages clinic financials including efficient utilization of supplies or equipment and regular profits and loss review.
* Responsible for all required network reporting and on-site state or federal surveys.
PATIENT CARE:
* Coordinates all aspects of patient car...
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Type: Permanent Location: College Park, US-GA
Salary / Rate: Not Specified
Posted: 2025-03-22 07:39:05
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Must have prior dialysis experience!
PURPOSE AND SCOPE:
Functions as part of the hemodialysis health care team as a Team Leader Registered Nurse to ensure provision of quality patient care on a daily basis in accordance with FMS policies procedures and training.
Support FMCNA's commitment to the Quality Enhancement Program (QEP) and CQI Activities including those related to patient satisfaction.
Actively participate in process improvement activities that enhance the likelihood that patients will achieve the FMCNA Quality Enhancement Goals (QEP).
Supports FMCNA's mission vision values and customer service philosophy.
Adhere to all requirements of the FMCNA Compliance Program and FMS patient care and administrative policies.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
General and Staff Related:
* Directs Patient Care Technician's provision of safe and effective delivery of chronic hemodialysis therapy to patients in compliance with standards outlined in the facility policy procedure manuals as well as regulations set forth by the corporation state and federal agencies.
* Delegates tasks to all direct patient care staff including but not limited to LVN/LPNs Patient Care Technicians and Dialysis Assistants.
* Ensures adequate staffing through daily management of staff scheduling when appropriate.
* Assesses daily patient care needs and develops appropriate patient care assignments.
* Routinely monitors patient care staff for appropriate techniques and adherence to facility policy and procedures.
* Assists Clinical Manager with staff performance evaluations.
* Participates in staff training and orientation of new staff as assigned.
* Participates in all required staff meetings as scheduled.
* Functions as Team Leader.
* Enforces all company approved policies and procedures as well as regulations set forth by state and federal agencies and departments.
* Maintains overall shift operation in a safe efficient and effective manner.
* Act as a resource for other staff members.
* Routinely meets with the Clinical Manager to discuss personnel and patient care status issues and information.
* Collaborate and communicate with physicians and other members of the healthcare team to interpret adjust and coordinate care provided to the patient.
* Provides assistance as needed to patients regarding prescription refills according to FMCNA Policies.
* Ensures all physician orders are transcribed and entered into the Medical Information system in a timely manner.
* Oversees all documentation of patient information.
* Maintains facility drug list for all required stock medications.
* Maintains competency with all emergency operational procedures and initiates CPR and emergency measures in the event of a cardiac and/or respiratory arrest.
* Ensures verification and availability of adequate emergency equipment.
* Ensures provision of appropriate vaccinati...
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Type: Permanent Location: Bronx, US-NY
Salary / Rate: Not Specified
Posted: 2025-03-22 07:38:24
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Your Job
Georgia-Pacific, LLC (GP) is now hiring a R&D Process Engineer for its Tolleson, Arizona Mailers facility.
The R&D Process Engineer supports manufacturing on site including equipment installation, training, acceptance testing, performance testing, and process and equipment upgrades.
The R&D Process Engineer must be able to present data in a concise way to both technical and non-technical audiences.
We believe in the challenge process and this person must be open to the ideas and recommendations of others to create the best outcome for both the site, R&D and i2.
Typical work schedule would be weekdays from 8am-5pm.
Our Team
The GP Tolleson facility employs about 115 people and serves converting customers throughout the Southwest with sustainable packaging products.
This position provides opportunities for promotion within GP Tolleson, as well as many other Georgia-Pacific and Koch facilities across the country.
Come join our team!
You know us already! Georgia-Pacific is one of the nation's leading corrugated sheet and box manufacturers.
Check out these videos/links to learn more about the Corrugated Business at Georgia-Pacific:
www.gppackaging.com
What You Will Do
* Actively engage with Operations, Maintenance, and R&D to identify opportunities for evolutionary changes to the process and equipment
* Update process control and troubleshooting procedures and train plant personnel on current and updated process procedures
* Identify and lead process improvement projects to improve OEE (Overall Equipment Effectiveness)
* Translate learnings and technology upgrades from other sites and work with EHS and site operations to deploy on site
* Support new customer and product trials and production campaigns
* Employ process control best practices and strategies to centerline the process
Who You Are (Basic Qualifications)
* Bachelor's degree in engineering or science
* Previous experience using Microsoft Office programs and other software programs to present data (Word, Excel, Outlook, Teams, Power Bi, etc.)
* Previous experience in a manufacturing facility
* Previous experience moderating meetings and training sessions
* Must be willing and able to travel up to 25%
* Must have legal authorization to work permanently in the United States for any employer without requiring a visa transfer or visa sponsorship
What Will Put You Ahead
* Bachelor's degree or higher in Mechanical, Chemical or Electrical Engineering
* 2+ years of hands-on experience in a manufacturing facility interfacing with quality, operations leadership, maintenance and hourly employees
* Previous experience within a corrugated and/or converting manufacturing facility
* Previous experience developing and executing experiments and monitoring process data
* Previous experience leading process improvement initiatives
* Previous experience in data analysis and/or statistical software (JM...
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Type: Permanent Location: TOLLESON, US-AZ
Salary / Rate: Not Specified
Posted: 2025-03-22 07:37:16
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POSITION SUMMARY:
The Assistant Director of Parks & Recreation is responsible for assisting the Parks & Recreation Director in the overall management and administration of the Department and may act as the Director in their absence. The Assistant Director provides logistical, strategic and coordination support to management, staff and volunteers in diverse areas including recreation, maintenance, public outreach, special event programming, education, safety, security, personnel, stewardship, budget, capital improvements, historic preservation and environmental conservation efforts. Special emphasis in knowledge and experience with maintenance and care of all historic buildings and collections. Identification, evaluation, and preservation of County Historic resources
POSITION RESPONSIBILITIES:
Essential Functions
The duties and responsibilities of this position include, but are not necessarily limited to:
* Provide logistical, strategic and coordination support to all aspects of Park operations, public activities, services and events, as well as oversight, planning and management of parks, trails, recreation facilities, natural resources and historic properties.
* Oversee the maintenance and preservation of the Departments historic buildings, related facilities, and collections with knowledge of current preservation standards
* With Director, supervise Parks Maintenance, Recreation & Special Events, Historic Resource, Park Ranger and Natural Resource Supervisors, along with all other Department full-time, and part-time staff members.
Project manage capital and planning projects, working in coordination with the Director of Parks
* In association with Director of Parks and Parks Maintenance Supervisor, develop and manage scoping, bid requests and cost estimates for repair, replacement and infrastructure improvement.
* Assist in the preparation of annual operation and capital budgets; oversee the budgetary and financial elements of the Department to include Federal, State and private grants and donations.
* Collaborate with the Director in researching and securing grants and other appropriate revenue sources as well as then ensuring the department is operating in compliance with grant requirements and filing necessary reports.
* Oversite of Heritage Center Country Store and Snack Bar
* Prepare and deliver content for workshops, webinars, videos, publications
* Working with the Historic Resource Supervisor, organize, analyze, and synthesize data and information and prepare guidance related to historic resources
* Coordinate, manage, and evaluate vendor contracts and procurement requests.
* Along with department supervisors train, assign and supervise volunteers for maintenance and improvement projects.
* Provides direction to those who are responsible for proper care and maintenance of Archives, collections, research, and management of Heritage Center/ Canal Center/...
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Type: Permanent Location: Reading, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-22 07:33:46
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Under the guidance of the Recreation Supervisor, the Recreation Program Assistants create, plan, and implement program and office support on Department-wide special events and programs on and off site of Berks County Parks.
Hours vary - must be available weekdays, weekends and weeknights.
Must have excellent people and customer service skills, as well as a strong work ethic. The ability to problem solve, adapt to changing situations, and a willingness to learn are necessary.
Must be able to work independently, plan, implement and follow-through with responsibilities. Must also enjoy working outside, in all types of weather.
Applicants must have an appreciation of nature and outdoor recreation programs and a commitment to public service.
Those with experience with graphic design and marketing a plus!
Minimum Age Requirement - 18 years of age.
Rate: $15.86/hr
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Type: Permanent Location: Reading, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-22 07:33:45
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If you are a Quality professional looking for an opportunity to grow, Emerson has an exciting opportunity for you! Based in Louisville, KY, you will maintain customer and will perform the required quality control inspection and testing to ensure product compliance to specifications.
TopWorx is the global leader in valve control and position sensing for the process industries.
In This Role, Your Responsibilities Will Be:
* Apply knowledge of measurement science, mathematics, physics, and electronics to calibrate inspection, measurement, and test equipment (IM&TE).
* Identify and utilize appropriate measurement procedures (including CMM, optical comparator, micrometers, etc.).
* Perform corrective actions to address identified measurement problems.
* Follow equipment, standards, and procedures to accomplish unique measurements.
* Responsible for maintaining calibration standards / records.
* Perform laboratory and/or departmental housekeeping.
Who You Are:
You effectively communicate in various settings: one-on-one, small and large groups, or among diverse styles and position levels.
For This Role, You Will Need:
* High school diploma or equivalent
* Must have good understanding of Geometric Dimensioning and Tolerancing (GD & T) skills.
* Mechanical proficiency and the ability to read and interpret drawings.
* Must have the ability to analyze and interpret data and other information in order to complete calibration procedures.
* Fluent in English (reading and writing)
* Ability to complete basic math functions (addition/subtraction/multiplication/division)
* Ability to lift 40 pounds intermittently
* Ability to sit and/or stand daily up to 10 hours
* Legal authorization to work in the United States without sponsorship now or in the future.
Our Culture & Commitment to You
At Emerson, we prioritize a workplace where every employee is valued, respected, and empowered to grow.
We foster an environment that encourages innovation, collaboration, and diverse perspectives—because we know that great ideas come from great teams.
Our commitment to ongoing career development and growing an inclusive culture ensures you have the support to thrive.
Whether through mentorship, training, or leadership opportunities, we invest in your success so you can make a lasting impact.
We believe diverse teams, working together are key to driving growth and delivering business results.
We recognize the importance of employee wellbeing.
We prioritize providing flexible, competitive benefits plans to meet you and your family’s physical, mental, financial, and social needs.
We provide a variety of medical insurance plans, with dental and vision coverage, Employee Assistance Program, 401(k), tuition reimbursement, employee resource groups, recognition, and much more.
Our culture offers flexible time off plans, including paid parental leave (maternal and paternal), ...
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Type: Permanent Location: Louisville, US-KY
Salary / Rate: Not Specified
Posted: 2025-03-22 07:29:01
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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:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
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 surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world.
Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer.
Patients are waiting.
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 our MedTech Surgery, Manager of Global Strategic Marketing position, based out of Santa Clara, CA.
The Manager - Global Strategic Marketing, Robotics will play a key role in leading and executing customer-facing visits at our Santa Clara facility.
This position demands close collaboration with various departments, including Marketing, Professional Education, R&D, Medical Affairs, Human Factors, Regional Marketing, Field Sales Organization, and external partners, to create a best-in-class customer-centric experience.
Additionally, developing and maintaining strong relationships with key stakeholders will be vital for the success of this role.
Key Responsibilities:
* Collaborate with cross-functional teams to implement the Healthcare Provider (HCP) Engagement strategy.
* Lead daily activities related to HCP Engagement, including organizing onsite visits and labs (scheduling, logistics, contracting, and follow-ups).
* Maintain tracking systems and dashboards for HCP engagements.
* Recruit, retain, and cultivate long-term relationships with key HCPs.
* Provide Voice of the Customer (VOC) insights to inform go-to-market strategies and contribute to the development of platforms, products, and procedures.
* Have a strong understanding of the program and deliver platform reviews to onboard strategic HCPs.
* Monitor and analyze market trends to identify opportunities for enhancement in HCP Engagement strategies and experiences.
* Develop and ...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-22 07:17:14
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, 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 Principal Scientist, Analytical Comparability & Product Characterization – Advanced Therapies to be in Malvern, PA.
Purpose:
The Biotherapeutics Development - Analytical Development (BioTD - AD) group is seeking an upbeat, highly motivated Principal Scientist to focus on analytical comparability and product characterization for advanced therapy modalities. The individual would work with team to develop product comparability study approaches for advanced therapy modalities that will be endorsed by the health authorities. A successful candidate will have experience with the design, execution and optimization of a broad range of characterization assays and will have the opportunity to engage in multi-functional teams.
They will learn from and contribute to industry-leading drug discovery/development programs that has brought numerous quality therapeutics to patients and has made significant contributions to human health.
Primary Responsibilities:
·Design and lead the execution of analytical comparability studies for advanced therapy modalities across various stages of development.
·Lead the execution of the advanced methodologies associated with comparability and deep characterization of cell and gene therapy.
·Author or coordinate appropriate IND/IMPD/BLA/MAA sections & interact with regulatory agencies to address CMC-comparability and product characterization related inquiries.
·Optimally communicate comparability study plans, statistical justifications, and results and scientific data to cross-functional teams, project teams, and health authority as needed.
·Collaborate to develop innovative approaches to challenging solutions for analytical comparability strategy and product characterizati...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-22 07:16:25
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SUMMARY:
The Armstrong Company is seeking a high-energy Crew Member/Mover who will be responsible for preparing, packing, loading, unloading, and moving household goods or office equipment with an objective of delivering an excellent customer experience from start to finish. The Mover will be involved with both Household Goods and Commercial moves.
The right candidate will be one who works well under pressure and is highly self-motivated.
KEY RESPONSIBILITIES:
* Pack & Prepare: Help prepare and pack customer items to prevent damage during transit.
This includes disassembling furniture, wrapping items, packing items in boxes, and using straps to secure large items.
* Load & Unload: Use equipment such as dollies and ramps to load customer items from their buildings to the moving truck.
Strategically arrange items in the truck to prevent objects from falling or getting damaged.
Move items off the truck, reassemble, and place them in the location the customer requests.
* Customer Service: Provide excellent customer service by interacting with customers in a friendly and professional manner. Answer customer questions and address specific move requests.
* Housekeeping: Before leaving the customer’s loading site, clean up any supplies or garbage left behind during the packing/unpacking process.
Keep moving trucks and work sites free from debris.
* Safety: Follow all safety policies and procedures at all times, including use of proper safety equipment and PPE. Use proper lifting, carrying, pushing, and pulling techniques at all times to avoid potential injury.
* Other Duties: When not in the field completing customer moves, assist with tasks needed in local warehouse and operations.
Complete all other duties as assigned by Manager.
MINIMUM QUALIFICATIONS:
* Excellent interpersonal and customer service skills.
* Must possess a positive attitude for interacting with customers, staff, and management.
* Punctual, results oriented, and focused on problem solving.
* Physical stamina for sustained periods of lifting, carrying, pushing, pulling, walking, and bending.
PHYSICAL REQUIREMENTS:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job:
* Requires the ability to communicate effectively using speech, vision, and hearing.
* This position requires excellent physical stamina and the ability to regularly lift, carry, push, or pull up to 80 pounds.
* Sustained periods of lifting, standing, sitting, walking, bending, and kneeling.
HOURLY RATE OF PAY:
$17 per hour
The Armstrong Company is an Affirmative Action / Equal Opportunity Employer (EOE).
Our employment decisions are made without regard to race, color, religion, sex, marital status, pregnancy, national origin, citizenship, age, physical or mental disability, genetic information, sexual orientation, veter...
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Type: Permanent Location: Canton, US-MA
Salary / Rate: 17
Posted: 2025-03-21 07:34:56
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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: Sr.
Analytical Scientist, Biologics
As an Sr.
Analytical Scientist, Biologics you will be part of Elanco’s R&D team, driving the development of chromatographic, electrophoretic, and LC/MS analytical methods for biopharmaceutical products.
In this role, you’ll be responsible for advancing analytical techniques for therapeutic proteins and vaccines, supporting bioprocesses, and leading method development, validation, and transfer efforts across global sites.
If you are passionate about advancing analytical methodologies and playing a key role in biopharmaceutical development, we invite you to apply and join our innovative team!
Your Responsibilities:
* Develop and optimize chromatographic, electrophoretic, and LC/MS analytical methods for vaccine and therapeutic protein products.
* Innovate and implement analytical solutions for diverse drug formulations and bioprocess support.
* Lead method validation, verification, and transfer activities across global sites and CROs.
* Train and mentor associates and scientists globally to ensure consistency in analytical practices.
* Author technical reports, review scientific documents, and maintain laboratory safety standards.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree with 12+ years or Master’s Degree with 10+ years of experience in Analytical Chemistry, Biochemistry, Biophysics, or a related scientific field.
* Experience: Extensive hands-on experience developing HPLC/UPLC-based, electrophoretic, and LC/MS analytical methods for large molecule characterization.
* Top 2 skills: Strong expertise in analytical method development and validation, with excellent problem-solving and communication skills.
What will give you a competitive edge (preferred qualifications):
* Expertise in recombinant proteins, monoclonal antibodies, oligonucleotides, and peptides.
* Experience with method validation, transfer, and qualification under GMP conditions.
* Strong statistical knowledge and proficiency with statistica...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-21 07:25:42
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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: Analytical Scientist, Biologics
As an Analytical Scientist, Biologics you will be part of the Analytical Development Team at Elanco, supporting the development of innovative biopharmaceutical products.
In this role, you’ll be responsible for advancing analytical method development, optimization, and validation, ensuring high-quality analytical support for product and process development.
Your Responsibilities:
* Lead the development and optimization of analytical methods, including chromatographic, electrophoretic, and ligand-binding assays.
* Design, execute, and oversee analytical method qualification for release, characterization, and stability assays.
* Provide rapid analytical support for bioprocess and formulation development activities.
* Train and mentor associates and scientists globally, fostering knowledge sharing across sites.
* Author reports, SOPs, and technical documents, ensuring compliance with regulatory guidelines.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree in Biochemistry, Chemistry, Biotechnology, Biology, Microbiology, Analytical Chemistry, Cellular Biology, or a related field.
* Experience: A minimum of 3 years of experience in the Biotech/Biopharmaceutical industry with a focus on large molecule analytical characterization.
* Top 2 skills: Strong analytical method development expertise and excellent problem-solving and communication skills.
What will give you a competitive edge (preferred qualifications):
* Experience with recombinant proteins, monoclonal antibodies, oligonucleotides, and peptides.
* Practical knowledge in method development, optimization, and validation.
* Ability to work effectively in an interdisciplinary team environment.
* Experience with electronic laboratory notebooks (ELN).
* Strong organizational and decision-making abilities.
* Ability to independently plan and conduct experiments while ensuring regulatory compliance.
* Expertise in method transfers, troubleshooting, and pr...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-21 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!
Devenez notre futur(e) Expert Investigations Analytiques !
Venez rejoindre une équipe dynamique et riche de sa diversité dans un laboratoire de pointe, modèle de l’excellence opérationnelle !
RÉSUMÉ DE LA FONCTION
* Etre responsable de la coordination et de la rédaction des investigations du laboratoire de contrôle.
* Identifier les besoins en actions d’améliorations continues du laboratoire.
ACTIVITÉS PRINCIPALES
Réaliser et coordonner les investigations analytiques du laboratoire
* Concernant les investigations atypiques ou de niveau 1 gestion par les opérationnels (technicien senior et manager CQ laboratoire) de l’investigation avec le support potentiel d’un expert investigateur analytique mais assurer la revue et l’approbation technique (Veeva) systèmatique.
* Concernant les investigations niveau 2 plus complexes et impactantes réaliser l’ensemble de l’investigation.
* Récolter les informations nécessaires aux investigations auprès des techniciens laboratoire, des managers CQ, des responsables libérations analytiques et des autres experts du laboratoire.
* Par une démarche d’investigation structurée, déterminer la cause racine de la problématique.
* Concevoir si nécessaire des protocoles d’essais complémentaires.
* Rédiger de manière claire et structurée le rapport d’investigation.
* Vérification des déviations étendues (niveau 2) suite à une investigation de laboratoire relecture des déviations process sous l’angle analytique.
* Participation aux réunions transversales d’investigation (PSM, Deviation Review Board TSMS et fabrication) si besoin.
* Réunion PSM CQ : Organiser, animer et identifier et solliciter les personnes ressources (experts et les opérationnels) en lien avec la problématique à résoudre.
* Mettre en place et suivre les indicateurs liés aux investigations.
* Former tout nouveau collaborateur au processus d’investigation du laboratoire, y compris dans le système électronique.
* Effectuer la...
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Type: Permanent Location: Huningue Cedex, FR-68
Salary / Rate: 46000
Posted: 2025-03-21 07:25:36
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PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) process.
...
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Type: Permanent Location: Aiken, US-SC
Salary / Rate: Not Specified
Posted: 2025-03-21 07:23:25
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Accounting Analyst II - Fixed Assets - 12 Months Contract (Global Business Services)
Job Description
Accounting Analyst II - Fixed Assets (Global Business Services)
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:
* Develop and maintain a detailed fixed asset register, through audit, and the timely and accurate recording of additions, retirements, transfers, depreciation, for local and US GAAP, and tax, to meet Corporate and Tax requirements.
* Provide reporting, analysis, and assist in the control of Fixed Assets and Capital Projects for Corporate, Site, and Project Management
* Maintain assigned systems, processes, or process components in good working order and identify and recommend system improvements to ensure timely, relevant and accurate Financial Accounting Information
* Co-ordinate, and assist in the preparation of site property, plant, and equipment capital budgets and forecasts (CAPEX)
Expectation: -
* The incumbent is responsible for the integrity of the property, plant, and equipment records and processes through the ongoing maintenance of the asset register and implementation of procedures, work instructions, and training programs for site management, finance, and project engineers.
* The position is expected to act independently and with minimal supervision, liaising directly with local and remote site management, finance, and project engineers, in maintaining the framework in which the processes operate, providing reporting and advice, and working with local management to resolve any issues as they arise.
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 care...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-03-21 07:22:53
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We are seeking a dedicated and experienced Environmental Health and Safety (EHS) Manager to join our team.
This role is responsible for developing, implementing, and maintaining the company’s safety, health, and environmental policies and standards.
The EHS Manager will oversee all Environmental, Safety, and Health (ESH) activities for our large, special-order engineered manufacturing facility located in Marshalltown, Iowa.
Emerson offers generous benefits, and flexible work schedules, and we are committed to a diverse workforce!
In this Role, Your Responsibilities Will Be:
* Manage ES&H Department and Medical Department.
* Maintain regulatory compliance for OSHA-required regulations, IDNR, City of Marshalltown as well as Emerson Corporate Standards.
* Review and implement revisions of ESH processes, guidelines, programs, and policies and communicate/train plant personnel.
* Supervise Velocity Safety Software system and ENVIRON Environmental Compliance database.
* Complete risk assessments for accurate machine guarding.
* Recommend safety initiatives, solution options, and compliance programs to management.
* Develop, coordinate, and facilitate ES&H communications and design/revise training programs for OSHA-required programs, BBS implementation, and general safety awareness.
* Maintenance of monthly safety and health inspections/internal audits and disposition of open action items.
* Conduct Industrial Hygiene exposure assessments, conduct sampling, and communicate monitoring results.
* Recognition, evaluation, and mitigation of workplace hazards including development and implementation of processes, JHA/SOPs, work procedures, programs, and training.
* Active participation in safety/environmental and security teams.
* Assist Environmental Engineer with air, waste, wastewater, stormwater, EPCRA and SARA compliance, monitoring and regulatory reporting.
* Implement Emerson Operation Excellence Safety Audits, Environmental Compliance Audits, and self-assessments and maintain/improve current ratings.
* Ability to communicate with a variety of audiences including company and corporate personnel, union, and government officials.
Who You Are:
You step up to handle tough issues. You carefully consider all relevant factors and use appropriate decision-making criteria and principles. You understand that different situations may call for different approaches. You partner with others to get work done.
For This Role, You Will Need:
* Bachelor's degree in Occupational Safety and Health, Industrial Hygiene, Safety Engineering or related field, or a combination of education and related experience.
* 3-5 years of experience with manufacturing processes and identifying safety and health risks associated with manufacturing operations.
* Knowledge of manufacturing safety elements including OSHA federal and state standards.
* Familiarity with...
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Type: Permanent Location: Marshalltown, US-IA
Salary / Rate: Not Specified
Posted: 2025-03-21 07:22:01
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Kaiser Aluminum Warrick has been on the path of innovation, embracing the latest technologies for almost 60 years! We have revolutionized the industry and lead the way in the development of sustainable aluminum products the you use every day for food and drinks.
Our people are the bedrock for our operations.
Along with their dedication to excellence and integrity, our people are drivers of continuous improvement who build on new ideas while flourishing within our growing business.
We provide opportunities for you to think outside the box and bring creative and progressive solutions to our operations.
Our passion for inclusion, diversity and equity is a value at the core of our organization and people.
Are you ready to start your journey with us and be the future of Kaiser Warrick Aluminum?
aiser Aluminum is known around the world for its superior quality.
Our secret is what we put into it—innovative thinking, industry-leading reliability, and a world-class commitment to customer service.
In short, the same qualities we look for in our people.
We are looking for a Safety Training Coordinator to join Kaiser Aluminum Warrick Operations in Newburgh, Indiana!
The Safety Training Coordinator plays a critical role in developing and implementing safety training programs in an aluminum sheet manufacturing environment.
This position ensures all employees, contractors, and visitors are properly trained on workplace hazards, regulatory compliance, and company safety policies.
The ideal candidate will be an experienced safety professional with a strong background in OSHA, NFPA 70E, molten metal safety, LOTO, machine guarding, and hazardous materials handling. They will collaborate with plant leadership, operations, and EHS teams to maintain a proactive safety culture and reduce workplace incidents.
What’s in it for you!
To support our teams and their families beyond the workplace, we provide an outstanding benefits package effective day one of employment!
* Industry leading compensation program.
* 401K options that begin vesting day 1.
* First-rate vacation plan for valuable work-life balance.
* Relocation assistance for new team members.
* Employee resource groups.
What you will work on:
Safety Training Program Development & Implementation
* Design and deliver manufacturing-specific safety training for new hires, existing employees, supervisors, and contractors as needed.
* Ensure compliance with OSHA 1910, ANSI, NFPA, and industry-specific regulations related to aluminum sheet manufacturing.
* Develop and maintain training materials for critical safety topics, including molten metal safety, hot work, mechanical hazards, PPE, ergonomics, and emergency response.
* Oversee all safety related training programs, ensuring compliance with applicable regulations and corporate policies.
* Utilize hands-on demonstrations, e-learning, toolbox talks, and safety simulations to enhance engagement and re...
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Type: Permanent Location: Newburgh, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-21 07:20:37
