-
Werde Lagermitarbeiter / Sortierer für Briefe in Frankfurt -
kein Minijob !!!!
Dienstag – Samstag 00:15 Uhr - 06:00 Uhr und
17:15 - 20:45
Was wir bieten
* 16,28 € Tarif-Stundenlohn
* + 25% Nachtzulage steuerfrei schon ab 20:00 Uhr (bis 6:00 Uhr, entspricht 17,25 € Stundenlohn)
* Ein krisensicherer Arbeitsplatz, bezahlte Einarbeitung, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Du kannst sofort als Aushilfe / Abrufkraft starten, mind.
18 Stunden/Woche
* Kostenlose Ausstattung, wie z.B.
Sicherheitsschuhe und Schutzhandschuhe
* Übernahme bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote, wie z.B.
Rabatte bei Mobilfunkanbietern, Fitnessstudios, Modemarken etc.
Deine Aufgaben als Sortierer bei uns
* Sortieren der Briefsendungen nach verschiedenen Kriterien
* Bedienen der Sortieranlagen
* Heranholen der zugeführten Briefbehälter
* Leeren der Fächer und Abtransport der Briefbehälter
* Unsere Schichten:
WAZ 18 Dienstag – Samstag 00:15 Uhr - 06:00 Uhr
Was du bietest
* Du hast mindestens 6 Wochen am Stück Zeit, für uns tätig zu sein
* Du möchtest im Anschluss als Abrufkraft an einzelnen Tagen tätig sein
* Du arbeitest zuverlässig und bist engagiert
* Du kannst anpacken und hast Spaß an körperlicher Arbeit
* Du kannst dich auf Deutsch unterhalten
* Du arbeitest gern im Team
Werde Sortierer bei Deutsche Post DHL
In deinem Nebenjob als Briefsortierer sorgst du dafür, dass unsere Briefe pünktlich ankommen.
Bei uns sind auch Quereinsteiger oder Studenten herzlich willkommen, denn du zählst, wie du bist!
Wir freuen uns auf deine Bewerbung als Sortierer, am besten online.
Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#werdeeinervonunssortierer
#werdeeinervonunslagerhelfer
#jobsnlfrankfurt
....Read more...
Type: Contract Location: Frankfurt am Main, DE-HE
Salary / Rate: Not Specified
Posted: 2025-06-02 08:13:06
-
Responsibilities:
* Handles inbound calls from designated client accounts, ensuring a responsive and personalized experience.
* Accurately and thoroughly documents all client interactions within internal systems.
* Reviews assigned client accounts regularly to identify trends and insights, preparing detailed reports that highlight performance metrics, identify areas for improvement, and demonstrate the value Resolv Dental provides.
Maintains consistent and proactive communication with clients via scheduled value calls or emails.
* Maintains a working knowledge of software supported by Resolv Dental to confidently address client questions and provide training on company services, processes, and policies.
* Demonstrates a solid understanding of Resolv Dental’s core business model, including the company’s mission, value proposition, and service offerings, to effectively communicate the company’s impact to clients.
* Stays up to date on company policies and procedures to ensure all client interactions are aligned with internal standards and regulatory requirements.
* Collaborates with team members to investigate and resolve client concerns effectively.
* Actively participates in departmental meetings and contributes to team discussions.
* Demonstrates strong communication skills and works collaboratively with colleagues, management, and clients to maintain a positive work environment.
* Adheres strictly to HIPAA guidelines in handling and protecting client information and data.
* Effectively prioritizes and manages multiple responsibilities in a fast-paced environment.
* Engages with third-party vendors or partners as needed on behalf of clients to facilitate issue resolution or coordination.
* Participates in monthly one-on-one meetings with their manager for performance reviews and support.
* Takes initiative in professional development by regularly participating in training sessions to enhance skills and stay informed on best practices.
....Read more...
Type: Permanent Location: Mumbai, IN-MH
Salary / Rate: 27500
Posted: 2025-06-02 08:09:41
-
Primary Responsibilities
1.
Receives inbound calls from assigned clients.
2.
Documents all Client calls thoroughly and accurately.
3.
Prepares value findings by reviewing assigned Client accounts, analyzes practice reports for trends and delivers comprehensive overviews via value calls or emails to Clients on a regular basis.
They would be required to have regular proactive communication with their assigned clients.
These would entail going over how well the office is performing, pointing out any problem areas that they notice when reviewing the clientâs metrics as well as helping to show the value that Resolv Dental has provided to the clients.
4.
Possesses basic knowledge of Resolv Dental supported software to answer inquiries from assigned clients and training clients on Resolv Dentalâs services, policies, and procedures.
5.
Collaborates with coworkers to research and resolve client issues.
6.
Attends and participates in regularly scheduled departmental meetings.
7.
Ability to effectively communicate, work positively and cooperatively with co-workers, managers, and clients.
8.
Upholds Company HIPAA guidelines pertaining to client files and data.
9.
Able to effectively manage multiple tasks simultaneously.
10.
Communicates with third party partners on behalf of, and/or with the client.
11.
Meets with Manager monthly.
12.
Actively seeks and participates in on-going training exercises to develop and maintain necessary knowledge and skills.
Secondary Functions
Knowledge of and potentially participates in new client staff member software training and demonstrations for clients as assigned.
Provides standard support and duties as assigned.
Cross trains with various departments to enhance knowledge of Resolv Dental and third-party programs.
Job Complexity
This position requires an organized individual with strong communication (written and oral) and analytical skills to handle a low degree of complex duties.
 Individual must also possess flexibility to adapt to the changing needs of the department and company.
Supervisory Responsibilities
None
Interpersonal Contacts
This position requires daily communication with doctors, doctorâs staff, sales team, and other internal staff. Contacts within the company are usually with immediate associates and supervisors. Contacts are regularly initiated at the supervisorâs request and at the employeeâs own initiative.
Specific Job Skills
Skills necessary for this position include:
           Demonstrates strong work ethic
Strong communication skills both oral and written
Self-Starter\Take Initiative       Â
           Good telephone etiquette
           Good organizational skills
           Strong interpersonal skills
           Ability to work well with different personalities and varying skill sets
           Ability to make decisions and problem solve in a timely manner
       Â...
....Read more...
Type: Permanent Location: Mumbai, IN-MH
Salary / Rate: 37500
Posted: 2025-06-02 08:09:39
-
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: Supervisor – Operations
As the Supervisor for Operations you’ll directly lead the operations team to deliver the demand for monoclonal antibody bulk protein production.
In this role, you’ll lead personnel within a manufacturing unit operation to achieve the business productivity goals with a focus on safety, quality, and manufacturing excellence.
Your Responsibilities:
* Lead an operations staff to achieve business demands with a “Safety first and quality always” mindset.
* Effectively staff and work-plan the organization to ensure compliance in training and personnel capability on the manufacturing floor.
* Represent operations in cross-functional collaboration throughout the site to uphold a manufacturing, quality, safety, and technical agenda.
* Engage in documentation processes for manufacturing record lifecycle management, change and deviation management, personnel performance, and production execution.
* Passionately engage in personnel development, organizational development, and manufacturing process development.
* Role-model and create an accountability culture to Elanco’s core values of respect, integrity, and excellence.
What You Need to Succeed (minimum qualifications):
* Education: Highschool diploma or equivalent
* Experience: 3+ years experience in a regulated, commercial manufacturing environment.
* Must be able to wear appropriate gowning and personal protective equipment in manufacturing and support areas.
What will give you a competitive edge (preferred qualifications):
* Bachelor’s degree in biomanufacturing related field
* Biomanufacturing experience
* Monoclonal antibody manufacturing
* Understanding of USDA, FDA, EU GMP, cGMP regulatory standards
* Operational excellence, lean manufacturing, six sigma, TPS experience
* Demonstrated success in leadership
* Experience with SAP, OSI PI, VEEVA
Additional Information:
* Travel: minimal 0-5%
* Location: Elwood, KS
* This role is a day shift 5a-5p 12 hour, 2 week r...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: Not Specified
Posted: 2025-06-02 08:09:30
-
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 Assurance Associate - Process Team
The Quality Assurance Associate is responsible to oversee the Quality Assurance responsibilities for the associated process team and quality operations process, to provide daily assistance and guidance to issues such as non-conformance investigations, change controls, quality training, review and approval of documents and to ensure the adherence to Elanco Quality standards and Regulatory agencies. The QA Associate works as a team member within the operations teams to achieve site goals while maintaining a strong quality mindset.
Your Responsibilities:
* Quality Guidance and Oversight: Provides routine and non-routine quality guidance, training, and batch record review within the manufacturing environment.
This includes a daily presence on the production floor and assisting with batch disposition for incoming, semi-finished, and finished materials.
* Document Review and Approval: Reviews and approves a variety of process team quality documents, such as SOPs, forms, protocols, MPRs, and OJTs to ensure documentation accuracy and adherence to quality standards.
* Distribution and Product Release Support: Oversees distribution area quality, including label approvals, issuing Certificates of Analysis (CoAs), managing retain samples, and coordinating SAP quality movements.
* Deviation and CAPA Management: Manages deviations and corrective/preventative actions (CAPAs), including preparation, review, approval, and effectiveness verification.
This addresses non-conformances and drives continuous improvement.
* Quality System Support and Representation: Supports the quality system through SAP expertise, training, participation in meetings and projects, and mentoring site personnel on quality matters to ensure quality system effectiveness and promote a quality-conscious culture.
What You Need to Succeed (minimum qualifications):
* B.S.
Degree (Microbiology/Biology/Chemistry/Engineering degree preferred)
* Root cause analysis and troubleshooting skills
* Techni...
....Read more...
Type: Permanent Location: Winslow, US-ME
Salary / Rate: 79400
Posted: 2025-06-02 08:09:29
-
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: Senior Project Manager
The project manager is responsible for the development, execution and discipline support for capital projects.
They may support the technical needs of operational areas in accordance with all guidelines to improve safety, compliance, efficiencies, quality, unit production costs, reliability, capacity or infrastructure.
Your Responsibilities:
* Manages Capital Projects: Oversees all project phases from identification and scoping through execution, qualification, and closeout, ensuring alignment with customer needs.
This includes working with external consultants and contractors.
* Financial Responsibility: Develops cost estimates, manages budgets, controls costs, and handles procurement of equipment and materials.
* Collaboration and Communication: Works proactively with project owners and stakeholders, maintaining consistent communication throughout the project lifecycle and seeking feedback for continuous improvement.
* Safety and Environmental Focus: Prioritizes safety and environmental considerations in all project activities, including ergonomic assessments, audits, and addressing safety concerns.
* Technical Expertise: Provides technical support and troubleshooting within their assigned discipline, assists with investigations and change controls, and contributes to technical development and analysis.
What You Need to Succeed (Minimum Qualifications):
* B.S or equivalent in Engineering or related field, or equivalent level of experience.
* Working experience with building mechanical systems.
Including: HVAC, refrigeration, compressed air, steam, water and electrical.
* Previous project management experience
What Will Give You a Competitive Edge (Preferred Qualifications):
* CAMP, PMP or MS in project management a plus
* Experience in SAP and Veeva systems
Additional Information:
* Day shift with some flextime required to support weekend, evening or unusual hours to support projects execution
Don’t meet every single requirement? Studies have shown u...
....Read more...
Type: Permanent Location: Winslow, US-ME
Salary / Rate: 122000
Posted: 2025-06-02 08:09:23
-
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: Director, Quality Operations
The Quality Operations Director at the Winslow site provides comprehensive leadership for the Quality Operations team, covering strategic direction, administrative management, and technical expertise.
Their oversight spans the entire manufacturing process, from incoming inspection to product distribution, encompassing key areas such as cell culture, fermentation, downstream processing, packaging, labeling, and laboratory operations.
This role is crucial for ensuring market release of only top-quality products, achieved through effective staff management and rigorous adherence to regulatory, corporate, and site quality standards.
As a Director, you will drive continuous improvement initiatives, foster a culture of quality excellence, and ensure both operational efficiency and full regulatory compliance.
Your Responsibilities:
* Leads and oversees all aspects of Quality Operations, including developing and implementing SOPs, providing technical guidance and training, managing budgets, ensuring compliance with regulations and Elanco standards, escalating quality issues, overseeing documentation practices, and fostering a culture of continuous improvement within a high-performing team.
* Provides comprehensive Quality oversight of all manufacturing and operational processes, including finished product release, conducting audits and walkthroughs, managing event reporting and resolution, guiding documentation practices, coordinating contamination risk mitigation, and collaborating with Sterility Assurance on improvements.
* Manages all aspects of supplier quality, including audit planning and follow-up, maintaining the supplier qualification list, conducting risk assessments, collaborating with stakeholders on supplier selection and approval, overseeing change controls and specification maintenance, and ensuring compliance of incoming materials.
* Oversees and implements the department's training program, including curriculum development and review, collaboration with Operations, compliance with Ela...
....Read more...
Type: Permanent Location: Winslow, US-ME
Salary / Rate: 155000
Posted: 2025-06-02 08:09:23
-
Your Job
Georgia-Pacific is now hiring for a Converting Production Leader for our Operations Department in the Plattsburgh, NY Mill.
This Leader is responsible for providing leadership with accountability for all hourly employees on the shift, safety, and environmental compliance.
They will also coach, train and develop personnel in safety, quality, production, problem solving and technical skills.
This role will have roughly 12 direct reports and will report to the Operations Manager.
The shift for this position is 12 hour rotating shifts that fluctuate from 2 weeks of day shift to 2 weeks of night shift.
Our Team
The Plattsburgh Tissue Mill is situated on the shores of Lake Champlain in the Northeast region of upstate New York and is rich in history.
GP made its historic entry into the world of consumer paper products when it purchased this facility in 1963 as GP's first tissue mill.
Georgia-Pacific's Plattsburgh facility uses state of the art innovation and technology to manufacture Quilted Northern Ultra Plush Tissue.
What You Will Do
* Build and develop capability of on-shift personnel
* Be a business partner with Manufacturing Engineers in their respective areas
* Ensure safety and environmental ownership and compliance
* Identify and correct unsafe conditions and acts, recognizing positive safety performance as well as individual and team contributions to a safer workplace
* Lead operational and shift maintenance initiatives in accordance with the Asset Strategy to achieve maximum asset capability
* Provide performance feedback and coaching: appraising performance and providing feedback as needed
* Assist in resolving complaints and issues; hold employees accountable in a fair and consistent manner, and communicate issues and results daily
* Act as a positive change agent for continued transformation and improvement
* Develop and foster an environment where employees are contribution motivated
* Work within the bounds of a union contract (USW)
Who You Are (Basic Qualifications)
* Continuous improvement experience
* Knowledge and experience with reliability systems and work processes
What Will Put You Ahead
* Bachelor's Degree or higher in Engineering or Paper Science
* Experience initiating, executing, commissioning and starting-up capital projects
* Experience managing product systems
* Leadership experience with responsibility for direct reports
For this role, we anticipate paying $85,000 to 100,000 per year.
This role is eligible for variable pay, issued as a monetary bonus or in another form.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's ...
....Read more...
Type: Permanent Location: Plattsburgh, US-NY
Salary / Rate: Not Specified
Posted: 2025-06-02 08:09:08
-
Your Job
The desired candidate must demonstrate customer focus as well as strategic & economic thinking, possess good problem-solving skills, and enjoy collaborating across the organization.
This position supports all control systems (DCS, PLC, VFDs, Instrumentation, etc) throughout the mill and will be responsible for designing and implementing control improvements while working with others to maintain and troubleshoot the mill's control systems.
Our Team
Georgia-Pacific is seeking a Process Control Engineer to join our team at the Big Island, Virginia Mill.
Big Island is located near Lynchburg in central Virginia.
What You Will Do
• Support process operations (your customer) by troubleshooting installed systems to improve the effectiveness and efficiency of these systems.
• Partner with operations to implement new technologies that support advanced manufacturing.
• Work closely with mill personnel to identify opportunities and solve problems
• Be involved in the controls and automation design, implementation, and support of hardware and software systems for mill process equipment i.e.
ABB DCS/QCS systems and Rockwell PLCs, drives, and instrumentation.
• Develop and lead projects to migrate away from end of life control systems.
• Act as project resource for new instrumentation or control/automation systems.
• Implement, design, and configure advance process control strategies.
Maintain functional design specifications for process control systems.
• Support optimization and Advanced Process Control efforts.
• Support of the mill safety program both personally and through observation.
Who You Are (Basic Qualifications)
• Bachelor's degree or higher in engineering field plus internship/coop experience in controls-related assignment OR industrial experience working as an electrical or instrumentation technician.
What Will Put You Ahead
• Experience in the Pulp and Paper industry.
• Degree in Electrical Engineering or similar
• Experience with ABB DCS (AC800M, Bailey) platforms
• Experience with control system network topology (i.e.
Ethernet, EthernetIP, ProfiNET)
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based...
....Read more...
Type: Permanent Location: Big Island, US-VA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:57
-
Your Job
DEPCOM Power Inc.
is looking for a Site Manager to join the team in Fort Stockton, TX.
The Site Manager will support the O&M team on the Alamo & Pearl Utility Solar Site.
Our Team
The fast-growing DEPCOM Power O&M group is a collaborative, safety-oriented team that operates our customer's industrial solar power generating sites.
The O&M group rounds out the DEPCOM Engineering, Procurement, Construction (EPC) group's capability to give our customers the support they need from designing to the daily operations for industrial solar sites.
What You Will Do
* Oversee daily operations at the project site, ensuring adherence to safety protocols and project timelines.
* Communicate effectively with contractors, team members, and stakeholders, providing updates and addressing any concerns.
* Document daily site activities, including progress reports, safety inspections, and any incidents or challenges.
* Utilize Microsoft Excel to create and maintain project reports, track key performance indicators, and analyze data.
* Set up and facilitate meetings with contractors, project stakeholders, and team members to ensure alignment and resolve issues.
* Manage the team's expense reports and ensure accurate tracking of time worked by team members.
* Collaborate with the project management team to support contractor onboarding and performance evaluations.
* Identify challenges on-site and proactively seek solutions to optimize operations and efficiency.
* Assist in the coordination and management of resources, equipment, and materials necessary for project completion.
* Ensure compliance with all regulatory requirements and company policies related to site operations.
* Serve as the primary point of contact for customer inquiries and concerns, ensuring high levels of satisfaction and responsiveness.
Who You Are (Basic Qualifications)
* Previous experience in a team environment
* Experience with Microsoft Office ( Word, PowerPoint)
What Will Put You Ahead
* Previous experience in a leadership role within Utility Scale PV Solar
* Experience with PV systems utility scale operations & maintenance
* Knowledge of inverters, tracker systems & communications
* Knowledge of Medium Voltage (MV) and High Voltage (HV) power distribution equipment
* Knowledge of Commercial, Industrial and Utility Power Plant Operations
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
This position is not eligib...
....Read more...
Type: Permanent Location: Fort Stockton, US-TX
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:55
-
Your Job
Georgia-Pacific is looking for a Paper Machine Gatekeeper to join our team in Brewton, AL.
The Gatekeeper plays critical role in our organization and asset maintenance work process.
People in this role work with and through other mill leaders to balance competing maintenance priorities, forecasting spend plans, while focusing on the long-term success of operations within their departments and beyond.
Our Team
The Brewton Mill is an integrated paper mill producing product for Dixie® plates and various GP and external corrugated box facilities.
Brewton is located in south central Alabama, about an hour from Mobile, AL, Pensacola, FL, and the beautiful beaches of the Gulf Coast.
To learn more about Georgia-Pacific's packaging business please visit: www.gppackaging.com and view the video How Paper Is Made! Our culture is defined by the Principle Based Management™ philosophy which guides everyday decision making and provides employees with opportunities to contribute and personally benefit from the value they create.
What You Will Do
• Optimize value creation by managing maintenance and miscellaneous operations spend for the Paper Machine area.
• Actively participate in Mill Spend Evaluation meetings, presenting the planned and unplanned spend on a weekly and monthly basis.
• Actively participate in Work Prioritization meetings to ensure proper work is scheduled for execution.
• Review submitted work requests for need, accuracy, correct accounting codes daily.
Convert work requests to work orders and send to planning or execution as needed.
• Manage existing contracts, invoices, and accruals for correctness.
• Monitor Work Process Status & Aging dashboards and keep up to date.
• Effectively manage many high priority tasks / projects with a sense of urgency.
• Review and follow up on emergency work execution to ensure completeness and if follow up work is required.
• Manage forecast for Extraordinary Maintenance needs /spend plans as well as baseline spend and full year spend plans.
• Work with the team to review and analyze loss analysis and asset tracking data to identify equipment reliability and performance issues (gap analysis) and develop improvement plans.
• Help develop long-term reliability and asset strategies.
• Collaborate with manufacturing engineers, maintenance team members, and department leaders on critical equipment strategies.
• Ensure reliability activities are scheduled based on resource availability and priority.
Provide technical support on both capital and non-capital projects.
Who You Are (Basic Qualifications)
• Experience working within a manufacturing, industrial or military environment.
• Experience leading and facilitating meetings.
• Ability to respectively challenge co-workers at all levels of the organization when necessary.
• Ability to work collaboratively in fast paced 24/7 manufacturing environment, including multitasking and prioritization.
•...
....Read more...
Type: Permanent Location: Brewton, US-AL
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:50
-
Your Job
The Paper Area Manufacturing Leader will be responsible for leading the day-to-day operations of our two paper machines at the Brewton mill.
This will include leading a team of 6 salaried direct reports and indirect responsibility for the entire paper team of 160+ employees.
They will partner closely with, act as a strategic thought partner, and report to the Paper Production Leader.
Our ideal candidate will aspire for continued career growth and advancement, beyond this opportunity.
This position will provide strategic and tactical leadership to achieve key objectives in safety, environmental compliance, reliability, production, quality, and cost.
The successful candidate will utilize problem solving skills while focusing on safely improving productivity and reducing cost through process/equipment optimization and operator knowledge/skill improvement with a high sense of urgency.
Our Team
The Brewton mill is located in south central Alabama about an hour from Mobile, AL, Pensacola, FL, and the beautiful beaches of the Gulf Coast.
The team is made up of 450 employees who produce white top linerboard and solid bleached sulfate (SBS) paperboard.
The SBS material is used to make GP's Dixie plates.
White top linerboard is used in production of corrugated containers and displays.
This position is an opportunity to be part of a rapidly expanding organization with tremendous growth potential.
The most recent $160M capital investment is expected to be completed in late 2024.
The Brewton mill was also the first fully integrated pulp and paper mill in the US to receive an Energy Star designation from the U.S.
Environmental Protection Agency.
To learn more about Georgia-Pacific's packaging business please visit: www.gppackaging.com and view the video How Paper Is Made! Our culture is defined by the Principle Based Management™ philosophy which guides everyday decision making and provides employees with opportunities to contribute and personally benefit from the value they create.
Learn more about our Brewton facility and employees here: We Are: Brewton
What You Will Do
• Providing leadership through application of Koch's Principled Based Management (PBM) philosophy to achieve superior results.
• Drive a culture of safety and environmental excellence through critical hazard identification, risk reduction and risk mitigation.
• Work with Area Leader and other leaders to coach and develop employees.
• Lead teams in the identification, development, evaluation and implementation of safety, quality, and /or cost reduction initiatives and projects that has the highest value to the operation to drive continuous improvement.
• Demonstrate ownership for planning outages and routine maintenance.
• Understand, communicate, and align goals in the areas of safety, quality, production, and reliability.
• Drive process and equipment modifications that result in improved product quality, reduced variation, and higher customer satisfact...
....Read more...
Type: Permanent Location: Brewton, US-AL
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:49
-
Senior Retail Media / eCommerce Solution Architect
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.
In this role, you will:
* Lead digital shelf ecosystem architecture, development, integration, implementation and operations in collaboration with the content, Ad Tech and data & analytics product teams.
* Manage features timelines, budgets, and resource allocation for digital shelf.
* Provide technical support to internal stakeholders on digital shelf related tools and processes.
* Identify and resolve technical issues related to content syndication, data mapping, and platform integrations.
* Manage data mapping, validation rules and data quality checks to ensure accurate product listing in collaboration with the data & analytics product teams and downstream application owners.
* Analyze digital shelf performance metrics to identify areas for improvement.
* Develop and implement strategies to optimize content delivery and product discoverability on the digital shelf.
* Develop and maintain automated workflows to syndicate product content to various retailer websites and marketplaces in collaboration with Content Solution Architect.
* In collaboration with legal, privacy and compliance, ensure that all architectural designs comply with CPRA/CCPA, GDPR, and other data privacy regulations.
* Stay current with industry trends in digital experience platforms and architecture, applying relevant advancements to improve solutions.
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 more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
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 i...
....Read more...
Type: Permanent Location: Buenos Aires, AR-B
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:47
-
Your Job
Georgia-Pacific's Plywood facility located in Taylorsville, Mississippi is now hiring for Production Utility Associates.
Compensation:
* $20.05 per hour
* $1.50 shift differential for night shift
* This role is eligible for variable pay
You will work as a part of a team committed to safety and production excellence.
There are opportunities for long-term growth and fulfillment in a supportive environment.
You will be able to contribute to a team that encourages critical thinking, driving initiative, and working collaboratively.
Our Team
Georgia-Pacific employees strive for safety and health excellence while achieving an injury-free workplace.
Georgia-Pacific's Building Products business is consistently among the nation's top suppliers of building products to large warehouse retailers and building materials dealers.
To learn more about our Building Products division, visit http://www.buildgp.com .
What You Will Do
* Maintain strict adherence to safety rules and regulations, to include wearing safety equipment
* Perform basic housekeeping responsibilities throughout the mill
* Continuous knowledge development through shadowing and training in various roles
* Perform basic operator care and preventive maintenance tasks
* Engage in tasks such as lifting, walking, climbing, stooping, pushing and/or pulling for twelve (12) or more hours a day
* Work in a hot, cold, humid, noisy, industrial environment
* Work around dust, oil, grease, chemicals, and other substances
Who You Are (Basic Qualifications)
* Experience in a farming, carpentry, construction, warehouse, military, production or manufacturing environment
What Will Put You Ahead
* At least one (1) or more years of experience in a farming, carpentry, construction, warehouse, military, production or manufacturing environment
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based packaging, cellulose, specialty fibers, building products and much more, Georgia-Pacific works to meet evolving needs of customers worldwide with quality products.
In addition to the products we make, we operate one of the largest recycling businesses.
Our more tha...
....Read more...
Type: Permanent Location: Taylorsville, US-MS
Salary / Rate: Not Specified
Posted: 2025-06-02 08:07:43
-
At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.â¯Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
People Leader
All Job Posting Locations:
Beijing, China
Job Description:
1.
 Principal Duties and Responsibilities (General Summary, essential functions and authorities, etc.)
    主è¦å·¥ä½èè´£ï¼åºæ¬æ¦åµï¼ä¸»è¦åè½ï¼æéçï¼
ï§Â   Align with company and commercial strategy, direct, develop and manage project registration activities focused on the define registration (and renewal) strategy, registration project plan, supervision on project execution and delivery.
ï§Â   åºäºå
¬å¸åä¸å¡çç¥ï¼æ导ãå¼åå管ç项ç®æ³¨åå·¥ä½ï¼çéäºå¶å®æ³¨åï¼å延ç»æ³¨åï¼æç¥ã注å项ç®è®¡åï¼çç£é¡¹ç®æ§è¡ä¸äº¤ä»ã
ï§Â   Manage day-to-day operation to ensure registration related projects/programs progress.
Review and approve required information for the registration dossier and technical requirement document.
ï§Â  Â
ï§Â   管çæ¥å¸¸è¿è¥ï¼ä»¥ç¡®ä¿æ³¨åç¸å
³é¡¹ç®/计åçæµç¨å¦¥åå®æ½ã审æ¹æ³¨åèµæåææ¯è¦æ±æ件æéä¿¡æ¯ã
ï§Â   Assign and allocate resources and actively oversee departmental (team) projects.
Provides managerial leadership & direction to assigned team allowing appropriate prioritization of resources to achieve goals.
ï§Â   åé
åé
ç½®èµæºï¼ç§¯æçç£é¨é¨ï¼å¢éï¼é¡¹ç®ãç»æå®å¢éæä¾ç®¡çå±é¢çå¼å¯¼ä¸æ导ï¼å
许éå½çèµæºä¼åé
置以å®ç°ç®æ ã
ï§Â   Interact and proactively forge new relationships with external partners, including global regulatory functions, quality, R&D, manufacture and commercial partners, Effectively communicates with franchise and local cross functional leaders.
ï§Â   ä¸å
¬å¸å¤é¨åä½ä¼ä¼´ï¼å
æ¬å
¨çæ³è§é¨é¨ãè´¨éãç åãç产ååä¸ä¼ä¼´äºå¨å¹¶ç§¯æ建ç«æ°å
³ç³»ãåæ»é¨åå½å°è·¨èè½é¨é¨è´è´£äººæææ²éã
ï§Â   Establish and maintain relationship with NMPA and other authorities, manage and maintain clear and effective internal-external communication channel.
ï§Â   ä¸NMPA以åå
¶ä»ç管é¨é¨å»ºç«å¹¶ç»´æè¯å¥½å
³ç³»ï¼ç®¡ç并维æ¤å
-å¤é¨ä¹é´çæææ²éæ¸ éãÂ
ï§Â   Provide regulatory support for cross functional departments and cultivate company regulatory compliance environment.
ï§Â   为跨èè½é¨é¨æä¾æ³è§æ¯æï¼å¹¶è¥é...
....Read more...
Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-06-02 08:05:02
-
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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Shanghai, China
Job Description:
Principal Duties and Responsibilities (General Summary, essential functions and authorities, etc.)
主要工作职责（基本概况，主要功能，权限等）
* 法规事务专员由其直线经理监督管理。法规事务专员负责多个法规事务项目的计划、执行和交付，以实现公司重大目标。法规事务专员负责在直线经理的监督管理下计划并执行所分配项目的注册工作；负责协调不同跨职能部门之间的工作，包括研发、生产、质量、医学事务、临床、法务以及其他职能部门，以满足项目注册之需要。本职位要求具备相应的法规和产品知识、一定的协调能力、沟通能力与执行能力，这些都会直接影响业务部门的运营结果。
RA Specialist is under the supervision from their line manager.
They will be responsible for planning, execution, and delivery of multiple RA projects to achieve significant company goals.
RA Specialist plan and execute the registration activities for assigned projects under their line manager’s supervision.
They coordinate activities of various cross-functional departments including research & development, manufacturing, quality, medical, clinical, legal, and other functions to meet the needs of project registration.
This role requires regulation and product knowledge, coordination, communication skills and execution which directly impact the operational results of the business unit.
* 主要职责/任务（以时间的百分比表示）：
* Key responsibilities/tasks （indicate estimated % of time spent where possible）：
* 70% 产品注册准备和执行。
* 70% Product registration preparation & execution.
* 10% 制定注册项目计划。
* 10% Develop registration project plan.
* 10% 为法规合规工作提供支持。
* 10% Support regulatory compliance activities.
* 10% 法规信息收集、解读和政策制定。
* 10% Regulatory intelligence collection, interpretation and policy shaping.
* 职责/主要衡量指标：
* Accountabilities/Key measures：
* 根据注册（以及延续注册）策略和注册项目计划，计划并执行项目注册工作。
* Plan an...
....Read more...
Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-06-02 08:05:01
-
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:
Professional
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
Scientist, Quality Control
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to create 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/.
Johnson & Johnson Services Inc., a member of the Johnson & Johnson Family of Companies, is recruiting a QC Scientist.
This position will be located in Leiden, Netherlands.
The Leiden Quality Control (QC) Leiden department is a Business Unit within the Leiden site, a biotherapeutics and vaccines manufacturing site belonging to the Johnson & Johnson Supply Chain.
The Leiden QC department is responsible for raw material, in-process, and release testing for products manufactured at the site.
Additionally, the Leiden QC department has a unique global responsibility and exposure by being the stability testing hub for large molecule products within the Johnson & Johnson Supply Chain, and by partnering with multiple Contract Manufacturing Organizations to perform the release testing.
The department is structured in different testing laboratories and supporting teams, which are divided based on specific techniques and/or expertise.
The Scientist will be part of the testing teams within the Quality Control (QC) department, acting as the scientific responsible person to support the analytical testing aspects associated with Drug Substance and Drug Product manufacturing.
This role involves troubleshooting of analytical methods, ensuring smooth entry of new methods into QC, proactively making improvements to test methods to stimulate executional excellence, managing product related deviations, leading investigations and analytical method transfers, and providing subject matter expertise for new equipment.
Additional responsibilities include participating as a Subject Matter Expert (SME) in internal and external audits, writing observation responses, and developing the next generation QC Scientists.
The Scientist...
....Read more...
Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:55
-
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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Product Submissions and Registration
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Employer: Auris Health, Inc.
Job Title: Senior Regulatory Affairs Specialist, Program Lead
Job Code: A011.485
Job Location: New Brunswick, NJ
Job Type: Full-Time
Rate of Pay: $135,000 - $160,000
Job Duties: Author regulatory submissions and support product development stages to help the organization achieve US and international regulatory (NPD) approval goals.
Support health authority communications and contribute to strategy development.
Manage, prepare, and submit regulatory submissions required for device approvals and registrations in the US and globally.
Oversee SME resources preparation of submission deliverables to meet regulatory requirements or other project objectives.
Correspond and collaborate with international J&J colleagues on international approval efforts.
Conduct regulatory evaluation of changes to Auris devices in accordance with requirements of commercial/operating geography and generate the required regulatory submission.
Anticipate program risk and make recommendations for mitigations.
Function as a Regulatory Affairs subject matter expert on new product introduction and lifecycle management supporting cross functional partners including clinical, marketing, and engineering through design control activities.
Conduct reviews and provide expert regulatory feedback on specifications, device testing, risk management, and other relevant documentation in accordance with regulatory requirements and positioning for regulatory submission.
Assist research personnel, application specialists, and risk management specialists to ensure clinical research and clinical evaluations are performed in accordance with regulatory requirements.
Support quality system and technical file/design dossier audits.
Translate and simplify problems of considerable scope and complexity into manageable tasks with measurable requirements.
May telecommute.
Requirements: Employer will accept a Master's degree in Pharmacy Administration, Biomechanical Engineering, or related field and 4 years of experience in the job offered or in a Senior Regulatory Affairs Specialist, Program Lead-related occupation.
This job posting is anticipated t...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:55
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Finance Business Partners
Job Category:
Professional
All Job Posting Locations:
Cincinnati, Ohio, United States of America, Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson is recruiting a Senior Financial Analyst.
This position is based in Cincinnati, OH or Raritan, NJ.
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/.
Position Overview
The Senior Financial Analyst role is essential in developing deals for our US Surgery customers as well as developing creative pricing programs and solutions to grow our overall business.
A successful candidate will learn how the business directly interacts with the administration and clinical staff at the hospital systems.
Key Responsibilities:
* Leads the creation of financial models for customer deals in close connection with Offer Development, Account & Key Account Management teams.
* Fully owns and presents financial models at Pricing Committee meetings when requested.
* Develop a deep understanding of End User sales and how pricing decisions impact overall value for both the business and the customer
* Partners closely with Brand Marketing finance teams and Gross to Net teams to bring greater transparency to pricing decisions and impacts to overall business results.
* Works directly on, and shapes complex analytical pricing & marketing projects.
* Ability to independently manage timelines and deliverables to ensure customer response expectations are met.
* Presents ad hoc analyses and presentations for management as unique customer situations arise.
Qualifications:
* Minimum of a bachelor's degree required, preferably a major in Accounting, Finance or other related field
* At least 3 years of work experience in accounting, finance or related field required.
* Strong Excel and PowerPoint skills
* This position is based in Cincinnati, OH or Raritan, NJ and 10% of t...
....Read more...
Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:54
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Finance Business Partners
Job Category:
Professional
All Job Posting Locations:
Istanbul, Turkey
Job Description:
We are looking for a skilled and proactive Senior Financial Analyst to join our finance team.
This role is instrumental in driving financial performance and ensuring compliance with accounting standards.
The ideal candidate will collaborate with various business partners to provide strategic insights that support decision-making and enhance financial management.
Key Responsibilities:
* Monthly & Quarterly Reporting: Prepare and submit comprehensive close reports to meet organizational policies and deadlines, ensuring accuracy and transparency.
* Budgeting & Forecasting: Actively participate in the budgeting process and rolling forecasts, contributing valuable insights to enhance the financial planning framework.
* Internal Reporting: Monitor and track actual costs against budget, providing regular updates and insightful analyses to key stakeholders.
* Strategic Development: Collaborate with business partners to develop strategic business cases, offering financial insights and recommendations to drive organizational goals.
* Compliance Assurance: Ensure adherence to accounting policies and internal requirements, fostering integrity in all financial practices.
* Metric Management: Manage and monitor key performance indicators (KPIs), providing detailed tracking reports to facilitate performance assessment.
* Project Participation: Engage in local and regional special projects, including systems implementations, process improvements, and strategic data analysis.
Provide ad hoc support as needed.
Requirements:
* Bachelor’s or master’s degree in Business Administration, Accounting, or a related field.
* 3-5 years of experience in finance, preferably within the pharmaceutical industry; experience in a Reputable Audit Company is a plus.
* Strong understanding of accounting fundamentals, financial control, budgeting, and reporting processes.
* Proficiency in accounting software (SAP BPC, FM, FI, and CO) and advanced Excel skills.
* Excellent command of both oral and written English.
* Compliance-oriented with a strong commitment to ethical financial practices.
* Strong communication and analytical skills and a proactive mindset.
....Read more...
Type: Permanent Location: Istanbul, TR-34
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:47
-
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:
Ciudad Juarez, Chihuahua, Mexico
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Senior Trainer to be in Ciudad Juarez.
Purpose:
Along with the Training Coordinator, the trainer ensures that all manufacturing associates are trained to the corresponding specifications / procedures, as established in the training curriculum.
· Execute New Hire Orientation activities (NHO) as required.
· Assign exams to assess the training effectiveness.
· Document training activities and verify documentation related to training.
· Supports the development of programs and materials for the effectiveness of training for manufacturing personnel.
· Support in the maintenance of department files.
· Maintains reports and department records (matrix, records, reports, etc.)
· Supports manufacturing associates in solving machine and product / process problems.
· Supports manufacturing activities related to training as required.
· Participates in Site's safety initiatives.
· Know and comply with all safety regulations established by the company.
You will be responsible for:
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Along with the Training Coordinator, the trainer ensures that all manufacturing associates are trained to the corresponding specifications / procedures, as established in the training curriculum.
* Execute New Hire Orientation activities (NHO) as required.
* Assign exams to assess the training effectiveness.
* Document training activities and verify documentation related to training.
* Supports the development of programs and materials for the effectiveness of training for manufacturing personnel.
* Support in the maintenance of department files.
* Maintains reports and department records (matrix, records, reports, etc.)
* Supports manufacturing associates in solving machine and product / process problems.
* Supports manufacturing...
....Read more...
Type: Permanent Location: Ciudad Juarez, MX-CHH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:46
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Planning
Job Sub Function:
Demand Planning
Job Category:
Professional
All Job Posting Locations:
Markham, Ontario, Canada
Job Description:
Johnson & Johnson MedTech is recruiting for a Senior Demand Planner.
This position is located in Markham, ON Canada.
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
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
As a Senior Demand Planner, you will play a key role in the Sales & Operations Planning Process to drive the alignment among Supply Chain, Finance, and Commercial functions for the reliable demand forecast.
You will drive the monthly cadence of the S&OP Cycle (Demand Review, Supply Review) and will contribute to the maturity of the Demand Planning process towards IBP (Integrated Business Planning).
You also work closely with the Supply Planning team to deliver the outstanding service level, optimize inventory, and reduce obsolescence.
In addition, you are the key linkage point with the Global Planning organizations ensuring End-to-End visibility and synchronicity between global and local supply chain.
Responsibilities:
* Lead the Canadian S&OP process for the assigned portfolio of products aiming to align Commercial and Supply Chain plans.
* Own critical metrics related to product portfolio (OTIF, forecast accuracy, NPI on-time launch and Life Cycle Management) and contributes to other supply chain related measurements (Inventory, obsolescence and write-offs)
* Review statistical forecast generated and provide input on changes that may be required.
Collaborate with functions such as Sales, Marketing, Commercial Operations, and Finance to identify and incorporate market intelligence (events) into the demand forecast.
* Proactively identify and resolve directly or through business partnership any issue affecting the product flow.
* Collaborate with global supply chain teams on projects affecting the product portfolio and/or the supply network.
* Partner with the Field Assets Management team to find opportunities and implement solutions for field assets optimization - if applicable.
* Ensure positive rel...
....Read more...
Type: Permanent Location: Markham, CA-ON
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:42
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Leiden, Netherlands
Job Description:
Are you ready to take on a unique and exciting opportunity as a Specialist QA – GMP Quality Systems Compliance? Johnson & Johnson is seeking a highly motivated individual to join our team in Leiden, Netherlands with an unlimited contract.
This is your chance to be part of a world-class organization that is committed to innovation and delivering flawless quality in everything we do.
As the Specialist QA – GMP Quality Systems Compliance, you will play a crucial role in ensuring that our operations meet the highest standards of quality and compliance.
You will have the opportunity to work with a team of exceptional professionals and contribute to the success of our goals.
Ensures a professional, up to date, high quality level of JBV’s core Quality Systems and its application of these systems to maintain and improve the compliance status of JBV’s processes and systems in line with the regulatory, JBV, Janssen Supply Chain and J&J standards.
Develops and updates quality systems and procedures when appropriate.
Advises Q&C Management and the executing departments regarding compliance issues and ensure resolution.
Essential Job Duties and Responsibilities GMP Specialist
Acts as a Center of Expertise for GMP core quality systems.
Maintains and improves GMP core quality systems, ensuring that the JBV quality systems are compliant, state-of-the-art, and efficient.
Ensures consistency in the quality systems across processes and departments.
Has an outstanding knowledge of GMP regulations, Janssen and J&J standards and translates these requirements in JBV systems that are compliant.
Is responsible for the Inspection Readiness program for the quality systems under his/her responsibility ensuring that JBV is in compliance with the GMP regulations and has a high First Time Pass for all regulatory inspections.
Performs internal audits as a (lead/team) auditor.
Identifies critical areas for improvement through audits and assessments and prioritizes and executes the compliance improvements initiatives resulting from this.
Uses appropriate assessment tools (e.g., PE, Lean, Risk Management principles) in assessing the status of current quality processes and in introducing improvements.
Ensures that quality initiatives are implemented effectively across all relevant...
....Read more...
Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:42
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Sales Enablement
Job Sub Function:
Sales Operations & Administration
Job Category:
People Leader
All Job Posting Locations:
Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, West Chester, Pennsylvania, United States of America
Job Description:
We are searching for the best talent for a Senior Manager of Commercial Operations Systems to be in Raynham, MA, West Chester, PA or Palm Beach Gardens, FL.
About Orthopaedics
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 Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.
Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Purpose:
We are seeking a dynamic and experienced Senior Manager of Commercial Operations Systems to lead our key technology strategy and deployment initiatives within our Orthopaedics business.
This role will focus on the strategic alignment and deployment of technology solutions that drive operational efficiency and enhance sales and commercial effectiveness.
In this role, you will have the opportunity to lead the strategy, design, and delivery of new and innovative technologies, as well as enhancements to existing technologies, that will modernize the experience for our commercial teams.
These include field inventory management systems, set tracking capabilities, and ERP upgrades.
The role will interface with several connected organizations, providing the opportunity to gain exposure to the broader Orthopaedics organization.
Key Responsibilities
* Strategic Leadership: Develop and execute a comprehensive technology strategy for Orthopaedics Sales and Commercial Operations, ensuring alignment with overall business objectives.
* Business Process Ownership: Provide guidance and serve as subject matter expert on business requirements that Information Technology partners will use...
....Read more...
Type: Permanent Location: Raynham, US-MA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:39
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Professional
All Job Posting Locations:
Toronto, Ontario, Canada
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 an Associate Site Manager (Clinical Research Associate).
This position is a field-based role covering primarily the Greater Toronto Area, Ontario; occasional travel outside of this province as needed. Ideally, the Associate Site Manager should be located in the Greater Toronto Area.
Purpose:
As an Associate Site Manager (Clinical Research Associate), you will be part of the Global Clinical Operations (GCO) Canada team and will be responsible for study site management through the assessment/selection, initiation, maintenance and closure phases of a clinical trial (Phase 1 – 4 trials).
You will be responsible for:
* You are the primary point of contact for the study site; liaison with study teams.
* Your responsibilities include actively identifying and driving patient recruitment strategies at assigned sites.
* You are responsible for monitoring the study/site according to GCP standards and J&J GCO SOPs, both on-site and with remote contacts.
This includes source document verification, Investigator Site File (ISF) review and accurate drug accountability.
* You will provide site training, during site initiation and ongoing, to ensure compliance with all required regulations, SOPs, trial-specific tools and systems, and specialized procedures.
* You will ensure resolution of site-specific issues and will partner closely with investigator and site staff to meet all study timelines.
* You will work closely with the local study operations team to resolve protocol and site-specific issues.
* You will use and maintain the clinical trial tracking system (CTMS) and update the electronic Trial Master File (TMF) as required.
Qualifications / Requirements:
* Bachelor of Science, R.N., or equivalent degree in Biologica...
....Read more...
Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:37
