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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...
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Type: Permanent Location: Buenos Aires, AR-B
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:47
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
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...
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-06-02 08:05:01
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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:
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...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:55
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
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...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:55
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
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.
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Type: Permanent Location: Istanbul, TR-34
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:47
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
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...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:42
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Affairs
Job Category:
Scientific/Technology
All Job Posting Locations:
Horsham, Pennsylvania, United States of America
Job Description:
About Immunology
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.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases.
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 Associate Director, Global Medical Affairs Execution in our Global Commercial Strategic Organization (GCSO) Immunology Medical Affairs organization to be located in Horsham, PA.
Purpose:
The Associate Director, Global Medical Affairs Execution supports the strategic objectives of the J&J Innovative Medicine Immunology Global Medical Affairs (GMAF) team.
This individual will partner within designated Immunology disease areas ensuring execution of GMAF data generation and dissemination strategies in support of the GMAF Immunology team.
You will be responsible for:
* Partner with GMAF Leaders in preparing robust strategies (including integrated evidence generation plans) for compounds in development that reflect prioritized regional needs and support medical launch excellence
* Global Medical Affairs Team management and coordination
* Development and execution of globally funded medical strategies (i.e.
advisory boards, steering committees, external data landscapes, internal training, etc.)
* Development and execution of comprehensive scientific engagement strategies and congress plans (i.e.
manage internal congress websites, pre/post congress meetings, onsite HCP meetings, etc.)
Qualifications / Requirements:
* A minimum of a Bachelor’s degree is required, an advanced degree preferred
* A minimum of 6 years of relevant work experience is required
* Experience in a medical, clinical or scientific environment is required
* Project leadership and strong organizational skills are ...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:35
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Facilities – Operations, binnen onze afdeling “Engineering & Property services” beheert de kritische gebouwen, HVAC, nutsvoorzieningen (stoom, koelmedia, verwarmingsmedia, watersystemen, perslucht, hoogspanning…) en installaties (stoomvormers, koelcellen, luchtgroepen, clean rooms, magazijnen...) op de sites te Beerse, Geel, Olen, Merksem, La Louviere, Courcelles en Gent; vanaf de centrale productie en distributie tot in de chemische, farmaceutische productie- en R&D-gebouwen en Advanced Therapy labo’s.
Voor de groep welke verantwoordelijk is voor de onderhoudsystemen en compliance methodieken, voor de uitbating van kritische installaties/systemen/services op de verschillende Belgische campussen, zijn we op zoek naar een Senior Compliance Engineer:
Doel:
* Het managen van de compliance methodieken binnen E&PS.
* Expert in de levenscyclus voor computer system validation, level 1 tot en met level 4 systemen, binnen E&PS.
* Coordineren van de compliance status van verschillende services, zoals programma soft services beheer, pestcontrole, cleaning.
* Bewaken van de uitbestede services, operationele compliance en projectkwalificaties gedragen door commissioning en kwalificatie.
* Opvolgen van het inspectie readiness programma voor de E&PS organisatie.
* Expertise in de processen zoals mappingen, certificatie, calibratie en andere.
* Aanspreekpunt voor de verschillende compliance programma’s komende van J&J en E&PS globaal naar implementatie.
* Ondersteunen van andere E&PS sites, op vraag.
U bent verantwoordelijk voor:
* Ownership over het horizontaal proces “compliance”.
+ Coordineert de periodieke meeting met de Compliance Engineers uit de operationele zuilen;
+ Beheerder van het ontwikkelings- en overleg model voor de compliance methodieken.
* Aanspreekpunt computer system validation voor de bestaande E&PS systemen en de nieuwe ontwikkelingen.
+ Beheerder, vanuit het escalatie model, over de bestaande ticketten van de computer systemen;
+ Evalueert en ondersteunt nieuwe ontwikkelingsvragen vanuit E&PS.
* Coordineren en ondersteunen van de compliance activiteiten van de verschillende E&PS services tot een inspectie re...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:15
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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:
Legal & Compliance
Job Sub Function:
Health Care Compliance
Job Category:
Professional
All Job Posting Locations:
Bucureşti, Romania
Job Description:
Senior Health Care Compliance Specialist
Location: Romania
Full-Time - permanent contract
SUMMARY:
The Health Care Compliance Senior Specialist supports Health Care Compliance Programs to ensure business practices and activities are in compliance with related Johnson & Johnson internal guidelines, local laws and regulations and anticorruption laws, including the Foreign Corrupt Practices act.
Therefore, the candidate supports planning, trainings, assessments, testing & monitoring and other varied Health Care Compliance functions.
This position reports directly to the Health Care Compliance Officer.
Position is located in Bucharest and supports the Health Care Compliance Program in Romania.
PROFILE:
* Requires strong communication, organizational and analytical skills
* Proven track record in delivering results, self-starter and ability to manage complexity it is a must
* Industry related experience preferred, experience in the Pharmaceutical or Consumer industries
* Ability to work independently and in a detailed manner
* Ability to manage conflicts in an open and constructive manner
* Ability to work well between functions and across all levels of the business and effective time management skills are essential
* Understands the J&J Credo based culture and able to make things happen through managing a broad set of J&J Credo based values
* Background may include Compliance, Medical Affairs, Regulatory
* Fluent in English language
ESSENTIAL DUTIES AND RESPONSIBILITIES:
The Health Care Compliance Senior Specialist will work with Health Care Compliance Officer (HCCO) - to implement the company’s compliance program on various activities, which may include but not limited to the following:
* Assist HCCO in the update and implementation of all HCC policies (SOPs) and procedures on an ongoing basis.
* Support the HCCO in the implementation of education, training, and regular communications in compliance to all covered employees, including local sales, marketing, medical affairs, finance, HR, supply chain at the local level.
* Prepare the report of unplanned deviations, consolidate data & metrics relevant to Risk Assessment process and support HCCO in managing day-to-day inquiries, al...
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Type: Permanent Location: Bucureşti, RO-B
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:09
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Business Support
Job Sub Function:
Administration & Secretarial
Job Category:
Business Enablement/Support
All Job Posting Locations:
Amersfoort, Utrecht, Netherlands
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Administrator to be in Amersfoort!
The Administrator Service Center plays a crucial role in ensuring the smooth and efficient operation of the organization by managing administrative tasks, coordinating office activities, and providing support to various departments.
The primary goal of this position is to facilitate a well-organized and productive work environment so that the organization can achieve its objectives.
You will be responsible for:
* Office Management: Supervise daily office operations and ensure a clean and organized work environment.
Manage office supplies, equipment, and facilities to meet the needs of the staff.
* Communication and Correspondence: Manage incoming and outgoing communications, including emails, phone calls, and written correspondence.
* Record and Data Management: Maintain accurate records, files, and databases.
Assist with data entry and retrieval, ensuring the confidentiality and integrity of information.
* Support to Management: Provide administrative support to executives and managers.
Help prepare reports, presentations, and documentation as needed.
* Teamwork: Collaborate with various departments to facilitate cross-functional communication and cooperation.
Qualifications/Requirements:
* Secondary education; additional training or certification in office management or a related field is a plus.
* Full proficiency in Dutch and English, both written and spoken, at a professional level is required.
* Proven experience in administrative roles, with a successful track record in effectively managing office operations and familiarity with common office software and tools.
* Strong verbal and written communication skills to effectively connect with individuals at all levels within the organization.
* Outstanding organizational and multitasking skills with a focus on accuracy and completeness.
*...
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Type: Permanent Location: Amersfoort, NL-UT
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:02
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Manufacturing Pharmaceutical Process Operations
Job Category:
People Leader
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
Are you an enthusiastic leader who flourishes in a dynamic and fast-paced environment who like to be directly involved in the fight against complex diseases?
Do you possess the expertise and experience to drive operational excellence, foster a culture of inclusion, and deliver outstanding results? If so, an exciting opportunity awaits you!
The Fermentation department:
For our Fermentation department within Operations, we are looking for a driven Senior Supervisor working 16/7 shift schedule.
In this role, you are responsible for the production of monoclonal antibodies within a safe and controlled "cleanroom" environment.
You manage a team and contribute to achieving the production and quality standards, as laid down in the Master Production Schedule (MPS) or Shipment Schedule.
You work according to the standards in the field of Environment, Health, Safety & Sustainability (EHS&S), cGMP and LEAN.
Together with your fellow (Senior) Manufacturing Supervisors, you are responsible for achieving the core results of the department.
You are committed to continuously improving processes and working methods and creating a stimulating and learning work environment for your team.
Job Description:
As Senior Manufacturing Supervisor, you will lead a group of approx.
15 operators within the fermentation department, that is approx.
160 employees.
You work closely with the other (sr) manufacturing supervisors, manufacturing specialists, process engineers, trainers, QA, QC and MAM.
Leads processes and assignments for the Operations unit and supports organizational objectives and business goals.
Defines project terms to meet objectives and goals of the Operations unit.
Establishes workflow for strategic plans and serves as a primary point of contact for the Operations unit.
Maintains high standards of professionalism, efficiency, personal communication, discretion, and independent judgment.
The Senior Manufacturing Supervisor gets the best out of his or her people and is responsible for delivering a high-quality environment within the applicable standards in the field of safety and compliance.
Specific tasks and job duties of the position that are required daily:
* Be responsible for daily operations to...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:03:58
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Athens, Georgia, 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 Senior CQV (Commissioning, Qualification, and Validation) Engineer! This hybrid position will be located in Athens, Georgia!
Are you interested in joining a team that is helping improve patient care and drive innovation? At Johnson & Johnson, we blend heart, science, and ingenuity to profoundly change the trajectory of health for humanity.
Apply today for this exciting opening to support us at our pharmaceutical plant!
The Senior CQV Engineer is responsible for supporting the qualification of cleanroom facilities and large process equipment at pharmaceutical manufacturing sites in Athens, GA.
They will also be responsible for hands-on writing and executing of qualification protocols (IQ, OQ, PQ) and preparing final validation reports.
Key Responsibilities:
- Perform CQV activities for cleanroom areas and large process equipment, including but not limited to: Vessels (Bioreactors, Fermenters, Mixing Tanks); Centrifuges; Pharma Dryers; and/or CIP (Clean-in-Place) Skids.
- Develop, execute, and review Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
- Generate and maintain validation documentation, including final reports ensuring compliance with GMP, FDA, and industry standards.
- Work closely with engineering, quality, and operations teams to troubleshoot validation challenges and implement corrective actions.
- Support regulatory audits and inspections by providing validation documentation and justifications.
- Ensure compliance with cGMP, 21 CFR Part 11, ISPE Baseline Guides, and ASTM E2500 methodologies.
- Assist in risk assessments, change control evaluations, and impact assessments for equipment modifications.
QUALIFICATIONS:
EDUCATION:
- Minimum of a Bachelor's ...
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Type: Permanent Location: Athens, US-GA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:03:52
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
People Leader
All Job Posting Locations:
Philadelphia, Pennsylvania, United States
Job Description:
Johnson & Johnson Innovative Medicine is searching for the best talent for Senior Medical Science Liaison-Neuroimmunology for the Upstate region.
This is a field-based position located in the Upstate region. The ideal location is the Philadelphia area, and the territory covers the New York, Pennsylvania and West Virginia.
About Immunology
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.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases. 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
The Senior Medical Science Liaison (Sr.
MSL) is responsible for providing fair balanced, objective, scientific information, and education to opinion leaders (OLs), health care professionals, and to internal partners as required by scientific and business needs.
The Sr.
MSL is considered an established scientific and clinical knowledge lead on current and future J&J Innovative Medicine products per Therapeutic Area (TA) alignment. The Sr.
MSL is responsible for staying abreast of current scientific and treatment landscape trends in their therapeutic areas of interest. The Sr.
MSL provides research support for company and investigator-initiated research. The Sr MSL will function with high integrity and follow credo values.
The Sr.
MSL will be responsible for:
* Building external relationships with identified KOLs and health care providers (MD, PA, NP, RN, Pharm.D., bio coordinators) and developing and managing a geographical territory.
These relationships and engagements can include both virtual & in-person, with a prioritization of in-person engagements when appropriate.
* Developing and maintaining a territory strategic plan, which includes educational activities with identified OLs, HCPs, institutions, and community practic...
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Type: Permanent Location: Philadelphia, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:03:46
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Toronto, Ontario, Canada
Job Description:
We are searching for the best talent for our Manager, Regulatory Affairs position to be located in Toronto, Ontario under the flexible working model (at least 3 days in office).
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
Purpose:
The Regulatory Affairs Manager is responsible for managing and leading the regulatory activities to obtain and maintain drug product registration status in compliance with Canadian drug laws and regulations, as well as corporate policies and procedures.
As a subject matter expert and leader for Regulatory Affairs, the individual will provide guidance to local and global business partners.
This role may have direct report(s).
You will be responsible for:
* Developing and implementing regulatory strategic plans for product registration and lifecycle management.
* Leading the preparation of regulatory submissions including New Drug Submissions (NDSs), Supplemental New Drug Submissions (SNDSs), and ad hoc reports to Health Canada, and maintain the life cycle of currently marketed products.
The focus of this role is on the clinical/therapeutic claims and not the Chemistry, Manufacturing and Controls.
* Leading the development and review of responses to Health Canada queries in relation to clinical efficacy and safety, clinical pharmacology, biopharmaceutics and preclinical subject matter (e.g.
Clarifax, Notice of Non-Compliance [NON], and Notice of Deficiency [NOD]).
* Leading interactions with Health Canada throughout the submission review cycle to ensure timely regulatory approval and optimal labelling.
* Collaborating with global cross-functional teams and the Global Regulatory Affairs (GRA) function/teams to facilitate regulatory activities.
* Collaborating with internal partners to ensure alignment of regulatory affairs strategy with business priorities, and to meet strategic business obje...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-06-02 08:03:45
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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:
Medical Affairs Group
Job Sub Function:
Medical Affairs
Job Category:
People Leader
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
Johnson and Johnson is currently seeking a Senior Director, Medical Strategy, PH located in Titusville, NJ.
About Pulmonary Hypertension
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.
Our Pulmonary Hypertension team is focused on transforming the disease into a long-term manageable condition.
Bringing your passion for health to this team will help discover and develop effective treatments that help patients live their best possible life.
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
J&J Pulmonary Hypertension is a leader in the field of pulmonary arterial hypertension (PAH).
Our portfolio of PAH treatments covers the spectrum of disease, from WHO Functional Class (FC) II through to FC IV, with oral, inhaled and intravenous medications.
The Senior Director, Medical Strategy, PH, will lead a multifaceted critical function for the operating company by supporting multiple products in the broad PAH portfolio and pipeline, reporting directly into the VP, Medical Affairs, PH.
A strong insight into the PH therapeutic area and knowledge of the US market is required. The Senior Director, Medical Strategy will be part of the Medical Affairs Leadership Team. The Senior Director, Medical Strategy will be an expert in medical strategy development and will lead the overall medical strategy team to develop a portfolio medical strategy of products under his/her supervision with a goal to address medical and scientific issues and to ensure the appropriate use of all relevant J&J Medical Affairs supported products.
Duties and responsibilities include, but are not limited to:
* Identify and develop strategies to address crucial gaps using critical relationships with KOLs, Medical Societies, Global Medical Affairs, R&D, RW V&E (HEOR), Commercial, and others.
* Provides leadership and oversight on external engagement plan and represents US MAF with key external stakeholders.
* Helps to develop...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-02 08:03:36
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Automation Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
CH008 Cilag AG, Schaffhausen, Schaffhausen, Switzerland
Job Description:
Für die Welt sorgen … beim Einzelnen beginnen.
Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson.
Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.
Die Cilag AG ist ein internationales Entwicklungs- und Produktionsunternehmen der Pharmasparte von Johnson & Johnson mit Sitz in Schaffhausen und ist zuständig für die Herstellung von biotechnologischen, chemischen und pharmazeutischen Produkten.
Wir produzieren hochqualifizierte Wirkstoffe (Active Pharmaceutical Ingredients (APIs), Pharma- und Medizinprodukte.
Durch die kreative und innovative Vorgehensweise ist es uns möglich kontinuierlich die Einführung von neuen Produkten, Prozessen und Technologien zu gewährleisten.
Heute ist die Cilag AG eine der führenden Pharmaproduktionsunternehmen der Schweiz und beliefert alle bedeutenden Globalen Märkte.
Zur Verstärkung unserer Execution Systems-Gruppe suchen wir zum nächstmöglichen Zeitpunkt einen teamfähigen, fachlich ausgewiesenen:
Senior Execution System Engineer (w/m/d) 80-100%
Die Execution Systems-Gruppe ist verantwortlich für alle Systeme der Betriebsleitebene.
Dazu gehören die Schnittstellen zu Produktionsplanungssystemen (SAP), die Schnittstellen zu den Automationssystemen zur Anbindung der verteilten Systeme der Produktion, sowie die klassische Datenerfassung und Aufbereitung wie Betriebsdatenerfassung (BDE), Maschinendatenerfassung (MDE), aber auch alle anderen Prozesse, die eine zeitnahe Auswirkung auf Fertigungs- und Produktionsprozesse haben.
In diese Bereiche fallen Systeme zu Operational Intelligence/Business Intelligence (OI/BI), Manufacturing Execution Systems (MES WERUM PAS-X) und Data-Historian (OSI PI).
Hauptaufgaben
· Einführung, Betreuung und Optimierung der Level 3 Systeme wie MES PAS-X,
· Erstellung von GenericMasterBatch Records (GMBR)
· Erstellung von ParametrizeMasterBatch Records (PMBR)
· LifeCycleManagement von Parametervalue Listen
· Schnittstelle zwischen den Operation Support Gruppen und Execution Systems
· Mitarbeit in Projektteams für neue Produkteinführung.
· Unterstützung bei Qualifizie...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:03:34
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Your Job
We are seeking an Operations Manager to manage our Log Yard, Stranding, and Drying area to join our team at Georgia-Pacific's Clarendon OSB manufacturing facility mill in Alcolu, SC.
The Alcolu facility is critically important to GP's Building Products business, and the Operations Manager role supports the leadership team and Plant Manager in guiding operations and reliability measures to ensure operational excellence and preferred partner status.
The role works to develop and own key measures of success and drives accountability within the site.
This role also manages and supervises the Team Leads and develops a cadence of consistency to support the team, filling in for the Plant Manager as needed.
Our Team
Georgia-Pacific Clarendon OSB is one of the newest facilities using some of the most advanced technology to create the specialty brand of Blue-Ribbon Oriented Strand Board (OSB).
This type of OSB is used for floor, wall, and roof sheathing in residential and light commercial construction applications.
To learn more about Georgia-Pacific's OSB Division please visit: www.buildgp.com/plywood-osb .
What You Will Do
* Lead a wood products production team to work injury-free/incident free in a continuous manufacturing environment - consistent with our Principle Based Management philosophy and framework.
* Supervise/coordinate production efforts that result in long term improvement in work processes - including, but not limited to: Environmental, Health & Safety (EHS) compliance, variability reduction, reliability, quality, production, and costs.
* Facilitate team development and communication, employee skill development, problem-solving and resolution, and build employee commitment and ownership.
* Establish roles, responsibilities, and expectations for direct reports with appropriate coaching, feedback, and development, to achieve results.
* Drive cultural change in which employees take ownership for running the facility.
* Support a variety of shift schedules such as day / night / weekends / holidays, with the understanding that shift schedules can change during employment
* Work in a variety of environments such as, but not limited to: confined spaces, high spaces, hot/cold/humid/noisy
* Wear the necessary Personal Protection Equipment (PPE) - hard hat, safety glasses, face shield, chemical suit, respirator, ear plugs, hearing protection, steel-toe boots / shoes, and other PPE required for specific jobs.
Also must be able to work without wearing jewelry
Who You Are (Basic Qualifications)
* Supervisory experience in an industrial, manufacturing, or military environment that includes a strong understanding of not only production, but also day to day operations including, but not limited to the following: HR, EHS, Quality
* Must have a solid working knowledge of MS Word (creating, editing, formatting documents, preparing reports and tables) and Excel (creating, modifying spreadshe...
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Type: Permanent Location: Alcolu, US-SC
Salary / Rate: Not Specified
Posted: 2025-06-02 08:00:47
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At EVRAZ, our strength starts with our people! As a team we collaborate to solve problems, contribute ideas and challenge each other to ensure growth and ultimately success for the business and our employees.
Job Description and Responsibilities
Join EVRAZ North America’s Portland team as an Asset Maintenance Coordinator and play a pivotal role in ensuring the optimal performance and longevity of our industrial assets.
This position is integral to our operations, directly influencing efficiency and productivity across the company.
* Effectively manage and develop plans for inspections, monitor and evaluate results; plans should include predictive and preventative maintenance for assigned assets
* Develop maintenance budgets for assigned assets including maintenance CAPEX repair projects
* Monitor and manage Key Performance Indicators (KPIs) and metrics for assigned tasks
* Develop plans for maintenance downturns, major plant shutdowns and CAPEX repair projects for assigned assets
* Train staff as required
Requirements
* Minimum of five (5) years experience working as an Industrial Engineer, Journeyman Electrical or Mechanical Craftsperson or as a Maintenance Facility Coordinator in an industrial manufacturing environment
* Strong computer skills in MS Excel, Projects and PowerPoint
* Proven teamwork, communication (oral and written), administrative and organizational skills
* Understanding of equipment technologies and limitations and their effect on safety, quality, productivity and cost
* Ability to read blueprints and schematic drawings
* Good written and oral communication skills
* Good problem solving and analytical skills
* Familiarity with predictive maintenance tools (vibration analysis, thermographic imaging, ultra sound, laser alignment, etc)
Our total compensation package includes amazing benefits!
* Competitive wages and bonus opportunities
* Family medical, dental, and prescription coverage at minimal employee cost
* Short and long term disability programs
* Competitive retirement plans
* Flexible Spending and Health Savings Accounts
* Employer-provided and Voluntary Life Insurance options
* Paid vacation and recognized statutory holidays
* Apprenticeship and career advancement within the company
* Tuition reimbursement
* Wellness program
All applicants must be eligible to work in the USA.
While we thank all those who apply, only those being actively considered for employment will be contacted.
Equal Opportunity Employer
EVRAZ North America is an Equal Opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.
EVRAZ North America is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities.
If you need special...
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Type: Permanent Location: Portland, US-OR
Salary / Rate: Not Specified
Posted: 2025-06-01 08:11:39
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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!
Historically, the role of IT has been to provide a reliable ecosystem to run the business, drive efficiencies and reduce costs.
These areas remain integral, however, driven by the quickening pace of innovation, IT must evolve, proactively partnering with the business to enable new digital business models that power new types of customer engagement.
At Elanco, our engineer roles bring adaptive set of skills covering Software-as-a-Service (SaaS), Commercial-of-the-Shelf (CotS) and/or Custom Developed applications.
The role is part of our software engineering team established to deliver Engineering expertise to business facing products and services.
As an Engineer you will be deployed into a multi-disciplined product team applying your software engineering talent to Elanco’s biggest opportunities.
To be successful in an engineering role in Elanco requires a highly motivated individual, with an innovative mindset and a willingness to drive tangible outcomes.
The individual must be able to articulate complex technical topics and collaborate with the internal engineering organisation to improve engineering across the enterprise.
Your Responsibilities:
Engineering
* Join a diverse engineering organisation and contribute to growing our engineering capabilities across Software, and Platform Engineering.
* Develop full-stack solutions, building highly scalable distributed solutions that enable positive user experiences and measurable business growth.
* Implement and support modern digital products that are technologically sound, avoid technical debt, guarantee compliance, and enable the required business outcome.
* Collaborate across Platform Engineering teams to provide input to shaping their products allowing software engineers to deliver business value faster than ever before.
* Look for continuous improvement opportunities in our core ecosystem identifying new ways to enhance application team and developer experience.
* Embed security, privacy, data protection and quality assuran...
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Type: Permanent Location: Hook, GB-HAM
Salary / Rate: 48700
Posted: 2025-06-01 08:10:49
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Position Summary
Touchstone Advanced Composites, a subsidiary of Core Natural Resources, is a rapidly growing supplier of high-tech tools and composite parts to the aerospace, space, defense, and other industries. We are seeking a motivated individual for the position of Production Planner who enjoys developing, maintaining, and tracking detailed schedules and driving optimal utilization of resources and equipment while working in a team environment to produce high-quality products. This position will work closely with production, engineering, management and other stakeholders to produce and maintain optimal resource planning and tracking as well as inventory management in the manufacturing environment.
Target Responsibilities
* Accept, embrace, and promote the following Core Values of Core Natural Resources: Safety, Compliance & Continuous Improvement
* Develop and maintain production schedules that align with the business plan, customer demand and inventory levels
* Utilize MRP (Material Requirements Planning) systems and resource planning systems to manage resource utilization and material flow in a manufacturing environment
* Collaborate with cross-functional teams including procurement, production, engineering and management to streamline operations
* Scheduling – Identify capacity issues and provide feedback to engineering and management
* Monitor production performance metrics and adjust schedules as necessary to meet changing demands
* Maintain accurate records of inventory levels, production schedules, and resource allocation
Required Skills and Experience
* Must be at least 18 years of age.
* Proven experience in production planning or scheduling within a manufacturing environment.
Minimum 5 years of experience in inventory control, production control, purchasing or scheduling
* Strong knowledge of MRP/ERP systems
* Experience in inventory management practices, including forecasting and demand planning
* Ability to analyze data effectively to make informed scheduling decisions
* Excellent organizational skills with keen attention to detail
* Strong communication skills, both verbal and written, for effective collaboration across teams
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Type: Permanent Location: Triadelphia, US-WV
Salary / Rate: Not Specified
Posted: 2025-06-01 08:10:07
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Produktionsassistent (m/w/d) im Wareneingang Pharmalogistik
Bist Du bereit für Deine neue Herausforderung bei dem Weltmarktführer DHL Supply Chain im Bereich Kontraktlogistik? Dann bist Du genau richtig bei uns! Wir bieten als Experten unseren Kunden aus diversen Branchen maßgeschneiderte Lösungen entlang der gesamten Supply Chain an.
So verbinden wir Menschen weltweit und verbessern Leben.
Darüber hinaus leisten wir mit unseren Initiativen GoGreen, GoTeach und GoHelp einen positiven Beitrag für die Gesellschaft.
Klingt spannend? Dann bewirb Dich jetzt als Produktionsassistent im Wareneingang (m/w/d) und werde Teil unseres Pharmalogistik-Teams in Florstadt!
Das bieten wir:
* Unbefristeter Arbeitsvertrag in einem zukunftssicheren Wachstumssegment der Logistik
* Zuschläge und voller Ausgleich von Überstunden
* Vermögenswirksame Leistungen und betriebliche Altersvorsorge
* Arbeitskleidung sowie gezielte und personenbezogene Einarbeitung
* Fachschulungen, Spezialisierungs- und Weiterentwicklungsmöglichkeiten
* Großes Angebot an Rabatten und vergünstigte Urlaubsangebote über das ErholungsWerk Post Postbank Telekom e.V.
* Firmenfahrradleasing, Job-Ticket und vieles andere mehr
* Kostenfreie Mitarbeiterparkplätze unmittelbar vor der Niederlassung
* Verkehrsgünstige Lage: direkter Autobahnanschluss (A45)
Das sind Deine Aufgaben:
* Entladung und Abstellen im zugewiesenen Wareneingangsbereich
* Überprüfung und Protokollierung der Temperatur des Lieferfahrzeugs
* Prüfung der Liefer- und Frachtpapieren sowie Zuordnung der Ware
* Entpackung der Paletten und Prüfung auf Schäden
* Warenaufnahme mit Dokumentation (Warenaufnahmeformular)
* Buchung der Wareneingänge (inkl.
Prüfung der Bestelldaten)
* Erfassen / Änderung der logistischen Stammdaten im System
* Musterzug bei pharmazeutischen wie nicht-pharmazeutischen Artikeln
* Prüfung der Etikettierung und Kennzeichnung von Kartons
* Entladung von Transportmitteln (z.
B.
Umsetzung auf Europaletten, Austausch defekter Paletten)
* Aufsetzen der Paletten aus dem Wareneingang auf Fördertechnik
Das bringst Du mit:
* Berufs- oder Praxiserfahrung im Bereich Logistik, idealerweise im Wareneingang
* Ausbildung zur Fachkraft für Lagerlogistik oder vergleichbar qualifizierende Ausbildung von Vorteil
* Kenntnisse eines Lagerverwaltungssystems (idealerweise SAP)
* Staplerschein (oder Bereitschaft, diesen zu erwerben)
* Gute Deutschkenntnisse (zwingend erforderlich)
* Konzentrationsvermögen und akkurate Arbeitsweise
* Teamgeist, Belastbarkeit und Flexibilität
* Arbeitszeit: 2 Tagesschichten von Mo bis Fr im Wochenwechsel (7:00 bis 15:00 Uhr und 9:00 und 17:00 Uhr)
Kontakt:
Dein Ansprechpartner für diese Stelle ist Jörg-Alexander Kurdzel, der Dir gerne auch Fragen unter Tel.
+49 6035 70 92 793 beantwortet.
Wir freuen uns auf Deine Online-...
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Type: Permanent Location: Florstadt, DE-HE
Salary / Rate: Not Specified
Posted: 2025-06-01 08:08:11
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Join a great place to work with MissionSquare, a financial services corporation with approximately $79 billion in assets under management and administration and over 600 employees.
Founded in 1972, MissionSquare is dedicated to the retirement needs of public sector employees.
We focus on delivering results-oriented retirement and retiree health savings plans, education, investment options, personalized guidance, and related services to public sector participants in more than 9,200 plans and nearly 2 million participant accounts.
We strive to make the administration of retirement programs as easy and cost-effective as possible.
We have an extraordinary talent base and invite you to consider joining MissionSquare's Product & Strategy team.
The Director, Proposal Strategy manages the proposal development process, ensuring the creation and timely submission of high-quality, compliant proposals that align with MissionSquare’s business acquisition and retention goals.
The Director, Proposal Strategy is a dual-role position that combines leadership and hands-on involvement in managing strategic proposals.
This role manages a team of proposal professionals, fosters a collaborative relationship with cross-functional teams, and leads by example, demonstrating best practices in proposal development.
Essential Functions for this role include:
* Develop proposal strategy and approaches for the continuous innovation of the proposal management function
* Manage the proposal development process, ensuring the creation and timely submission of high-quality, compliant proposals that align with MissionSquare’s business acquisition and retention goals.
* Implement changes to improve the proposal management process, create efficiencies, and develop compelling responses that result in a higher close or retention rate
* Lead, develop and manage a high-performing team that creates best-in-class responses to support MissionSquare’s business strategy
* Partner with leaders across the corporation in sales, product, customer experience, and operations to understand priorities and to communicate our value to prospects during an RFP/RFI process
* Other duties as assigned
If you have the following skills, we encourage you to apply:
* BA/BS or equivalent experience.
* 10+ years of relevant work experience as a retirement proposal management leader in financial services.
* MBA/MA in Marketing, Communications, or similar relevant field, preferred.
* Understanding of the dynamics of the public sector, 457 and 403b retirement plans, the plan sponsors, and participants – their business practices and decision-making processes.
* Demonstrated expertise in “B to B” governmental retirement plan proposal management
* Confident and collaborative developer of proposal content management
* Exceptional planning, team management, and communication skills.
* Experienced working against firm deadlines.
*...
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Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2025-06-01 08:06:13
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Your Job
Georgia-Pacific Toledo Containerboard Mill has an exciting opportunity for a Power and Recovery Area Leader.
The identified candidate will be responsible for providing leadership to the Power & Recovery Operations Team as well as implement strategies that drive continuous improvement and support all elements of reliability.
In addition, the candidate will provide leadership and direction to their team - distributing a facilitation of knowledge, skill development, and ensuring the department is meeting the objectives in EH&S, quality, reliability, production, and costs.
The Power and Recovery Area Leader reports to the Operations Manager, leads a team of 6 salaried employees, and is responsible for supporting the Mill's Visions and creating long term value measured by improved equipment reliability using Operations Excellence.
Long-term value is created through the application of the company's business philosophy of Principle Based Management and Georgia-Pacific's Guiding Principles.
Our Team
Georgia Pacific Toledo is one of five containerboard manufacturing sites within our Packing & Cellulose division.
They are also a recycling leader in the Northwest United Sates.
The team is currently comprised of 480+ dedicated employees.
The Toledo Mill is located within a 10-minute drive to the Pacific Ocean and offers many local outdoor activities including fishing, hiking, mountain biking, kayaking, and boating.
What You Will Do
* Lead through the proactive and deliberate application of Market Based Management (MBM®) to capture and realize long-term value through the use of Operations Excellence
* Lead in creating an operation that is capable, stable and predictable
* Provide leadership and direction to direct reports to ensure the Mill is meeting its objectives in EHS, quality, reliability, production, and costs
* Lead the development and implementation of asset strategies that drives continuous improvement and supports all elements of reliability
* Facilitate knowledge and skills development of direct reports, which include Supervisors, Planners and Hourly (union) Technicians
* Work as a team member with operations to cost effectively plan, schedule, and execute work that creates real long-term value
Who You Are (Basic Qualifications)
* Five (5) years or more of operations or maintenance experience in an industrial plant or military environment
* Experience as an operations or maintenance leader directing a salaried and hourly work force
* Experience with power generation equipment (boilers, turbines, etc.)
* Experience using a computerized maintenance management system (CMMS), such as Passport or SAP
* Experience with Microsoft Word, Excel, Microsoft Project, and PowerPoint
What Will Put You Ahead
* Bachelor's Degree or higher in Engineering
* Experience in the pulp and paper industry
* Experience with asset reliability techniques to improve equipment reliability
...
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Type: Permanent Location: Toledo, US-OR
Salary / Rate: Not Specified
Posted: 2025-06-01 08:04:43
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Your Job
Georgia-Pacific is seeking to grow our team by adding an Operations Manager at our Savannah River Mill operation in Rincon, GA.
The vision for this position is centered around making a strategic investment in the hiring and development of exceptional leaders across the organization.
Our focus is on leaders who have the capabilities to lead their own site in the future, along with the mobility to relocate when the right opportunity presents itself.
The role, responsibilities, and expectations will offer unique challenges for the Operations Manager to tackle.
Ideally, this will be the first position of many exciting opportunities for you to grow within Georgia-Pacific!
Our Team
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 than 30,000 employees in over 150 locations are empowered to innovate every day - to make everyday products even better.
What You Will Do
* Develop key business relationships and be a strategic part of the plant leadership team
* Helping our teams get better through developing plans to close the gap between how we are doing and what is possible
* Be accountable for employee and organizational development plans and people management strategies
* Identify and align operational priorities with the business vision - ensure production and delivery of the highest quality products at the lowest costs, consistent with customer requirements, company plans and profit objectives
* Partner with plant leadership to enhance facility performance and metrics - lead and facilitate continuous improvement initiatives and develop innovative practices, methods and procedures that add value for the facility
* Keeping our employees and communities safe through safe work practices and upholding our compliance standard
Who You Are (Basic Qualifications)
* Proven experience leading successful operations teams in a manufacturing or industrial environment
* Experience leading improvement efforts in production, quality, or profitability
* Willing and able to relocate for future growth opportunities in the next 1-3 years
What Will Put You Ahead
* Bachelor's degree or higher
* Experience leading change management/transformation initiatives
* Experience working in a pulp or paper mill operating 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,...
....Read more...
Type: Permanent Location: Rincon, US-GA
Salary / Rate: Not Specified
Posted: 2025-06-01 08:04:07
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Your Job
Georgia-Pacific is seeking to grow our team by adding an Operations Manager at our Savannah River Mill operation in Rincon, GA.
The vision for this position is centered around making a strategic investment in the hiring and development of exceptional leaders across the organization.
Our focus is on leaders who have the capabilities to lead their own site in the future, along with the mobility to relocate when the right opportunity presents itself.
The role, responsibilities, and expectations will offer unique challenges for the Operations Manager to tackle.
Ideally, this will be the first position of many exciting opportunities for you to grow within Georgia-Pacific!
Our Team
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 than 30,000 employees in over 150 locations are empowered to innovate every day - to make everyday products even better.
What You Will Do
* Develop key business relationships and be a strategic part of the plant leadership team
* Helping our teams get better through developing plans to close the gap between how we are doing and what is possible
* Be accountable for employee and organizational development plans and people management strategies
* Identify and align operational priorities with the business vision - ensure production and delivery of the highest quality products at the lowest costs, consistent with customer requirements, company plans and profit objectives
* Partner with plant leadership to enhance facility performance and metrics - lead and facilitate continuous improvement initiatives and develop innovative practices, methods and procedures that add value for the facility
* Keeping our employees and communities safe through safe work practices and upholding our compliance standard
Who You Are (Basic Qualifications)
* Proven experience leading successful operations teams in a manufacturing or industrial environment
* Experience leading improvement efforts in production, quality, or profitability
* Willing and able to relocate for future growth opportunities in the next 1-3 years
What Will Put You Ahead
* Bachelor's degree or higher
* Experience leading change management/transformation initiatives
* Experience working in a pulp or paper mill operating 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,...
....Read more...
Type: Permanent Location: Savannah, US-GA
Salary / Rate: Not Specified
Posted: 2025-06-01 08:04:07
