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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Als Policy Lead (m/w/d) übernimmst Du eine Schlüsselrolle bei der Gestaltung der gesundheitspolitischen Zukunft in Deutschland.
Deine Arbeit legt den Grundstein dafür, dass innovative Diagnostik-Lösungen von Roche den Weg zu Patient:innen finden.
Du bist verantwortlich für die Entwicklung und Umsetzung unserer Health Policy-Strategie und stellst sicher, dass die Rahmenbedingungen für unser gesamtes Diagnostik-Portfolio vorausschauend optimiert werden.
Dein neues Team
Du wirst Teil des Teams Market Access & Health Policy.
Wir sind ein dynamisches und vernetztes Team, das eng mit der Geschäftsführung und bereichsübergreifenden Partner:innen zusammenarbeitet, um die gesundheitspolitische Landschaft proaktiv zu gestalten.
Außerdem verantwortet unser Team weitere Themenfelder, wie z.B.
Market Insights, Pricing und Payor Relations.
Verantwortlichkeiten | Das erwartet Dich
* Du entwickelst und implementierst die Health Policy-Strategie (Fokus: Diabetes) für Roche Diagnostics in Deutschland in enger Abstimmung mit internen (Diagnostics & Pharma) und externen Stakeholdern im Sinne von "OneRoche".
* Du analysierst kontinuierlich das politische Umfeld, identifizierst Handlungsbedarfe für das Diagnostik-Geschäft und kommunizierst relevante Insights in die Organisation.
* Du bewertest die Produkt-Pipeline frühzeitig auf politisch-gesetzliche Risiken und entwickelst mit dem Market Access Team proaktiv Strategien und Taktiken zur Markteinführung.
* Du initiierst, pflegst und etablierst ein starkes Netzwerk zu Entscheidungsträgern und gesundheitspolitischen Einflussnehmern in Politik und Verbänden (Governmental Affairs).
* Du vertrittst die Interessen von Roche in relevanten Gesetzgebungsverfahren und bist fachlicher Ansprechpartner für die Geschäftsführung, inklusive der selbständigen Erstellung von Briefings.
* Du übernimmst die Leitung komplexer Projekte und steuerst diese erfolgreich hinsichtlich Ressourceneinsatz, Budget und Zeitplan.
Qualifikationen | Das bringst Du mit
* Du verfügst über einen Masterabschluss (idealerweise Wirtschaftswissenschaften) und bringst mindestens 10 Jahre Berufserfahrung in der Diagnostik-, Pharma- oder Healthcare-Branche oder bei gesundheitspolitischen Institutionen mit.
* Das deutsche Gesundheitssystem und der Diagnostik-Markt sind Dir bestens vertraut und Du bringst Erfahrung in der Verbands- und Lobbyarbeit mit.
* Du besitzt ein tiefes Verständnis für das Diagnostik-Portfolio, i...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-10-31 07:40:22
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Harris Computer, the largest operating group of Constellation Software Inc.
(TSX:CSU), is looking for a Corporate Development professional, based in Canada, to join our expanding team on the mergers and acquisitions (M&A) team.
This team works closely with Harris’ senior management in continuing the company’s success in acquiring software businesses.
This role is a full-time, remote, work from home position.
We will consider candidates from anywhere in Canada (preferably Toronto/Ottawa and surrounding areas).
As a member of the Harris Corporate Development team, you will report to the Director of Corporate Development.
This role requires travel of up to 10% in North America, and a valid passport is required.
Help shape the future of government and public sector software.
Our Frontline Group is seeking a Corporate Development Associate to partner with senior leadership and advance our M&A strategy.
You’ll help identify and evalutate qualified acquisition opportunities, as we deploying capital into market-leading vertical software businesses.
The ideal candidate is a true people-person who is self-motivated and has a passion for developing and maintaining relationships.
Prior business development experience is a key asset.
Knowledge of basic financial literacy and software will contribute to your success.
In this role, you will:
* Originate & qualify opportunities: Research, cold call, and directly engage target companies to assess fit with our investment profile.
* Build relationships: Develop and maintain frequent contact with founders, executives, and our existing target network.
* Pipeline management: Track outreach activity in Salesforce, moving opportunities through the M&A funnel.
* Communicate our story: Represent Harris’ investment strategy with professionalism and care.
* Collaborate with leadership: Partner with the M&A team in due diligence, screening, and deal progression.
* (Some travel required, ....Read more...
Type: Permanent Location: Toronto, CA-ON
Salary / Rate: 80000
Posted: 2025-10-31 07:28:35
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
R&D Technician – ELYSIS
A New Era for the Aluminum Industry
Carbon Free Aluminum
The ELYSIS™ technology is the greatest breakthrough in the aluminum industry since its beginnings in 1886.
Work is underway now to further develop this revolutionary new way to produce aluminum, eliminating carbon dioxide and all other greenhouse gas emissions from the traditional smelting process.
The ELYSIS process eliminates the use of carbon anodes, replacing those with proprietary materials.
It is the first industrial process that emits oxygen as its by-product and has the potential to transform an entire industry.
In 2018, two international aluminum producers, Alcoa and Rio Tinto, came together to form the ELYSIS joint venture with the provincial government of Quebec.
With support from the Canadian Government and Apple, the technology is progressing and is currently being designed to support the construction of new smelters or retrofits.
ELYSIS is headquartered in Montreal, with Technology Research & Development locations in Alma, Quebec, (Canada), in Jonquiere, Quebec, (Canada), in New Kensington, Pennsylvania, (United States), and in France.
Commercial quality metal produced by ELYSIS during the ongoing R&D process is already being used by Apple in a variety of products (The 16-inch MacBook Pro and the iPhone SE); Ab InBEV (cans); Audi (e-tron GT wheels produced by the RONAL Group), and Corona (cans).
Join the ELYSIS team in this exciting work!
About the location
The ELYSIS US Research & Development facility is located in the Alcoa Technical Center (ATC) in New Kensington, Pennsylvania. Located near Pittsburgh, the carbon-free smelting process was first developed at ATC, where a dedicated team is working to reinvent the aluminum industry for a sustainable future.
About the Role
As the R&D Technician I at Alcoa Technical Center (ATC) in New Kensington, PA, you will be an integral member of the research and development team, responsible for conducting experiments, installing and commissioning new equipment, and recording and documenting results and observations systematically and completely in laboratory notebooks and computer databases.
This role will be part of a pilot-scale development team, focusing on manufacturing and testing advanced proprietary materials for the development of innovative technology.
Key Activities / Responsibilities:
* Manufacture powders and components and prepare and test samples using laboratory analytical equipment and methods, consisting of LECO chemical analysis, physical measurements, Archimedes density, and various other analytical equipment
* Conduct a variety of laboratory experiments to support technological development
* Collect, organize, and report data to engineering/manag...
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Type: Permanent Location: Alcoa Center, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-31 07:25:14
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
As a leader within Alcoa, you can help fulfill our purpose and realize our vision to reinvent the aluminium industry.
Be part of the team that is helping shape a better workplace with a better work-life balance and the equal opportunities that help everyone thrive.
You have the power to shape things and individuals to make them better.
You’re a strategic thinker ready to make a big impact—and this is your opportunity.
Reporting to the VP of Strategy, Business Development, and Joint Ventures, you’ll take the lead on major growth initiatives that define the future of our business.
From identifying and valuing opportunities, to negotiating and executing deals, you’ll be at the forefront of transformative projects.
About the Role:
As the Global Director of Business Development, Acquisitions and Ventures, you will collaborate across teams and functions, driving high-impact partnerships, acquisitions, and new ventures that align with our corporate strategy.
Key responsibilities include:
* Lead and deliver large-scale business development projects—including acquisitions, joint ventures, new business lines, and expansions.
* Drive the full deal lifecycle: from opportunity ideation and strategic assessment to valuation, due diligence, negotiation, and execution of agreements.
* Manage internal and external stakeholders to ensure alignment and successful project delivery.
* Oversee financial modelling and market analysis to support valuations and maintain competitive intelligence.
* Mentor team members and enhance business development processes to build a high-performing team.
* Support executive decision-making through special projects and complex, non-standard analysis.
What’s on offer:
* Be part of a global operation where you can play a pivotal role in our ongoing success
* Global Career development opportunities to pursue your passion
* Car allowance
* Health insurance
* Long- and short-term incentive programs
What you can bring to the role:
* Ideally you will have at least 10 years’ experience in corporate, business, joint venture development, or investment banking.
* Postgraduate qualifications and experience in mining, minerals processing, or manufacturing would be highly beneficial.
* Proven experience leading complex transactions, including acquisitions and joint ventures, from valuation through to execution.
* Strategic thinking capability teamed with strong financial acumen and deep knowledge of valuation methodologies and financial statement analysis.
* Demonstrated success managing multiple high-priority projects under tight deadlines.
* Well-developed communication skills, with a proven track record in working with global cro...
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Type: Permanent Location: Rotterdam, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-10-31 07:25:09
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FP&A COE Analyst - IFP
Job Description
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
This is a key role within the FP&A COE, supporting the IFP finance leadership.
The incumbent will be responsible for providing reliable and insightful reporting, leading the forecasting process, and developing analysis about the performance and outlook of the business and the broader market environment.
This role will demonstrate creativity and ability to challenge the status quo to improve processes to be more effective but also more efficient to deliver outcomes that will drive business results.
Role Overview & Primary Accountabilities:
* Financial Planning and Analysis:
Assist in the development and management of annual budgets, forecasts, and long-range plans.
Conduct variance analysis to compare actual results against forecasts and budgets.
Prepare and present financial reports and dashboards to senior management.
Provide presentation materials with high level commentary analysis.
* Data Analysis and Reporting:
Analyse financial data to identify trends, risks, and opportunities.
Develop and maintain financial models to support business planning and decision-making.
Ensure the accuracy and integrity of financial data and reports.
* Business Partnering:
Collaborate with business units to understand their financial needs and provide actionable insights.
Support various departments in managing and reporting.
Facilitate cross-functional discussions to drive financial performance.
* Process Improvement:
Identify and implement process improvements to enhance the efficiency and effectiveness of the FP&A function.
Ensure compliance with financial policies, procedures, and internal controls.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact.
We’re founded on 151 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fu...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-10-31 07:23:37
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About CORE
CORE Electric Cooperative is the largest member-owned electric distribution cooperative in Colorado dedicated to providing reliable, affordable, clean, and safe electric service to our communities.
With a commitment to innovation and member satisfaction, we strive to meet the evolving needs of our members while maintaining the highest standards of service excellence.
Job Summary
The Commercial Operations Program Manager oversees the Cooperative’s short term energy trading and scheduling activities to ensure reliable and cost-effective operations of CORE’s portfolio of owned and contracted generation resources.
This role is responsible for optimization of the energy portfolio, identifying near term resource and delivery needs, and compliance with operational resource adequacy program requirements.
Direct activities will include contract management, support for asset integration, pricing development, support for contract negotiations, and assisting with settlements.
Essential Duties and Responsibilities
* Oversee the short-term and long-term trading activities that are carried out by a contract real-time trading consultant/desk.
* Lead CORE’s efforts to procure and manage short-term power supply and portfolio optimization.
* Responsible for power trading activities for short-term power supply contracts.
* Ensure employees and consultants adhere to compliance requirements.
Ensure that risks are effectively evaluated and managed, and decisions appropriately and proactively presented.
* Works collaboratively with Control Center, Electric Resource Planning, Transmission Planning, Member Services, Accounting, Enterprise Risk and Regulatory Affairs.
* Sets clear expectations and holds consultants accountable for performance of energy portfolio goals and targets.
* Develops pricing models and recommends security requirements for large load development and off-system sales.
* Leads weekly trading meetings with consultant.
* Supports accounting and settlements, assists in preparation of reports concerning daily operation of generation resources, including owned and those under long-term contract.
* Responsible for origination activities for short-term power purchasing and sales.
* Responsible for overseeing the development and implementation of generation dispatch and portfolio optimization.
* Leads effective development and ongoing implementation of operational processes that deliver efficient, effective, and agile merchant activities.
* Supports analysis and development of an execution plan to manage transmission congestion, financial transmission rights and commercial aspects of COREs physical and contract transmission portfolio in an evolving structured power market.
* Leads development of advanced analytical techniques and tools that help the utility see and react to dynamic market conditions.
* Provides input on regu...
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Type: Permanent Location: Sedalia, US-CO
Salary / Rate: 140088
Posted: 2025-10-31 07:14:27
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POSITION SUMMARY:
This is position that is responsible for the operation and supporting activities surrounding a particular coating process. The primary equipment will be operated through HMIs (Human-Machine Interfaces) and a series of switches, pushbuttons, and other interactive control points. Successful Operators will be capable to produce the required amount of product in a defined period while ensuring all (Environment, Health and Safety (EHS) and Quality requirements are continuously satisfied. The Operator will be required to work as part of a team with Operations Support, Engineering, Maintenance, and Management personnel. Some overtime will be required on occasion to meet production and project schedules. Limited travel may be required in support of training program. Operators will be provided the opportunity to progress within the role as defined below.
DUTIES AND RESPONSIBILITIES:
* Perform complex and multi-level tasks from procedures and work instructions defining the tasks.
* Maintain timely and accurate record keeping using provided tools including digital and handwritten data entry and notes.
* Maintain 100% compliance with personal protective equipment (PPE) requirements while operating equipment and/or performing supporting operations, includes ensuring your personal protective equipment is functioning properly prior to starting a task.
* Effectively identify and communicate non-standard situations including (EHS) and Product Integrity concerns.
* Operate support equipment (pre/post coating) and support Coater Operators
* Maintaining metal coating fixtures for use in coater which including visually verifying condition, removing residual coatings, and removing any contamination that may have affected the fixtures.
* Cross training in other coating process areas as needed to support production requirements. Will be required to complete the training program for each process prior to performed assignments in that area.
QUALIFICATIONS:
* High school diploma or general education degree (GED).
* At least 2 years’ experience working in a production manufacturing environment
* Additional Education, Training, Certifications, or Licenses that are applicable will be considered and may be used to supersede either of the other two requirements.
* Must be able to read, write, and communicate in English.
* Read and interpret documents such as safety rules, operating instructions, and procedure manuals.
* Write routine reports and correspondence either in digital or handwritten formats.
* Good mathematical skills, scientific principles and reasoning ability
* Mechanically inclined individual that thrives in a hands-on, demanding environment with little direct supervision once assignments are handed out.
* May be required to operate of forklift (training provided).
PHYSICAL DEMANDS: Reasonable accommodat...
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Type: Permanent Location: Oldsmar, US-FL
Salary / Rate: Not Specified
Posted: 2025-10-31 07:14:23
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Nonclinical Safety
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium
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
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-036414
* Belgium - Requisition Number: R-038682
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Director, Global Nonclinical Writing and Submissions.
This position is a hybrid role and will be located in Beerse, Belgium.
The Director, Global Nonclinical Writing and Submissions, within the Preclinical Sciences and Translational Safety (PSTS) organization, will drive the nonclinical writing strategy and lead the team to deliver state-of-the-art submissions aligned with global requirements.
Principal Responsibilities:
* Lead and mentor the nonclinical writing team, including internal and contracted writers, to meet pipeline goals with timely and high-quality deliverables (e.g., Investigator’s Brochures, IND/CTA/NDA nonclinical modules, briefing books, health authority responses) across all programs and development phases.
* Review of documents prepared by writers and ensure adherence to standards, quality, and strong positioning of key messages and risk assessment.
* Maintain awareness of global submissions landscape and ensure nonclinical submissions strategy evolves to produce state-of-the-art, compliant deliverables.
* Ensure consistent support and implementation of best practices across portfolio and maintain adherence to standard operating procedures and reg...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-31 07:08:49
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Business Intelligence
Job Category:
Professional
All Job Posting Locations:
Warsaw, Masovian, Poland
Job Description:
Business Intelligence Manager
Loation.: Warsaw, Poland
Full time job
Business Intelligence Manager is responsible for supporting the company and therapeutic areas in leading & conducting business intelligence processes, facilitating key business decisions at product/ therapeutic area/ company level according with Brand Team/company strategy.
Plays a pivotal role as brand team member in shaping the right decisions for the brand / portfolio strategy short and long-term.
Provides strategic support for enhancing the quality of customer support services and developing the company in an extremely competitive and dynamic market.
Business Analytics & Forecasting:
• Driving and leading forecasting processes (FBP, LRFP, JU NU, MER, IBP, SOS)
• Adapting or designing Patient Based Models based on local needs
• Ensuring forecasting assumption alignment along IBVT and MSM guidelines
• Scenarios modeling and recommendation to enable information-based decision making
• Owning local business reports and dashboards to monitor performance, and enable to drive decisions in execution or strategy within the CVT
• Seeking, identifying, and introducing available market data to enable performance assessment.
• Ad hoc reports/analysis
Market Research:
• Developing and implementation of primary and secondary-type research
• Facilitating local participation in EMEA conducted market research.
• Designing and embedding market research process according to CVT decisions
• Leading vendor management process
• Providing interpretation, insights and recommendations for CVTs to influence marketing strategy and objectives.
• Administering MR process within relevant J&J systems
Competitive Intelligence:
• Integrating competitive data with available sources of information and delivers competitive insights and actionable recommendation.
• Maintaining focus on short & long-term issues such as key risks and challenges that can potentially affect the company and actively seeks new competitive opportunities.
• Participating in Pharma Europe CI expert and BI network group to share and activate relevant initiatives and best practice.
Requirements (knowledge, education, skills):
• Bach...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-10-31 07:08:41
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Capital Sales -- MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Chengdu, Sichuan, China
Job Description:
Supervises individual contributors and/or Supervisors, and is accountable for conducting effective performance management.
Leads processes and assignments for the Clinical Sales - Hospital/Hospital Systems team and supports organizational objectives and business goals.
Defines project terms to meet objectives and goals of the Clinical Sales - Hospital/Hospital Systems area.
Directs work flow for strategic plans and serves as a primary point of contact for the team.
Supervises individual contributors and/or Supervisors, and is accountable for conducting effective performance management.
Coordinates processes and assignments for supervisors and individual contributors to achieve sales goals.
Communicates information throughout the clinical sales area to ensure employees stay well-informed on product knowledge, launches, policies, and guidelines.
Supervises customer acquisition and retention process from identifying potential customers to maintaining positive relationships with existing customers.
Advises team on policies and procedures to ensure compliance and achievement of the organization's sales objectives for their designated area.
Responsible for managing operational aspects of their team (e.g., workflow, performance, and compliance), as well as ensuring achievement of team goals within expected standards.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
Job is eligible for sales incentive / sales commissions.
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Type: Permanent Location: Chengdu, CN-51
Salary / Rate: Not Specified
Posted: 2025-10-31 07:08:38
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
Job Description:
Position Title: Experienced Scientist, Therapetics, Development & Supply (TDS)
Department: TDS-AD Cork
Report to: Associate Manager, Bioassay, Bioassay and Avanced Therpy Stability Sciences
Location: Cork
Travel: 5-10%
Global Compensation Framework Band Number: 25
Company Summary: Johnson and Johnson Innovative Medicine (formerly Janssen Sciences Ireland UC) is a pioneer in the use of mammalian cells to manufacture monoclonal antibodies.
TDS Analytical Development Cork (TDS) Aanalytical Develeopemt (AD) is a department responsible for clinical release and stability testing for drug substance and drug product and stability management of the large molecule (therapeutic proteins) portfolio.
In addition to clinical release & stability activities TDS-AD Cork is responsible for analytical support for large molecules through troubleshooting, investigations, manufacturing support and analytical method transfer.
In addition to a range of therapeutic molecules (e.g.
monoclonal antibodies, Bi-specifics), J&J has an emerging Advanced Therapy portfolio (Gene Therapy, Car-T etc).
Position Summary:
Reporting to the Associate Manager, Bioassay TDS-AD Cork, the person will be focused executing analytical procedures for release & stability testing and process characterization for the clinical pipeline.
The successful candidate will also be responsible for the resolution of testing related issues in support of of the Bioassay and Advanced Therapy Stability Sciences team.
Main duties and responsibilities:
· Analytical Testing in a GMP laboratory for the purposes of release and stability testing of the clinical porfolio.
· Provision of technical expertise in support of release, stability & process characterization assays (e.g.
qPCR, ELISA and cell-based assays).
· Provision of technical support for process impurity assays (e.g.
Residual Host Cell DNA, Residual DNA and residual protein A).
· Analytical technology transfer, including co-validation/qualification.
· Perform, design and direct bench experiments as required.
· Troubleshooting and investigations.
· Drive continuous improvement initiatives.
· ...
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-10-31 07:08:28
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, 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 Associate Analyst, Quality Control CAR-T to be in Raritan, NJ.
Purpose: The QC Associate Analyst is responsible for conducting biochemical, microbiological, and/or general testing of final product samples submitted to the QC laboratories.
They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
They typically work with a team of 5 – 15 other Analysts within the functional laboratory of the Quality Control department.
You will be responsible for:
* Lab support and maintenance
* Sample handling (Supporting with the lifecycle of the samples outside of testing (Sample running-Disposal)
* Accountable for the review of equipment logbooks
* Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
* Responsible for the completion of QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP laboratory.
* Ensure testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
* Perform peer review/approval of laboratory data.
* Apply electronic systems (LIMS, MES) for execution and documentation of testing.
* Supports process improvement teams.
Qualifications / Requirements:
Education:
* A minimum of an Associates’s Degree in Engineering, Science or equivalent technical field is required.
Experience and Skills:
Required:
* Minimum of (0-1) years of relevant work experience
* Knowledge of cGMP regulations, Good Documentation Practices (GDP) and FDA/EU guidance related to manufacturing of cell-based products is required.
* Experience within Biopharmaceutical or Pharmaceutical...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-31 07:08:24
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Beerse, Antwerp, Belgium
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
About CAR-T
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
We are searching for the best talent for a EM/Logistic analyst - early-shifted late, to be in Beerse.
To support the CAR-T program in EMEA, Janssen has built two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories are located on the existing Janssen Beerse site.
The EM/Logistic analyst, QC CAR-T Europe is responsible for shipment of Environmental Monitoring samples, Drug Product samples and Critical Reagents. Next to that also the incubation and read-out of Environmental Monitoring samples will be part of your responsibilities. All activities should be following the applicable procedures, standards, and GMP regulations.
This job will be in a 2-shift regime: Early/Shifted late (6:00h-14:00h and 12:00h-20:00h)
You will be responsible for:
* Environmental Monitoring testing: Receival and unpacking of the shipment, incubation, read-out of result
* Perform EM testing in compliance with all applicable specifications, procedures, GMP regulations
* Drug Product Shipments, receival, unpacking and storage, including assigning the right storage locations to the different samples for all different temperature conditions (-120°C/-80°C/2-8°C)
* On-Site transport of Critical Reagents
* Copy of COA results in eLims for gowning, cleaning and other consumables
* General administrative related QC tasks
* Maintain a safe work environment in compliance with all applicable environmental, health, and safety regulations
* Support laborat...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-31 07:08:02
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Nonclinical Safety
Job Category:
People Leader
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-036414
* Belgium - Requisition Number: R-038682
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Director, Global Nonclinical Writing and Submissions.
This position is a hybrid role and will be located in Spring House, PA.
The Director, Global Nonclinical Writing and Submissions, within the Preclinical Sciences and Translational Safety (PSTS) organization, will drive the nonclinical writing strategy and lead the team to deliver state-of-the-art submissions aligned with global requirements.
Principal Responsibilities:
* Lead and mentor the nonclinical writing team, including internal and contracted writers, to meet pipeline goals with timely and high-quality deliverables (e.g., Investigator’s Brochures, IND/CTA/NDA nonclinical modules, briefing books, health authority responses) across all programs and development phases.
* Review of documents prepared by writers and ensure adherence to standards, quality, and strong positioning of key messages and risk assessment.
* Maintain awareness of global submissions landscape and ensure nonclinical submissions strategy evolves to produce state-of-the-art, compliant deliverables.
* Ensure consistent support and implementation of best practices across portfolio and maintain adherence to standard...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-31 07:07:58
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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:
Sales Enablement
Job Sub Function:
Sales Training
Job Category:
Professional
All Job Posting Locations:
Bangkok, Bangkok, Thailand, Jakarta, Indonesia, Kuala Lumpur, Kuala Lumpur, Malaysia, Singapore, Singapore
Job Description:
Position Overview:
The role will lead the development and execution of education strategies across Southeast Asia, including shape the learning experience for both internal teams and external healthcare professionals in the rapidly evolving field of robotic and digital-assisted surgery.
The current scope includes on the VELYS™ Robotic-Assisted Solution and the broader complementary orthopaedic portfolio.
Secondly, as the clinical lead, this individual will support VELYS funnel development in presenting clinical and technical advantages of VELYS during product demos and clinical evaluation.
He or she will also provide hypercare support during critical evaluation period as well as starting up first few cases.
Where necessary, this lead will also help to address technical questions around VELYS and to escalate clinicians concerns to the global R&D team.
Strategically, this role will support the development of product business plans, ensuring product-market relevance that marketing plans are grounded in sound clinical imperatives.
Key Responsibilities:
1.
Professional & Commercial Education Development
* Design and implement VELYS Professional Education programs to support surgical excellence and improved clinical outcomes in knee and hip arthroplasty.
* Create Commercial Education Programs tailored to sales and marketing teams to enhance technical knowledge and value-based selling capabilities.
* Collaborate with regional and global stakeholders to ensure alignment with APAC education standards and compliance requirements.
2.
Market & Content Strategy
* Assess market dynamics, customer insights, and training gaps across SEA to inform educational priorities.
* Translate clinical and commercial needs into engaging, data-driven educational content and tools that address surgeon concerns and support decision-making.
* Monitor clinical trends, competitive landscape, and surgeon feedback to proactively evolve the education strategy.
3.
Clinical Insight & Portfolio Strategy
* Act as a clinical subject matter expert for VELYS Knee and Hip solutions—helping address key clinical concerns and guiding internal teams on evidence-based posi...
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Type: Permanent Location: Singapore, SG-01
Salary / Rate: Not Specified
Posted: 2025-10-31 07:07:46
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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:
Quality
Job Sub Function:
R&D/Scientific Quality
Job Category:
People Leader
All Job Posting Locations:
Aachen, North Rhine-Westphalia, Germany
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com
The Supervisor of MQSA is responsible for leading the site Control Contamination, Environmental, Product Microbiology, Cleaning and Sterilization systems and practices through the implementation of the appropriate Medical Device standards and harmonization with J&J practices for the site.
Ensure all new product introductions are in compliance with all standard requirements and international regulations to provide the required information to Regulatory.
Mentor team members to ensure development of subject matter experts in all the related areas for Sterilization & Microbiology.
Principle Duties and Responsibilities:
* Manage the Environmental Monitoring, Sterilization Validations, Cleaning assessments and Microbiology product level testing plans for the timely completion.
* Lead the timely completion of annual re-qualification process for all sterilization processes for the site.
* Collaborates with engineering teams to assure timely closure of technical investigations.
* Works with MQSA leaders, R&D, manufacturing, and quality design to bring new product and changes to existing products to completion.
* Responds to Request from Regulatory bodies for supplemental information or clarification of existing submittals.
* Identifies and implements improvements and innovative ideas with end-to-end thinking for all the areas managed.
* Prepares metrics and trending reports for Sr.
Management monthly and annually.
* Provides direction regarding Corrective and Preventative Actions that relates to the product microbiology, contamination control, cleaning, sterilization, and environmental monitoring.
* Interprets updates to applicable international standards and guidelines and implement...
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Type: Permanent Location: Aachen, DE-NW
Salary / Rate: Not Specified
Posted: 2025-10-31 07:07:25
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ERM is hiring a motivated hands-on Senior Environmental, Health and Safety (EHS) Consultant to join our growing Performance & Assurance technical team in Sunnyvale, California. This position is expected to involve working a minimum of 3 days on-site. This is a fixed-term, full-time role (40 hours a week) for a duration of 4 months, renewable.
The ideal candidate will have experience developing and supporting implementation of Cal/OSHA requirements, Standard Operating Procedures, Job Hazard Analysis/ Risk Assessments, Emergency Response Plans, Behavioral Safety Programs and Contractor Safety Management. Candidates should also have familiarity with research laboratory safety requirements, waste management (hazardous, non-hazardous, universal/ electronic), environmental reporting (HMBPs), and chemical safety requirements.
RESPONSIBILITIES:
* Oversee and direct team members to effectively manage tasks for on-time delivery and quality of their deliverables.
* Perform compliance audits to assess client compliance with applicable health and safety or environmental regulatory requirements, client standards, or management systems.
* Support our clients’ desire to improve safety performance by providing training, field coaching, and targeted EHS assessments.
* Identify follow-up corrective actions to close audit findings.
* Provide technical assistance on EHS compliance and EHS management system projects on a range of areas such as R&D laboratory safety, chemical safety, machine guarding, laser safety, robotics safety, hazardous materials use/storage/waste, EHS auditing.
* Develop and implement EHS compliance procedures, plans, permits, and reports.
* Manage tasks within assigned scope/budget/schedule and ensure quality standards on project deliverables.
* Build client relationships and nurture repeat business by continuously striving to exceed their expectations.
* Support ERM Partners and Project Managers to effectively manage and deliver projects.
* Build strong collaborative relationships with other ERM employees.
REQUIREMENTS:
* BS in engineering, environmental science, occupational health and safety, or related discipline preferred.
* A minimum of 7 years of applicable experience providing EHS support with an emphasis on health and safety.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Ability to succeed in a fast-paced consulting environment, handling multiple assignments, meeting strict deadlines, and being able to re-prioritize tasks as-needed.
* Valid driver’s license and good driving record.
Pay Transparency:
For the Environmental, Health and Safety (EHS) Consultant position, we anticipate the annual base pay of $76,000– $97,400, $36.54/hr - $46.82/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on ...
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Type: Permanent Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-31 07:06:36
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ERM is hiring an Environmental, Health & Safety (EHS) Consultant to support a key technology client facility in San Jose, CA.
In this role, you’ll assist with day-to-day safety operations, compliance assurance, and continuous improvement initiatives across laboratory and facility environments.
This is a part-time (24-40 hours per week) limited-term onsite consulting role with a duration of 1 month, extendable.
RESPONSIBILITIES
* Support Energy Isolation Plan development, implementation, and verification.
* Assist with laboratory compliance: hazard communication, SDS management, and inspections.
* Conduct ergonomic assessments for lab and office staff.
* Manage hazardous waste labeling, accumulation, and disposal in line with regulations.
* Perform routine inspections and recommend corrective actions.
* Participate in safety committee meetings and support site initiatives.
* Collaborate with Micron’s EHS team to ensure policy and regulatory compliance.
* Maintain accurate records and prepare summary reports.
REQUIREMENTS
* Bachelor’s degree in Environmental Science, Occupational Health & Safety, Industrial Hygiene, or related field preferred.
* Minimum 3 years of EHS experience in lab, semiconductor, or manufacturing environments preferred.
* Knowledge of OSHA and Cal/OSHA regulations, including LOTO, hazardous waste, and ergonomics.
* Strong communication and teamwork skills in a client-facing environment.
* Ability to manage multiple priorities and adapt to dynamic site conditions.
* Proficiency in Microsoft Office; experience with EHS systems like Enablon or Intelex is a plus.
Pay Transparency:
For the EHS Onsite Support position, we anticipate the annual base pay of $88,236 - $132,849, $42.42/hr – $63.86/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/Flexforce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including Flexforce) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible.
See your recruiter for more details.
You can apply for this role through https://www.erm.com/careers/apply/ ...
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Type: Permanent Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-31 07:06:27
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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
032492 Safety Coordinator (Open)
Job Description:
Founded in 1877, Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world’s most demanding and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life’s essentials – and creates lasting value for its colleagues, customers, and other stakeholders.
OUR VISION:
Be the best performing customer service company in the world.
OUR PURPOSE:
We create packaging solutions for life’s essentials.
ROLE OVERVIEW: Under general supervision, performs generally non-routine risk assessments for processes and new equipment.
Submits corrective solutions to risks while also making fiscal and operational considerations.
Assists in safety and quality activities and improvement projects as directed by the manager.
Informs managers and supervisors of regulatory changes with which the company must comply.
Key Responsibilities
* Ensures that safety and environmental rules and regulations are followed.
* Advises managers regarding safety, compliance, and environmental issues.
* Implements compliance requirements and control procedures as prescribed by regulatory agencies.
* Performs safety orientation and conducts training updates for employees.
* Completes reports required by regulatory agencies and maintains environmental records.
* Implements safety and environmental programs in conjunction with corporate initiatives.
* May train employees on safety aspects of machine operations.
* Maintains system processes that support the safety and environmental function.
* May be responsible for quality processes.
* Incorporates and maintains safety observances, including but not limited to, use of all PPE by employees, ensuring guards and safety features are working, and promoting good safety practices and habits.
* May be responsible for regulatory water testing and reporting.
* May support site trails for process optimization and improvements.
* May conduct field sampling safely from various sampling points in and around Greif location(s).
* May perform customer service, purchasing, scheduling or other duties as required.
* Performs other duties as assigned.
Education and Experience
* High School Graduate or equivalent. Bachelor’s degree preferred.
* A minimum of 3 years of experience as a Safety or EHS Coordinator in an industrial manufacturing or plant facility is required. Over 4+ years of experience preferred.
Knowledge and Skills
* Solid knowledge of relevant safety regulations.
* Ability to identify unsafe work practices and/or able to recognize ...
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Type: Permanent Location: Tacoma, US-WA
Salary / Rate: Not Specified
Posted: 2025-10-30 08:21:52
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Company
Federal Reserve Bank of Cleveland
The Federal Reserve Bank of Cleveland is part of the nation’s central bank.
We’ve provided many opportunities for professional growth during our history.
For twenty-six years in a row, we’ve been named “One of Northeast Ohio’s Best Places to Work” by North Coast 99.
This prestigious award honors organizations with outstanding employment practices, including compensation, benefits, training, recruitment, retention, community services, and employee communications.
Our People Make the Difference! The Federal Reserve Bank of Cleveland is seeking innovative thinkers with vision to build the framework that will carry the Bank into the future.
Follow us on LinkedIn, Twitter, Instagram, and our YouTube channel – Cleveland Fed
To be considered for this role, candidates must be a U.S.
citizen, permanent resident, or green card holder.
Our interns will work onsite at our Cleveland, Ohio location.
We’re looking for collaborative and innovative full-time students entering their sophomore year or beyond.
Our student interns work 40 hours per week for the duration of a 10- to 12-week internship that starts as early as June and ends as late as September, depending on student schedules and business needs.
The expected starting salary range for this position is between $20 and $23 hourly.
Final salary and offer will be determined by the applicant’s background, experience, skills, internal equity, and market data
Audit Intern Duties:
You will work with audit team members to enhance and protect organizational value by providing risk-based and objective assurance, advice, and insights in the evaluation of the effectiveness of risk management, internal control, and governance processes.
As an intern you may:
* Assist on IT audits or projects for business areas within the Fourth District.
* Conduct interviews with clients, staff, and management to understand their control environment.
* Analyze data and business processes to evaluate and verify compliance with established policies or procedures.
* Assist IT audit staff in determining if internal controls and processes are effective for assigned audit steps.
* Prepare workpapers for auditor-in-charge and audit management.
* Complete projects and ad hoc assignments (e.g., flowcharting new processes, helping with developing new audit tools, updating department websites, etc.).
* Engage in leadership and career development activities for your future.
* Perform other duties as assigned or requested.
Requirements for Internships:
* Currently pursuing an undergraduate or graduate degree in Business, IT/Cyber Security, or a related field with a minimum GPA of 3.0.
* Strong computer/technical skills required.
Proficiency with Microsoft Office products, specifically Excel and Access (or familiarity with other data access tools).
* Need to have one semester remaining upon completion of the internsh...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-10-30 08:20:27
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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.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
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: SIAM Analyst
As Elanco grows, the SIAM Business Systems Analyst will play a key role in stabilizing and optimizing the IT Operating Model through data-driven process improvement, service integration, and reporting.
This role is responsible for developing IT governance reports, managing dashboards in ServiceNow and Power BI, supporting vendor management reporting, and driving continuous improvement initiatives.
By partnering across IT and vendor teams, the analyst ensures process alignment, monitors performance metrics, and contributes to the ongoing evolution of Elanco’s IT governance, collaboration and processes.
Your Responsibilities:
* Generate, validate, and distribute monthly IT governance reports
* Develop and maintain ServiceNow Performance Analytics (PA) dashboards and Power BI (PBI) reports
* Assist in the development and delivery of vendor management reports for the VMO
* Contribute to the creation and tracking of ServiceNow enhancement stories and platform upgrade initiatives
* Set up, monitor, and manage ServiceNow SLA definitions and reporting
What You Need to Succeed (minimum qualifications):
* Minimum of three to five years of IT Service Desk experience.
* Minimum of three to five years of experience in data aggregation and reporting.
* Minimum of three to five years of experience and demonstrable proficiency using and developing reports within ServiceNow
* Education: A bachelor’s degree in IT, computer science, business, management or a related field is required
What will give you a competitive edge (preferred qualifications):
* Comprehensive understanding of an ITSM/ITIL governed support model.
* Proficiency in the analysis and interpretation of data and how to effectively utilize that information to drive efficiencies, maturation, and improvement.
* A solid understanding of IT Vendor deliverables and obligations through contracted SOWs, SLA/KPI measurement, and contractually binding credit generating stipulations
Additional Information:
* Travel: 0%
* Location: India, Bangalore
Don’t meet every singl...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-10-30 08:14:30
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Job Category:
Manufacturing/Operations
Job Family:
Sanitation
Work Shift:
Days (United States of America)
Job Description:
This is a day shift position, 6am-6:30pm on a 2-2-3 rotation schedule.
* Responsible for equipment, CIP and Sanitation of the Processing and Production lines, pieces of equipment and plant infrastructure.
* Responsible for minimizing product loss.
* Responsible for drain sanitizing on a daily basis.
* Responsible for effectively taking care of and operating the floor scrubber.
* Maintain a clean work environment.
* Follow all plant safety, USDA, SQF and GMP guidelines.
* Responsible for all record keeping and documentation reviews for sanitation programs.
* Knowledge of SDS and how to read and find SDS.
* Responsible for promoting open, honest communication between partners.
* Responsible for maintenance of equipment.
* Responsible for JHAs, and SOPs for processes specific to their job tasks.
* Responsible for working with Production, Processing, QA, and Maintenance Partners to meet line performance goals
* Responsible for proper handling, storage and sanitation procedures.
* Responsible for accounting and communicating MSS program outages to Production, Processing, QA, and Maintenance leaders.
* Responsible for auditing environmental clean ups during CIP for improvements.
* Special Event tracking and reaction swabbing.
* Responsible investigations for PEM outages.
Back up for maintaining PEM program.
* Maintaining the Food Safety Plans for construction projects.
* May be required to come in on another shift, if there is a large clean up event happening.
* May be required to perform other sanitation tasks in other areas as needed.
* Required to become skilled in the use of Process Excellence Tools and to demonstrate these skills as part of their daily functioning as operators in support of achieving continuous improvement of line results
* Perform all process CCP, PC, QCP, QPs checks required for the position.
Follow reaction plans for Food Safety, Food Quality and customer requirement deviations.
Be able to identify and understand customer requirements and assist in assuring proper production operation.
Demonstrate identity of product and record accurate data on production reports
* Other duties as assigned by leadership
JOB REQUIREMENTS
* Operate equipment to ensure proper sanitation and CIP functions of lines, tanks and production equipment.
* Operation of CIP systems, including tanks, lines and equipment.
* Equipment disassembly and assembly as needed.
* Perform general sanitation of the overall plant
* Lead cleanup efforts, maintain records and documentation.
* Ability to read and write, and communicate effectively
* Ability to follow oral and written instructions
* ...
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Type: Permanent Location: Beloit, US-WI
Salary / Rate: Not Specified
Posted: 2025-10-30 07:59:20
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
Como líder na Alcoa, você pode ajudar a cumprir nosso propósito e realizar nossa visão de construir um legado de excelência para as gerações futuras.
Faça parte da equipe que está ajudando a moldar um ambiente de trabalho melhor, com flexibilidade e oportunidades iguais que ajudam todos(as) a prosperar.
Você tem o poder de moldar as coisas e as pessoas para torná-las melhores.
Sobre a função:
Alcoa está buscando profissional de Medicina do Trabalho para integrar nosso time na Unidade de Juruti/PA.
Como Gerente de Saúde Ocupacional Sênior, você desempenhará um papel estratégico e essencial na promoção da saúde e segurança das(os) nossas(os) funcionárias(os), garantindo o cumprimento rigoroso das normas legais e dos protocolos corporativos.
Você também contribuirá com estratégias integradas alinhadas às diretrizes da Alcoa e às necessidades da região, bem como terá atuação em emergências, auditorias e investigações de incidentes.
As principais responsabilidades da função incluem:
* Garantir conformidade legal e corporativa com normas de saúde ocupacional, protocolos EHS e certificações aplicáveis;
* Gerenciar o absenteísmo e coordenar o Programa de Reabilitação Profissional, realizando o acompanhamento de ações, apoiando a definição de estratégias e promovendo programas de inclusão;
* Coordenar programas de saúde ocupacional e de prevenção, incluindo ergonomia, saúde mental e fadiga;
* Supervisionar serviços médicos da unidade, atuando como responsável técnica(o) pelos ambulatórios e contratos médicos;
* Apoiar a gestão da saúde assistencial, garantindo qualidade dos prestadores, auditorias, programas de prevenção e oncologia;
* Liderar ações emergenciais e de vigilância epidemiológica, incluindo acidentes de trabalho e ameaças à saúde pública.
O que você pode oferecer para a função:
* Formação Superior completa em Medicina e Pós-Graduação em Medicina do Trabalho;
* Experiência prévia em posições de liderança na área de Saúde Ocupacional;
* Domínio da legislação trabalhista e das Normas Regulamentadoras (NRs) aplicáveis à Saúde Ocupacional;
* Perfil hands on, visão estratégica e habilidade para construir relacionamentos positivos e colaborativos;
* Disponibilidade para residir em Juruti-PA (área remota);
* Regime de trabalho: presencial.
Disponibilidade para atendimento de demandas fora do expediente (urgências).
O que está sendo oferecido:
* Nossa Essência e Cultura: somos movidos por valores sólidos - agimos com integridade, operamos com excelência, cuidamos das pessoas e lideramos com coragem;
* Segurança em Primeiro Lugar: a segurança não é...
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Type: Permanent Location: JURUTI, BR-PA
Salary / Rate: Not Specified
Posted: 2025-10-30 07:57:20
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Finance Manager - Distribution
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.
The Finance Manager - Distribution, you will help drive current year cost delivery, connecting operational execution with brand ambitions.
You will lead the monthly forecast, budget, and strategic planning cycles and providing detailed and comprehensive financial analysis, partnering with cross functional leaders to influence key decisions, drive measurable results, and support current year cost savings.
In this role, you will:
* Drive Supply Chain Results – Partner with North America and Enterprise Supply Chain Leaders to deliver results, utilizing standardized processes to enable seamless end-to-end supply chain integration.
* Lead Financial Analysis – Deliver financial insights on major initiatives - identifying trends, influencing decisions, and translating data into clear, actionable recommendations.
* Deliver Financial Leadership – Lead the monthly NA Distribution forecast, budget, and strategic planning cycles.
Integrate inputs from cross-functional teams to develop accurate, driver-based forecasts.
Ensure timely and transparent communication of financial outlooks to all key stakeholders.
* Advance Cost Transformation Initiatives – Actively contribute to North America transformation initiatives to meet in-year productivity targets and build a robust, multi-year cost savings pipeline in partnership with supply chain stakeholders.
* Influence Financial Decision-Making – Collaborate with Supply Chain and Brand leaders, providing comprehensive Total Delivered Cost insights, including monthly actuals and forecasted outlooks, supporting NA Logistics Operations in achieving financial objectives.
* Develop and Foster Learning – Deliver targeted training to cross-functional business partners to enhance Distribution financial acumen and foster a culture of continuous learning and collaboration.
* Ensure Financial Control and Compliance – Uphold strong financial controls and compliance standards, reinforcing the organization’s commitment to operational excellence and governance.
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 ...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-10-30 07:54:29
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Finance Manager - Amazon
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:
* Provide the Customer Development team with financial advice and counsel on all pertinent business matters by supplying ongoing, timely, and meaningful financial analysis, both routine and as needed of business results, trade promotion, and other expenses.
* Complete financial reporting for Amazon teams to include Net Sales, Trade, Contribution, and other key metrics vs.
targets and provide status updates to Customer Development and Finance Leadership as appropriate
* Support and lead customer and business unit requests, analytics, reporting, and business plan development.
* Ensure application of efficient and effective financial and operating controls within the Corporation.
Promote sound internal control programs and support the Corporation's requirement for strong central financial control by reporting to the Director of Finance – Customer Development, whenever Corporate Financial Policies or instructions are not being followed or appear inappropriate, inadequate or out-of-date.
* Demonstrate a commitment to quality performance through personal example by adopting a customer-based approach to business support.
* Communicate fully with superiors, subordinates, and others who have need to know.
Be informative without being obtrusive or vexatious.
Communicate in a way that is timely, yet prompt; complete, yet concise; and clear, yet responsive.
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.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark,...
....Read more...
Type: Permanent Location: Bellevue, US-WA
Salary / Rate: Not Specified
Posted: 2025-10-30 07:54:25
