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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:
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 the Analyst 1, Lab Quality Control role to be in Athens, GA.
Benefits you will enjoy starting your first day:
* Competitive pay based on experience, night shift differential, plus an annual performance bonus.
* Full medical, dental and vision coverage, competitive 401k, HSA/FSA, and company paid Pension plan.
* 120 hours paid vacation, plus 40 hours paid sick leave and an additional 40 hours paid personal leave.
* Tuition Reimbursement for eligible degree programs.
Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting role!
The Associate Analyst is responsible for testing and analyzing raw materials, in-process samples, and products such as chemicals and Active Pharmaceutical Ingredients (API) to determine stability, purity, chemical content, and other characteristics.
They follow standardized test-methods, procedures, and work instructions, document test results, and communicate status of test results.
Key Responsibilities:
* Set up, operate, and clean laboratory equipment used to support production of intermediate, raw material, and finished products for API, medical device raw material components, and other products as directed; complete all associated support activities in the laboratory.
* Assure that QC laboratories run in a safe, clean, and environmentally sound manner.
* Review peer laboratory data to ensure accuracy and completeness.
* Demonstrate and develop experience on HPLC, UPLC, Karl Fischer, UV analysis, NIR, and other analytical techniques and train other laboratory personnel on these techniques.
* Develop skills to troubleshoot and perform minor maintenance, calibration, and repair of lab...
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Type: Permanent Location: Athens, US-GA
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:05
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Sei pronto/a ad entrare a far parte di un’organizzazione in crescita, globale, specializzata nella produzione e sviluppo farmaceutico, che mette le persone al primo posto? Unisciti ad Adare! Noi lavoriamo a stretto contatto con i nostri partner nell’industria farmaceutica durante tutte le fasi di sviluppo e produzione dei farmaci destinati alla commercializzazione, con l‘intento di migliorare le vite dei/delle pazienti e dei farmaci essenziali per le persone di tutto il mondo.
Ogni ruolo all’interno di Adare ti offrirà un’esperienza unica e personalizzata nonché l’opportunità di avere un grande impatto, fondamentale per il successo della nostra azienda. Con l’aiuto di persone come te che si dedicano alla nostra missione, Adare migliora vite migliorando la somministrazione dei farmaci !
Unisciti alla nostra missione, unisciti ad Adare!
La nostra proposta:
* Assicurazione sanitaria
* Piano pensionistico
* Benefit previsti da accordo interno
* Crescita professionale e opportunità di avanzamento all’interno dell’azienda
* Premio di partecipazione
* Programma di riconoscimento dei/delle dipendenti
Siamo alla ricerca di un un/una Analytical Method Validation Analyst che si unisca al nostro Team di Quality Control Compliance.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE:
Il/la Analytical Method Validation Analyst svolge le attività di convalida di metodi analitici su API, intermedi e prodotti finiti all’interno del reparto di Controllo Qualità, in accordo con quanto previsto dalle GMP, dalle normative ICH e dalle Procedure Operative Standard, riportando direttamente al/alla Quality Control Compliance Lead.
COMPITI E RESPONSABILITA’:
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati.
* Svolge il proprio lavoro nel rispetto delle procedure aziendali e delle disposizioni di legge in materia di sicurezza sul lavoro e delle Norme di Buona Fabbricazione.
* Partecipa e fornisce supporto, per quanto di competenza, al Transfer di nuovi Progetti, elaborando una valutazione di fattibilità e successivamente Protocolli e Report della convalida.
* Convalida metodi analitici per API, intermedi di produzione e prodotti finiti in bulk o in confezionamento di mercato.
* Consulta in autonomia linee guida, quali ICH, EurPh e documentazione inerente alla convalida di metodi analitici, ne assicura la corretta applicazione individuando eventuali disallineamenti tra i metodi esistenti e le richieste regolatorie o linee guida.
* Revisiona i dossier nella parte che compete le attività analitiche e del Controllo Qualità in collaborazione con il reparto Affari Regolatori.
* Aggiorna i documenti analitici in conformità alle principali farmacopee ed ai dossier di riferimento in caso di cambi.
* Monitora e redige peri...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:01
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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
Internship IP2TIS 2025 - For students in the field of Business Administration, Sustainability, Chemistry
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love. That’s what makes us Roche.
Our Global Internship Programme in Innovation & Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.
Are you ready to join a global network spanning 20+ countries, where bright minds collaborate to tackle real-world challenges in Innovation & Sustainability? Do you want to work on impactful projects, shape the future , and drive change from within?
The Opportunity
Are you passionate about sustainability and eager to make a meaningful impact in the world of green chemistry? Join our innovative team as an intern in the direct procurement team, where you'll play a key role in shaping our procurement portfolio with a focus on green chemicals!
In this hands-on role, you'll delve into evaluating our chemical procurement practices, ensuring they align with our stringent sustainability criteria.
You'll analyze supply chains, assess environmental impacts, and propose solutions that promote the use of green chemicals.
This is your opportunity to drive sustainable change while gaining invaluable experience in the dynamic field of green chemistry.
Who You Are
You are enrolled or have completed your Bachelor's studies at a university, preferably in the field of Business Administration, Sustainability, Chemistry within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 3 months and getting to know the pharmaceutical industry.
Furthermore you are
* Passion for Sustainability: Evident interest and enthusiasm for the sustainability topics.
* Analytical Skills: Ability to analyze data, evaluate problems, and provide solutions.
* Communication Skills: Strong written and verbal communication abilities.
* Teamwork: Demonstrated ability to work well in a team environment.
* Procurement / Supply chain management experience preferred
If you meet most but not all qualifications, we still encourage you to apply.
Technical details:
The start date for the internship...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:45
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love. That’s what makes us Roche.
Our Global Internship Programme in Innovation & Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.
Are you ready to join a global network spanning 20+ countries, where bright minds collaborate to tackle real-world challenges in Innovation & Sustainability? Do you want to work on impactful projects, shape the future , and drive change from within?
The Opportunity
The project GreenTwin develops a digital twin to optimize supply processes for production.
By modeling logistics flows, we aim to reduce resource consumption, improve efficiency, and lower CO₂ emissions.
The project will enhance transparency, enable data-driven decision-making, and support a more sustainable global supply chain.with three key goals:
Reduced Carbon Footprint & Resource Efficiency; Improved Supply Chain Efficiency & Cost Savings; Data-Driven Decision Making & Process Transparency: The project enhances visibility into supply chain performance, allowing for real-time monitoring and ranking of logistics efficiency.
This enables proactive decision-making, reduces risks, and ensures a more reliable production supply.
Who You Are
You are enrolled or have completed your Bachelor’s / Master’s studies at a university, preferably in the field of Logistics and Supply Chain Management, Information Systems, Industrial Engineering and Management or Sustainable Resource Management within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 3 months (extension to 6 months possible) and getting to know the pharmaceutical industry.
Furthermore you are
* Simulation & Modeling skills – Tools like AnyLogic, MATLAB, or Python-based simulations are required
* Open-minded, conscientious, independent attitude, and driven by solving problems
* Critical Thinking, effective communication and proactive engagement with colleagues
* German language skills are required, English is a plus
* Data Analytics & AI – Skills in Python, R, SQL for data-driven decision-making is a plus
If you meet most...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:37
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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:
Cambridge, Massachusetts, 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
Johnson & Johnson is currently seeking an Associate Scientist II, In Vitro Display located in Cambridge, MA.
We are seeking an outstanding Associate Scientist for our protein engineering and in vitro discovery group, who can support the development, implementation, and utilization of phage naïve or immune libraries for antibody discovery, or other emerging molecular optimization techniques to support the development of biologics (multi-specific antibodies, CAR-T, ADCs, etc.) in various disease areas.
The position will offer an exciting opportunity to engage in the discovery and molecular engineering of biotherapeutics while also developing new processes and technologies for biologics discovery.
This role will also include portfolio project leadership and interaction with world-class scientists in different therapeutic areas, including Oncology, Immunology, Metabolic Diseases, Neurology, and Infectious Diseases.
Principal Responsibilities:
* Perform and optimize in vitro display techniques such as phage display and yeast display for molecule discovery and selection.
* Conduct experiments involving DNA/RNA library construction, DNA purification, protein expression, purification, and characterization.
* Execute assays to evaluate the binding, off-rate, and functionality of selected candidates (flow cytometry, ELISA, Octet, etc.).
* Analyze, interpret, and document experimental data while maintaining accurate and detailed records.
* Collaborate with cross-functional teams to support project objectives and timelines.
* Contribute to troubleshooting, protocol development, and the continuous improvement of laboratory workflows.
* Prepare technical reports, presentations, and summaries for internal discussions and ex...
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Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:36
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biological Research
Job Category:
Scientific/Technology
All Job Posting Locations:
US026 PA Spring House - 1400 McKean Rd
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
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.
We are searching for the best talent for Principal Scientist, Respiratory-Discovery to be located in Spring House, PA.
We are currently seeking a Principal Scientist specialized in respiratory biology to join our Immunology Discovery team within the Immunology Therapeutic Area to be based in Spring House, PA.
You will be integral to our mission of developing novel therapies targeting respiratory diseases.
The ideal candidate will possess deep knowledge and subject matter expertise in immune pathways implicated in pathogenesis of respiratory diseases.
Recent lab-based experience in T2 and non-T2 immune cell analysis, primary cell culture, lung organoid and in vivo models relevant to asthma and COPD.
We are looking for someone with a strong sense of scientific curiosity and innovation, who thrives in a collaborative, multi-disciplinary environment.
A talent that is ambitious, aspires to learn, open-minded and transparent will succeed in this role.
Key Responsibilities:
* Plays a critical role in shaping discovery respiratory strategy and providing technical expertise and leadership in an interdisciplinary environment.
* Builds, aligns and executes tec...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:31
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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:
US121 NJ Raritan - 1000 Highway 202 S
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 to be in Raritan, NJ.
Purpose: Entry to developing individual contributor, who works under close supervision.
Assists staff in various processes in the Quality Control function.
Supports day-to-day laboratory activities such as sample management, supply ordering and receipt, and general housekeeping.
Assists with analysis, qualification/validation activities, and lab investigations.
Supports data review and metrics reporting.
Executes continuous improvement projects with supervision.
May execute testing under supervision.
You will be responsible for:
* Ensure testing is completed in compliance with all applicable procedures, standards, and current Good Manufacturing Practices regulations.
* Conduct analytical testing of final product samples submitted to the QC laboratories.
* Perform peer review/approval of laboratory data.
* Use electronic systems (LIMS, iLAB) for execution and documentation of testing.
* Build, review, and approve relevant QC documents, SOPs, and WIs.
Qualifications / Requirements:
Education:
* Minimum of a Bachelor’s or equivalent University Degree required; focused degree in Biology, Biochemistry, Microbiology, or related scientific field is preferred
Experience and Skills:
Required:
* 0 - 2 years of relevant work experience
* Knowledge and understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
* Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, ELISA, Cell Culture, and/or Potency assays
* Experience with Manual Sample Processing
* Excellent written and verbal communication skills
Preferred:
* Experience in a Quality Control setting
* Experience withi...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:27
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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:
Technology Product & Platform Management
Job Sub Function:
Technical Product Management
Job Category:
People Leader
All Job Posting Locations:
DE029 Aachen, US345 MA Danvers - 22 Cherry Hill Dr
Job Description:
J&J Heart Recovery (Abiomed) , is currently recruiting for a Technology Leader Global & Americas, to be located in Danvers, MA.
This is a hybrid role.
Key Responsibilities:
Business & Technology Strategy
* Support vision, align/prioritize business & IT strategies and co-shape strategic demand with the business
* Shape and define annual objectives, roadmaps and outcomes informed by business and technology for selected areas / functions
* Translate business vision/strategies and customer needs to products, empowering products and squads to innovate and create solutions to meet business / customer / user needs
* Unite varied products into cohesive end-to-end digital business strategies and solutions for function/franchise/region
* Co-drive continuous improvement and seek opportunities for business process improvement through technology, data and automation.
Be a change agent that drives digital transformation.
* Understand competitive landscape and how competitors use technology.
Value Management
* Governance and prioritization of the investment processes, and management of the technology budget.
* Define and actively measure the value being created and delivered to customers / users / stakeholders (e.g., define, refine and measure OKRs on a regular cadence)
* Maintain a pulse on performance metrics to focus on business value realization and pull-through, including end user/customer KPIs, product group performance, technical performance (e.g., available / up time), product maturity and revenue/market growth
* Co-create business cases with business partners, supporting socialization and/or funding request activities
* Support selected initiatives and any planning cycles (e.g., BP, JU, NU LRFP)
* Owns budget assigned to scope
Internal and External Partnerships
* Represent J&J in strategic technology discussions with key external and internal stakeholders
* Foster an environment to increase digital acumen and drive data-driven culture for business partners and product teams across markets
* Build strong partnerships and connections with technology providers to shape policies & deliver innovative solutions
Experiment...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:20
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Classification:
Exempt
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The District Manager is responsible to meet or exceed Service goals in the management of a district of routes.
Reports to the Service Manager.
A DM may manage a service center and if the service center has more than 7 routes, the DM becomes classified as a Senior DM.
Our full-time employees enjoy:
401K Plan with Company Match
Medical, Dental, Vision, FSA/HSA
Life Insurance, Disability Insurance
Vacation, Sick Time, Holidays
Choice of Global Cash Card or Direct Deposit
Career Advancement
Learning & Development Opportunities
Inclusive and Diverse Team Environment
Essential Functions:
- Develop and motivate a district to be a highly productive team through continual training, regular meetings, daily check-in, fostering a positive work environment, route rides, and building strong relationships with each RSR.
- Ensure customer loyalty and outstanding customer service through customer visits, audits, new installs, problem solving, open communication and negotiating with customers.
- Ensure all company policies and procedures are followed in their district, including safety and Service SOP.
- Manage retention and growth by motivating their district to solicit new customers, up-sell/cross-sell/sample all lines of service or product and ensure a profitable product mix.
Monitor and report competitive activity.
Oversee promotions, contests and continued excellent customer relationships.
- Leading their district to success, communicate changes and policies, oversee route organization, project a professional image and require of their district likewise, and cooperatively work with other departments in the branch.
- Complete general route responsibilities when necessary.
Safely operate a delivery vehicle, following all applicable laws and company policy.
- Follow written and verbal instructions and perform other tasks as directed by supervision.
- A Senior DM performs the above functions as well as oversees a service center.
This includes securing the facility, managing inventory to ensure sufficient s...
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Type: Permanent Location: Reno, US-NV
Salary / Rate: Not Specified
Posted: 2025-04-02 08:11:34
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SBA Communications is a leading independent owner and operator of wireless communications infrastructure, including towers, buildings, rooftops, DAS and small cells.
We offer a competitive benefits and compensation package and are looking for team members who will thrive in our dynamic environment.
We welcome your interest in SBA.
Let us know a little about you by checking all that apply:
* You are a self-starter.
* You are resourceful and thrive in a fast-paced environment.
* You have a strong work ethic.
* You are passionate and driven to achieve results.
* You are a team player who enjoys working in a collaborative environment.
* You continuously challenge yourself to find innovative ways to improve.
You may be a perfect fit.
At SBA, we operate with the highest sense of integrity and commitment to quality.
We focus on achievement and operate with responsiveness, timeliness and accountability.
Our culture of excellence incorporates working collegially, where every team member can contribute meaningfully and make a difference.
If you are ready to make an impact, join our team!
Job Profile Summary
The position will be responsible for leading the Competitive Intelligence (CI), Geographic Information Systems Group (GIS), and Revenue Defense projects for the assigned region.
The position is responsible for researching and analyzing the site level internal and external data to create and implement a plan to optimize the performance of the international tower portfolio.
This position will work closely with other internal departments, including Site Leasing, Services, Sales, Real Estate, Legal, Accounting, Taxes, Mergers & Acquisitions, Business Development, solutions, technology, IT
and New Tower Builds and will present to the executive leadership regularly or as needed.
Your Next Career Opportunity – Principal Specialist, International Competitive Intelligence
The position will be responsible for leading the Competitive Intelligence (CI), Geographic Information Systems Group (GIS), and Revenue Defense projects for the assigned region.
The position is responsible for researching and analyzing the site level internal and external data to create and implement a plan to optimize the performance of the international tower portfolio.
This position will work closely with other internal departments, including Site Leasing, Services, Sales, Real Estate, Legal, Accounting, Taxes, Mergers & Acquisitions, Business Development, solutions, technology, IT
and New Tower Builds and will present to the executive leadership regularly or as needed.
What You Will Do – Primary Responsibilities
Be the regional leader of the Competitive Intelligence (CI), Geographic Information Systems Group (GIS), and Revenue Defense projects for the International Competitive Intelligence area, which will include the review of all relevant business intelligence information, including extracting data from multiple servers (external an...
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Type: Permanent Location: Boca Raton, US-FL
Salary / Rate: Not Specified
Posted: 2025-04-01 08:18:41
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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.
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*English version to follow
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ELYSIS – Directeur(trice) global(e) approvisionnement
Une nouvelle ère pour l’industrie de l’aluminium – ELYSIS
Aluminium sans carbone
La technologie ELYSIS™ représente la plus grande avancée dans l’industrie de l’aluminium depuis 1886.
Des efforts sont présentement déployés afin de perfectionner cette nouvelle façon révolutionnaire de produire de l’aluminium, qui élimine le dioxyde de carbone et toutes les autres émissions de gaz à effet de serre du procédé conventionnel d’électrolyse.
Le procédé ELYSIS élimine l’utilisation d’anodes de carbone, en les remplaçant par des matériaux brevetés.
En tant que premier procédé industriel qui émet de l’oxygène comme sous-produit, il a le potentiel de transformer toute l’industrie.
En 2018, deux producteurs d’aluminium de calibre international, Alcoa et Rio Tinto, ont uni leurs forces afin de créer la coentreprise ELYSIS avec le gouvernement du Québec.
Bénéficiant du soutien du gouvernement du Canada et d’Apple, la technologie progresse et elle est actuellement conçue pour être utilisée aussi bien dans des projets de construction que de modernisation d’alumineries.
ELYSIS a son siège social à Montréal, avec des centres de recherche et de développement à Alma et à Jonquière, au Québec (Canada), ainsi qu’à New Kensington, en Pennsylvanie (États-Unis) et en France.
Du métal de qualité commerciale produit par ELYSIS durant le processus de R et D est déjà utilisé par Apple dans un éventail de produits (comme le MacBook Pro 16 po et l’iPhone SE), par AB InBev (canettes) et par Audi (roues du e-tron GT, fabriquées par le RONAL Group).
Joignez-vous à l’équipe d’ELYSIS !
À propos du poste
ELYSIS est à la recherche d’un(e) Directeur(trice) Global(e) des Approvisionnements hautement expérimenté(e), basé(e) à Montréal, Québec.
Relevant de la cheffe de la direction financière, il ou elle sera chargé(e) de gérer l’ensemble des achats de l’entreprise, en menant des initiatives stratégiques, en développant des solutions adaptées aux besoins de l’organisation et en dirigeant une équipe performante.
Principales activités et responsabilités :
* Gérer la fonction d'approvisionnement d'ELYSIS en respectant les normes de conformité et les meilleures pratiques établies pour l’achat de biens et services.
* Diriger les activités d'approvisionnement en fonction des besoins commerciaux de l’entreprise.
* Gérer et encadrer une équipe de professionnels dynamiques.
* Favoriser un environnement d'équipe positif, collaboratif et productif.
* Développer des stratégies pour la chaîne d'approvisionnement mondiale et apporter des ...
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Type: Permanent Location: Montreal, CA-QC
Salary / Rate: Not Specified
Posted: 2025-04-01 08:18:30
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Your Job
Georgia-Pacific, LLC is now hiring a Process Improvement Analyst (PIA) for our McDonough, GA Mailer's facility.The ideal candidate will be a self-driven individual with a passion for excellence in Safety, Continuous Improvement, Manufacturing, and Customer Focus.
The PIA is a key addition for the Mailer facility, responsible for improving the corrugated facility's manufacturing performance through technology implementation, raw material qualifications and production line enhancements.
It's the perfect opportunity for someone on a steep growth trajectory who is ready to stretch a little.
The PIA will normally work a weekday (M-F) 8a-5p shift with potential for coverage during off-shift hours as needed including potential Saturdays.
Our Team
Georgia-Pacific's Mailers is a part of the Packaging and Cellulose business, the Mailers business is expanding its product lines, working with key customers to create and launch one or more new products to complement our already thriving recyclable padded mailer business.
Watch a short 60 sec video to see what we do at Mailers: How We Make Mailers | Georgia-Pacific - YouTube
What You Will Do
* Identify and implement cost-saving opportunities after validation
* Assist with new product development and ensure compliance through the New Substance Request (NSR) process
* Facilitate the Change Request process by receiving requests, uploading them to the PLEX change module, monitoring approvals, and collaborating with requestors to update SOPs on SharePoint
* Assist the Product Quality Supervisor by:
* Maintaining accurate BOMs and Specifications in PLEX and keeping SOPs and OPLs updated in SharePoint.
* Training new plant personnel on current Product Quality procedures and updating all personnel on revised procedures.
* Collaborating with the Quality Manager to maintain training logs.
* Providing timely recommendations (Release/Scrap/Rework) for products on "Hold" using a risk management approach and entering resolutions into Plex.
* Managing lab equipment calibration and ensuring the R&D lab adheres to 6S standards.
* Supporting customer complaint resolution through collaborative root cause analysis and documenting in Plex
* Evaluating and testing incoming raw materials for specification adherence, documenting results, and facilitating early invoice payments for contractual price discounts
Maintain regular structured and informal communication with Product Quality Specialists, the R&D team, Quality Manager, and Operations team
Troubleshoot issues and develop Design of Experiments (DOE) to identify and resolve recurring manufacturing challenges
Who You Are (Basic Qualifications)
* Previous experience in a quality or process improvement role within a manufacturing/ industrial environment or lab setting
* Previous e xperience documenting procedures and data and communicating to technical and non-technical audiences
* Must ha...
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Type: Permanent Location: McDonough, US-GA
Salary / Rate: Not Specified
Posted: 2025-04-01 08:14:40
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Safety Specialist PDS Primoris Distribution Services – Denton, TX
Job description
SUMMARY: Responsible for all area activities involving safety and compliance with company policy and regulatory requirements.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
· Responsible for performing field safety audits for all divisions and all products primarily in Denton Tx.
Area
· Perform accident and incident investigations and reporting as directed.
· Assists in documentation collection for driver qualification files while in the field.
· Assists in training functions.
· Investigates instances of non-conformance and facilitates the determination of the root cause.
· Provides input to management.
· Additional duties as assigned.
SUPERVISORY RESPONSIBILITIES - None
QUALIFICATIONS/EXPERIENCE
*Must be Bilingual (fluent in Spanish), OSHA 30 hours
*Some travel required for the position- up to 25%
· Risk management degree, safety professional certification, construction surface restoration, or utility construction experience preferred.
· Basic computer skills particularly Microsoft Office programs (Word, Excel and PowerPoint) for input and output of data.
· Knowledge of computers and Windows based software, or the ability and willingness to learn.
· Ability to identify and suggestion resolution of problems in a timely manner.
· Ability to coordinate multiple tasks simultaneously.
· Effective communication skills, both oral and written.
· Respond promptly to customer needs and resolve all issues satisfactorily.
· Maintain confidentiality at all times.
· Demonstrate accuracy and thoroughness in all tasks.
· Treat people with respect and uphold the organizational values.
· Follow policies and procedures, with attention to detail.
· Prioritize and plan work activities and use time efficiently.
· Ability to consistently meet or exceed deadlines.
· Ability to deal with frequent changes, delays or unexpected events.
· Effectively provide guidance, maturity and foster positive attitudes about the job and the company.
· Strong interpersonal skills with the ability to relate to all types of people.
· A demonstrated willingness to work hard and at times physically demanding work in the elements.
Some of the physical demands are:
1.
Must be able to lift 50 pounds on a daily and continual basis.
2.
Ability to drive on a stop and start basis daily and continually.
3.
Lifting, placing of materials, standing, walking – particularly on uneven surfaces, turning, stooping, kneeling, crawling, reaching, crouching, speaking and hearing are required continuously.
4.
Close vision is required for some functions and distance and peripheral vision is required for safety.
WORK ENVIRONMENT
· Employee will be subjected to both outdoor and indoor environments
EEO Statement:
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, n...
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Type: Permanent Location: Denton, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-01 08:11:32
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Sr.
Specialist - Downstream Operations Technician
The Downstream OpTech is technical process leader on the Downstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of the Clarification, Chromatography, and Tangential Flow Filtration operations.
Your Responsibilities:
* Executes the operation with team serving as process leader, coach, trainer, and responsible party
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Operations representative for cross-functional process support team, engaging in process
* Real-time problem solving, process intervention, and technical experiment delivery
* Ensures process documentation is prepared and completed with accuracy and concurrence
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: A minimum of 3 years of experience in Liquid Protein A Chromatography at manufacturing scale
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Proficiency with SAP
* GMP manufacturing
* Tangential Flow Filtration
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights incl...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 40
Posted: 2025-03-31 08:08:57
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Coordonnateur R&D - Description du poste
Depuis 1980, PG SOLUTIONS, une filiale de Harris Computer, est un chef de file du marché québécois dans le domaine des solutions d'affaires et de gestion pour le domaine public et parapublic.
Notre mission est de concevoir, développer et déployer des solutions de gestion les plus performantes sur le marché afin de contribuer à l’atteinte des objectifs de gestion des organisations que nous desservons.
Présentation du poste
Tu es à la recherche d'une opportunité professionnelle stimulante au sein d'une entreprise novatrice et en pleine croissance ? Ce poste est fait pour toi !
En tant que Coordonnateur d’une équipe de développement, tu seras au cœur de notre mission d'innovation.
Tu participeras activement à la planification, à l’organisation et au suivi de toutes les activités de ton équipe.
Ton rôle sera essentiel pour analyser les opérations de développement, superviser les projets et proposer des méthodes de travail innovantes.
Avec ton leadership inspirant, tu guideras ton équipe vers l'excellence, en favorisant une approche axée sur le soutien et l'efficience.
Tu seras un pilier pour assurer la mobilisation et la motivation de ton équipe.
Nous recherchons une personne rigoureuse, curieuse et avide de nouveaux défis.
Si tu te reconnais dans cette description, cette opportunité est faite pour toi !
Tâches et responsabilités :
* Participer à l’analyse, la planification, la coordination et la supervision des activités nécessaires à l’atteinte de tous les objectifs des projets, en respectant les ressources allouées;
* Participer au suivi d’avancement des projets auprès de la direction R&D;
* Au besoin, répondre aux demandes complexes et décider des priorités quotidiennes des équipes;
* Assurer les bonnes relations entre les intervenants à tous les niveaux hiérarchiques;
* S’informer sur les bonnes pratiques et nouveautés dans le développement logiciel autant au niveau des processus que des langages;
Responsable du personnel de développement :
* Mesurer la « performance » des équipes (Engagement, respect des estimés, qualité);
* Définir, évaluer et gérer les objectifs, les compétences et les besoins de développement des membres des équipes afin de voir à leur croissance;
* Participer au recrutement de personnel;
* Mobiliser les équipes autour des objectifs et enjeux de l’entreprise.
Responsable des activités Scrum/Agile :
* Collaborer avec le « Product Owner » pour maintenir un carnet de produit sain et planifier les tâches des sprints en fonction de la capacité de l’équipe;
* Organiser et animer les réunions « Scrum / Agile » pour assurer une communication efficace au sein de l’équipe;
* Encourager l’autonomie de l’équipe et promouvoir une amélioration continue pour atteindre son plein potentiel;
* Guider l’équipe dans l’identificati...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 80000
Posted: 2025-03-31 08:08:25
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Austin Industrial delivers premier maintenance, construction, and soft craft services to leading industrial companies across the U.S.
An industry leader for more than 60 years, we offer single-source solutions to our customers in the oil, gas, chemical, food, agriculture, power, and manufacturing industries.
Our team of employee-owners, equipped with innovative technology and optimized procedures, helps owners optimize safety, productivity, profit margins, and cost-efficiency.
This is a full-time maintenance job working 40 hours a week (4/10's). There is no per diem and no relocation funding.
Industrial Insulator
The Industrial Insulator will layout, fabricate, assemble, install and repair insulation and sheet metal around pipes, maintenance parts, fittings, equipment and systems.
Responsibilities
* Must be an experienced Industrial Insulator with 3 or more years of experience.
* Must be able to install temp mat and pads and install pipe covering and fittings (Calcium Silicate).
* Must have experience forming sheet metal materials around pipes, ductwork and industrial equipment.
* Must be able to install insulation and fittings, pipe cover and board materials, such as perlite and calcium silicate.
* Install sheet metal around insulated pipes with screws/ bands to protect the insulation from weather conditions or physical damage.
* Makes flat sheet metal layouts of finished parts, such as sheet metal "square-to-round" transitions, offsets, flashing, tapered elbows, transitional elbows, "Y" branches and compound fittings.
* Brush adhesives and mastic application to insulation material.
* Using tape measure or other measuring device, measure and cut metal material to specified size and shape for covering flat or round surfaces.
* Must be able to use hand tools and equipment to form, crimp, or roll metal in place.
* Must be able to perform work wearing personnel protective equipment.
Including but not limited to the following: rain gear, chemical protective clothing, supplied air and air purifying respirators, safety harness, fire resistant coveralls, hard hat, ear plugs and safety glasses.
* While performing the duties of this job, the employee is regularly required to have full range of mobility in upper and lower body, able to reach overhead, able to work in various positions, including, but not limited to, stooping, standing, bending over, sitting, kneeling, squatting; use hands to handle, or feel objects, tools or controls; reach with hands and arms; climb stairs; work at heights, balance for extended periods of time. Must be able to climb ladders and lift a minimum of 50 pounds.
* Other duties as assigned.
Qualifications
Education – no minimum education requirements.
Experience - 3 years of Insulator experience.
Must pass drug screen and background check, as a condition of employment.
This is a full-time maintenance job working 40 hours a week (4/10's). There is n...
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Type: Permanent Location: Orlando, US-FL
Salary / Rate: 26
Posted: 2025-03-31 08:03:29
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Submissions & Regulatory Intelligence Manager
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Submissions & Regulatory Intelligence Manager (hybrid) located within commutable distance of High Wycombe, United Kingdom; Beerse, Belgium; Leiden, Netherlands; Bangalore or Hyderabad, India; Springhouse or Titusville NJ, United States.
Purpose:
Contributes to the Clinical Data Standards team as an individual contributor who is a developing subject matter expert, and who works independently with minimal supervision and who takes a leadership role in the collaboration with various internal and external partners.
Consults on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy.
Applies in-depth knowledge of Clinical Data Standards to install best in class policies, procedures, and plans for the area.
Ensures consistency of clinical data standards across clinical trials and in compliance with regulatory requirements.
The Submissions & Regulatory Intelligence Manager is responsible for providing significant expertise to the IDAR department (and GD if applicable) in clinical study data regulatory submission requirements and strategies.
Examples of this content are:
* Newly released or updated Regulatory Health Authority (RHA) and industry guidance documentation
* Identification of clinical study data submission information critical to IDAR submission processes and procedures, including providing an interpretation of such information if needed
* IDAR submission requirements and rules.
The position serves as the single Point of Contact for any stakeholder on data management, clinical and statistical programming, and global re...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-31 07:59:00
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Bangalore, Karnataka, India, Beerse, Antwerp, Belgium, Leiden, South Holland, Netherlands, PENJERLA, Telangana, India
Job Description:
Submissions & Regulatory Intelligence Manager
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Submissions & Regulatory Intelligence Manager (hybrid) located within commutable distance of High Wycombe, United Kingdom; Beerse, Belgium; Leiden, Netherlands; Bangalore or Hyderabad, India; Springhouse or Titusville NJ, United States.
Purpose:
Contributes to the Clinical Data Standards team as an individual contributor who is a developing subject matter expert, and who works independently with minimal supervision and who takes a leadership role in the collaboration with various internal and external partners.
Consults on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy.
Applies in-depth knowledge of Clinical Data Standards to install best in class policies, procedures, and plans for the area.
Ensures consistency of clinical data standards across clinical trials and in compliance with regulatory requirements.
The Submissions & Regulatory Intelligence Manager is responsible for providing significant expertise to the IDAR department (and GD if applicable) in clinical study data regulatory submission requirements and strategies.
Examples of this content are:
* Newly released or updated Regulatory Health Authority (RHA) and industry guidance documentation
* Identification of clinical study data submission information critical to IDAR submission processes and procedures, including providing an interpretation of such information if needed
* IDAR submission requirements and rules.
The position serves as the single Point of Contact for any stakeholder on data management, clinical and statistical programmi...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:57
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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:
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-000701
* Canada - Requisition Number: R-002921
* United Kingdom, Belgium, Switzerland - Requisition Number: R-002952
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 an Associate Director, Global Labeling Product Leader.
This position is a hybrid role and will be located in Toronto, Canada.
The Associate Director, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provides advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation.
Ensure high quality and compliant labeling documents.
This role may collaborate with external partners.
* Contribute to and implement the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeli...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:54
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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 Systems
Job Category:
Professional
All Job Posting Locations:
Latina, Italy
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/
J&J Innovative Medicine is recruiting for a Analyst Quality Systems.
Principle responsibilities:
This role is part of the eLIMS Center of Excellence (CoE) Small Molecules (SM) and serves as a subject matter expert in the configuration and maintenance of master data within the eLIMS system.
This role supports key processes such as the release of pharmaceutical, raw, and packaging materials, as well as Certificate of Analysis (CoA) generation in translating specifications into the eLIMS system using current business processes.
The incumbent independently creates, maintains, and reviews high-quality master data, conducts system testing and supports the creation and updating of system-related documentation.
Additionally, the role identifies opportunities for process improvements and drives their implementation.
This role is responsible for managing and executing incoming requests promptly and effectively.
To ensure the accuracy and integrity of master data, it is essential to have a comprehensive understanding of the site’s master data requirements and laboratory processes.
Additionally, the position involves the creation of training materials to foster knowledge sharing within the team, and actively participates in the development of team members through training and continuous personal growth.
The individual in this role is expected to support various projects within QC Operations, which could include the implementation of iLAB (paperless lab execution program) initiatives, process harmonization and standardization, master data support for consumer products and contract manufacturing organizations (CMOs).
Furthermore, this position offers critical support to the Supervisor in managing COMET nonconformance investigations and proactively...
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Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:51
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Issy-les-Moulineaux, Hauts-de-Seine, France
Job Description:
En tant qu’acteur majeur du bloc opératoire, Johnson & Johnson MedTech développe et commercialise des dispositifs médicaux utilisés notamment en chirurgie générale, orthopédie, traumatologie, neuroradiologie et électrophysiologie.
Nous innovons en permanence pour apporter aux professionnels de santé des produits à la pointe de la technologie et des solutions innovantes qui visent à améliorer la qualité de vie des patients et répondre à leurs besoins.
Nous recrutons un(e) Spécialiste Qualité dans le cadre d'un contrat en alternance pour une durée de 12 mois à partir de septembre 2025 (Issy-les-Moulineaux (92))
Principales responsabilités :
* Être garant de la conformité du traitement des réclamations qualité et des vigilances relatives aux produits (dispositifs médicaux et médicaments) commercialisés par Johnson & Johnson MedTech, dans le respect de la réglementation française et européenne et des procédures de l’entreprise :
+ Recueil et enregistrement des réclamations qualité produits et signalements de matériovigilance et pharmacovigilance.
+ Contribution aux investigations en suivant les demandes d’informations complémentaires en lien avec les fabricants
+ Elaboration des réponses aux clients sur la base des conclusions d’investigations faites par le fabricant
* Contribuer à la mise en place et au suivi des informations et actions de terrain et de sécurité.
* Participer au maintien et au développement du système de Management de la Qualité en supportant l’exécution des processus suivants :
+ Gestion documentaire
+ Gestion des enregistrements qualité dans le respect de la protection des données personnelles
+ Participation aux audits et inspections
+ Suivi des Non-conformités et des CAPA
+ Gestion des changements
Qualifications
Formation :
* Formation scientifique, Management de la Qualité
Expérience et compétences :
Requis :
* Bon niveau d’anglais
* Connaissance de la réglementation française et européenne relative aux dispositifs médicaux
* Connaissance du système de management de la qualité
* Bonnes capacités relationnelles et...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:47
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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:
Career Programs
Job Sub Function:
Post Doc – R&D Product Development
Job Category:
Career Program
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a (3 years) PostDoc position, located in Beerse, Belgium
To continue a rich legacy in the field of neuroscience, we are building on our proven track record of innovative precision discovery approaches with a long-term commitment to neurodegenerative and neuropsychiatric diseases.
Our scientists are an integral part of the Johnson & Johnson Innovative Medicine Research and Development community and conduct research in collaboration with a broad network of academic leaders in the field.
At Johnson & Johnson, we strive to attract passionate and talented scientists who can drive change and deliver real value to patients.
We focus on innovation, collaboration and impact and by working with us, you will discover a place where you can grow and realize your full potential.
Through our culture of recognition and motivation for exceptional work, we care for and value our employees, just as we do the patients we serve.
At our exciting scientific research site with an interdisciplinary team of scientists, our goal is to understand the dysfunctional neural pathways that underlie psychiatric and neurodegenerative disorders to implement precision therapies.
We now have the opportunity within the Department of Neuroscience to take up a 3-year postdoctoral research position to contribute to the evaluation and implementation of innovative, context-specific animal models of disease using cutting-edge and advanced analytics.
Key Responsibilities:
* Perform neurophysiological experiments, implement and validate novel technologies for EEG data collection and analysis in rodents.
* You will also have access to a
* Ability to independently plan, organize and prioritize own work to make the most effective use of time and resources emphasis on innovation, collaboration, and timely delivery of results.
* Seek innovative ideas that add value to the project activities and provide ad hoc support for coordinating operations with external preclinical imaging collaborators on combined EEG/MRI recording modalities.
* Act as a “team player” contributing to achievement of the project’s objectives, build effective collaborative working relationships with team members, understa...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:46
-
At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.â¯Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
Business Improvements/ä¸å¡æ¹å
* Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
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* Conduct benchmarking to develop more effective inspection methods for improving quality.
      æ§è¡åºåï¼ä¸ºäºæé«è´¨éå¶å®æ´ææçè´¨éæ£éªæ¹æ³ã
Compliance/Regulatory/åè§/æ³è§
* Support Quality Engineer to review/analyze whether current product and processes (including actions or decisions conducted) are in compliance to standards.
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* Support Quality Engineer to conduct periodic line audits to assess for production controls such as lot segregation. Review results of area audits to ensure that corrective and preventive actions are adequate.
      æ¯æè´¨éå·¥ç¨å¸è¿è¡å®æçç产线审计以è¯ä¼°ç产æ§å¶ï¼å¦æ¹æ¬¡é离ãæ£æ¥åºå审计çç» Â Â æï¼ç¡®ä¿çº æ£åé¢é²æªæ½æ¯å
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* Support Quality Engineer to ensure the documentation and business process compliance, such as: handle the documentation approval process in PLM system, support training system maintenance, ECR process in SAP, dashboard creation/update, data processing, sample retention etc.
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Product Quality, Control & Disposition and Performance Standards/产åè´¨éï¼æ§å¶&å¤ç½®åæ§è½æ å
* Supports activities related to the Material Review Board.
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* Support Quality Engineer to conduct actions of non-conformances, CAPAs and customer complaints.Â
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* Support Quality Engineer for material identification, material segregation, and classification of defect types including the successful application of these techniques on a day-to-day basis in manufacturing.åå©è´¨é...
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:45
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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:
Project/Program Management Group
Job Sub Function:
R&D Project Management
Job Category:
Professional
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for the role of Director, Global Functions, Data Science Digital Health. We have a strong preference for this hybrid position to be located at one of the following offices; Titusville, NJ; Raritan, NJ; New Brunswick, NJ; Spring House, PA; Horsham, PA; Cambridge, MA; or San Diego, CA.
Remote work options in the US may be considered on a case-by-case basis and if approved by the Company.
At Johnson & Johnson Innovative Medicines R&D, the Data Science & Digital Health (DSDH) function is charged with applying analytic approaches to drug discovery and development across Therapeutic Areas.
We drive and shape internal and external collaborations, working across Janssen’s Therapeutic Areas and R&D functions, including Global Development and other areas.
The Global Functions, Data Science & Digital Health (GF, DSDH) group within the R&D Data Science organization has the accountability for full scale impact across the Development pipeline via AI/ML-driven site recommendation trial design optimization, real-world evidence (RWE) generation, digital endpoints, decentralized trials, and external policy, with the key pillars being:
* Manage the development of solutions for the purpose of driving Trial Acceleration & Optimization using data science, including but not limited to:
* Enrollment modeling, feasibility analytics, country footprint expansion, advanced AI/ML modeling for predictive site recommendations
* Leverage real-world data for pat...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:38
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Submissions & Regulatory Intelligence Manager
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Submissions & Regulatory Intelligence Manager (hybrid) located within commutable distance of High Wycombe, United Kingdom; Beerse, Belgium; Leiden, Netherlands; Bangalore or Hyderabad, India; Springhouse or Titusville NJ, United States.
Purpose:
Contributes to the Clinical Data Standards team as an individual contributor who is a developing subject matter expert, and who works independently with minimal supervision and who takes a leadership role in the collaboration with various internal and external partners.
Consults on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy.
Applies in-depth knowledge of Clinical Data Standards to install best in class policies, procedures, and plans for the area.
Ensures consistency of clinical data standards across clinical trials and in compliance with regulatory requirements.
The Submissions & Regulatory Intelligence Manager is responsible for providing significant expertise to the IDAR department (and GD if applicable) in clinical study data regulatory submission requirements and strategies.
Examples of this content are:
* Newly released or updated Regulatory Health Authority (RHA) and industry guidance documentation
* Identification of clinical study data submission information critical to IDAR submission processes and procedures, including providing an interpretation of such information if needed
* IDAR submission requirements and rules.
The position serves as the single Point of Contact for any stakeholder on data management, clinical and statistical programming, and global regulatory affairs, for data submission deliverable requir...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:37
