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Key Responsibilities:
Assist in the preparation of ingredients (e.g., chopping vegetables, preparing sauces).
Support chefs in basic cooking and food plating under supervision.
Maintain cleanliness and hygiene in the kitchen area in accordance with food safety standards.
Store food and ingredients according to proper procedures.
Assist in receiving and stocking kitchen supplies.
Learn and adhere to kitchen operations, recipes, and presentation standards.
Qualifications:
Education: High school diploma or equivalent required.
A diploma or certificate in Culinary Arts from a recognized hospitality or culinary institute is preferred.
Experience: Previous kitchen or food service experience is an advantage but not mandatory.
Skills: Basic knife skills, willingness to learn, ability to work in a team, good communication, and time management.
Work Conditions:
Fast-paced kitchen environment
Standing for extended periods
Flexible to work shifts, weekends, and holidays
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Type: Contract Location: Beirut, LB-BA
Salary / Rate: Not Specified
Posted: 2025-05-24 08:31:27
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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.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Technician
The position will include routine testing of in process antigens and final product samples for the release of veterinary vaccines. The individual will be responsible for ensuring all methods are performed as written and filed with regulatory agencies and standard operating procedures.
Your Responsibilities:
* Perform required tests for bulk antigens, final products, and raw materials, as well as other procedures necessary to support company and laboratory objectives to meet specified timelines.
* Maintain aseptic laboratory technique at all times and ensure accuracy of test results through precision and attention to detail.
* Maintain accurate and concurrent testing records and ensure compliance with Company SOPs and specifications, USDA, and cGMP regulations. Assist with updating, writing, and maintaining SOP’s, bench records and data entry for the department.
* Environmental monitoring of clean rooms and personnel: assisting in and/or performing microbial and particulate tests (air sampling).
* Provide effective training as requested, confirming that individuals are trained on the procedure at hand and all required training documentation has been completed.
What you need to succeed (minimum qualifications):
* High School Diploma or equivalent required.
* Experience in working in a team environment and handling multiple tasks simultaneously.
* Proficient in Microsoft Word and Excel, capable of using a controlled informatics system.
What will give you the competitive edge (additional preferences):
* Bachelor of Science degree in Microbiology, Virology, Bacteriology, Biology, or related field
* Minimum of four (4) years of laboratory experience.
* Fundamental experience in cell culture, viral and/or bacterial propagation.
* Experience in biotechnology and aseptic technique.
Other Information:
* Location: Winslow, ME (Onsite)
* Shift: Monday-Friday, 7am-3:30pm (evening, weekend, and holiday hours may be required)
* Must b...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: 27.12
Posted: 2025-05-23 08:36:21
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At MTM Transit, it is never just a ride, it's personal.
We understand that our passengers deserve personalized attention and exceptional care and to us, every trip is important.
We have exciting opportunities to join our growing team where your work has a direct impact on the communities we serve.
Our company culture is one of innovation, collaboration, and growth.
If you are passionate, driven, and ready to join a team where your work will directly transform and shape our industry, then we want to talk to you!
What Will Your Job Look Like?
The Manager, Safety and Training is responsible for implementing safety and training programs as defined by the Leadership of Safety Administration and will ensure compliance with State and Federal regulations, as well as corporate, client guidelines and policies.
This position is contingent upon award of contract.
Location: Grand Rapids, MI
What you’ll do:
* Manage a consistent safety culture that incorporates various departments, such as operations, safety and maintenance
* Oversee Corporate Safety Incentives and programs effectively and consistently, including assignment of Safety Points
* Implement and support the company and client’s safety management system (SMS) safety plan and initiatives Manage and monitor the FTA’s drug and alcohol DAMIS reporting requirements
* Monitor and support all location insurance claims activities to ensure effective communication with claimants, to help control claims costs and support claims closure
* Lead and support the local safety committee and SMS Ambassador group
* Oversees the locations worker compensation program to ensure compliance and effectively reduce/eliminate claims
* Deliver proper classroom, behind the wheel and mobility management training in accordance with contractual and company requirements
* Promote employee self-responsibility to achieve all safety goals and training requirements
* Ensures all new hires meet minimum qualifications for each division including, background and DMV checks
* Ensure all safety manuals, programs and policies and practices are current and meet the needs of the operating divisions; updating as appropriate
* Successfully complete all related audits including those conducted by the Company, the Client, internal staff members, and state and federal regulatory agencies
* Review, determine and respond to all vehicular, passenger and employee accidents/incidents, indicating the cause and preventability, identifying potential trends to be addressed in future training efforts
* Provide functional expertise in safety regarding hiring of safety department employees
* Collaborate with local Leadership to deliver comprehensive safety meetings and plans
* Act as the location drug program manager, ensuring compliance of FTA/DOT regulations
What you’ll need:
Experience, Education & Certifications:
* High School Diploma or G.E.D.
* Bach...
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Type: Permanent Location: Grand Rapids, US-MI
Salary / Rate: Not Specified
Posted: 2025-05-23 08:27:34
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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 dipendenti.
Siamo alla ricerca di un/una Senior Formulation Scientist che si unisca al nostro Team di Pharmaceutical Development.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Senior Formulation Scientist svolge le attività concernenti lo sviluppo formulativo di prodotti solidi orali dalla scala pilota alla scala industriale, ivi inclusi lotti destinati a studi clinici.
Prepara la documentazione tecnica ed interagisce con i clienti.
Inoltre fornisce formazione, affiancamento e tutoring a scienziati meno esperti, oltre che interagire con i clienti in riunioni dedicate.
La posizione riporta direttamente al Director I, Pharmaceutical Development.
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.
* Elabora ed esegue studi di sviluppo formulativo mirati allo sviluppo di forme solidi orali definite dai clienti o dal Management
* Sviluppa nuovi prodotti impiegando le tecnologie nuove o disponibili dalla pre-formulazione alla produzione su scala industriale
* Esegue in autonomia o supervisiona la produzione di lotti destinati a studi clinici
* Esegue in autonomia attività di technology transfer
* Collabora con le funzioni di Project Management e Business Development nelle attività di progetto quali sviluppo formulativo o technology transfer
* Collabora con Operation, Quality e Regulatory nelle attività di scale up di prodotti dalla fase pilota alla fase industriale
* Esegue in autonomia la stesura di procedure...
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Type: Permanent Location: Pessano Con Bornago, IT-MI
Salary / Rate: Not Specified
Posted: 2025-05-23 08:12:45
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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:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
In the R&D Microbiology Centre of Excellence (Beerse, Antwerp, Belgium) there is currently a full-time opening for a microbiology analyst conducting microbial method development, GMP method qualification/validation, and release and stability testing in support of the clinical development portfolio.
R&D Microbiology Analyst
Your Function
* Execute method development and GMP method qualification/validation for a diverse range of microbial assays, such as bioburden testing, bacterial endotoxin testing, sterility testing, etc.;
* Perform release and stability testing on clinical products;
* Coordinate and execute Low Endotoxin Recovery (LER) studies;
* Coordinate and execute Microbial Challenge studies to determine hold time of sterile preparations;
* Author, review and approve development reports, qualification/validation reports and test method descriptions;
* Coordinate laboratory investigations;
* Ensure compliance with regulatory requirements, GMP and safety.
Your Profile
* Bachelor’s degree in Biomedical Laboratory Technology, or equivalent through experience;
* Good knowledge of and experience with aseptic and microbiological techniques;
* Experience with GMP;
* Meet high quality standards when executing experiments;
* Efficient, flexible and dynamic.
Capable of dealing with changes in the planning;
* Team player yet able to organize and execute the work independently;
* Demonstrate sense of urgency;
* Good knowledge of English, both spoken and written.
You will be welcomed in a diverse and coherent team, and will receive proper training by experienced analysts in order to fulfill your role.
Departmental responsibilities
As part of Johnson & Johnson Innovative Medicine, R&D - Discovery, Product Development, and Supply (DPDS) – Analytical Development (AD), the Microbiology CoE has the following responsibilities:
* Providing global support for all microbiology-related aspects during clinical development (R&D) and life cycle management (commercial) of the J&J Innovative Medicine product portfolio (Biotherapeutics and Synthetics).
* Coordinating microbial method development, validation/qualification and transfer activities with internal and external microbi...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:06
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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:
Pharmaceutical Product R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
In the Microbiology Centre of Excellence (Beerse, Antwerp, Belgium) there is currently a full-time opening for a pharmaceutical microbiology expert with a proven track record of project management related to microbial method validation, specification setting and control strategy in support of the Biotherapeutics R&D portfolio.
As part of Johnson & Johnson Innovative Medicine, R&D - Discovery, Product Development, and Supply (DPDS), the Microbiology Subject Matter Experts (SME) are responsible for:
* Providing global support for all microbiology-related aspects during clinical development (R&D) and life cycle management (commercial) of the J&J Innovative Medicine product portfolio (Biotherapeutics and Synthetics)
* Coordinating microbial method development, qualification/validation and transfer activities with internal and external microbiology laboratories in compliance with regulatory and internal requirements, GMP and safety regulations
* Microbial specification setting and control strategy
* Author regulatory documents and supporting health authority inquiries in the field of microbiology
* Validation and implementation of innovative microbial technologies for established and new product platforms
* Provide on-demand expertise and solutions for investigations on R&D and commercial products.
Qualifications
Education:
* You hold a PhD degree in Bioscience Engineering, Biology, Biomedical Sciences or similar with a strong expertise in the field of microbiology, or you hold a Master degree in combination with a proven track record in the specific area of pharmaceutical microbiology, in particular in the biopharmaceutical industry.
* The following experience and expertise are considered as important assets:
+ Detailed knowledge of general microbiology as well as familiar with microbiological requirements relevant to the pharmaceutical industry
+ Biological production process knowledge
+ Thorough GMP knowledge
Other:
* Ability to work independently yet also a good team player in an international setting
* Have high moral standards and assure scientific quality
* Good project management skills and able to handle multipl...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:05
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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:
Pharmaceutical Product R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
In the Microbiology Centre of Excellence (Beerse, Antwerp, Belgium) there is currently a full-time opening for a pharmaceutical microbiologist with a passion for innovative technologies in support of the Biotherapeutics R&D portfolio.
As part of Johnson & Johnson Innovative Medicine, R&D - Discovery, Product Development, and Supply (DPDS), the Microbiology CoE is responsible for the validation of microbial test methods and the microbial specification setting to assure safety and quality of (bio)pharmaceutical products across the J&J Innovative Medicine portfolio.
Novel therapies require innovative ways of testing, and hereto we are seeking an Innovation Lab lead with a passion for microbiology and new technologies, who manages and coordinates laboratory activities (overseeing 2 analysts) and also participates in the execution, summarizes and reports study results to the local and global project teams, and defines strategic validation and implementation plans in a GMP environment.
Qualifications
Education:
* You hold a PhD degree in Bioscience Engineering, Biology, Biomedical Sciences or similar with a strong expertise in the field of microbiology, or you hold a Master degree in combination with a proven track record in the specific area of pharmaceutical microbiology, in particular in the biopharmaceutical industry.
* The following experience and expertise are considered as important assets:
+ Detailed knowledge of general microbiology as well as familiar with microbiological requirements relevant to the pharmaceutical industry
+ GMP
Other:
* Ability to work independently yet also a good team player in an international setting
* Good project management skills and able to handle multiple projects simultaneously
* People management skills
* Have high moral standards and assure scientific quality
* Strong sense of urgency
* Efficient and flexible attitude
* Excellent communication skills (written and oral)
* You have good knowledge of English (written and oral)
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:04
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ERM is hiring an Archaeological Field Technician to support future needs of survey efforts for projects located in Northern California or Southern California.
Archaeological Field Techs will assist with or conduct archaeological field surveys or monitoring.
This is a fixed-term consulting role with a duration of Six months and the possibility of renewal.
RESPONSIBILITIES:
· Digging shovel tests and screening soil;
· Conduct intensive pedestrian surveys consisting of visually inspecting the land surface for presence of artifacts;
· Monitoring alongside construction crews to avoid impacts to resources;
· Bagging recovered artifacts and recording the provenience of the finds;
· Maintaining field notes;
· Compliance with corporate HSE; and
· Performing other duties as assigned or required.
REQUIRED:
· B.A.
in Anthropology
· 2 years of related experience
· Ability to travel extensively throughout Northern or Southern California
· Archaeological field school or prior archaeological field survey experience;
· Ability to work outdoors in variable weather conditions and on varied terrain;
· Ability to work weekends and over 40 hours per week when needed;
· Working knowledge of archaeological survey and monitoring protocols;
· Ability to work in the field for extended periods of time;
· Ability to work independently and as a part of a crew
· Must meet criteria identified in Job Demands & Conditions Analysis for Office and Field Positions.
· Permitted BLM Field Director preferred;
· Master’s in Anthropology preferred
For the Archaeological Field Technician position, we anticipate the annual base pay of $73,207 – $95,761 $35.19/hr – $46.03/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/ or through the internal careers portal if you are a current employee.
Note: No amount of pay is considered to be wages...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:25
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Alternant(e) Assistant Manager Operations
Job Description
A propos du poste
En tant que personne, vous êtes un apprenant – quelqu’un qui prend toujours l’initiative d’améliorer les choses et d’entraîner les autres avec vous.
Vous vivez votre vie en accord avec les valeurs les plus élevées d’intégrité et de qualité, en veillant toujours à ce que vos responsabilités deviennent une réussite à long terme.
Dans le cadre de ce rôle d’apprenti opérateur de production, vous nous aiderez à fournir de meilleurs soins à des milliards de personnes dans le monde.
Cela commence par VOUS.
Nous recherchons un(e) alternant(e) Assistant Manager Operations en contrat d’apprentissage de deux ans au sein de notre usine Kimberly-Clark de Villey Saint-Etienne (54).
Vous serez au cours de votre contrat d’apprentissage amené(e) à travailler sur les missions suivantes :
* Déploiement des Indicateurs de Performance :
Déployer des indicateurs de performance pour la sécurité, l'environnement, la qualité, l'adhérence au planning de production, la performance des machines et les ressources humaines.
Déployer des paretos sur les indicateurs de panne, déchets et perte de vitesse concernant la performance des machines.
Sensibiliser les équipes de production à l'importance de la performance et assurer le déploiement des indicateurs dans toutes les équipes.
* Accompagnement au Déploiement de l’outil SAP PM :
Aider l'équipe projet SAP PM à déployer notre nouvel outil de GMAO (Gestion de Maintenance Assistée par Ordinateur).
Constituer les nomenclatures de pièces.
Accompagner les équipes dans l'utilisation du nouvel outil SAP PM.
A propos de nous
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
Vous connaissez déjà nos marques légendaires, tout comme le reste du monde.
En fait, des millions de personnes utilisent les produits Kimberly-Clark tous les jours.
Nous savons que ces incroyables produits Kimberly-Clark n’existeraient pas sans des professionnels talentueux, comme vous.
Chez Kimberly-Clark, vous ferez partie de la meilleure équipe qui s’engage à stimuler l’innovation, la croissance et l’impact.
Nous sommes fondés sur plus de 150 ans de leadership sur le marché et nous sommes toujours à la recherche de nouvelles et meilleures façons de performer - c’est donc là que vous avez une porte ouverte sur les opportunités.
Tout est là pour vous chez Kimberly-Clark.
Guidé par un objectif.
Piloté par vous.
A propos de vous
Vous performez au plus haut niveau possible et vous appréciez une culture de la performance alimentée par une bienveillance authentique. Vous voulez faire partie d’une entreprise qui se consacre activement à la durabilité, à l’inclusion, au bien-être et au développement de carrière.
Vous aimez ce que vous faites, surtout lorsque le travail que vous faites fait une diff...
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Type: Permanent Location: Toul Cedex, FR-54
Salary / Rate: Not Specified
Posted: 2025-05-22 09:27:47
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium, Breda, Netherlands
Job Description:
We are looking for a driven Manager Clinical Operations to join our growing Clinical Operations team in Belgium (Beerse) and The Netherlands (Breda).
As a Clinical Research Manager, you will manage a team of Local Trial Managers (Local project managers), Site Managers (Clinical Research Associates) and Clinical Trial Assistants, with a strong focus on staff performance, people development, training/onboarding and resource management.
You are responsible for the successful implementation and execution of phase Ib-IIIb trials from country feasibility through study close-out while keeping clear oversight of timelines, budget, quality & performance indicators and compliance with Standard Operating Procedures (SOPs), Health Care Compliance (HCC) and local regulatory requirements.
We are seeking to hire a strong leader, who is a team player, with quick learning and problem-solving abilities.
You will contribute to the creation of the country strategy in order to optimize ways of working, drive innovation, and strive for continuous improvement and future readiness.
You will be part of a hardworking, enthusiastic, and committed team eager to deliver and helping to improve the lives of millions of patients.
Principal Responsibilities:
* People management: Provide line management to your team including goal setting, performance evaluation and talent development; Build, hire and train a fully effective team; Conduct accompanied site visits; Evaluate and forecast resource needs and manage your team's workload.
* Trial delivery & oversight: Accountable for robust feasibility processes and oversight of site selection.
Responsible for implementation, execution and monitoring of trials in assigned therapeutic area(s).
Empower your team to deliver on your team's quality and performance objectives.
Ensure inspection readiness at all times, adherence to ICH-GCP, local legislation and relevant SOP's.
Support your team in issue resolution and stakeholder management.
Support audits, inspections and timely CAPA resolution.
Build and shape internal and external network in assigned therapeutic area.
* Continuous improvement & organizational change: Lead implementation of innovation and change in the local organization; Cul...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-22 08:49:27
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Principal Scientist, Analytical Comparability & Product Characterization – Advanced Therapies to be in Malvern, PA.
Purpose:
The Biotherapeutics Development - Analytical Development (BioTD - AD) group is seeking an upbeat, highly motivated Principal Scientist to focus on analytical comparability and product characterization for advanced therapy modalities. The individual would work with team to develop product comparability study approaches for advanced therapy modalities that will be endorsed by the health authorities. A successful candidate will have experience with the design, execution and optimization of a broad range of characterization assays and will have the opportunity to engage in multi-functional teams.
They will learn from and contribute to industry-leading drug discovery/development programs that has brought numerous quality therapeutics to patients and has made significant contributions to human health.
Primary Responsibilities:
·Design and lead the execution of analytical comparability studies for advanced therapy modalities across various stages of development.
·Lead the execution of the advanced methodologies associated with comparability and deep characterization of cell and gene therapy.
·Author or coordinate appropriate IND/IMPD/BLA/MAA sections & interact with regulatory agencies to address CMC-comparability and product characterization related inquiries.
·Optimally communicate comparability study plans, statistical justifications, and results and scientific data to cross-functional teams, project teams, and health authority as needed.
·Collaborate to develop innovative approaches to challenging solutions for analytical comparability strategy and product characterizati...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-05-22 08:46:24
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At EVRAZ, our strength starts with our people! As a team we collaborate to solve problems, contribute ideas and challenge each other to ensure growth and ultimately success for the business and our employees.
RESPONSIBILITIES:
We are seeking a new crew member that is an enthusiastic team player with a strong desire to learn, high safety consciousness, and good time management skills. Under minimal supervision, this person will cut, mill, and handle steel plate and samples in preparation for laboratory properties testing. Key responsibilities include but are not limited to:
* Cuts test coupons to required dimensions using CNC plasma/oxy-fuel burn table and hand torch
* Prepares steel test samples using CNC and manual lathes, saws, milling machines, and grinders
* Verifies, collects, transports, and checks in samples from other departments to the laboratory
* Inventories samples, including identifying, labeling, organizing, and other material handling concerns
* Performs other duties as they might be assigned
REQUIREMENTS:
* Able to read and follow detailed procedures, roll pages, and quality prints (work documents)
* Maintains accuracy of material identifying labels and descriptors legibly and without transposing figures
* Robust math skills: addition, subtraction, multiplication, division, accurate number identification
* Valid driver license
* High school diploma/GED or equivalent experience
* CNC burn table and hand torch cutting experience preferred
* Experience defining quality sample dimensions using micrometers and precision measuring equipment preferred
* Shop experience, including saws, sanders, cranes and forklift operation preferred
* Machine shop experience, including CNC and manual lathes, mills, grinders, broaches, and laboratory testing preferred
* Must be able to work in an environment subject to fluctuations in heat, humidity, fumes, odors, dust and noise
* Able to regularly lift up to 50 pounds
* Able to stand up to 12 hours per shift
Our total compensation package includes amazing benefits!
* Competitive wages and bonus opportunities
* Family medical, dental, and prescription coverage at minimal employee cost
* Short and long term disability programs
* Competitive retirement plans
* Flexible Spending and Health Savings Accounts
* Employer-provided and Voluntary Life Insurance options
* Paid vacation and recognized statutory holidays
* Apprenticeship and career advancement within the company
* Tuition reimbursement
* Wellness program
All applicants must be eligible to work in the USA.
While we thank all those who apply, only those being actively considered for employment will be contacted.
Equal Opportunity Employer
EVRAZ North America is an Equal Opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, nati...
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Type: Permanent Location: Portland, US-OR
Salary / Rate: Not Specified
Posted: 2025-05-21 08:49:48
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Primary Function
The Global EHS Manager is responsible for developing, implementing, and maintaining innovative EHS programs and systems that foster a robust safety culture, proactive analytics, risk mitigation and ensuring compliance across all AAG facilities worldwide.
This role requires strategic leadership, regulatory expertise, and a proactive approach to health, safety, and environmental stewardship.
Who We Are
At Amsted Automotive, we’re more than just a company—we’re a community of innovators, creators, and dedicated professionals who take pride in our work and each other.
As an employee-owned organization, every team member has a vested interest in our success and shares in our achievements.
This unique ownership culture fosters a collaborative, supportive environment where your ideas and contributions truly matter.
Come join us and be part of a dynamic team that’s transforming the industrial and automotive industries while shaping the future of mobility!
What’s In It for You
We create a supportive environment where employees thrive! With a range of benefits designed to enhance your health, well-being, and financial security, we’re here to support you every step of the way.
Join us and experience the exceptional perks that make Amsted Automotive a great place to work!
Health And Wellness
• Medical Insurance
• Dental and Vision Insurance
• Prescription Drug Benefits
• Wellness Reimbursement
• Telehealth
• Onsite health screenings
• Mental health resources
• Employee Assistance Program that includes counseling and support services for mental health, family support, financial advice, legal guidance, and more
Financial Benefits
• Competitive Salaries
• Employee Stock Ownership Plan
• Annual Bonus Opportunity
• 401k with Company Match
• Health Savings Account with Company Contribution
• Life and Disability Insurance
Work-Life Balance
• Paid Time Off
• Parental Leave
• 14 Annual Company Paid Holidays
Professional Development
• Training Programs
• Education Expense Reimbursement
• Career Advancement Opportunities
Additional Benefits
• Pet Insurance and Discount Program
• Legal Insurance
• Employee Discounts
• Recognition and Rewards
• Community Involvement
• Workplace Giving Matching Gift Program
Duties and Responsibilities
• Develops, in conjunction with plant operations personnel, safety risk assessments to proactively address potential serious injury and fatalities (SIFs).
Creates short-term and long-term safety improvement plans and actions that can be executed by operations.
• Leads the implementation of global safety projects, respective reporting tools, and ensures key stakeholders remain updated.
Establishes and tracks key safety performance indicators to drive continuous improvement.
• Assists in the development and communication of the overall EHS strategy and roadmap with periodic status updates to stakeholders, ensuring alignment across all globa...
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Type: Permanent Location: Saginaw, US-MI
Salary / Rate: Not Specified
Posted: 2025-05-21 08:31:17
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Liberty POST is currently seeking a motivated and energetic Early Childhood School Psychologist for per diem employment to work with children who are birth-5 years old through Early Intervention and Preschool Special Education programs.
Immediate positions are available throughout Syracuse.
Liberty POST has offered its clients a range of high-quality and individualized services since 1994.
Backed by Liberty Resources Inc.
and part of a large social services circle, originally POST was a speech-language practice in Syracuse NY, and has grown to provide a range of services throughout all of New York State and New Jersey.
We employ over 500 professionals in a variety of settings and offer a collaborative team approach to provide evaluation, direct therapy, and family education through child-directed play.
We are focused on the importance of a child’s natural learning environment, a family’s unique strengths and needs and the diverse population we serve.
Job Duties and Responsibilities:
* Effectively communicates and works with related agencies, community members, clients, families and co-workers.
* Establishes and maintains a rapport with clients/family members/caregivers and co-workers.
* Review client information prior to evaluation and complete necessary client forms in collaboration with family, other evaluators and current service providers.
* Complete IEP direct including goals, outcome summary and results.
* Gather outside information regarding child’s performance in a variety of settings.
* Utilize Provider Soft to record notes and evaluation results and submit evaluation write up to team leader.
* Attends and participates in ongoing staff in-services and mandatory quarterly meetings.
* Attend CPSE meetings.
Qualifications, Knowledge and Experience:
* Master’s Degree in School Psychology or Doctor of Psychology
* Evaluation and assessment experience required. Familiarity with a variety of preschool assessment tools.
* Effectively communicates via phone, e-mail, in public, and in large groups.
* Proficient on assessment tools necessary for evaluations.
* Works independently, manages time and prioritizes tasks appropriately.
* Strong organizational skills necessary
* Evidence of independence, initiative and forward thinking related to clinical expertise.
* Willingness to give insight.
* Open to feedback and commitment to quality of provided services.
* Communicates problematic clinical issues with respective supervisor.
* Responds positively to suggestions/directions, maintains a flexible attitude and generates new ideas and process improvements.
* Maintains confidentiality of client records.
Benefits for this position:
* Health Benefits and Retirement packages available for FT positions
* Accrual of sick time based on NYS Sick time Laws
* Mentoring is offered to all providers
*...
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Type: Permanent Location: Syracuse, US-NY
Salary / Rate: Not Specified
Posted: 2025-05-21 08:29:40
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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:
Pharmacokinetics & Pharmacometrics
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
We are searching for a talented Principal Scientist pharmacokinetic/pharmacodynamic modeling expert in Translation Pharmacokinetic Pharmacodynamic and Investigative Toxicity (TPPIT) group within Preclinical Safety and Translational Sciences (PSTS), to be located in Beerse, Belgium.
The successful candidate will be employed within our PBPK/PD modelling team in TPPIT.
Key responsibilities:
* Represent PSTS/TPPIT as pharmacokinetic/pharmacodynamic modelling expert in cross-functional project teams and external collaborations
* Independently, develop and apply PBPK/PD models to explore the effects of target and pathway modulation, defining candidate drug target profiles and projection of human exposure profiles.
* Predict human dose and regimen, contribute to exposure and pharmacodynamic biomarker-based decision-making for early clinical trials.
* Interpret and communicate modelling results and impact to project teams
* Designs, conducts, interprets and prepares study and regulatory summaries of PBPK and PKPD M&S activities
* Prepare PBPK and/ PKPD M&S-based strategies to support discovery and development programs
* Drive learning through back-translation of clinical exposure and pharmacodynamic data, offering strategic options for future clinical testing.
* Acts as a main contact for team members in discussions relating to the design of their studies and data analysis to support, clinical candidate selection, development and approval of medicines
* Guides junior colleagues through consultation and mentoring in techniques and processes, and provides functional (matrix) supervision
You will be encouraged to have a desire for learning and innovation, and to continue career development through participation in internal and external scientific meetings, and increase visibility for self, J&J IM R&D, and J&J through publications, participation in external organizations, and presentations at major scientific, industry, and regulatory meetings.
Qualifications / Requirements:
Required:
* PhD in a relevant life science subject area, e.g.
pharmaceutical sciences, pharmacometrics, computational biology, chemical/biomedical engineering, or a related field
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-21 08:27:26
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ERM is looking to hire an experienced Principal Technical Consultant, Environmental Toxicologist and Ecological Risk Assessor to join our growing Risk Assessment practice. The successful candidate will produce and direct expert ecological risk assessments with a focus on oil and gas exploration locations in Gulf Coast wetland habitats.
Candidates will be considered for offices located in Baton Rouge, LA, New Orleans, LA, Houston, TX, Austin, TX or Dallas, TX, depending on the applicant’s qualifications.
RESPONSIBILITIES:
* Write, manage, and produce ecological risk assessments.
* Design and implement biological field investigations.
* Manage, direct, and train junior environmental staff.
* Research toxicities and physical/chemical properties of oil and gas constituents and develop and implement site specific risk assessment methods.
* Write expert reports, design field investigation plans, write technical papers for clients, conduct large scale ecological risk assessments.
* Work collaboratively with other senior level staff to achieve client goals.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Provide support in ensuring compliance with all federal, state and local regulations.
* Communicate daily with clients, regulatory agents, and subcontractors.
REQUIREMENTS:
* Master’s Degree or Ph.D.
in toxicology, environmental toxicology, chemistry, ecology, or related life science discipline.
* 6-8 years (10+ years preferred) of relevant experience; consulting experience preferred.
* Experience testifying as an expert witness is preferred.
* Strong commitment to safety, including following established Health and Safety protocols.
* Excellent verbal, written, and personal communication skills.
* Strong quantitative skills and experience managing and analyzing large datasets using MS EXCEL.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Ability to succeed in consulting by working efficiently, handling multiple project assignments, maintaining flexibility, and meeting strict deadlines.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solutions for our clients.
Our diverse team of world-class experts supports clients across the breadth of their or...
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Type: Permanent Location: Metairie, US-LA
Salary / Rate: Not Specified
Posted: 2025-05-20 08:57:45
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ERM is looking to hire a motivated, detail-oriented Managing Technical Consultant, Environmental Toxicologist and Risk Assessor to join our growing Risk Assessment practice in Austin, TX. Working under the direction of project managers and partners, the successful candidate will work on interesting ecological risk assessments and projects focused on oil and gas exploration in Gulf Coast wetland habitats.
This position is being offered in our Austin, TX office.
However, candidates may also be considered for offices located in Houston, TX, Baton Rouge, LA, New Orleans, LA, or Dallas, TX, depending on the qualifications of applicants.
This is a great opportunity to work with ERM's technical experts to grow your career providing environmental consulting services.
RESPONSIBILITIES:
* Support ecological risk assessments and site investigations.
* Manage, query, review, and analyze large chemical and biological data sets.
* Conduct literature searches and reviews on toxicological, biological or other risk assessment subject matters.
* Prepare work plans, figures, and technical reports.
* Focus on team project delivery, taking direction primarily from Task Managers and Project Managers.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Support in ensuring compliance with all federal, state and local regulations.
* Assist in communication with clients, regulatory agents, and subcontractors.
REQUIREMENTS:
* Bachelors in toxicology, environmental toxicology, chemistry, public health, ecology, or related life science discipline.
Minimum 3.0 GPA.
Advanced degree (MS or higher) preferred.
* 4 to 5 years of relevant experience; consulting experience preferred.
* Strong commitment to safety, including following established Health and Safety protocols.
* Effective written/verbal communication and organization/analytical skills are required; experience recording/writing detailed technical data and reports a plus.
* Strong quantitative skills and experience managing and analyzing large datasets using MS EXCEL.
* Ability to work independently and as part of a team.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Ability to succeed in a consulting pace, handling multiple project assignments, and maintaining flexibility, while meeting strict deadlines.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an esse...
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-05-20 08:57:44
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Classification:
Non-Exempt
Job Summary:
As a Sales Consultant, you’ll be the driving force behind the top-line growth of the branch you report into.
In this position, you will report to a Regional Sales Manager that will train you, coach you and assist you in closing new business.
After your 13-week training period, you will be ready to identify and secure new customers, build relationships, and deliver customized solutions for all types of businesses in food & beverage, industrial and healthcare industries that use linen, uniforms, and facility services like first aid and restroom supplies. With the support of a dedicated team, you’ll develop your skills, meet your financial goals, and help your branch achieve its growth goals.
About Us:
At Alsco Uniforms, we don’t just sell uniforms and linen laundry services – we offer solutions to help businesses maintain a safe and clean environment for their employees and customers.
Since 1889, Alsco Uniforms has been a family-owned company that is headquartered in Salt Lake City, Utah.
Today, the company operates over 80 laundry facilities throughout North America and proudly serves more than 125,000 customers in all industries.
What makes Alsco Uniforms special? It’s our people.
Our team members are the driving force behind our success, fueling decades of strong financial performance, innovation, and unmatched service.
We’re looking for ambitious sales professionals who are ready to grow their careers with us.
If you’re seeking competitive pay, excellent benefits, and a company that invests in your success, Alsco Uniforms is where you belong.
Your sales mission is simple: Showcase to prospects why It Pays to Keep Clean with Alsco Uniforms.
This is done by offering tailored solutions that keep businesses safe, spotless, and ready to thrive, ensuring a healthier and more professional environment for their employees and customers.
Join our team and take the next step toward a fulfilling and dynamic career path!
Why Choose Alsco Uniforms?
* The solutions we offer are essential laundry services to all types of businesses.
Any business is a prospect of ours, and we give our Sales Consultants territories with plenty of prospects.
* We operate over 80 laundry facilities across North America and have a global presence in more than 13 countries.
Despite our worldwide reach, our culture remains people-focused, prioritizing stability while offering a career with strong growth potential and clear paths for advancement.
* Professional training along with ramp-up quotas to ensure you are successful from day one.
* The corporate marketing team and local service team that is dedicated and compensated to provide high quality leads to you.
* Opportunities for professional growth and leadership development.
* An inclusive and diverse team environment that values your unique contributions.
Our full-time employees enjoy:
* 401K Plan with Company Match
* Medical...
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Type: Permanent Location: New Castle, US-DE
Salary / Rate: Not Specified
Posted: 2025-05-20 08:57:35
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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!
Scope:
The account person is responsible for developing business relationships with targeted poultry farm, swine farm and vaccine product distributions, veterinarians that are involved in vaccine business.
Responsibilities:
* Develop annual business plans for targeted key account incorporation execution plans by species and products.
* Accountable for achieving annual sales quotas within allocated expenses.
* Incorporate the Concepts of Customer Selling Skill (CVS) and Strategic Account Management (SAM).
* Apply territory management to optimize time and selling efforts.
* Submit monthly forecast by customer
* Work to satisfy customers’ needs – for example recommending solutions to the problems regarding diseases, managements, food safety, etc.
* Convey solutions/recommendations to customer’s management from the farm, technical, procurement, manufacturing, sales and distribution to the top of a complex organization.
* Propose ideas to build up high quality tailored-made technical service to each KA feed millers including training/consultancy, technical materials and lab analysis support
* AE/PC – Report adverse events and product complaints as per global and local regulatory requirements.
* Adhere to company policies and procedures when interacting and promoting products to customers, to protect the Elanco brand and business.
* Adhere to safe working practices and take reasonable care of self and others.
* Comply with other policies sated in Elanco Code of Conduct as well as Elanco SOPs.
Ensuring myself and my subordinates (if any) comply with the company rules and regulations including Ethics and Compliance and external laws and regulations.
Minimum Qualification (education, experience and/or training, required certifications):
Education/Experience
Graduate of any four year course preferably business or science course. Degree in Veterinary Medicine, Animal Science or any related course is an advantage
Skills and Knowledge:
With at least three years sales experience with proven...
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Type: Permanent Location: Ho Chi Minh City, VN-SG
Salary / Rate: Not Specified
Posted: 2025-05-20 08:51:16
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Your Job
Georgia-Pacific, LLC (GP) is now hiring a R&D Process Engineer for its Tolleson, Arizona Mailers facility.
The R&D Process Engineer supports manufacturing on site including equipment installation, training, acceptance testing, performance testing, and process and equipment upgrades.
The R&D Process Engineer must be able to present data in a concise way to both technical and non-technical audiences.
We believe in the challenge process and this person must be open to the ideas and recommendations of others to create the best outcome for both the site, R&D and i2.
Typical work schedule would be weekdays from 8am-5pm.
Our Team
The GP Tolleson facility employs about 115 people and serves converting customers throughout the Southwest with sustainable packaging products.
This position provides opportunities for promotion within GP Tolleson, as well as many other Georgia-Pacific and Koch facilities across the country.
Come join our team!
You know us already! Georgia-Pacific is one of the nation's leading corrugated sheet and box manufacturers.
Check out these videos/links to learn more about the Corrugated Business at Georgia-Pacific:
www.gppackaging.com
What You Will Do
* Actively engage with Operations, Maintenance, and R&D to identify opportunities for evolutionary changes to the process and equipment
* Update process control and troubleshooting procedures and train plant personnel on current and updated process procedures
* Identify and lead process improvement projects to improve OEE (Overall Equipment Effectiveness)
* Translate learnings and technology upgrades from other sites and work with EHS and site operations to deploy on site
* Support new customer and product trials and production campaigns
* Employ process control best practices and strategies to centerline the process
Who You Are (Basic Qualifications)
* Bachelor's degree in engineering or science
* Previous experience using Microsoft Office programs and other software programs to present data (Word, Excel, Outlook, Teams, Power Bi, etc.)
* Previous experience in a manufacturing facility
* Previous experience moderating meetings and training sessions
* Must be willing and able to travel up to 25%
* Must have legal authorization to work permanently in the United States for any employer without requiring a visa transfer or visa sponsorship
What Will Put You Ahead
* Bachelor's degree or higher in Mechanical, Chemical or Electrical Engineering
* 2+ years of hands-on experience in a manufacturing facility interfacing with quality, operations leadership, maintenance and hourly employees
* Previous experience within a corrugated and/or converting manufacturing facility
* Previous experience developing and executing experiments and monitoring process data
* Previous experience leading process improvement initiatives
* Previous experience in data analysis and/or statistical software (JM...
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Type: Permanent Location: TOLLESON, US-AZ
Salary / Rate: Not Specified
Posted: 2025-05-20 08:46:29
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We are seeking to hire a QC Chemist to join our Quality Control team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required.
Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance.
Responsible for timely analytical data reporting based on project timelines.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
• Demonstrate a more advanced knowledge of various test methods and instrument analysis techniques and be proficient with all sample types and test methods.
Perform more advanced troubleshooting/maintenance of the instrumentation.
• Responsible for more complex physical and chemical testing of raw material, intermediate, and finished products as described in the documented procedures to support product release and process validation protocols.
• Demonstrate proficient ability to operate the instrument software applications, set up advanced sequences, troubleshoot software and report data while executing the higher complexity test methods that utilize instruments such as UV, FTIR, GC, and HPLC, and IC.
• As required, perform swabbing and analysis of more complex manufacturing equipment with no supervision in accordance with cGMP guidelines.
Provide input on cleaning related issues and investigations.
• Evaluate and maintain assigned calibrations for equipment in the laboratory as required and review the required documentation for compliance.
Review instrument qualification documents to support system change control actions and assist vendors during installation and PM’s.
• Investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines.
• Assist Management with writing and completion of investigation sections and product impact as required.
Train others as required as it pertains to LIR/OOS procedures.
• Perform method validation and method transfer activities as required.
• Train other Chemists, Lab Assistants, and temporary personnel.
• Assist with customer and regulatory audits as required for Data Integrity and/or instrument file review.
• Author, revise and update laboratory test methods and Standard Operating Procedures.
• Accurately maintain notebooks and files compliant with current GMPs and internal Standard Operating Procedures.
Peer review and/or audit others work as required for verification of GMP compliance.
• Auditing of laboratory testing data as required.
• Demonstrate consistent ability to perform testing with limited investigations and repeat analyses.
Ability to accurately report test data in various formats along with advising less experienced Chemists.
• Perform cost savings and process improvement ...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-20 08:43:54
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Per il potenziamento del Laboratorio Analisi Centrale, che opera al servizio ed in sinergia con i dipartimenti formulativi della sede R&S di Milano ricerchiamo un/una:
R&D Analysis Technician
Principali attività:
* preparare soluzioni reagenti e campioni per le analisi di laboratorio
* lettura schede tecniche e schede di sicurezza dei reagenti di laboratorio
* calibrazione e utilizzo di strumentazione analitica (titolatore, spettroscopie FT-IR, UV-VIS, TOC, analisi chimico-fisiche)
* eseguire analisi in base a norme e procedure interne prestabilite
* registrare nel software di gestione i dati relativi alle analisi
* housekeeping dell’ambito del laboratorio dopo il suo utilizzo
Requisiti richiesti:
* Diploma tecnico a indirizzo chimico/biologico o similari
* Gradita eventuale breve esperienza nel ruolo in settori affini
* Buona conoscenza della lingua inglese
* Approccio metodico e preciso, senso di responsabilità, proattività
* Buone capacità relazionali e team working con diversi interlocutori e livelli
* Curiosità e capacità analitica per portare avanti progetti in autonomia
* Buona conoscenza del pacchetto Office
Ulteriori informazioni:
* Sede di lavoro: Milano
* Contratto da valutare in base alla seniority del candidato
Filosofia aziendale:
* Innovazione e specializzazione
* Internazionalizzazione
* Sostenibilità sociale e ambientale
* Persone al centro
* Pari opportunità e inclusione
Benefits:
* Formazione continua e sviluppo
* Welfare aziendale
* Fondi CCNL (Assicurazione sanitaria e pensionistica)
* Convenzioni aziendali
Chi siamo:
Mapei, fondata nel 1937 a Milano, è una realtà leader nello sviluppo, nella produzione e distribuzione di prodotti chimici e soluzioni per l'edilizia, con oltre 24 Linee di Business in grado di rispondere a qualsiasi necessità nel mondo delle costruzioni.
Attualmente il Gruppo coinvolge oltre 12.000 persone nel mondo ed è composto da 102 Consociate con 81 stabilimenti produttivi nei 5 continenti e 32 centri di ricerca.
Lavorare in Mapei significa far parte di una squadra vincente con grande senso di appartenenza e valori.
Cerchiamo persone con una forte motivazione, flessibilità e passione orientate a sviluppare le proprie competenze ed essere sempre un passo avanti.
MAPEI, il cantiere più importante per il tuo Talento!
L’azienda garantisce il trattamento dei dati ai sensi del Regolamento Europeo n.
2016/679, rinviando all’informativa privacy disponibile proseguendo con la presente candidatura.
La ricerca è rivolta a candidati di entrambi i sessi.
(L.
903/77).
Esplora le Opportunità di carriera sul sito www.mapei.com
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Type: Contract Location: Milano, IT-MI
Salary / Rate: Not Specified
Posted: 2025-05-20 08:31:38
