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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 Quality Control Junior Analyst (tempo determinato 12 mesi) che si unisca al nostro QC Team di Pessano con Bornago.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Quality Control Junior Analyst svolge le attività analitiche e affini all’interno del reparto di Controllo Qualità, in accordo con quanto previsto dalle GMP e dalle Procedure Operative Standard, Procedure Analitiche Standard, metodi di analisi, ed altri regolamenti interni, riportando direttamente al/alla Quality Control Laboratory Supervisor.
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.
* Tiene in ordine ed aggiornati i propri quaderni di laboratorio e i propri documenti analitici.
* Esegue operazioni di base di laboratorio, quali: preparazione di reattivi e soluzioni, campionamenti di materie prime, prodotti semilavorati e prodotti finiti, ecc.
* Segue scrupolosamente le disposizioni impartite dai superiori.
* Esegue analisi con tecniche analitiche semplici e complesse, seguendo metodi definiti, in autonomia operativa.
* Adempie alle funzioni per la corretta gestione dei reagenti in accordo alle specifiche procedure.
* Lavora in modo efficace nel rispetto delle scadenze.
* Agisce come rappresentante dell'azienda mostrando rispetto e come ambasciatore /ambasciatrice delle convinzioni e dei comportamenti aziendali.
* Rispetta le politiche, le procedure e le normative in vigore in azienda.
* Svolge ...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-05-23 08:12:43
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Beijing, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% in compliance.
Stra...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:33
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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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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
People Leader
All Job Posting Locations:
Shanghai, China
Job Description:
* Please kindly note this is an Individual contributor role.
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program...
....Read more...
Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:43
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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:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
Professional
All Job Posting Locations:
Limerick, Ireland
Job Description:
An experienced Environmental Specialist who is passionate about their role and has the ambition and drive to develop and continually improve the JJVC Environmental Program while ensuring compliance with the IE Licence, Environmental Regulations, and Corporate standards.
KEY RESPONSIBILITIES
* Lead the sites Environmental Program.
* Ensure compliance with the IE License and other regulatory requirements.
* Ensure compliance with Corporate Environmental Standards, Goals and Objectives.
* Ensure the timely and complaint submission of required reports to the EPA, Corporate and other partners.
* Collect, analyse and report Environmental data as per IE Licence and Corporate requirements.
* Develop and achieve Environmental Goals and Objectives in partnership with Senior Management and other partners.
* Maintain the ISO14001 registration and ensure compliance with all requirements.
* Lead preparations for and execution of Environmental Audits with Regulators, Corporate and Certifying bodies.
* Conduct regular environmental inspections of the facility and systems audits to identify opportunities for improvement.
* Submit all necessary reports to the EPA and Corporate and act as the primary Environmental site contact.
* Collaborate closely with the Sustainability and Energy Teams on site sustainability strategies and initiatives.
* Ensure the effective oversight and management of Key environmental equipment in conjunction with the Facilities department.
* Ensure the effective investigation of any Environmental Events, identification of root cause and putting in place corrective and preventative actions to prevent recurrence.
* Provide Environmental Awareness and training to employees as required.
* Build and maintain strong relationships with stakeholders.
* Support other aspects of the wider EHS Program as required.
EDUCATION AND SKILLS
* Third-level qualification in Environmental Science, Engineering, or a related discipline (B.Sc./B.E.
preferred).
* 5 years of relevant experience managing an Environmental Program at an IE Licensed Facility
* Practical experience of implementing and maintaining an ISO14001 Ma...
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Type: Permanent Location: Limerick, IE-LK
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:39
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Kibbutz Shefayim, Center District, Israel
Job Description:
About Oncology
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 Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
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 MSL to be in Shefayim.
Key Job Activities:
* Keeping abreast of medical and scientific knowledge
* Creating and fostering a network of partnerships with experts
* Working cross-functionally within the company to become a valuable team member
* Providing high level scientific engagement with experts, while utilizing multichannel platforms
* Initiator and coordinator of medical education activities and advisory boards, in alignment with Medical Manager
* Scientific support and training to company sales representatives and other peers
* Supports and initiates evidence generation via research and publications
* Gains valuable scientific insights contributing to the short & long-term strategic plans of the therapeutic area
* Skillful in implementing innovative solutions and ideas for multichannel engagement and data-collection
* Champions medical benefits of products and contributes to the fostering of innovative therapeutic approaches for patient's benefits
* Actively involved in strategy and action plans related to local reimbursement of products
The role is mainly field-based ( 85%) , requires agility with regards to travel & work hours
Requirements:
Education
MD, D.M.D, D.V.M, Ph.D.
(Pharmacy or Science)
Experience:
With preference for:
* Previous experience working in the pharmaceutical industry or research company- an advantage
* High-competency in project & customer-affairs management
Knowledge:
* Deep scientific & clinical kn...
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Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:35
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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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ERM is hiring a Health & Safety Specialist to support a aerospace client facility in Redmond, WA.
In this critical role, you will be responsible for ensuring safety compliance with applicable regulations and existing company standards and contributing to an environment where employee health and safety is paramount.
This is a full-time (40 hours), limited-term role with a duration of 12 months and the possibility of renewal.
RESPONSIBILITIES:
* Providing health and safety oversight for an aerospace manufacturing facility.
* Oversee general safety and risk programs in an aerospace manufacturing environment – machine safety, LOTO, electrical safety, PPE, fall protection, confined space, etc...
* Communicating with internal stakeholders.
* Developing, reviewing, and/or updating health and safety documentation such as SOPs, JHAs, and safety plans.
* Conduct inspections and audits.
* Participating in the Emergency Response Team.
* Conduct safety training.
* Participate in incident investigation, root cause analysis, and report writing.
* Participating/leading meetings to support ongoing compliance and safety initiatives.
* Writing and submitting status update reports, and other communications.
REQUIREMENTS:
* Bachelor’s in safety or related discipline preferred.
* 3+ years of health and safety experience in a manufacturing environment, aerospace experience preferred.
* Certification such as ASP/CSP highly preferred.
* Experience with High Hazard Work Activity, Confined Space, LOTO, Machine Guarding, and Fall Protection.
* Familiarity with federal/state health and safety regulations.
* Strong MS Office computer skills.
* Excellent written and verbal communication skills.
For the Health & Safety Specialist position, we anticipate the annual base pay of $80,691 – $97,410, $47.56/hr – $55.19/hr, 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 ...
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Type: Permanent Location: Seattle, US-WA
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:18
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Manager of Analytics and Data Science
Location: Niagara Falls, NY (Flexible work options available)
Reports to: Vice President, Research & Developmen, Frank Ortiz
Collain is seeking a skilled and experienced Manager of Analytics and Data Science to join our team.
In this role, you will design and lead the development of innovative software solutions that support healthcare providers in the Long Term and Post Acute Care (LTPAC) sector.
You will collaborate with cross-functional teams to translate business needs into scalable, high-performance software systems and provide technical leadership across projects.
This position will report to Frank Ortiz, Vice President, Research & Development of our Collain business unit.
What your impact will be:
* Lead the design and architecture of scalable software solutions.
* Translate business requirements into technical specifications and system designs.
* Evaluate and recommend tools, frameworks, and technologies.
* Collaborate with cross-functional teams to align architecture with business goals.
* Mentor and support junior engineers and architects.
What we are looking for:
* Bachelor’s or Master’s degree in Computer Science, Engineering, or a related field.
* 10+ years of experience in software architecture and development.
* Proven experience designing complex, scalable systems.
* Strong knowledge of software design patterns and system integration.
* Proficiency in at least one modern programming language.
What would make you stand out:
* Experience in the healthcare technology industry.
* Familiarity with EHR systems or interoperability standards.
* Background in AI or data analytics integration.
What we can offer:
* Opportunity for challenging projects and professional growth
* 3 weeks’ vacation and 5 personal days
* Comprehensive benefit package
* Lifestyle rewards
* Flexible work options
About us:
Collain Healthcare operates in the healthcare technology industry, specializing in solutions for the Long Term and Post Acute Care (LTPAC) sector.
Founded in 2011 and based in Niagara Falls, NY, the company provides electronic health records (EHR) and interoperability solutions designed to help healthcare providers improve operational efficiency and financial performance.
Collain leverages advanced analytics and artificial intelligence to transform healthcare data into actionable insights, supporting better decision-making and aligning with the industry's goals of improved access, outcomes, cost efficiency, satisfaction, and employee well-being.
Our clients primarily include healthcare providers navigating complex care environments.
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2025-05-22 09:30:32
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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.
This is your opportunity to shape your career through the skills and experience you bring to the role now and by training for the roles you may want in the future.
Our success depends on great teams, where you can thrive and do your best work in a supportive environment.
About the Role
Shape your career by joining Alcoa’s Vacation Student program! Based in WA at our Pinjarra refinery, you’ll have the chance to put your university knowledge into practice, propelling you toward a career path that exceeds your wildest expectations.
Throughout your 12-week paid summer placement, you’ll experience professional growth, technical expansion, and become an integral part of our vibrant community, where inspiration and daily challenges await.
During the program, you will be matched with a senior specialist who will offer hands-on training, mentoring, and coaching.
The program is designed to support you in becoming a creative problem solver, assisting you in completing meaning projects that will be assigned to you.
What’s on offer?
* Exposure to industry and a future career at Alcoa.
* An attractive hourly rate of pay for the hours you work.
* Meaningful project work that provides you with valuable hands-on work experience
* Working locally, in an onsite environment enabling you to return home to friends and family every night.
* Inclusion and diversity networks; shaping a culture where everyone is welcome, respected and heard.
* Be part of our commitment to sustainability, delivering world class technology and innovations that lead the aluminium industry!
* A workplace culture that strongly values your safety.
* Increased opportunity to gain a place in the Alcoa Graduate Program after you have completed your degree
* Access to the Alcoa Live Well program with a selection of health & wellbeing discount offers to help you live your best life!
What you’ll be doing
As an Occupational Hygienist Vacation Student at Alcoa, you will learn, grow and develop hands-on experience and expertise in:
* Based on site at our Pinjarra Alumina Refinery.
* Assigned a project that both delivers real value to the business and provides you with hands-on industry experience.
* Involved in conducting ongoing surveillance programs including workplace exposure monitoring.
* Exposed to hazardous materials risk assessment and management.
* Assisting in the identification and verification of exposure controls for chemical, physical and biological hazards.
You will be given an appropriate level of responsibility to handle assigned project(s), utilizing your innovative thinking, eagerness to learn, and passion for growth to make meaningful contributions to the business.
In our open-minded...
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Type: Permanent Location: Pinjarra, AU-WA
Salary / Rate: Not Specified
Posted: 2025-05-22 09:30:17
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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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SRI Healthcare, LLC, a Subsidiary of NOVO Health Services offers a healthcare service that provides a total and unique opportunity for hospitals to source their Sustainable Reusable Sterile Packs as well as other sustainable healthcare linens such as DermaTherapy®, Isolation Gowns, Sterilization Wrap, and cubicle/privacy curtains.
SRI's products and services help Healthcare providers attain their sustainability goals, improve surgeon and staff satisfaction while ensuring continuity of supply.
SRI operates three regional processing facilities located in Raleigh, NC, Chattanooga, TN, and Mason, OH.
Our state-of-the-art, FDA-regulated service centers provide daily processing, assembly, and delivery of reusable products required for surgery.
SRI is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with Sterilized Reusable Surgical Solutions.
Get to know us: SRI Health Care, with headquarters in Atlanta, GA, offers linen management solutions to the healthcare industry.
SRI keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen utilization by department to eliminate excess internal costs.
SRI’s wide range of service programs offer a variety of options to provide a seamless, single source distribution system.
SRI’s regional healthcare linen facilities are HLAC accredited and operate with state-of-the-art processing equipment and processes.
SRI Health Care is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with both Healthcare Laundry Services as well as Sterilized Reusable Surgical Solutions.
Job Summary:
We are currently looking for a Team Lead Soil Sort, at our Chattanooga, TN Healthcare Laundry facility.
We are looking for someone who is confident in decision making, can act quickly, and has excellent communication skills.
If you are ready to make a commitment to measurable performance and continuous improvements, then we want to hear from you!
The successful candidate:
* Know all soil sort operations, including Standard Operating Procedures and Q.A.
functions, and ensure adherence by soil sort personnel to established standards.
* Train all new soil sort employees.
* Make recommendations to facility management on soil sort methods or production standard changes.
* Assist facility management in employee hiring process and evaluations as needed.
* Keep accurate records to comply with written Standard Operating Procedures.
* Facility management in scheduling of any testing, validation, etc.
* Maintain cleanliness
* Ability to read and understand all Standard Operating Procedures.
* Other duties as assigned.
Job Requirements:
* Extremely organized and detail-oriented.
* Able to keep precise records.
* Good interpersonal skills.
* Able to train new...
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Type: Permanent Location: Chattanooga, US-TN
Salary / Rate: Not Specified
Posted: 2025-05-22 09:24:03
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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:
Enterprise Management
Job Sub Function:
R&D Management
Job Category:
People Leader
All Job Posting Locations:
Galway, Ireland
Job Description:
Johnson & Johnson MedTech Neurovascular are looking for an R&D LCM (Lifecycle Management) Manager / Principal Engineer
Location: Ballybrit, Galway
Johnson & Johnson MedTech Neurovascular
J&J MedTech Neurovascular is a global leader in neurovascular care.
Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship.
J&J MedTech Neurovascular offers a broad portfolio of devices used in the endovascular treatment of hemorrhagic and ischemic stroke.
What is it like to work at J&J MedTech Neurovascular Galway?
* Culturally, we are putting the needs of Our Credo stakeholders first through pursuing the highest standards of quality, compliance, and ethics, ensuring everyday actions contribute to Our Purpose.
* We are continuing to better our understanding of clot science, through our Neuro Thromboembolic Initiative (NTI).
This is a commitment to advance the treatment of stroke through interdisciplinary collaboration and investment in clot and stroke research.
How we understand clots and their behaviour enhances our opportunity to design devices that improve patient outcomes and, overall, advance the treatment of acute ischemic stroke.
* Strong new product pipeline and the fastest growing medical device company within J&J in 2021.
* From a People perspective, we invest in our people, and take great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation.
This is empowered through our employee resource groups (ERGs) focused on further balances of gender, nationality, capability and more, including the additional attracting of qualified diverse candidates for our open roles.
Job Summary:
Johnson & Johnson MedTech Neurovascular is recruiting for a R&D LCM Manager in Galway Ireland.
The R&D LCM Manager will be responsible for managing design changes and sustaining activities providing technical leadership and judgment to a team of engineers in the life cycle of a portfolio of devices to treat ischaemic and haemorrhage stroke.
The R&D LCM Manager is also responsible for co-ordinating the activities of a multi-disciplinary team to ensure the successful compl...
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Type: Permanent Location: Galway, IE-G
Salary / Rate: Not Specified
Posted: 2025-05-22 08:48:52
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Post Doc – Drug Discovery & Pre-Clinical/Clinical Development
Job Category:
Career Program
All Job Posting Locations:
Lisbon, Portugal
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
The GSSRM Pharm.D.
Fellowship is a training program designed to prepare the Fellow to become proficient at safety analyses and ad hoc report writing.
The Fellow, in partnership with the Medical Safety Officer (MSO) and under the mentorship and support from the preceptor, is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.
The Fellow will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a product’s safety strategy, complete safety analyses and evaluations, proactively review safety data/lead safety data review meetings and interpret safety information to make a recommendation, supporting SMT deliverables as required.
The Fellow will gain a high-level understanding of case processing, safety surveillance, and review of medical literature and clinical trial data.
The Fellow will function under the guidance/support from the preceptor, and other team members, be able to link discussions to content, and deliver quality results with guidance from the preceptor and the team.
Key Responsibilities:
* Support safety evaluations, including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)/MSO and other stakeholders as necessary, data retrieval, data analysis, report writing, and report revision.
* With mentorship from the preceptor and/or Safety Analysis Scientist (SAS), ensure high quality safety evaluations and reports with moderate comments from stakeholders and moderate revisions required.
* Provide support to SAS for novel projects, to bring value through completion of task-based activit...
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Type: Permanent Location: Lisbon, PT-11
Salary / Rate: Not Specified
Posted: 2025-05-22 08:47:42
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Specialty Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States, Columbus, Ohio, United States, Detroit, Michigan, United States, Pittsburgh, Pennsylvania, United States of America
Job Description:
This is a field-based role available in multiple states within the US.
While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
We invite candidates from various locations to apply and encourage you to review the following states/cities where this opportunity is available:
Cleveland, OH
Columbus, OH
Pittsburg, PA
Michigan
Johnson & Johnson is recruiting for a District Business Manager to support our J&J Vision business, responsible for key distributor and direct accounts. The district for this position will include Cleveland OH, part of Columbus OH, Pittsburgh PA and Michigan.
This is a field-based position with the ideal candidate residing in Cleveland, OH.
About Johnson & Johnson
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/.
About Vision
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medte...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-22 08:46:27
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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 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:
Communications & Corporate/External Affairs
Job Sub Function:
External Communications
Job Category:
Professional
All Job Posting Locations:
US017 NJ New Brunswick - 1 J&J Plaza
Job Description:
Johnson & Johnson is recruiting for a Director, Global Finance Communications.
This position is in New Brunswick, New Jersey.
Position Summary
The Director, Global Finance Communications will lead communications strategies that amplify J&J’s narrative regarding its financial positioning, business focus and strategic direction to external, financial and investor community and business media audiences.
The Director will be responsible for partnering directly with Investor Relations, business segments, communications colleagues, media relations and key stakeholders to develop, manage, optimize and executive communications strategies for quarterly earnings, financial reporting, M&A Announcements, and other key financial events.
The Director will serve as the direct partner to the VP, Investor Relations, and Media Relations team, triangulating key messages and communications approaches to critical investor engagements and financial media opportunities for the CFO and other Finance leaders.
Responsibilities
* Lead communications strategies that amplify J&J’s financial positioning, business focus and strategic direction to the external, financial and investor community and business media audiences.
* Partner with Investor Relations and across business segments, communications colleagues, media relations and key stakeholder groups to develop, manage, optimize and executive communications strategies for quarterly earnings, financial reporting, M&A Announcements and other key financial events such as the annual shareholders meeting and investor days.
* Serve as the direct partner to the VP, Investor Relations and Media Relations team, triangulating key messages and optimal communications approaches to critical financial engagements, business and industry media and media opportunities for the CFO and other Finance leaders.
* Develop and maintain relationships with key media, trade, influential stakeholders, and communication partners.
* Lead a matrixed team of indirect resources, peer groups and agency vendors.
Required
* A minimum of bachelor’s degree
* 10+ years of experience in Communications
* People management with a focus on engagement and development
* E...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-22 08:45:50
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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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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: SFE & Market Intelligence Analyst
As a Sales Force Excellence & Market Intelligence Analyst, you will be part of the Commercial team to deliver data-driven insights to optimize sales execution.
In this role, you'll be responsible for advancing CRM optimization, performance analytics, and customer segmentation strategies.
Your Responsibilities:
* CRM Management: Maintain, improve, and provide support for CRM systems, ensuring data accuracy and consistency.
* Sales Force Enablement: Train and support sales teams on CRM usage and data-driven decision-making, monitoring key performance indicators.
* Territory Management: Implement and optimize territory strategies, including segmentation, sizing, and route optimization.
* Performance Reporting: Generate reports and dashboards to track and analyze sales execution performance.
* Market Analysis: Collect, analyze, and interpret market, sales, pricing, and competitor data to provide actionable insights.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor's degree in management, finance, technology, or similar field
* Required Experience: A minimum of 2 years of experience in CRM software proficiency (e.g., Salesforce), data management, customer service, Power BI, Microsoft Office Suit.
English is a must
What will give you a competitive edge (preferred qualifications):
* Experience in pharma or animal health
Additional Information:
* Travel: 0% - 10%
* Location: Bogota, Colombia
Don’t meet every single requirement? Studies have shown underrepresented 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 wh...
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Type: Permanent Location: Bogota, CO-DC
Salary / Rate: Not Specified
Posted: 2025-05-21 08:48:36
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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
