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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.
About the Location
The Alumar Consortium, managed by Alcoa, located 25 kilometers from the center of São Luís - MA, began its operations in 1984.
It is made up of companies with a tradition in the areas of alumina and aluminum production, with different participations in the two factories that make up the Complex.
At Alcoa, we are committed to generating value in our relationships with all stakeholders in our business, communities and environment.
We build inclusive and secure environments so that our people can live and express themselves as they please.
With the aim of attracting and retaining diverse talent, the company maintains the inclusion groups that promote internal and external activities to value human diversity and plurality as a way of enriching one's own values.
We are values led, vision driven and united by our purpose of transforming raw potential into real progress. Our commitments to Inclusion, Diversity & Equity include providing trusting workplaces that are safe, respectful and inclusive of all individuals, free from discrimination, bullying and harassment and that our workplaces reflect the diversity of the communities in which we operate.
This is a place where you are empowered to do your best work, be your authentic self, and feel a true sense of belonging.
Come join us and shape your career!
Your work.
Your world.
Shape them for the better.
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Type: Permanent Location: Sao Luis, BR-MA
Salary / Rate: Not Specified
Posted: 2026-02-13 07:56:03
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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.
Faça parte da equipe que está ajudando a moldar um local de trabalho melhor, com um melhor equilíbrio entre a vida pessoal e profissional e com oportunidades iguais que ajudam todos (as) a prosperar.
Você tem o poder de moldar as coisas para torná-las melhores.
Sobre a Função
A Alcoa está com uma oportunidade aberta para Eletricista Industrial Portuário na área do Retroporto da unidade Alumar, em São Luís (MA).
A pessoa selecionada será responsável por realizar manutenções corretivas e preventivas em equipamentos elétricos diversos, incluindo motores elétricos de alta e baixa tensão, gavetas e chaves seccionadoras, inversores de frequência, redes DeviceNet, Ethernet e ControlNet, cabos de força, comandos elétricos, controladores lógicos programáveis, relés de sobrecorrente e sensores.
Também fará a manutenção de instrumentos indicadores de variáveis de processo, como transmissores de temperatura, fluxo, densidade e vazão, além de executar leitura e interpretação de diagramas elétricos
Outras responsabilidades importantes incluem:
* Manutenção em cabos de força e inversores de frequência;
* Interação básica com PLC’s;
* Leitura e interpretação de desenhos elétricos;
* Manutenção em sistemas de proteção em Transportadores de correias
* Manutenção elétrica em altura;
* Manutenção em Retomadoras de bauxita e Empilhadores de Bauxita;
* Manutenção em motores elétricos, comandos elétricos.
O que você pode oferecer para a função:
* Formação: Técnico em Eletrotécnica, Eletrônica, Eletromecânica ou Eletroeletrônica (CFT – Conselho Federal dos Técnicos Industriais – Ativo)
* Desejável: Treinamento NR10 e conhecimento em manutenção corretiva e preventiva em equipamentos elétricos industriais;
* Necessário facilidade na elaboração de relatório e histórico de equipamentos e Habilidades práticas em inspeções de ferramentas elétricas;
* Conhecimento em Informática – nível básico;
* Disponibilidade para trabalhar em regime de turno.
O que está sendo oferecido
Para apoiar você e sua família além do local de trabalho, a Alcoa fornece um pacote excepcional de benefícios a partir do primeiro dia de trabalho.
Além dos benefícios médicos, oferecemos programas estruturados de trabalho em casa, oportunidades de grupo de recursos para funcionários, opções de planos de pensão e um plano de férias de primeira linha para um valioso equilíbrio entre a vida pessoal e a profissional.
* Como uma empresa baseada em valores, agimos com integridade, operamos com excelência, cuidamos das pessoas e lideramos com coragem
* Reconhecida como uma das melhores empresas para se trabalhar pelo pro...
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Type: Permanent Location: Sao Luis, BR-MA
Salary / Rate: Not Specified
Posted: 2026-02-13 07:56:02
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Company
Federal Reserve Bank of Chicago
About the Federal Reserve Bank of Chicago
The Chicago Federal Reserve Bank is a non-governmental entity that conducts economic research, bank supervision, community outreach and education, and central bank services.
The fundamental mission of the Federal Reserve System is to foster the stability, integrity, and efficiency of the nation’s monetary, financial, and payment systems so as to promote optimal macroeconomic performance.
Job Description:
We are seeking applicants for a Senior Multimedia Technician position for our Detroit Branch.
As a Senior Multimedia Technician, you will provide technical consultation, coordinate tasks, support on-site and virtual events where AV is needed, and manage communications for small to mid-scale Video Conferencing and Audiovisual projects.
You will provide user support and assist in the development, setup, monitoring, testing, and maintenance of technical conferencing solutions and equipment for our Detroit branch.
You will ensure the quality of processes, procedures, and standards to ensure consistent and high-quality service.
The level of work required is considered advanced and you will operate under minimal supervision.
Your Responsibilities:
* Determines the appropriate troubleshooting of basic AV, videoconferencing, and audio-conferencing issues and provides complex audio, video, and data conferencing solutions.
* Consults with IT groups, internal stakeholders, and vendors to validate design and architectural recommendations as they relate to AV systems.
* Evaluates equipment requirements and cost analyses for installations ranging from simple to broad complexity.
* Develops, recommends, and maintains technical standards for the design, equipment, and support of multimedia systems.
* Determines the development and implementation of quality control processes and procedures.
* Provides technical consultation and coordination of tasks for small to mid-scale video conferencing and audiovisual projects.
* Conduct installation, set up, monitoring, testing, and maintaining audio conferencing, videoconferencing, and audiovisual technologies and equipment.
* Designs scheduling and customer communications for audio conferencing and videoconferencing calls.
* Plans the identification and development of manual processes or automated, scripted solutions for common videoconferencing issues.
* Develops, organizes, and maintains standard operating procedures and workflow processes and procedures for AV systems.
* Provides on-site and remote technical support for corporate events, meetings, and hospitality functions, ensuring seamless AV integration and high-quality user experience.
* Coordinates with event planners and hospitality teams to assess AV requirements, set up multimedia equipment, and troubleshoot issues during live events.
* Advises on best practices for AV solutions in event spaces, including li...
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Type: Permanent Location: Detroit, US-MI
Salary / Rate: 99000
Posted: 2026-02-12 07:38:40
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Join the dynamic and diverse team at La Jolla Beach & Tennis Club, Inc., where tradition meets opportunity.
Our family of properties includes the iconic La Jolla Beach & Tennis Club, a private oceanfront club with world-class tennis courts and direct beach access; the inviting La Jolla Shores Hotel, a beachfront getaway beloved for its relaxed coastal charm; and the internationally acclaimed Marine Room, celebrated for its fine dining and dramatic surfside views.
These landmark destinations are cherished La Jolla institutions, built on a legacy of family values, exceptional service, and a deep commitment to our community.
As part of our team, you’ll enjoy a supportive and collaborative work environment, competitive pay, outstanding benefits, and the chance to grow your career in a setting as inspiring as the coastline we call home.
Whether you’re starting your career or ready to take it to the next level, we’re passionate about helping our employees thrive in one of California’s most beautiful destinations.
What we offer:
* Free daily meal and salad bar
* Benefits including: Medical, Dental, Vision, 401K (based on employment status)
* Paid vacation, sick, and holiday time
* Dining discounts for employees (and up to 6 guests) at the Marine Room, The Shores Restaurant, and our Club Dining!
* Property retail shop and hotel discounts
* $500 referral bonus for referring new employees to The La Jolla Beach & Tennis Club
What we ask:
* Consistently provide professional, attentive, and genuinely friendly service
* Promote and follow LJBTC, Inc's Signature Service standards and requirements to ensure a lasting impression of exemplary service resulting in satisfied and loyal members and guests
Hourly Rate
$19.50
Summary
The Locker Attendant maintains locker room and guest areas in a clean and orderly condition.
This position upholds and promotes LJBTC, Inc’s Signature Service standards to ensure an exceptional member and guest experience.
The Locker Attendant contributes to creating a lasting impression of exemplary service, resulting in highly satisfied and loyal members and guests.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
* Receives schedules and work assignments from Housekeeping Supervisory staff.
* Scrubs guest and employee rest room walls, floors, mirrors, fixtures, sinks, vanities, toilets and urinals.
Replenishes restroom supplies.
Records tasks performed on cleaning log posted in each rest room.
* Cleans public restrooms.
* Sweeps, cleans, waxes, and polishes floors.
* Empties wastebaskets, empties and cleans ashtrays and transport trash and waste to disposal area.
* Sorts linens into bins by type and loads and starts the washer on the appropriate cycle.
* Removes linen from washers and loads and starts dryer, setting the correct temperature and time.
* Removes linen from dryers and removes linen that is stained and spotted for trea...
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Type: Permanent Location: La Jolla, US-CA
Salary / Rate: 19.5
Posted: 2026-02-11 07:34:25
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Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.
Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission.
Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.
By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.
Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.
It’s our work, our passion, and our legacy.
We invite you to join us.
Remote
Employee Value Proposition:
At Taiho Oncology, the compassion we practice for our patients extends to our team, empowering and motivating them to do their best work for those who need it most.
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment.
Position Summary:
The Senior Medical Writer, Medical Writing is accountable for the timely delivery of high quality, regulatory-compliant documents including but not limited to protocols, IBs, clinical study reports, for assigned program and ensures documents are delivered per corporate objectives, from planning through internal approval.
Performance Objectives:
* Responsible for the development of high-quality clinical documents submitted to Regulatory Authorities (e.g.
FDA and EMA) including but not limited to Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments,.
* Collaborate with Global Development Teams and Clinical Development to ensure alignment with program objectives.
* Participates in Global Medical Writing initiatives on clinical development cross-functional teams.
* Assists with development and implementation of Medical Writing processes improvement in line with SOPs.
* Owns and updates assigned Medical Writing SOPs, as necessary.
Education/Certification Requirements:
* Bachelor’s Degree in life science, health-related or pharmaceutical field, or the equivalent in experience.
Knowledge, Skills, and Abilities:
* Minimum of 3 years combined experience in academic/clinical and/or industry setting writing clinical protocols, CSRs and/or medical and/or scientific documents.
* Previous experience in Medical Writing in clinical drug development, preferably some experience in oncology.
* Working knowledge of Medical Writing requirements and document components.
* Experience with templates and temp...
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Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2026-01-08 07:28:15
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Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.
Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission.
Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.
By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.
Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.
It’s our work, our passion, and our legacy.
We invite you to join us.
Remote
Employee Value Proposition:
At Taiho Oncology, the compassion we practice for our patients extends to our team, empowering and motivating them to do their best work for those who need it most.
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment.
Position Summary:
The Manager, Medical Writing is accountable for the timely delivery of high quality, regulatory-compliant documents including but not limited to protocols, IBs, clinical study reports, health authority briefing books and clinical summary documents for assigned program and ensures documents are delivered per corporate objectives, from planning through internal approval.
Performance Objectives:
* Responsible for the development of high-quality clinical documents submitted to Regulatory Authorities (e.g.
FDA and EMA) including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and clinical summary sections of Common Technical Documents (CTDs) in support of worldwide (outside of Asia) regulatory submissions.
* Collaborate with Global Development Teams and Clinical Development to ensure alignment with program objectives.
* Participates in Global Medical Writing initiatives on clinical development cross-functional teams.
* Assists with development and implementation of Medical Writing processes improvement in line with SOPs.
* Owns and updates assigned Medical Writing SOPs, as necessary.
Education/Certification Requirements:
* Bachelor’s Degree in life science, health-related or pharmaceutical field, or the equivalent in experience.
Knowledge, Skills, and Abilities:
* Minimum of 4 years combined experience in academic/clinical and/or industry setting writing clinical protocols, CSRs and/or medical and/or scientific documents.
* Previous experience in...
....Read more...
Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2026-01-08 07:28:13
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Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.
Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission.
Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.
By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.
Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.
It’s our work, our passion, and our legacy.
We invite you to join us.
Remote
Employee Value Proposition:
At Taiho Oncology, we are driven by our mission to improve the lives of cancer patients.
As an Associate Director, Medical Writing, you will work on various document types and play a critical role in transforming scientific data into compelling narratives that contribute to innovative cancer treatments.
Join a dedicated team that fosters a collaborative, patient-first environment, where your expertise and passion will directly impact patient care and advance oncology research.
We believe in empowering our employees through continuous learning, career development, and a supportive culture that values diverse perspectives and encourages innovation.
If you are ready to take on new challenges and make a meaningful difference, Taiho Oncology offers you the opportunity to grow, excel, and be a part of something bigger.
Together, we are relentless in our pursuit of better cancer treatments. Join us in putting patients at the heart of everything we do.
Position Summary:
The incumbent is responsible for authoring Taiho Oncology, Inc., (TOI), documents submitted to Regulatory Authorities including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and relevant summary sections of Common Technical Documents (CTDs) in support of worldwide (outside of Asia) regulatory submissions for drugs in line with regulatory requirements and internal standard operating procedures.
Performance Objectives:
* Responsible for authoring TOI documents submitted to Regulatory Authorities (e.g.
FDA and EMA) including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and clinical summary sections of Common Technical Documents (CTDs) in support of worldwide (outside of Asia) regulatory submissions.
* Prepare documents in line with regulatory requirements in conjun...
....Read more...
Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2026-01-08 07:28:09
