Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to large sized studies that are moderate to complex in scope of work with moderate support from senior staff.

What you will do

• Author Safety Management Plan for assigned studies
• Attend and present at Investigator Meetings
• Review incoming SAE data for completeness and accuracy
• Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
• Perform QC of SAEs processed by other PV Associates
• Generate regulatory reports and perform safety submissions as needed

What you will bring to the role

• Strong understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements
• Strong understanding of computer technology, and management of relational database systems, including extraction of data
• Excellent organizational skills and ability to handle multiple competing priorities within tight timelines
• Consistently demonstrates commitment, dependability, cooperation, adaptability and flexibility in executing daily tasks and responsibilities

Your experience

• Minimum of 3 years of pharmacovigilance experience (pre-approval clinical trials)
• Bachelor’s degree in science related field, nursing or equivalent combination of relevant education and experience
• Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)
• Excellent written and verbal communication skills
• Excellent organization skills and attention to detail
• Demonstrated ability to handle multiple competing priorities while adhering to applicable timelines
• Ability to work independently, prioritize work effectively and work successfully in matrix team environment
• Ability and willingness for potential limited travel (domestic and international) as needed (attend Investigator Meeting, project kick-off meeting and/or bid defense meeting)
• Fluent in written and verbal English

Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to large sized studies that are moderate to complex in scope of work with moderate support from senior staff.

What you will do

• Author Safety Management Plan for assigned studies
• Attend and present at Investigator Meetings
• Review incoming SAE data for completeness and accuracy
• Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
• Perform QC of SAEs processed by other PV Associates
• Generate regulatory reports and perform safety submissions as needed

What you will bring to the role

• Strong understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements
• Strong understanding of computer technology, and management of relational database systems, including extraction of data
• Excellent organizational skills and ability to handle multiple competing priorities within tight timelines
• Consistently demonstrates commitment, dependability, cooperation, adaptability and flexibility in executing daily tasks and responsibilities

Your experience

• Minimum of 3 years of pharmacovigilance experience (pre-approval clinical trials)
• Bachelor’s degree in science related field, nursing or equivalent combination of relevant education and experience
• Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)
• Excellent written and verbal communication skills
• Excellent organization skills and attention to detail
• Demonstrated ability to handle multiple competing priorities while adhering to applicable timelines
• Ability to work independently, prioritize work effectively and work successfully in matrix team environment
• Ability and willingness for potential limited travel (domestic and international) as needed (attend Investigator Meeting, project kick-off meeting and/or bid defense meeting)
• Fluent in written and verbal English

Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools, contributing to our success in a collaborative environment.

We are looking for a Technical Project Manager (AI Portfolio).

In this role you will:

• Manage intake of AI use cases from CMC business and digital leadership, ensuring initiatives are clearly defined, prioritized, and actively managed
• Ensure alignment between AI initiatives, business outcomes, and enterprise priorities
• Drive portfolio-level actions, decisions, and follow-ups across multiple AI programs and workstreams
• Identify interdependencies, risks, and capacity constraints across the portfolio and proactively drive resolution
• Maintain standardized tracking for portfolio actions, statuses, risks, issues, and dependencies
• Track and report on portfolio KPIs to provide insight on the portfolio status
• Produce executive-ready reporting for leadership forums
• Implement and evolve portfolio governance mechanisms, including intake, prioritization, and escalation processes
• Drive continuous improvement in portfolio management practices, tooling, and reporting maturity
• Facilitate portfolio-level forms, working sessions, and reviews
• Lead projects as necessary:
• Develop and maintain detailed project plans, milestone tracking, RAID logs, and governance materials
• Drive execution of work, report on project statuses, and elevate risks, issues, and decisions to governing bodies
• Ensure assigned projects adhere to applicable regulatory, validation, security, and data governance requirements
• Influence without authority to drive accountability, resolve blockers, and maintain momentum

We have some requirements:

• Background/previous experience in Pharmaceutical or Life Sciences Industry
• Solid experience as PMO - ability to manage multiple projects simultaneously
• Experience working with AI/ML initiatives
• Demonstrated experience building and maintaining portfolio-level reporting and dashboards
• Compliance-focused mindset
• Familiarity with GxP, validation, or regulated environments
• A bachelor’s degree in STEM or another relevant academic discipline
• Fluent English

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What do we offer?

TCS Benefits – Brazil:

• Health insurance
• Dental Plan
• Life insurance
• Transportation vouchers
• Meal/Food Voucher
• Childcare assistance
• Totalpass
• TCS Cares – free 0800 that provides psychological assistance (24 hrs/day), legal, social and financial assistance to associates
• Partnership with SESC
• Reimbursement of Certifications
• Free TCS Learning Portal – Online courses and live training
• International experience opportunity
• Discount Partnership with Universities and Language Schools
• Bring Your Buddy – By referring people you become eligible to receive a bonus for each hire
• TCS Gems – Recognition for performance
• Xcelerate – Free Mentoring Career Platform
• Tata Consultancy Services is an equal opportunity employer, our commitment to diversity & inclusion drives our efforts to provide equal opportunity to all candidates who meet our required knowledge & competency needs, irrespective of any socio-economic background, race, color, national origin, religion, sex, gender identity/expression, age, marital status, disability, sexual orientation or any others. We encourage anyone interested to build a career in TCS to participate in our recruitment & selection process.

At TATA Consultancy Services we promote an inclusive culture, we always work for equity. This applies to Gender, People with Disabilities, LGBTQIA+, Religion, Race, Ethnicity. All our opportunities are based on these principles. We think of different actions of inclusion and social responsibility, in order to build a TCS that respects individuality. Come to be a TCSer!

#Buildingonbelief

Acompanhar try- out nos processos de produção, realizando ajustes em moldes, afiando corte, verificando circuito de refrigeração, polimento, jateamento, troca de moldes, polimento/ajustes de cabeçotes e acabamento em geral, bem como verificar pontos de melhorias.

PRINCIPAIS RESPONSABILIDADES / ATIVIDADES

- Ter conhecimento em máquinas operatrizes, torno, fresa, retífica e eletroerosão.

- Preparar, regular e operar máquinas e ferramentas para usinar e fresar peças metálicas e similares.

- Conhecimento aprofundado de metrologia, leitura de projetos e desenhos técnicos.

- Examinar as peças produzidas, observando a precisão e acabamento das mesmas, através de instrumentos de medição e controle.

- Identificar falhas no ferramental (Moldes).

- Avaliar desgastes de moldes, estampos e dispositivos.

- Fazer ajustes dimensionais em bucha de corte, pinos sopro, anel corte e ponteira.

- Zelar pela guarda, conservação, manutenção e limpeza dos equipamentos, instrumentos e materiais utilizados, bem como do local de trabalho;

- Cumprir as normas da empresa, segurança, boas práticas de fabricação, código de ética, POP’s (Procedimentos Operacionais Padrão) e IT (Instruções de Trabalho).

BENEFICIOS

• Rota da empresa ou vale transporte;
  
• 7% de assiduidade;
  
• Vale alimentação - 350 (Ifood benefícios);
  
• Plano de saúde e plano odontológico - Unimed;
  
• Alimentação na empresa;
  
• Wellhub - Desconto academia;
  
• 40% de descontona lojinha da empresa.

Quais serão as suas funções?

• Realizar o onboarding e treinamento de novos clientes.
• Oferecer suporte via e-mail e telefone
• Fazer o acompanhamento proativo dos clientes atuais, identificando necessidades e aumentando a adoção de nossos produtos.
• Criar e atualizar conteúdos e manuais de treinamento para clientes.
• Maximizar a satisfação e retenção de nossa base de clientes em toda América Latina.

O que oferecemos?

• Home office 100%.
• Jornada flexível: O horário geral é de segunda à sexta das 9h às 18h com 1 hora de almoço, mas diga-nos caso precise de adaptações.
• Formação contínua.
• Possibilidades reais de crescimento.