Trabajos quality en LaredoCrear alertas

DescriptionDir, Epidemiology Pipeline (TA-Oncology)Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.Discover what our 29,000 employees, across 110 countries already know:WORK HERE MATTERS EVERYWHEREWhy Syneos HealthWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job ResponsibilitiesJOIN OUR TALENT NETWORK. This position is part of an ongoing talent pipeline; while there is noimmediate opening, qualified candidates will be considered as opportunities become available. Looking for SME in Oncology Clinical Trials-Serves as a scientific resource for RWLP management, Company senior management, and other Functions within Company providing expertise in multiple scientific areas.- Works hand-in-hand with RWLP management, business development, and operations personnel to develop and win global business opportunities; helps to lead thedevelopment and delivery of project proposals, bid defenses, and represents capabilities presentations.- Provides overall scientific oversight of selected projects, responsible for meeting or exceeding customer expectations for timelines, budgets, quality, and overall satisfaction.- Coordinates with the project manager to oversee the scientific aspects of study start-up and ongoing study management. Leads the development of and/or peer-review essential study documents including the protocol, case report forms, statistical analysis plan, study management plans, and interim/final study reports. Facilitates scientific advisory boards for safety studies and produces scientific reports/manuscripts/abstracts/presentations.- Maintains a strong working understanding of clinical and epidemiological practice guidelines, clinical research models, protocol designs, real-world research development trends, and regulatory expectations and develops trainings for RWLP/Company organization to enhance their familiarization of epidemiologic study designs and applicable guidelines.- Responsible for the continued building of organizational capacity, improvement of scientific and operational processes and methodologies for non-traditional site management tasks (i.E., remote or central monitoring approaches, minimized regulatory document collection, etc.), integrated RWLP technology solutions including secondary database resources, and RWLP Standard Operating Procedures (SOP) development and maintenance.- Works collaboratively across the organization to help develop business opportunities in the area of post marketing safety commitments and/or risk management; develops and recommendstechniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.- Works to develop collegial relationships with sponsors, thought-leaders and clinical investigators.- Develops abstracts, provides podium presentations, and leads authorship of articles, manuscripts, etc. in industry and peer-reviewed journals to promote Company services.Requirements:SME in Oncology Clinical Trials- Requires graduate degree in Epidemiology, Statistics, or Public Health; (Masters; Preferred Doctorate); - Requires in-depth knowledge of and experience with a variety of study designs; familiarity with post-marketing and late phase study designs as well as relevant guidelines preferred; - Requires basic knowledge of statistical programming language(s) (e.G., SAS, R, Python); - Excellentcommunication, presentation, both written and spoken; - Strong personal communication and team-oriented skills; - Demonstrated leadership and technical skills.We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.Salary Range:The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.Get to know Syneos HealthOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.http://www.Syneoshealth.ComAdditional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

DescriptionClinical Scientist - CardiovascularSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.Discover what our 29,000 employees, across 110 countries already know:WORK HERE MATTERS EVERYWHEREWhy Syneos HealthWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities- Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans.- Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the datato identify risks and data patterns/trends and supports documentation of medical reviews.- Authors medical data queries and reviews query responses, approves query closure in association with Medical Director.- May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed.- Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed.- Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review.- Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner.- Attends at Trusted Process meetings and may participate in internal and external audits.- Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology.- Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans.We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.Salary Range:The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.Get to know Syneos HealthOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.http://www.Syneoshealth.ComAdditional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.SummaryPartners with Medical Director to provide clinical and scientific input to early and late-stage clinical development programs, with an emphasis on protocol-specific requirements, and ensuring the scientific integrity and data quality of clinical trials by using scientific knowledge. Collaborates with Medical Directors and other team members on data reviews and other Medical Management activities to ensure the successful execution and conduct of clinical trials.

SQA - Supplier Quality Assurance Engineer. Buscamos incorporar un/a SQA - Supplier Quality Assurance Engineer para asegurar la calidad de nuestros proveedores, liderando la gestión de reclamaciones y la resolución estructurada de problemas mediante metodologías de mejora continua.

Provide support in project audits, reviews, and approvals of suppliers' quality systems, if required by the customer Report quality and safety alerts and manage NCs (Non-Conformities) and safety issues. Ensure that the project team is aware of the Project Quality Plan and its deliverables, regularly

Además, con todos los desafíos a los que los que nos estamos enfrentando, es un momento muy emocionante y especial para unirte a nosotros El Supplier Quality Engineer es el representante de STELLANTIS en las plantas de los proveedores. Oferta de empleo como Supplier Quality Engineer en Stellantis

Técnico/a Funcional POS – Retail Madrid (Gran Vía) | Presencial | Proyecto estable Antes de solicitar este puesto, por favor, lea la siguiente información sobre esta oportunidad que encontrará a continuación.Si vienes de soporte, implantaciones o despliegues y quieres dar el salto a un rol f

Consultor BI – Especialista en Azure.Si eres un consultor de Business Intelligence con experiencia trabajando en la nube de Azure, ¡en.Responsabilidades principales:.Identificar y comprender las necesidades de negocio para definir soluciones de BI adecuadas.Diseño y desarrollo de soluciones BI:.

Oliver Bernard are currently working with a Tech for Good client of ours who are looking to take on an Agentic Quality Lead / Manager to drive their Quality Engineering team towards a 'Quality as a Service' model and integrate / embed their processes into broader centralised Quality function. The in

Ampliamos nuestro equipo! Se pueden requerir diversas habilidades interpersonales y experiencia para el siguiente puesto.Por favor, asegúrese de consultar la descripción a continuación con atención.Buscas un nuevo reto donde desarrollar tu carrera y aprender nuevas tecnologías? Entonces sigue

The role combines Business Analytics, Data Quality and analytical modelling, contributing to both business decision-making and data-driven initiatives. Improve data quality through validation processes, monitoring and issue resolution. Nice-to-have Experience in Data Quality and data governance.

You should have a risk-based testing mindset, strong analytical capabilities, and a focus on ensuring billing accuracy, financial reconciliation, and high-quality releases. Define and execute test strategies, plans, estimates, coverage models, and quality gates aligned with project risks and deliver

En LHH Recruitment Solutions estamos seleccionando un/a Quality Manager (Automotive) para incorporarse a una compañía multinacional líder en su sector, con un proyecto industrial sólido, estable y de largo recorrido, ubicada en la zona de Vallés Oriental.

The RoleDo you seek out problem-solving at the intersection of business and technology within Quality and Compliance? Do you readily identify how modern platforms can eliminate the friction slowing down quality processes? Do you desire to work at the forefront of Quality Management within the Pharma

Business Analytics, Data Quality and analytical modelling. Improve data quality through validation processes, monitoring and issue resolution.

Key ResponsibilitiesSupplier Quality LeadershipOwn supplier quality performance throughout the full lifecycle: development, qualification, and serial production. We are seeking a Senior Supplier Quality Engineer (SQE) – Composite Materials to take end-to-end ownership of supplier quality for compo

What your responsibilities will beIssue and review Global Quality Policies and ensure its implementation in all the sites within Biopharma Business UnitStay updated on industry trends and advancements in quality management practices to drive innovation and improvementFoster harmonization of Quality

Your role:Coordinate with production in order to plan and execute inbound and production checksManage relations with customers or third party inspectorsParticipate in external supplier quality testing and auditsParticipate in Continuous Improvement Process (CIP) eventsMonitor product portfolio KPIs

Your ResponsibilitiesStrategic Program Development:Identify training and service quality improvement opportunities by collaborating with regional Customer Support hubs, Business Implementation Specialists, and other GPC functions to ensure services evolve with business needsDesign, enhance, or disco

En LHH Recruitment Solutions buscamos un/a Ingeniero/a de Calidad para incorporarse a una compañía industrial internacional, referente en su sector y en pleno proceso de crecimiento y mejora continua.Si te apasionan los entornos industriales, la gestión de la calidad y la colaboración con provee

SpainWelo Data – Data Quality /Contract /RemoteOverviewAre you an experienced quality assurance professional with a passion for language quality, AI, and team leadership? We are looking for a Spanish (Spain)-speaking Quality Control Lead to join a large-scale AI training program. In this role, you

The Supply Chain & Quality Manager role typically includes the following tasks:Act as interface with suppliers for operational activitiesAssess suppliers during tendering phase and contribute to the selection decision Manage/contribute to supply chain & quality aspects of the contract being respons

Job descriptions may display in multiple languages based on your language selection.What we offer:At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies.We invest in our employees, providing them with the support and resou

Proven experience with SAP QM functionalities including Quality Inspection, Quality Planning, Quality Certificates, Quality Notifications, and Audit Management. Job Description:Airbus Defence and Space is seeking an experiencedIT- SAP ERP QM specialist to support and enhance our Quality Management p

Partner with engineering, operations, suppliers, and customers to ensure the highest standards of product and process quality. Lead problem-solving activities using structured methodologies to eliminate recurring quality issues and strengthen customer satisfaction. Contribute directly to operational

The selected candidate will join the Quality Logistics and Transport Team (part of Procurement Quality). The jobholder will reinforce our warehouse and certifying activities, taking part in material certification processes, quality inspections, and new initiatives to improve material management for

ISO 9001Hands-on experience with supplier quality management processes (PPAP, 8D, deviations, engineering changes, quality claims)Experience participating in or supporting NPI phases from an industrial quality perspective6–8 years experience in:Electronics manufacturing (EMS preferred)Industrial q

Promoting a preventive quality mindset within the production/AIT teams, ensuring the implementation of basic quality processes (Non Conformities management, Root Cause Analisis, NRB, quality authorization, operational surveillance, etc…). Ensure the QA team provides the quality documentation such

As Lead Quality Engineer, you'll architect the test automation infrastructure, quality gate logic, and shared tooling that make high-quality testing the path of least resistance for every engineering team. What We're Looking ForYou may be a good fit if you have:6+ years of experience in software qua

Mimica is seeking a Quality Engineer to establish robust quality foundations for a fast‑moving product engineering team. You will own quality from day one, shaping testing approaches, identifying gaps, and defining scalable processes that balance speed and reliability in a rapidly evolving LLM-pow

Veeva Systems invites a Solution Consultant to demonstrate Vault Quality across QMS, document control, Training, and more. You will lead demonstrations, engage with cross-functional teams, and guide customers to best-in-class quality solutions.

People deserve more from their money.More visibility, more control, and more freedom.Since 2015, Revolut has been on a mission to deliver just that.Our powerhouse of products— including spending, saving, investing, exchanging, traveling, and more—help our 75+ million customers get more from thei