Empregos atuais relacionados a Quality Operations Sr. Manager - Campinas - Zoetis
-
Quality Operations Sr. Manager
Há 3 horas
Campinas, Brasil Zoetis Spain Sl Tempo inteiro**Summary of the Position**Responsible for product quality, regulatory compliance, quality systems, and processes at the Campinas site.Accountable for all aspects related to Quality according to Brazilian and international Good Manufacturing Practices (GMP) and other applicable standards and regulations, as well as Zoetis Global Quality Standards.Responsible...
-
Quality Operations Sr. Manager
41 minutos atrás
Campinas, São Paulo, Brasil Zoetis Tempo inteiroSummary of the PositionResponsible for product quality, regulatory compliance, quality systems, and processes at the Campinas site. Accountable for all aspects related to Quality according to Brazilian and international Good Manufacturing Practices (GMP) and other applicable standards and regulations, as well as Zoetis Global Quality Standards. Responsible...
-
Operations Manager
Há 3 horas
Campinas, Brasil Buscojobs BR C2 Tempo inteiroJob Summary The Operations Manager is responsible for overseeing and optimizing day-to-day manufacturing operations to ensure efficient production, high-quality output, cost control, and compliance with safety and regulatory standards.This role plays a critical part in improving operational performance, managing cross-functional teams, and driving continuous...
-
Operations Manager
Há 3 horas
Campinas, Brasil Buscojobs BR C2 Tempo inteiroJob SummaryThe Operations Manager is responsible for overseeing and optimizing day-to-day manufacturing operations to ensure efficient production, high-quality output, cost control, and compliance with safety and regulatory standards. This role plays a critical part in improving operational performance, managing cross-functional teams, and driving continuous...
-
Quality Operations Sr. Manager Manufacturing
14 minutos atrás
Campinas, São Paulo, Brasil Zoetis Tempo inteiroSummary of the PositionResponsible for product quality, regulatory compliance, quality systems, and processes at the Campinas site. Accountable for all aspects related to Quality according to Brazilian and international Good Manufacturing Practices (GMP) and other applicable standards and regulations, as well as Zoetis Global Quality Standards. Responsible...
-
Datacenter Operations Manager
Há 4 dias
Campinas, Brasil Microsoft Tempo inteiroAs a Microsoft Datacenter IT Operations Manager (ITOM), you will lead and manage a team of managers and individual contributors in charge of logistics, area management, and technicians. You will manage data center site services and logistics across multiple buildings. Microsoft’s mission is to empower every person and every organization on the planet to...
-
Sr Project Manager
4 semanas atrás
Campinas, Brasil GE Vernova Tempo inteiroJob Description Summary We are seeking an experienced Sr Project Manager to lead complex multidisciplinary projects involving the design manufacture testing and delivery of large rotating machines with a particular focus on synchronous condensers. The selected candidate will be responsible for end-to-end project execution from engineering through...
-
Sr Project Manager
41 minutos atrás
Campinas, São Paulo, Brasil GE Vernova Tempo inteiroWe are seeking an experienced Sr Project Manager to lead complex, multidisciplinary projects involving the design, manufacture, testing, and delivery of large rotating machines, with a particular focus on synchronous condensers.The selected candidate will be responsible for end-to-end project execution — from engineering through manufacturing, factory...
-
Supplier Quality Manager
5 minutos atrás
Campinas, São Paulo, Brasil GE Vernova Tempo inteiroJob Description SummaryJob DescriptionMain ResponsibilitiesIncludes supplier qualifications, action plans, audits, performance monitoring, and assisting key suppliers towards industrial standards of excellence. SQEs have various levels of differentiation which are related to level of technical understanding of engineering drawings and ability to manage...
-
Supplier Quality Manager
4 semanas atrás
Campinas, Brasil Ge Vernova Tempo inteiroOverview Main ResponsibilitiesIncludes supplier qualifications, action plans, audits, performance monitoring, and assisting key suppliers towards industrial standards of excellence. SQEs have various levels of differentiation which are related to level of technical understanding of engineering drawings and ability to manage vendors. Developing in-depth...
Quality Operations Sr. Manager
Há 24 horas
Summary of the PositionResponsible for product quality, regulatory compliance, quality systems, and processes at the Campinas site.Accountable for all aspects related to Quality according to Brazilian and international Good Manufacturing Practices (GMP) and other applicable standards and regulations, as well as Zoetis Global Quality Standards.Responsible for compliance with regulatory requirements, including global regulatory requirements, global quality policies, company policies, procedures, and other applicable guidelines.This position reports to the Quality Lead - PharmaAmericas with interface to the Site Leader.Main ResponsibilitiesDrive the establishment of quality systems and culture to create lasting regulatory compliance and provide guidance and leadership to other site managers to enhance compliance with GMP systems.Maintain site compliance through continuous improvement processes focused on technology, people, and/or processes.Supervise the design and implementation of information systems for data storage and retrieval.Review, identify, and manage changes in technology, people, and processes to increase efficiency and compliance, ensuring regulatory and company policy requirements are met.Approve or reject all incoming production materials, in-process products, and finished products to ensure compliance with company, industry, and government policies.Make final decisions and provide advice in resolving production process issues, in-process products, final product release, and product complaints to ensure timely resolution.Establish and maintain programs for product development, including sampling materials and products for testing, monitoring filling and labeling activities, and stability testing.Maintain adequate laboratory facilities for biological, serological, chemical, and physical testing of marketed and developing products for release and/or stability evaluation, components, and control of aseptic production facilities.Additional ResponsibilitiesManage Quality Systems including audits and follow-up on corrective/preventive actions, production deviations, and atypical events related to customer complaints, change control, and all out-of-specification (OOS) or atypical analytical results, according to Brazilian or other applicable GMPs.Review and investigate (when necessary) all quality complaints from internal and external customers.Ensure compliance with GMP and Zoetis quality procedures across all departments.Approve the Validation Master Plan and verify execution of validation protocols and reports for new and existing facilities.Coordinate the review of Batch Records for marketing authorization requirements.Prepare, evaluate, and approve all GMP documentation including Site Master File, procedures, record sheets, various data collection methods by QA, Production, Engineering, and Maintenance, etc.Review local production and filling operations according to Good Production Practices.Coordinate documentation control to ensure availability, use, and periodic updating of Standard Operating Procedures (SOPs) for all relevant production and quality processes.Manage issuance of printed components, including labels and seals for production, and compliance with established requirements.Train colleagues in GMP and manage all training information in the appropriate database.Regulatory and Team ManagementCoordinate supplier qualification according to Zoetis operational procedures.Manage release for marketing of finished products, including preparation of Certificates of Analysis and export-related documents.Coordinate all regulatory activities at the plant, acting as the link to the Global Regulatory group, with direct relations to local regulatory authorities and inspections by external authorities.Contribute to process improvement efforts, quality enhancement, and cost reduction.Report to the Quality Lead – Pharma Americas Platform any occurrences outside normal standards, for corrective measures as necessary, following Escalation to Management Process.Ensure quality and robustness of processes through continuous improvement plans.Identify and develop people/talents, motivate and engage the team in meeting continuous improvement goals, according to company values.Comply and ensure compliance with legal and regulatory requirements regarding EHS—Environment, Health, and Safety, such as use of PPE, medical exams, and others, according to SOPs.Encourage the team's participation in EHS strainings, events, and campaigns.Encourage reporting of risk situations to the EHS area, using the GoodCatch program.Prevent unsafe acts at work, preparing operational procedures, including risk observations and prevention methods, involving EHS if necessary.Ensure good condition of equipment in the area of responsibility.Promote order, cleanliness, and ensure workplace safety in responsible areas through use of 5S methodology.Ensure confidentiality of information under responsibility.Comply and ensure compliance with the company's Code of Conduct.Manage related activities of the team under responsibility.Managed ResourcesFinancial Responsibility: Annual budget for the Quality Operations departmentSupervision: Direct Reports-1 QA Manager and 1 QC Manager (Organization with around 60 colleagues)Education and ExperienceBachelor's degree in pharmacy, biology, chemistry, or related fields.Thorough knowledge of GMP, regulations for biological and pharmaceutical products, company policies related to employees, accounting, SOPs, and safety regulations.Senior Manager with extensive and solid experience in pharmaceutical and biological Quality Assurance and people management.Fluent written and spoken English.Required Technical SkillsExperience managing regulatory requirements and audits.Knowledge of Quality Control testing and manufacturing processes performed by the company.Knowledge of Engineering and Maintenance processes performed by the company.Knowledge of Supply Chain, Logistics/Storage processes performed by the company.Solid experience in a manufacturing environment.Experience in establishing and managing business objectives and achieving superior results.Effective business management experience focused on results.Excellent oral and written communication.Skills in conflict management and time management.Full time#J-*****-Ljbffr
