85 Testing & Quality Assurance in Tamaulipas lowest at $2080.0+

Tecnico de Mantenimiento64631192758274120

Indeed

Tecnico de Mantenimiento

**About Convatec** **Pioneering trusted medical solutions to improve the lives we touch:** Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at\-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com Manages and/or operating manufacturing machinery, including: * Inspection, and operation of machining and finished products * Repair \& maintenance of machine shop operations and inspecting finished parts, tools, and dies against specified tolerances * Reviewing work orders and scheduling resources * Monitoring and adjusting machine shop tool/equipment setups, calibrations, and alignments where required Requires broad knowledge of operational procedures and tools obtained through extensive work experience and may require vocational or technical education. May require the following proficiency: • Works under limited supervision for routine situations. • Provides assistance and training to lower level employees. • Problems typically are not routine and require analysis to understand. **Responsibilities and powers – international**General Responsibilities: Make sure that equipment and processes have been properly validated. (4705007 Procedure for the maintenance of machinery and equipment in production area.) Make sure that all Test and Measurement equipment have been calibrated by QC. Process control specifications are followed and process control is properly recorded. Ensure proper implementation of preventive maintenance as well as filling appropriate, timely and routines according to good documentation practices. Meet 5\`s routines for the areas of drawers and tool carts assigned to the maintenance department as well as the due registration routines established for it. He is responsible for fulfilling the goals and objectives set out in its annual assessment and submit accurate and timely evidence of such compliance. The Technician is responsible to fix any problems regarding supplies (electricity and compressed air at the foot of the machine) and equipment, and contacting suppliers of machine components and technical personnel in Denmark, in case of requiring support for failures. Research and analysis of malfunctions of equipment and systems from prompt repair. To make sure that production requirements are met. Comply with those applicable requirements of the ISO 13485 \& FDA GMP Standards. Hi is responsible for train and register the training to new technicians. Also responsible to train and document the training of the operators in the safety handling of the equipment.. To comply with our quality policy. Powers To take corrective actions when process is out of specification limits. To repair, maintain and make any changes necessary to make the equipment work properly. Report immediately any mal function of the equipment and systems to the immediate supervisor or immediate Leader Technician. To be the Safety leader in the handling of the equipment. Stop and fix process when it is out of specification limits or quality could be compromised. To report delays in delivery due to problems that needs to be fixed. Safety, Health, and Environment Responsibilities Comply with safety, health and environmental policy, procedures established by the EHSMS. Maintain applicable documented information related to the EHSMS up to date. Participate in committees, trainings, and awareness, to ensure proper competency of their position if applicable. Be aware of and support compliance with applicable significant environmental aspects and associated significant environmental impacts. Understand EHS risk and legal requirements relating to job responsibilities and appropriate requirements. Execute job responsibilities with professional care and in compliance with legal requirements and internal standards without compromising the safety of self and others. Be alert to EHS hazards in the workplace, responding to them as appropriate and communicating them to responsible management as soon as they are identified (e.g. spills). Help drive continuous performance improvement in EHS areas, recommending potential improvements to responsible management. Participate in identifying opportunities for improvement and implementing the necessary actions to achieve the intended results of their activities. **Reporting – international** Preventive maintenance reports. Correct filling and capture order corrective maintenance. 4905204 Filling routine cleaning maintenance areas. 4902119\. **Success criteria – international** Maintain and improve the availability or reliability of assigned equipment according to the established metrics. Analysis and solution of repetitive issue that affect the availability of equipment assigned for production. That production never stops due to equipment malfunction. That the planned and required quantity of products in the machinery be produced among the specifications. Require or communicate adequately to planning and production personnel when the machinery will be taken for maintenance. The QA system is fulfilled following the specifications and the requirements in the good practices of documentation and manufacturing (5S's). Production requirements and company objectives are met. **Demands for education, training, and competence – international.** Job profile * Finished Technical Studies or engineering in Mechanics, Mechatronics, Electronics or related. * 1\-3 years of experience * English preferred * Software utilization skills / Computer skills * knowledge of basic requirements of FDA QSR's GMP's and ISO 13485 or similar regulations, preferred. * Knowledges in mechanics, electrical control and pneumatic. * Interpretation of electrical, pneumatic and electronic diagrams * Basic knowledge of PLC, HMI (screens). * Tools for analysis and solution of machinery problems. * Knowledge in LOTO system and EPP. * Induction to ISO 14001:2015\. Induction on Environmental Legal Requirements, Training on Applicable Environmental Management System Documents, Disaster Care and Response, Applicable Operational Controls, Determination of Applicable Significant Environmental Aspects and Impacts, EHS Policy and Environmental Objectives. Internal training * Compliance with document 4908028\. **Beware of scams online or from individuals claiming to represent Convatec** A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. **Equal opportunities** Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. **Notice to Agency and Search Firm Representatives** Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. **Already a Convatec employee?** **If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site \- Find Jobs". Thank you!**

Manuel Acuña 116, Nuevo Santander, 88302 Cdad. Miguel Alemán, Tamps., Mexico

Negotiable Salary

Supply Chain Superintendent64541514212739121

Indeed

Supply Chain Superintendent

**About Convatec** **Pioneering trusted medical solutions to improve the lives we touch:** Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at\-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com About the role To secure to follow the valid stablished procedures with the purpose to follow with the different authorities and the different regulations from FDA CGMP, ISO 13485 and OEA. Monitor the material movements, from receiving raw materials to shipping finished products. To secure that purchase of indirect materials in MX are planned based on the level of usage and in compliance with annual budget. To secure that transportation of goods is done under good conditions and for as low a cost as possible. To secure that any report, requested or permit is delivered in time to the authorities. To collect, handle and communicate information as to Logistics group in DK needs. To handle forecast as an asset in planning in the long run. Ensure order planning is successful and that the capacity is used in efficient manner. Investigation and development of the market. Knowledge of materials Vendor sourcing for new and existing categories. Work with sourcing team to implement VMI with local suppliers. Ensure that all applications and other purchasing documents comply with established processes, policies, and procedures. **Key Duties and Responsibilites** Define and deploys initiatives to improve the skills of the SCM Professionals (Planning, Inventory Control, etc.) Support and participate on continuous improvements activities such as: Kaizen, VSM, cost reduction, workshops. Responsible for communicating stock levels to BUID. Responsible to attend audits froe different customers. To follow, develop and acting according to Quality Assurance System based on ISO 13485 \& FDA CGMP regulations. Follow approved budget by the Business Units. To maintain the procedures, formats, and work instructions according with the different authority’s regulation. Identify potential suppliers to improve costs and quality. Support to the logistics department in commercial matters. Negotiate prices with existing and new suppliers. Negotiate contracts with the assistance and support of sourcing. Efficient communication with suppliers on commercial matters. Continue to develop and maintain partnership with suppliers on strategic matters. Participate in the physical inventory. Receive, handle, and confirm order confirmations from Logistics in DK Coordinate the preparation and release of order list/packing plan for all the productions lines in MX. Clear communicate with production site about capacities, plan, and orders in progress. Communicate with Logistics in DK about capacities, requirements, and shipping methods. Inform data about orders and shipping plans for VMI\-customers to shipping department. Supervision of Purchasing \& planning \& MRO Purchasing personnel. Complying with the Convatec quality policy **Skills and Experience** University Degree required. 5 years minimum experience on Supply Chain Fully English MRP system experience. Personnel management experience. Inventory and warehousing experience. Software utilization knowledge. Experience in the Medical Industry or other regulated industry (Preferred). Knowledge in GMP’s FDA, QSR and ISO 13485 and/or similar regulations (Preferred). **What you’ll** **g****et:** * Competitive salary \+ bonus * Training \& development * Collaborative, supportive culture **Ready to join us?** At Convatec, we’re pioneering trusted medical solutions to improve the lives we touch. If you’re ready to make a real impact, apply today and help us bring our Forever Caring promise to life. \#LI\-ML1 **Beware of scams online or from individuals claiming to represent Convatec** A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. **Equal opportunities** Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. **Notice to Agency and Search Firm Representatives** Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. **Already a Convatec employee?** **If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site \- Find Jobs". Thank you!**

Manuel Acuña 116, Nuevo Santander, 88302 Cdad. Miguel Alemán, Tamps., Mexico

Negotiable Salary

Product Quality Engineer64358211433730122

Indeed

Product Quality Engineer

**About Convatec** **Pioneering trusted medical solutions to improve the lives we touch:** Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at\-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at\-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com **About the role** Participate in changes within the project portfolio in SEG MX ensuring compliance with internal and external requirements according to standards, customer, and authorities; ensuring quality system is developed, maintained, and improved; assuring Process Validation and CCR system is followed accordingly and supporting as leader on quality issues or non\-conformities raised from the project\-change **Key responsibilities** * Update and develop quality procedures, quality specifications as required in the project\-change. * Draw up and/or follow up on internal deviations, rationales, statements, and preventive actions. Supporting the quality system in the adequate handling, for instance, non\-conformities activities, CAPA activities. * Responsible for Updating Risk Management Plan, including Use/Design FMECA and Process FMECA within a new project/change. * Responsible to ensure adequate communication/information between departments and sites to secure a complete DMR before qualification starts. * Assist project team regarding external tests and verifications, including biocompatibility and stability testing, when required. **Requirements** * Bachelor’s degree in engineering or related careers. * 2 years of experience in manufacturing industries, working with project/processes implementations and new products introduction. * Knowledge of Quality Control Systems. * Experience working in process lines. \- English proficiency: Intermediate \- Advanced. \- Microsoft Office proficiency: Intermediate \- Advanced. * Desirable knowledge on Trackwise, Lotus or related softwares. \#LI\-AA1 \#LI\-OnSite **Beware of scams online or from individuals claiming to represent Convatec** A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. **Equal opportunities** Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. **Notice to Agency and Search Firm Representatives** Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. **Already a Convatec employee?** **If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site \- Find Jobs". Thank you!**

Manuel Acuña 116, Nuevo Santander, 88302 Cdad. Miguel Alemán, Tamps., Mexico

Negotiable Salary

Ingeniero de Calidad en Proyectos64211374013827123

Indeed

Ingeniero de Calidad en Proyectos

**About Convatec** **Pioneering trusted medical solutions to improve the lives we touch:** Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at\-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at\-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com **About the role** The Quality Assurance Engineer will have a key position to support production as main leader, assuring the compliance for regulations, standards, QMS internal procedures on new projects, process improvements, validation \& re\-validations, risk management and customer complaints investigations. In relation to quality issues from nonconforming material, maintain quality indicators and internal deviations to coordinate and perform needed activities for a good follow up of a quality system. **Key responsibilities** Process Control related * Assure the process control is followed during product manufacturing. Monitor the process output and organize activities to meet and maintain the product quality standards. * Support the quality system by being focused on adequate handling of non\-conformity activities, corrective and preventive actions. * Define a classification of all Non\-Conformities based upon the risk. * Coordinate and lead the investigation / root cause, with the team member involved (maintenance, production, logistic, engineering, etc.). * Review, update and develop procedures, instructions, quality specification as needed. * Collect and review the objective evidence to complete the investigation and therefore the correct NC closure and assure the effectiveness of the actions established. * Follow up the QA roll as per NC procedure require (for instance, Originator, Owner, Quality Reviewer, Approver, etc.) as needed. * Monitor the process KPIs (PPMs, NCs, etc) and present any trending to the NCRB and take actions if needed. * Make sure the actions are being supported or referenced to the quality system. * Promote ideas for continuously improvement of Quality with the end achieve the fulfillment across of the systems simplicity. * Support at several areas where his/her experience and technical knowledge about the problem can be usefully (production, microbiology, systems, etc). * Perform internal process audits, when required. * Keep communication with other departments MX / DK in relation to any quality problem. * Create Quality alerts and Provide support on the definition of quality criteria, when needed. Projects \& Validation related * Participate in development teams having as main responsibility the quality and fulfillment with the regulations or other applicable standards. * Update and develop PFMEcA from the Risk management related with changes from projects, internal inputs, etc. * Support on the risk assessment preparation, when needed. * Support on the development of verification and validation of products. * Establish and maintain VMP (Validation Master Plan) for re\-validation of process equipment, including validation history and assure it is approved by and communicated to relevant areas. * In cooperation with the Production and Eng Department ensure resource planning for re\-validation activities. * Filling of validation documentation is following procedures and applicable regulations. * Review of acute maintenance on process equipment for evaluation of need for re\-validation according to document 4705007\. * Management of software validations in all systems applied, in collaboration with project leader * Collaborate on validation of molds and molding machines providing the support as Quality Engineering * To comply with the company quality policy. * Support on review IQ, OQ and PQ validations of test equipment validation. Safety, Health, and Environment Responsibilities * Comply with safety, health and environmental policy, procedures established by the EHSMS. * Maintain applicable documented information related to the EHSMS up to date. * Participate in committees, training's, and awareness, to ensure proper competency of their position if applicable. * Be aware of and support compliance with applicable significant environmental aspects and associated significant environmental impacts. * Understand EHS risk and legal requirements relating to job responsibilities and appropriate requirements. * Execute job responsibilities with professional care and in compliance with legal requirements and internal standards without compromising the safety of self and others. * Be alert to EHS hazards in the workplace, responding to them as appropriate and communicating them to responsible management as soon as they are identified (e.g. spills). * Help drive continuous performance improvement in EHS areas, recommending potential improvements to responsible management. * Participate in identifying opportunities for improvement and implementing the necessary actions to achieve the intended results of their activities. **Requirements** * Bachelor’s degree (Mechanical, Electronic, Industrial area or similar education) * Min. 3 years’ experience on Engineering areas * Strong Experience on handling of QMS (Quality management system) * Strong Experience on Quality Control Charts (histogram, pareto, process capability calculations, controls charts, etc) * Strong Experience on Quality Management Tools (brainstorms, flow diagrams, cause and effect diagrams, etc.) * Focus on continues improvement mindset * **Verbal and written English, C1 level minimum** * Training/Knowledge on FDA QSR's and GMP's, ISO 13485, J\-PAL/Ordinance No.169, EU and Canadian medical devices regulation, or similar regulations, preferred * Familiar with common computers software packages. MS Office, etc. required * Availability to work in different shifts. * Molding process knowledge * Able to travel, if required \#LI\-AA1 \#LI\-OnSite **Beware of scams online or from individuals claiming to represent Convatec** A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. **Equal opportunities** Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. **Notice to Agency and Search Firm Representatives** Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. **Already a Convatec employee?** **If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site \- Find Jobs". Thank you!**

Manuel Acuña 116, Nuevo Santander, 88302 Cdad. Miguel Alemán, Tamps., Mexico

Negotiable Salary