Temascalcingo Laboratory & Technical Services Job Listings

Indeed

Senior Purchaser

**Senior Purchaser** **Job Description:** Responsible for purchasing supplies, materials, equipment, and tools necessary for the operation of the company in the **electrical and civil** sector. **Main Responsibilities:** * Purchase supplies and materials. * Search for, evaluate, and select new suppliers. * Request quotations from authorized suppliers. * Generate purchase orders, manage payments, invoices, and payment complements. * Track purchases made and their shipment. * Operate the **Odoo** system. * Apply knowledge of **ISO 9001:2015 standard**. * Organize activities and safeguard documentation related to the purchasing area. * Prepare and deliver **KPIs** for performance. **Requirements:** * Proven experience in purchasing and supplier management. * Knowledge of Odoo and administrative systems. * Negotiation, leadership, and decision-making skills. * Knowledge of ISO 9001:2015 standard. **We Offer:** * Salary: **$14,000 net** * Schedule: **Monday to Friday, from 9:00 to 18:00 hrs** * Statutory benefits * Uniforms * Location: **Col. Las Américas, Querétaro** Employment type: Full-time Salary: $14,000.00 - $15,000.00 per month Benefits: * Free uniforms Work location: On-site

Fidel Velázquez 5, Los Miradores, 76850 Amealco de Bonfil, Qro., Mexico

MXN 14,000-15,000/year

CHEMICAL CONTROL COORDINATOR64151269157762121

Indeed

CHEMICAL CONTROL COORDINATOR

**We are looking for you** 'BRULUAGSA' is a leading Mexican company in the health sector, dedicated to the manufacturing and distribution of high-quality pharmaceutical products for over 25 years. Our commitment to excellence and innovation has positioned us as a recognized company in the market. **What do you need for the position?** * Degree in Pharmaceutical Chemistry, Industrial Pharmacy, Chemical Engineering or related fields (DEGREE HOLDER) * 2 years of experience as Validation Leader. * Knowledge of BPD, BPF and BPL **Knowledge and Functions to perform** * HPLC, GC techniques * Knowledge of NOM\-059\-SSA1 and NOM\-073\-SSA1 * Development and execution of validation protocols * Guidelines applicable to validation * Analytical transfers **Bruluagsa offers** * Base salary of $20,000\.00 gross per month. * Benefits above legal requirements: 30-day Christmas bonus, vacation premium above legal requirement, savings fund, grocery vouchers, subsidized cafeteria, major medical insurance, company transportation and more. * Opportunities for growth and professional development. **JOIN OUR TEAM AND BE PART OF BRINGING HEALTH TO ALL MEXICO!** Job type: Indefinite term Benefits: * Study assistance * Company parking * Free parking * Medical expense insurance * Major medical expense insurance * Cafeteria service * Grocery vouchers Work schedule: * Monday to Friday (Saturdays) Work location: On-site job Job type: Indefinite term Salary: $20,000\.00 \- $22,000\.00 per month Benefits: * Company parking * Free parking * Medical expense insurance * Life insurance * Cafeteria service * Additional vacations or paid leave * Grocery vouchers Work location: On-site job

Calle Lic Isidro Fabela Alfaro 14C, 50450 Atlacomulco de Fabela, Méx., Mexico

MXN 20,000-22,000/year

Documentation Coordinator64150694593283122

Indeed

Documentation Coordinator

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. **Your role at Vantive:** You will be responsible for managing quality in processes, systems, and plant products according to standards established by applicable current regulations and standards (ISO 9001, ISO 13485, FEUM, and NOM 241), as well as maintaining and complying with quality systems in accordance with established indicators. **What you will do:** * Evaluate and make decisions to resolve problems. * Integrate and collaborate with different work areas. * Ensure compliance with Vantive's corporate policies. * Verify compliance with the quality management system according to current standards NOM-241, ISO 9001, and ISO 13485. * Comply with procedures related to Documentation and GMP. * Manage the handling and analysis of complaints to ensure that for each received complaint, appropriate investigations are conducted, necessary corrective and preventive actions are implemented, and a system is established to measure the effectiveness of the actions taken. * Develop and implement an audit system. * Contribute to compliance with applicable current regulations by immediately notifying the Regulatory Officer of any detected health-related irregularity. * Manage the nonconformities process to ensure that any deviation from established procedures is investigated, reviewed, and resolved. * Manage the product recall process from the market and follow up on its execution. * Ensure compliance with safety procedures for activities and personnel under your responsibility, in accordance with international standards ISO 14001, 45001, and Mexican Official Standards on safety. * Manage and develop a comprehensive process to evaluate, identify, monitor, and reduce risks. * Manage the change control process impacting the Quality Management System. * Ensure regulatory compliance based on current legal provisions. * Identify compliance and legal risks for Vantive within the country/cluster. * Promote the implementation of the ethics and compliance program and prevent, detect, and correct violations of laws, Vantive policies, and the code of conduct. **What you will bring:** Bachelor's degree in Chemistry and Pharmaceutical Biology, Pharmaceutical and Industrial Chemistry, Chemical Engineering, Chemistry, or related chemical and/or pharmaceutical fields. Solid knowledge in Good Documentation Practices, Good Manufacturing Practices, Quality Management Systems, and the Mexican Official Standard NOM-241, ISO 9001, ISO 13485 (current version). 2 years of experience in quality management systems. **Reasonable Accommodation** Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link **Recruitment Fraud Notice** Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

R4QC+9V, 50487 San Bartolo el Arenal, Méx., Mexico

Negotiable Salary