Fire & Security Lead Saltillo, Coahuila Department: Security & Fire Prevention Reports to: México Power train & Assembly Security Lead / Mexico Security head / Facility Manager Location: Saltillo Truck Assembly Light Duty (STLD) Security Position
Job Description Propósito General de la Función Esta posición existe para liderar el diseño, escalamiento e industrialización de procesos para productos estables a temperatura ambiente, incluyendo salsas, condimentos y productos vegetales. La persona será responsable de
Meaningful Work From Day One: The Senior Finance Analyst (SFA) serves as the Subject Matter Expert for the General Ledger (GL)master data components and hierarchies (account-cost center-territories and profit centers). The SFA manages the month-end close
Are you ready to work hard, have fun and make history! As a Physical Security Manager you will be tasked with driving operational security excellence in the company that is changing the world! Your constant vigilance
Overview The Purchasing Manager is responsible for overseeing the procurement of materials, supplies, and services necessary for the companys operations. This role ensures cost-effective purchasing decisions, supplier negotiations, and inventory management while maintaining quality and compliance
Regulatory Affairs Specialist Within International Regulatory Affairs, as Regulatory professionals, we take innovative regulatory approaches to bring life-changing medicines to patients in international markets. We work across the AZ pipeline and business to accelerate Regulatory approvals
A Day in Your Life at MKS: The Security Manager oversees all physical security, asset protection, and risk‑mitigation operations for a high‑volume manufacturing campus in Nogales, Sonora. This role ensures the security of employees, protection of
Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in
Previous Pharmaceutical/Biotech experience is mandatory for this role MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in
Who we are At Twilio, we’re shaping the future of communications, all from the comfort of our homes. We deliver innovative solutions to hundreds of thousands of businesses and empower millions of developers worldwide to craft
Misión Liderar las actividades de seguridad y gestión de crisis en el sitio de Airbus Helicopters en Querétaro, fortaleciendo los fundamentos de seguridad, mitigando riesgos y garantizando un entorno seguro para el personal y los activos
Location: Multi-site Ciudad Juárez, Chihuahua and El Paso, Texas. Process Engineer General Purpose of the Position Design, analyze, optimize, and control production processes to improve efficiency, quality, safety, and operating costs while ensuring compliance with technical
Descripción y detalle de las actividades The Purchasing Manager is responsible for overseeing the procurement of materials, supplies, and services necessary for the companys operations. This role ensures cost-effective purchasing decisions, supplier negotiations, and inventory management
Previous Pharmaceutical/Biotech experience is mandatory for this role MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in
Previous Pharmaceutical/Biotech experience is mandatory for this roleMMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.MMR Consulting has offices in Canada, USA,
At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.Job Description: Job Overview We are looking for a highly organized Project Manager
Previous Pharmaceutical/Biotech experience is mandatory for this role MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation. MMRConsulting hasofficesinCanada,USA,andAustralia. This is an
Analyst, Reporting page is loaded# Analyst, Reportinglocations: Guadalajara, JALtime type: Full timeposted on: Posted Todayjob requisition id: Req- *About Ingredion: Join Ingredion, where innovation impacts lives worldwide! Without even realizing it, you have experienced our work
Join a team recognized for leadership, innovation and diversity : Essential Responsibilities- Partner with the Global Pricing Leader to devise price setting and executions strategies to meet business price targets and enable profitable business growth- -
Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in Canada, USA, and Australia. This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems, and facilities. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers. This role is for C&Q Manager will require to work on the validation of upstream and downstream bioprocess systems/equipment in the biopharmaceutical industry, as well as process equipment in pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers. The work will require working out of client’s facilities, which are in US (company offers TN Visa sponsorship). Responsibilities Provide technical guidance into the commissioning, qualification and start-up of various equipment and facilities used in life science manufacturing, such as bioreactors, tanks, CIP, Buffers, Media, Chrom, TFF, washers & autoclaves, etc. Lead the development of key qualification deliverables during the project lifecycle to ensure project is well defined, and the action plan to test the system is applicable and relevant. Lead qualification processes throughout the project lifecycle such as VPP, Risk Assessments, RTM, DQ, FAT, SAT, IQ, OQ and PQ as appropriate to ensure timely completion and to ensure all specifications are met. Prepare protocols, execute protocols, summarize data, resolve deviations, prepare final reports. Experience with C&Q of upstream or downstream bioprocess systems is required. Experience with C&Q of other process equipment, utilities, facilities is an asset. Thermal Validation experience is an asset. Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates. Engage other departments, as required, for design reviews and decisions. Travel may be occasionally required for meetings with clients, equipment fabrication vendors or Factory Acceptance Testing (FATs). Work may require occasional support over shutdowns or extended hours, specifically during installation and commissioning / validation phases. Client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc. Visit construction and installation sites following all site safety requirements. Other duties as assigned by client, and/or MMR, based on workload and project requirements. Qualifications Excellent written and spoken English is required including the preparation of technical documents in English Years of experience: 8+ years for years of experience in commissioning, qualification or validation of various systems within the pharmaceutical/biotech industry.