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- Specialist QA with experience in regulated industry and knowledge in: Environmental Monitoring, Microbial Identification (Micro ID), Critical Utilities (CU) monitoring Sampling monitoring: equipment and techniques Data trending and evaluation Microbiological...ContratoTrabajar en la oficina
- We are seeking a Sr. Engineer responsible for: • Own change controls for manufacturing g process changes • Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive...ContratoTrabajo por turnos
- We are seeking a highly motivated and experienced Senior Engineer to support engineering initiatives, equipment development, validation activities, and project execution within a regulated manufacturing environment. The successful candidate will play a key role in driving...Contrato
- Overview: The Project Field Engineer is responsible for providing technical engineering information to the Project Manager, Craft Supervisors, and Corporate Functional Managers to ensure design development and construction work complies with all engineering standards,...ContratistaSubcontratistaContratoTrabajar en la oficina
- For Maintenance services. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's degree in Engineering with (3) years within the Pharmaceutical or Medical Device Industry. Shift: Administrative and according to business needs. Good communications skills...ContratoTrabajo por turnos
- DESCRIPCIÓN- REPRESENTANTE DE SERVICIO ES RESPONSABLE DE VISITAR, EDUCAR, OFRECER SEMINARIOS Y MANTENER RELACIONES PROFESIONALES CON LOS CONTACTOS IDENTIFICADOS EN LOS PUEBLOS ASIGNADOS, QUE INCLUYE, PERO NO SE LIMITAN A: OFICINAS MEDICAS, HOSPITALES, HOGARES DE ENVEJECIENTES...Trabajar en la oficina
- QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...Contrato
- • Experience supporting sterile drug product manufacturing within the pharmaceutical or biotechnology industry. • Hands-on experience with aseptic filling operations, process characterization, process validation (PPQ), technology transfer, and commercial process support...ContratoTrabajar en la oficina
- Validation experience in highly regulated industry, If possible filling validation and work on technical documentation. Requirements Doctorate PhD OR PharmD OR MD OR -Master + 3 years of Scientific experience OR -Bachelors + 5 years of Scientific experience...Contrato
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...ContratoTrabajo por turnos
- For Quality services in the Engineering a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering with four (4) years of Assembly and Packaging Process experience. Bilingual (English & Spanish). Project Management skills. Shift...ContratoTrabajo por turnos
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...ContratoTrabajo por turnos
- JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them...Pago diarioPrácticaTemporalInicio inmediatoTrabajo por turnosFin de semana
- For C&Q services in the Business Operations area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Science, or Engineering field with at least 2 years of proven experience in commissioning and qualification processes, protocol generation and...ContratoTrabajo por turnos
$18,75 - $24,5 por hora
In accordance with state and federal regulations, assists the pharmacist, under direct supervision, in the practice of pharmacy. Assists the pharmacist in the performance of other Pharmacy Department duties in accordance with Company policies and procedures. Responsible...Inicio inmediatoTurno de tarde- QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...ContratoTurno de mañanaTurno de tardeFin de semana
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...ContratoTrabajo por turnos
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing to a world...ContratoTrabajo por turnos
- QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...Contrato
- QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...Contrato
- EQVAL Group, Inc. is a company that provides services to the manufacturing industry ( Medical Devices, Pharmaceuticals, Biotechnologies, others ). We work with an extraordinary group of professionals ( employees and contractors ) to accomplish the requirements established...ContratistaTiempo completoRemotoTrabajo híbrido
- Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical...ContratistaTiempo completoContratoCAS
- For Packaging & Supervisory services WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s degree in Engineering and at least three (3) years of prior experience in the pharmaceutical sector and in a supervisory role. Bilingual (Spanish and English) Shift...ContratoTrabajo por turnos
- For Technical Services in the Scientist a rea. WHAT MAKES YOU A FIT: The Technical Part: ~ Bachelor's Degree with four (4) years of experience as a Scientist or Engineer within the pharmaceutical or regulated industry. ~ Bilingual (English & Spanish). ...ContratoTrabajar en la oficinaTrabajo por turnos
- Se solicitan gondoleros(as) "grocery clerks" con disponibilidad de 12:00 p.m. en adelante a tiempo parcial para Amigo San Lorenzo. Para Solicitar: Completa la Solicitud de Empleo en Amigo San Lorenzo o Envía tu resumé a: ****** Requisitos: Escuela Superior ...Tiempo parcialTrabajo por turnosFin de semana
- Req ID: 373645 NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now. We are currently seeking a Senior Manufacturing...Trabajar en la oficinaRemotoTrabajo híbrido
- We are seeking a Sr. Engineer to develop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements. 1. Commissioning & Qualification Strategy and Planning Develop and implement the overall Commissioning &...ContratistaContrato
$77 700 - $129 500 por año
Join a high-impact engineering function focused on tooling development, mold performance, and injection molding processes within a regulated manufacturing environment. This role supports the full lifecycle of tooling programs—from design and validation to maintenance and...Tiempo completo- # Develop and communicate work scope for planned corrective and preventative maintenance tasks that involve multi-crafts. # Work with craft supervisors to identify contract support as needed to complete planned corrective and preventative maintenance tasks # Responsible...Tiempo completoContrato
- Bachelor's degree in engineering is a plus Deviations management Deviation assessments Track wise Biotech and manufacturing experience Requirements Doctorate OR Master’s + 2 years of Manufacturing Operations experience Alternatively, Bachelors + ...ContratoTrabajo por turnos