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- 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...SugeridoContratoTrabajo 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...SugeridoContratoTrabajo por turnos
- • Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner. • Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions...SugeridoContratoTrabajo por turnos
- To support the installation of several manufacturing solid dosage equipment such as but not limited to: Encapsulator Checkweigher Compression machine Hardness tester Encapsulation machine Auxiliary equipment Main activities should include: Verification...SugeridoContratoTrabajar en la oficina
- Asistir en las situaciones diarias de la empleomanía, brindando soluciones optimas que aporten a su experiencia laboral en La compañia. Contribuir en el compromiso de los empleados y los objetivos de la empresa. Deberes Básicos Los empleados de La compañia tendrán...SugeridoContratoTrabajar en la oficina
- ...Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation activities (Protocols, Tests, Reports). Familiarized with IQ, OQ and PQ validation phases for molds and equipment....SugeridoContrato
- ...qrcgroup.com / to learn more about our services and solutions! Job Description We are seeking a Senior Quality Systems Specialist who will be responsible for supporting and executing the Quality Management System (QMS) Remediation Plan in compliance with...SugeridoContrato
- ...requests from other plants/sites Complete assessment for new or changes in BOM's (Bill of Materials) Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining methodologies in that area. Qualifications: Bachelor's...SugeridoContratoTrabajo por turnos
- ...relevant experience to a new industry, join our team as we help shape a brighter way forward. Sr. Health, Safety and Environmental Specialist JOB SUMMARY: The HSSE Senior Specialist directs the development, implementation, and continuous improvement of the JLL HSSE...SugeridoPago diarioSubcontratista
- ...We are seeking a Quality Assurance Specialist to perform critical QA oversight activities, ensuring compliance with regulatory requirements, internal quality standards, and site procedures. This role requires the ability to work with minimal supervision while collaborating...SugeridoContrato
- This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining...SugeridoTemporal
- ...For Laboratory Validation Specialist services in the Quality Assurance/Validation area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Life Sciences or related discipline and at least two (2) years of previous exposure to laboratory qualification...SugeridoContratoTrabajo por turnos
- ...We are seeking a Specialist QA. The responsibilities include: • Perform On-the-floor Plant Quality Assurance (PQA) review, approval, and tracking of cGMP processes, procedures, testing methods in manufacturing, documents and records, batch record review, MES, EBR,...SugeridoContratistaContratoTrabajo por turnos
- For Validation services in the Manufacturing Operations and Business Process area WHAT MAKES YOU A FIT: The Technical Part: ~ BS in Computer Science, Computer Engineering, Electrical Engineering, or Information Technology and 5+ years of IT experience in pharmaceutical...SugeridoContratoTrabajo por turnos
- ¡Únete a algo grande! ¿Quiénes somos? En Premier no solo protegemos autos, ¡revolucionamos la industria! Con más de 18 años marcando la pauta en el mercado , combinamos la solidez de la experiencia con la energía de la innovación. Aquí no solo resolvemos problemas...Sugerido
- ...remote procedure review; ON ISLAND for startup, inspection, testing, and integrated commissioning REPORTS TO Lead Commissioning Specialist through independent Commissioning Firm EMPLOYMENT Contingent specialist pipeline; compliant independent-firm engagement...ContratistaTiempo completoContratoRemotoTrabajo híbridoTrabajo por turnosFin de semana
- For QA Services in the Drug Substance a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with four (4) years of experience within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. ...Trabajo por turnos
- o Knowledge in document handling on Veeva Vault (CDOCs) or similar platforms o Technical writing expertise o Change control handling (owner) o Project handling o Use of Smartsheet or similar platform Requirements -Doctorate OR Master’s + 2 years...Contrato
- Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico . Administrative Shift Shift: (M-F | 8am to 5pm | OT may be requested...Trabajo por turnos
- Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico . Administrative Shift Shift: (8hrs shift | Availability to work...Trabajo por turnos
- ...for civil, geotechnical, mechanical, electrical, structural, environmental, concrete/pavements/soils, or IT/communications work. Specialists are responsible to the CQC System Manager, must be physically present during work in their assigned area, and perform no duty other...ContratistaSubcontratistaTiempo completoContratoTrabajo por turnosFin de semana
- ...Position Summary: IEM is looking to bring on Full Time- Grants Management Specialist II (GMS II) to join our Homeland Security and Emergency Management team. The Grant Management Specialist II manages the full lifecycle of Public Assistance grants, including application...ContratistaTiempo completoTrabajar en la oficina
- ...Objetivo del Rol Buscamos una Human Resources Specialist con enfoque práctico (hands-on), altamente asertiva, positiva y activa, que gestione directamente todos los asuntos relacionados con el personal. Este rol es clave para mantener una cultura organizacional sólida...Práctica
- For Validation & Qualification services in the Manufacturing and Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Life Sciences or Engineering and previous exposure to Validation and/or Qualification activities within the pharmaceutical...ContratoTrabajo por turnos
- For Quality services in the Manufacturing/Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering or Life Sciences and at least five (5) years of experience in Quality activities within the medical device industry. Bilingual...ContratoTrabajo por turnos
- 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...Tiempo completo
- For Manufacturing Services in the Quality Systems a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with five (5) years of experience as a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project...ContratoTrabajo por turnos
- For Automation services in the Capital Project area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's degree in Engineering, Computer Science, Information Systems, or related field. 5+ years in pharmaceutical operations/manufacturing with project management...ContratistaContratoTrabajo por turnos
- ...PACIV, a global leader in industrial automation solutions servicing the Life Sciences sector, is seeking a IT / CSV Specialist to provide technical support for laboratory applications, systems, infrastructure, and validation activities within a pharmaceutical manufacturing...Tiempo completoHorario flexible
- 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...Tiempo completo