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- ...For Process Validation services in the manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's in Life Science or Engineering with five (5) years of experience in Process Validation activities within the Pharmaceutical Industry. Excellent...SugeridoContratoTrabajo por turnos
- ...For Validation services in the Manufacturing areas. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and at least four (4) years of exposure to Validation Engineering activities within the Pharmaceutical or Medical Devices industry....SugeridoContratistaContratoTrabajo por turnos
- ...Job Description Purpose Describe the primary goals, objectives or functions or outputs of this position. The Senior Validation Engineer/Analyst functions as the lead for maintenance, engineering, and validation activities within the assigned site/area of responsibility...SugeridoTemporalTiempo completo
- ...Validation Specialist — Equipment Location: Barceloneta, Puerto Rico (On-site) Shift: Day (7:00 a.m. – 5:00 p.m.) Start: ASAP Role Overview Execute and support validation for new and existing equipment , partnering closely with Construction, Utilities...SugeridoTrabajar en la oficinaInicio inmediatoTurno de mañanaTrabajo por turnos1 día a la semana
- ...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...SugeridoContrato
- JOB DESCRIPTION Responsibilities may include the following and other duties may be assigned. Provides technical and sustaining engineering support in a manufacturing area. Recommends and implements equipment and process modifications to meet quality standards and improve...Sugerido
- ...contractors) to accomplish the requirements established by our customers, to perform and provide a highly effective service. The Validation Engineer will support Validation/Installation activities in a Medical Devices manufacturing environment. Minimum Requirements:...SugeridoContratistaTiempo completoContrato
- For Packaging services in the Engineering area WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering with five (5) years of Engineering experience within the pharmaceutical or medical device industry. Bilingual (English & Spanish). ...SugeridoContratoTrabajo por turnos
- ...contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Perform and/or review process validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV] (not laboratory...SugeridoTemporalTrabajo por turnosFin de semana
- Validation Engineer – Job Requirements Education & Certifications • Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical, Biomedical, or related field). • Advanced degree or professional certifications (e.g., Six Sigma, ASQ, CQE) is a plus. Technical...SugeridoHorario flexible
- ...For Validation services in the Global Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Life Sciences or Engineering (preferrable)and at least eight (8+) years of experience in the execution of facility/utility protocol within...SugeridoContratoTrabajo por turnos
- ...English & Spanish). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert: Risk-based qualification methods (ASTM E 2500) for pharmaceutical manufacturing equipment and utilities Sterilization...SugeridoContratoTrabajo por turnos
- Qualified resources must have packaging engineering experience with knowledge of carton and blister packages that have background to propose changes to the materials, improve technically the designs, evaluate 2 nd supplier projects for packaging, execute troubleshooting...SugeridoContratoRemotoTrabajo híbridoTurno de mañana
- ...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...SugeridoContratoTrabajo por turnos
- ...Position Overview Weil Group is seeking a Laboratory Equipment Validation Specialist to support the qualification and validation of Quality Control (QC) laboratory instrumentation, with primary responsibility for the Thermo Scientific™ Nicolet™ FTIR system . The...Sugerido
- ...Description With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance...
- Description: Perform, Qualification life cycle. Protocol & Report Change Control Generation Troubleshooting Experience in GMP workplace. Experience in Manufacturing and Packaging equipment.Contrato
- ...withbusiness requirements ensuring implementation of sustainable solutions. Essential Duties and Responsibilities Perform periodic validation exercises to ensure data and operational process integrity. Alert of changes in trends, behavior, or productivity levels....PrácticaTiempo completoPatrocinio de visaInicio inmediatoTrabajo híbrido
- ...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...Tiempo parcialContrato
- ...jornada parcial; * Descripción de deberes y naturaleza del trabajo; Toda certificación de empleo está sujeta a verificación y validación, antes del proceso de selección final. * Se adjudicará puntuación adicional a la nota obtenida por concepto de Preferencia de...Tiempo completoTrabajar en la oficina
- ...experience working as a Pharmacist; or any combination of education and experience, which would provide an equivalent background. * Valid Registered Pharmacist license required. Preferred Skills, Capabilities and Experiences: * Minimum of 5 years of experience...TemporalTiempo completoTrabajar en la oficinaInicio inmediatoTrabajo híbrido
- ...scheduled along with appropriate line clearance procedures to meet cGMP compliance. · Ensure that batches are manufactured within the validated set up at all times and the quality team are provided with samples for outgoing testing throughout the batch. · Lead area 5S...Trabajar en la oficinaInicio inmediatoTrabajo 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
- ...Automation specifically tailored to pharmaceutical or biotechnological manufacturing. Solid background in Computerized Systems Validation (CSV) , ensuring systems comply with GAMP 5 and 21 CFR Part 11 requirements. The Personality Part: ~ Our Next Piece is...ContratoTurno rotativoTrabajo por turnosFin de semana
- ...Nutanix, VMware, Microsoft Hyper-V, or others) * Design, implement and maintain comprehensive BCDR frameworks * Establish and validate world-class recovery metrics * Manage cloud-based failover environments for disaster scenarios across global regions....Tiempo completoTrabajo híbrido
- ...Summary: Prepare and validate load files to support conversion and testing. Understand payroll system integrations to and from multiple vendors and sources. Key Responsibilities: Analyze, audit, reconcile, and resolve complex payroll processing and employee...Contrato
- ...highly effective service. The Microbiologist will support microbiological testing, environmental monitoring, and sterilization validation activities within a Medical Devices manufacturing environment. This role involves ensuring compliance with regulatory standards,...ContratistaTiempo completoContrato
- ...problems in an accurate and prompt manner. Manage incoming calls and referrals from other departments, also generating outbound calls to validate customer transactions when necessary. Essential Duties and Responsibilities • Provide exceptional customer service by...PrácticaTiempo completoPatrocinio de visaTrabajar en la oficinaInicio inmediatoTrabajo híbridoTrabajo por turnosLunes a viernes
- ...understanding fractions and percentages * Strong verbal and written communication skills * Basic computer skills * Must have a valid Driver's License and acceptable driving record * Ability to travel locally and overnight You'll thrive at IPS if you... *...ContratistaTurno de nocheHorario flexibleFin de semana
- ...environment. The ideal candidate will have 2–4 years of experience, with knowledge in nonconforming product handling, SPC, process validation, and quality documentation. Employment Type: Full-Time (On-site) Shift: 1st and 2nd Shift Schedule: Must be able to work...ContratistaTiempo completoTurno de tardeTrabajo por turnosFin de semana