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- ...The Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment used in a regulated pharmaceutical environment. This role ensures compliance with cGMP regulations through the planning, execution, and...SugeridoContrato
- ...For Validation services WHAT MAKES YOU A FIT: The Technical Part: Bachelor's in Life Sciences with five (5) years of experience in Validation activities within the Medial Devices Industry. Bilingual: English and Spanish Soft Skills: Great attitude and...SugeridoContratoTrabajo por turnos
- ...improvements Required Qualifications: * At least 2 years of experience in: manufacturing field, pharmaceutical industry * Valid Electrical License * Experience with uninterruptible power systems and emergency power systems * Ability to read HVAC, electrical...SugeridoPago diarioTurno rotativoTurno de nocheFin de semana
- ...3+ proven leadership experience managing or supervising technical teams, preferred Bilingual (Spanish and English), preferred Valid Driver's license, required KNOWLEDGE SKILLS AND ABILITIES Strong background in supporting operations within regulated industries...SugeridoContratistaTrabajar en la oficina
- ...For Validation services WHAT MAKES YOU A FIT: The Technical Part: Bachelor's in Engineering with five (5) years of experience in Validation activities within the Medial Devices Industry. Bilingual: English and Spanish Soft Skills: Great attitude and strong...SugeridoContratoTrabajo por turnos
- ...technical procedures and policies. Negotiates contracts with suppliers and clients. Evaluates managers of the Service, CMC and Validation departments. Organizes, coordinates, and participates in conventions and promotion activities for the company. Provides...SugeridoContratistaTemporalTrabajar en la oficina
- ...Collaborate extensively with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance, and/or validation departments. Work under the direct supervision of project managers to complete design, engineering, and construction projects...SugeridoContratoTrabajo por turnos
- .... Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description Purpose : The Senior Validation Engineer/Analyst functions as the lead for maintenance, engineering, and validation activities within the assigned site/area of responsibility...SugeridoTemporal
- ...of functional and safety testing to confirm proper operation following the upgrade. Key Responsibilities Provide on-site validation support during shutdown and installation activities . Execute IQ and OQ protocols for the new robotic system and associated...SugeridoContrato
- ...AbbVie, please visit us at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The QA Validation Analyst/Engineer is responsible for planning and overall approval of validation tasks. Responsibilities may also include...SugeridoTemporalContrato
- ...requirements, cGMP, and data integrity best practices. Evaluates and closes change control requirements and documentation, assuring the validated and compliant state of the environments. Assist with quality events investigations, internal audits, CAPA, and standalone...SugeridoContratoTurno rotativoTrabajo por turnosFin de semana
- ...voltage electrical systems, demonstrating comprehensive knowledge of electrical infrastructure operation and troubleshooting * Current valid Electrical License (required and non-negotiable for this position) * Proven expertise in building automation systems (BAS)...SugeridoPago diarioContratistaInicio inmediato
- ...Manufacturing Practices (cGMP) and other regulatory requirements. More than 5 years of experience in Equipment and Computer System Validation within pharmaceutical facilities. Experience with digital validation solutions (e.g., ALM or equivalent). Excellent...SugeridoTiempo completoTrabajar en la oficina
- ...inventory analysis to define the scope of remediation across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM) by leveraging automated tools and site-level expertise. This role will ensure data...SugeridoContrato
- ...MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Science or Engineering with five (5) years of experience in the validation life cycle, within the pharmaceutical industry. Bilingual (English & Spanish). Shift: Administrative, and according to business...SugeridoContratistaContratoTrabajo por turnos
- ...PIECE OF FITS, YOU WILL: (The day-to-day on the job) Support IQ/OQ/PQ and process performance qualification activities; develop validation protocols, reports, and master validation plans. Design and develop in‑process and receiving inspection systems for new...ContratoTrabajo por turnos
- ...Performs a variety of routine sample preparation and analysis procedures to support Manufacturing and Quality Operations. Follows validated or experimental analytical procedures with periodic direct supervision. Revision and compilation of results and data comparison against...TemporalTiempo completo
- ...Experience supporting new product introductions (NPI/NPD), including process development, equipment qualification, and process validation. Hands-on experience with risk management (FMEA, hazard analysis), root cause investigations, and CAPA systems. Proven collaboration...ContratoTrabajo por turnos
- ...FIT: The Technical Part: Bachelor’s Degree in Engineering and 5 years of experience in the review and approval of life cycle validation documentation in the regulated industry. Bilingual: Spanish and English Soft Skills: Attention to detail, organization, and...ContratoTrabajo por turnos
- ...bulk biologics products. Perform cleaning and sterilization procedures. Perform process tests and participate in qualification and validation activities as required. Assemble and inspect equipment in the manufacturing area to confirm operational status. Work is performed...TemporalTiempo completoTrabajo por turnos
$20 000 - $27 000 por año
...punctuality and consistency for all scheduled transport QUALIFICATIONS REQUIRED: ~ Strong reliability and punctuality ~ Valid driver’s license ~ Highly organized and detail-oriented ~ Able to follow direction and execute tasks efficiently ~...Tiempo completoContrato- ...regulated industries. ~ Strong understanding of PLCs, SCADA, DCS, and automation systems. ~ Experience with GMP environments and validation processes. ~ Excellent communication and stakeholder management skills. The Personality Part: ~ Picture yourself...Contrato
- ...coordination with project managers & portfolio master scheduler integrating scope, schedule, risk, and resource requirements. Monitor, validate, and report actuals, commitments, and forecasted costs at both project and portfolio levels. Provide root cause analysis for...PrácticaContrato
- ...· Experience supporting new product introductions (NPI/NPD), including process development, equipment qualification, and process validation. · Hands-on experience with risk management (FMEA, hazard analysis), root cause investigations, and CAPA systems. · Proven...Contrato
- ...Documentation: Maintaining accurate and detailed laboratory records and documentation. Method Development: Developing and validating new analytical methods and techniques. Qualifications: Strong analytical, problem-solving, and communication skills....ContratoTurno de tardeTrabajo por turnosFin de semana
- ...United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Responsibilities: Review and audit validation, qualification, and verification activities across manufacturing, packaging, utilities, facilities, laboratories, and systems....Tiempo completoTrabajar en la oficina