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Resultados de la búsqueda: 34 vacantes
- ...Job Title: CSV & Change Control Specialist Location: Manatí, PR Duration: 6‑month initial term (renewable up to 3 years) Position Overview WeilGroup is seeking two seasoned CSV & Change Control Specialists to support the Business Insights & Technology (BI&T)...SugeridoTrabajar en la oficina
- ...Responsibilities: Author, revise, and maintain SOPs and related controlled documents in accordance with regulatory and company standards.... ...document management systems (EDMS), including version control, approvals, and archival. Support internal and external audits...SugeridoTiempo completo
- ...@abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description Purpose Ensures quality control and quality assurance compliance across the manufacturing site. Serves as an integral member of site leadership team with a focus on...SugeridoTemporalTiempo completo
- ...process tolerance evaluation. Process Instrumentation/ Calibration to manage calibration... ...or Electronics. AD, Tecnología de Instrumentación y / o Electrónica. Physical Requirements... ..., or operate equipments, tools, or controls. The employee frequently is required to...SugeridoTiempo completoTurno de mañana
- For Change management services in the manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor in Life Science or Engineering with two (2) years of experience in a biopharmaceutical regulated Industry. Excellent written and verbal skills in both...SugeridoContratoTrabajo 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...SugeridoTiempo completoCASTrabajar en la oficina
- ...services.The resources will work with oversight from the Quality Control Laboratory, Computer System Validation Information Technology... ...Project Management and MS Visio programs. Experienced in Instrument Performance qualification, and method configuration Excellent...SugeridoTiempo completoDe duración determinadaTrabajar en la oficina
- ...Technology (IT), IT/CSV, Manufacturing Validation Team (MT), Quality Control (QC), Environmental Health & Safety (EHS), Engineering /... ...Project Management and MS Visio programs. Experienced in Instrument Performance qualification, and method configuration Excellent...SugeridoTrabajar en la oficina
- ...experience in the pharmaceutical industry or equivalent in an analytical laboratory. • Knowledge and abilities in managing analytical instruments. • Must have previous experience working with: FTIR ID testing • Bilingual preferred What type of environment is this...SugeridoTurno de tardeLunes a viernes
- ...De-trashing, Order processing, and shipping. Second level responsibilities to include, but not limited to the following: Inventory control (FIFO rotation, stock counts, cycle counts and manual monitoring of stock levels and usage). Work stock frequency reports to minimize...SugeridoContratistaTrabajar en la oficina
- ...SOPs, calibration procedures, and policy documentation. Lead corrective and preventive action (CAPA) initiatives and drive quality control improvements. Manage internal and external audits related to calibration and metrology compliance. Supervise lab personnel...SugeridoContratista
- ...in Excel spreadsheet design and validation. The ideal candidate will play a critical role in analyzing data to support our quality control and validation initiatives, ensuring data integrity and compliance with industry standards. Key Responsibilities: Validation: Develop...SugeridoTiempo completo
- ...Bachelor’s degree in Engineering, Computer Systems or related disciplines, combined with at least five (5) years of CSV and Change Control Management within a Pharmaceutical / Biotechnology Environment. Experience in: Change Control Management Reading and...SugeridoContrato
- ...Insights and Technology (BI&T) Department in the following key activities or tasks, such as but not limited to: Develop Change Control records, as required, following Electronic Change Control (e-CC) Procedure for the Manati Site. Perform Computerized System Validation...Sugerido
- ...Decommissioning of a temperature monitor sensor (System and Software), among others. Duties will include: Develop Change Control records, as required, following site Electronic Change Control (e-CC) Procedure. Perform Computerized System Validation (CSV)...SugeridoContrato
- ...set standards ~ Make sure that any loose wires are connected and secured properly ~ Ensure calibration of thermostats and other controls ~ Perform checks on motors and belts and handle lubrication duties ~ Change filters and replace any parts as they wear out...Tiempo completoCASInicio inmediatoFin de semana
- ...job) Evaluate and qualify product and process reworks by approved protocols and regulatory requirements. Review and revise controlled documents (e.g., SOPs, work instructions, protocols, batch records) as part of remediation efforts. Support impact assessments...ContratoTrabajo por turnos
- ...approved protocols and regulatory requirements. Review and revise controlled documents (e.g., SOPs, work instructions, protocols, batch... ...electronic quality management systems (eQMS) and document control tools. Excellent attention to detail, organizational skills...Contratista
- ...Process Development during new product introduction by defining traceability and inspection requirements, developing statistical process control criteria, developing manufacturing instructions, and creating training sheets and certifications. May also train operators on...Por horaPrácticaTemporalTiempo completoTurno de tarde
- ...assessments to support that validated critical operating parameters are within qualified parameters. Support the evaluation of Change Controls to establish qualification assessments and performance qualification requirements during process and/or modifications. Support...ContratoTrabajo por turnos
