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- ...America. Responsibilities: 1. Performs all functions listed below with direct supervision. 2. Perform activities related with Documentation according to project assignment, customers’ needs and requirements and in compliance with cGMP’s and Safety procedures 3....SugeridoTiempo completo
- ...Responsible for managing and maintaining the project's official document-control system, including drawings, contracts, change orders, reports, permits, revision records, and documentation required for audits and reimbursements. Key requirements: * Associate...SugeridoTrabajar en la oficina
- ...Manufacturing Support Specialist to support manufacturing operations by managing controlled documentation, coordinating Engineering Change Orders (ECOs), and assisting with... ...areas with the implementation of document changes through Engineering Change Order (ECO...SugeridoContratoTrabajar en la oficina
- ...quality procedures . Key Responsibilities Develop and execute IQ, OQ, and PQ protocols . Author and review validation documents, including: Validation Plans URS Risk Assessments Traceability Matrices Validation Summary Reports (VSR) Validate...SugeridoTiempo completo
- ...preventive maintenance forms. Development and approval of GxP and automation impact assessments. Provide alternatives to resolve documentation situations. Establish project communication and documentation controls. Assure consistent quality of activities that meets...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
- ...on the job) 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...SugeridoContratoTrabajo por turnos
- ...in the Manufacturing area. FITS is looking for a Validation Specialist to support a leading pharmaceutical manufacturer. You’ll be... ...equipment and washers in a qualified state through accurate, well-documented protocol execution. If you’ve spent years in the field running...SugeridoContratoTrabajo por turnos
- ...What Makes You A Fit: FITS is looking for a Manufacturing Specialist to support a leading biotechnology manufacturer. This is a hands... ...or initiatives As a Piece of FITS You Will Serve as document owner, keeping manufacturing procedures aligned with current operations...SugeridoContratoTrabajo por turnos
- ....com / to learn more about our services and solutions! Job Description We are looking for a qualified Jr. Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing: Validation protocols. Validation...SugeridoContrato
- ...Responsible for executing and documenting procurement activities involving construction, equipment, materials, and professional services while ensuring compliance with project policies and applicable federal requirements. Key requirements: * Bachelor...SugeridoContrato
- ...Possess excellent writing skills that include closing the gap between a highly technical investigation into a simple and concise document that can be understood by non-technical reviewers. Communication and escalation of complaints, site representation on the product...SugeridoContratoTrabajar en la oficinaTrabajo por turnos
- ...YOU A FIT: FITS is looking for a C&Q Specialist to support a leading biotechnology... ...enjoy hands-on testing and take pride in documentation that holds up to any review, this role... ...utilities Experience with electronic document, training, and project systems such as...SugeridoContratoTrabajo por turnos
- ...operation as the owner of supplier change control. In this role, you’ll ensure every change to a raw material or component is assessed, documented, and implemented correctly, and you’ll manage supplier-related non-conformances and CAPAs through closure. The Technical Part:...SugeridoContratoRemotoTrabajo por turnos
- ...experienced Computer System Validation Specialist to support validation and... ...validation, implementation, testing, and documentation . Key Responsibilities Support... ...Develop and execute test scripts and document test results, deviations, and exceptions...SugeridoTiempo completoHorario flexibleTrabajo por turnos
- ...Responsibilities: 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...Trabajo por turnos
- ...of cGMP manufacturing processes, procedures, testing methods, documents, and production records . Review and approve batch... ...deviations and quality events are properly triaged, investigated, documented, and resolved in accordance with procedures and cGMP requirements...ContratistaContratoTrabajo por turnos
- ...REQUISITION FBMG-009 CSS CAM LCAT 8A - Program Support Specialist (nonexempt administrative) DUTY LOCATION Fort... ...specification revisions, correspondence, meeting records, closeout documents, and the site document repository. The role supports CQC certification but does...ContratistaSubcontratistaTiempo completoContratoTrabajar en la oficinaRemotoTrabajo por turnosFin de semana
- ...process development, and quality. Proficiency in GDP (Good Documentation Practices) on a regulated environment. Knowledge in... ...Ensure all procedures reflect current operations. Serve as a document owner. Assess process performance by observation of floor...Trabajo por turnos
- ...Ensure all procedures reflect current operations. Serve as a document owner. Assess process performance and review of performance... ...changes in BOM's (Bill of Materials) Serves as a peer-recognized specialist in at least one area, with overall responsibility for...ContratoTrabajo por turnos
- ...Position Summary: Responsible for supporting manufacturing operations through technical investigations, process monitoring, documentation review, and continuous improvement initiatives within a regulated biopharmaceutical environment. The role requires collaboration...Contrato
- ...Responsibilities: Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under appropriate federal regulations. Coordinates activities with clients,...Trabajar en la oficinaTrabajo por turnos
- ...AUTOCAD SPECIALIST Ponce, PR | Full-Time | Hourly Create Precise Drawings. Support Critical Inspections. At Scientific Safety... .... • Prepare drawing packages, tables, and supporting documentation for final client reports. • Maintain organized drawing files...Tiempo completo
- ...Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description Validation Specialist with experience in regulated industry validating/qualifying laboratory equipment, manufacturing equipment, processes, utilities and...Contrato
- ...QualityReviews (PQR), Drug Master Files (DMF) or any other regulatory document to assure compliance and proper documentation according to... ...Industry with at least 2 years as Regulatory / Compliance Specialist ~ Willing to work irregular and/or extended shifts if needed...ContratoTrabajar en la oficinaTrabajo por turnos
- ...2 + years of experience in HSE roles, preferably in a plant or industrial setting. ~(Optional) Experience working as an HSE Specialist with ISO 14001 & 50,001 International standard certifications , PROSHA VPP Programs, in a industrial manufacturing environment....Tiempo completoVisa de trabajoLunes a viernes
$18 - $21 por hora
...Job Title: Collection & Risk Mitigation Specialist Employment Type: FLSA hourly non-... ...reviewing transactions and supporting documentation, identifying potential recovery... ...organizing complex information into clear, well-documented cases that support effective recovery...Por horaTiempo completoTrabajar en la oficina- ...We are seeking a SAP Implementation Support Specialist to support the deployment of SAP within a regulated medical device manufacturing... ...(production, quality, warehouse) Create compliant documentation: Work Instructions (WIs), SOPs Job aids and training materials...ContratoTrabajo por turnos
- ...Ensure all procedures reflect current operations. Serve as a document owner. Assess process performance and review of performance... ...changes in BOM's (Bill of Materials) Serves as a peer-recognized specialist in at least one area, with overall responsibility for...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