- ...EHS Specialist Are you passionate about construction safety and creating a workplace where everyone goes home safely? We are seeking... .../Tagout. Maintain accurate safety records, training documentation, inspections, and equipment certifications. Represent the...SugeridoTiempo completoTrabajar en la oficina
- ...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
- ...enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities Perform general document control and administrative support activities in an office environment. Review, organize, and maintain documents and records....SugeridoTemporalTrabajar en la oficina
- ...For Senior Microbiologist Specialist services in the Laboratory area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's... ...Laboratory procedures. Prepare and approve technical reports documenting investigation findings, qualification activities, and...SugeridoTiempo completoTrabajo 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...SugeridoTrabajo 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...SugeridoContratistaContratoTrabajo por turnos
- ...South America . Position Summary We are seeking an EHS Specialist to support environmental, health, and safety compliance... ...damage events. Ensure follow-up actions are completed and documentation is maintained properly. Conduct, coordinate, and track EHS...SugeridoTiempo completo
- ...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...SugeridoContratoTrabajar en la oficinaTrabajo 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...SugeridoContratistaSubcontratistaTiempo completoContratoTrabajar en la oficinaRemotoTrabajo por turnosFin de semana
- ...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
- ...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
- ...manufacturing procedures. -Provide process troubleshooting support. -Participate in the NPI process to assess requirements for documentation, materials, training. -Assist manufacturing change owner on CCRB packages impacting the process -Participate in the...SugeridoContratoTrabajo por turnos
- ...Support equipment installation, qualification, process validation, and implementation activities. Develop and maintain process documentation, procedures, and technical reports. Participate in investigations, troubleshooting, root cause analysis, and corrective/...SugeridoTemporal
- ...talented, dedicated individual committed to work under the highest ethics standards for the following position: Talent Acquisition Specialist I This is an on-site position at Guaynabo, PR. Description: Handle hiring requests including: Collecting the...SugeridoTiempo completo
- ...Computer System and Equipment Validation. Risk Assessments and Change Control. KNEAT, CDOCS, Scada, Trackwise, Maximo. Documents revision and approval. T he Personality Part: ~ Picture yourself in a lab… with all the equipment you need to put your...SugeridoContratoTrabajo por turnos
$1 - $2 por año
...monitoring, Wireshark, SNMP, ping, and traceroute You will also have the opportunity to *support and develop our Tier 1 team*, document solutions, and escalate complex issues to Network Engineering (Tier 3) or equipment vendors when necessary. *What are we looking...Tiempo completoTrabajar en la oficinaRemotoTrabajo por turnosFin de semanaLunes a viernes- Inteldot has over 15 years in the life sciences industry, with operations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico. Administrative Shift Job Description: Under minimal ...Tiempo completoTrabajo por turnos
- ...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....Contrato
$17 - $20 por hora
Responsible for executing, monitoring, and training inventory best practices and standard operating procedures for the entire store, including both front end and pharmacy. Supports pharmacy inventory management activities, including receiving, counting, ordering, and facilitating...Tiempo completoTurno de tardeTrabajo 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
- ...our services and solutions! Job Description We are seeking a Sr. Specialist QA with experience in Commissioning and Qualification, Equipment validation, QRAES, Kneat, Good Documentation Practices, Change Controls, SOP’s etc Qualifications Education:...Contrato
- ...Supports and assists in the trouble shoot of projects and equipment as required. Also assists validations process. Completes all documentation and reports on a timely basis as required (daily, weekly, monthly and annually). Keep and develop strong working team,...TemporalInterinoTrabajo 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
- -Manufacturing Operation experience, (not quality) -Document Management, create new documents, review and approval of documents. This resource must work with manufacturing operators Requirements -Doctorate OR Master’s + 2 years of Manufacturing Operations...ContratoTrabajo por turnos
- ...We are seeking a Specialist QA with GMP manufacturing experience in Quality Assurance, including review and approval of change controls, deviations, CAPAs, protocols, reports, and procedures. Experience supporting packaging/inspection operations, strong knowledge of...Contrato
- ...( A summary of the purpose of the position) Our Compliance Specialist will perform administrative tasks to ensure all compliance functions... .... Generate product certificate of compliance or test documents for required customer orders. Work with all necessary internal...Tiempo completoContratoTrabajar en la oficina
- ...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
- ...cGMP processes, procedures, testing methods in manufacturing, documents and records, batch record review, MES, EBR, SAP, EDMQ, DQMS, Trackwise... ...deviations from established procedures are investigated and documented per procedures and ensure on-the-floor triage is completed,...ContratistaTiempo completoTrabajo por turnos
- ...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...ContratoTrabajar en la oficinaTrabajo por turnos
- ...Description We are seeking a SAP Implementation Support Specialist to support the deployment of SAP within a regulated medical... ...(production, quality, warehouse) Create compliant documentation: Work Instructions (WIs), SOPs Job aids and training materialsm...ContratoTrabajo por turnos
Empleos de Document specialist en Puerto Rico
357 vacantes