Resultados de la búsqueda: 296 vacantes
...For Documentation Support services.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree with 3-5 of experience in document control within the Pharmaceutical or Medical Device industry.
Bilingual, Spanish and English
Shift: Administrative and according...
...Responsabilidades:
Recopilar documentos, informes y métricas para evaluar el cumplimiento de los estándares operacionales.
Generar informes de planes y estatus de procesos departamentales para el Gerente de Cumplimiento y Calidad.
Realizar auditorías sobre el...
...Canada, and South America.
Responsibilities:
Review contractor's Job Hazard Analisys.
Review contractor's qualification documents
Inform any deviation on SOP’s from Project Engineering and EHS Departments. Support in the implementation of health and safety...
...between a highly technical investigation into a simple and concise document
The Personality Part:
~ Complaints…. Everybody has one,... ...depending on the nature and complexity of the complaint, the specialist may be responsible of conducting and documenting the...
...preferably experience with Minitab
Ability to speak, write and understand English to comply with written procedures, instructions, SOPs and other documents
Works with minimum supervision.
**Weil Group is proud to be an Equal Employment Opportunity Employer**...
...We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
~Document Control Representative
The Document Control Representative will play a critical role in maintaining and organizing...
...for businesses.
The Cybersecurity Risk & Incident Response Specialist is responsible for the information security analysis,... ...information security risk management program.
Analyze and document each alert received to identify the existence of any intrusion...
For Quality services in the PQA area
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree with five (5) years of directly experience as Quality Professional in the regulated industry.
Bilingual (English & Spanish)
Project Management skills
Shift...
...cGMP processes, procedures, testing (methods) in manufacturing, documents and records, batch record review, MES, EBR, SAP, Trackwise;... ...that deviations from established procedures are investigated and documented per procedures
• Ensures that production records and testing...
...dynamic and forward-thinking team, we are on the l
Job Description:
We're in search of a highly skilled Performance Marketing Specialist with expertise across multiple channels, particularly Google Ads, Facebook Ads, GetApp, Capterra, and SourceForge. The ideal...
...America.
Responsibilities:
Participates and support all activities related with documentation store, supply, etc.
Administers the electronic documentation system (check in, document/CRs release, and controlled documents issuance).
Qualifications Requirements/...
...have established a Quality Management System which provides a framework for measuring and improving our performance. Compliance Specialist 2018 2 Job Description GIDEP).
Act as a point of contact for customers, suppliers, and internal employees with regard to all contracts...
Our Client is looking for a highly motivated, organized and energetic Recruiter to join our team in our Puerto Rico office. The Recruiter will research, develop and implement effective recruiting and staffing strategies to attract a diverse pool of qualified talent for...
...Review and approval of Electronic Batch Records and related documentation to support Drug Substance Disposition Process. • Performs SAP... ...deviations from established procedures are investigated and documented per procedures • Collaborates cross functionally as needed to...
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...
...fields.
Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description
CSV Specialist for validation of laboratory instruments with LIMS connection (HPLC, Gas Chromatographer, Instron pull testers)...
mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services...
...Validation Specialist with experience in regulated industry, validating/qualifying laboratory equipment, manufacturing equipment, processes, utilities and facilities.
Tasks:
Execute complete validation cycle
Change Control
Equipment qualification (manufacturing...
...Expertise
1. Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
2. Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and...
...CSV Specialist for laboratory equipment.
Skills:
Laboratory instruments qualification
Validation Cycle
Requirements
Bachelor Degree in Science
At least 5 years of experience in related area
Biligual (Spanish/English)
Technical Writing...
