19.02.2015 Views

¿BUSCANDO EMPLEO?

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

• Proficient in cGMP's, OSHA and FDA Regulations as it applies to <br />

pharmaceutical industry. <br />

• Capability to challenge the status quo to simplify work. <br />

INSIGHT RADIOLOGY PUERTO RICO <br />

Enviar currículo vitae con historial de salario a : <br />

InSight Radiology Puerto Rico <br />

P.O. Box 1633, Canóvanas, P.R. 00729 <br />

Fax: 787-­‐256-­‐0437 <br />

BATCH RECORD REVIEWER (Guayama) <br />

• BD Science <br />

• Provides project support with current Good Manufacturing <br />

Practices to clinical supply packaging operations. <br />

• Provides guidance on procedures and training necessary to be in <br />

complete compliance with current GMPs. <br />

• Evaluate all materials, packaging components and master <br />

packaging records and release of them. <br />

• Evaluate all raw materials and packaging components to release. <br />

Identified complex technical problems and provided guidance <br />

and support to quality system development to ensure alignment <br />

with departments. <br />

• Reviewed packaging records. <br />

• Previous experience in similar positions. <br />

COMPLIANCE SPECIALIST (Humacao) <br />

• BD Science <br />

• Minimum five (5) years’ experience in the pharmaceutical <br />

industry for oral dosage manufacturing <br />

• Broad knowledge of cGMP governmental regulations and <br />

guidelines and the ability to interpret and apply them. <br />

• Ability to communicate effectively with the wide range of <br />

personnel, written and verbal <br />

• Fully Bilingual 0Spanish/English) writing and speaking <br />

• Solid technical writing and interpretation skills related to <br />

investigations, process & equipment validations/qualifications, <br />

computer system validations, regulatory filings, and customer <br />

complaints. <br />

• Ability to create/organize cGMP systems and procedures based <br />

on regulatory compliance requirements <br />

• Knowledge to conduct and lead GMP audits (internal and <br />

external) and regulatory inspections <br />

• Computer skills (require using computerized systems) <br />

• Handle multiple task and comply with agreed or established <br />

completion due dates Quality certifications by recognized <br />

organizations is highly desired. <br />

ENVIRONMENTAL TECHNICIAN (Área Este) <br />

• AD or BD Science <br />

• 1 year of experience and Hazwoper 40 hours’ certification. <br />

MANUFACTURING TECHNICIAL (Guayama) <br />

• AD in Technical Degree <br />

• Compression expertise in Dietary Supplements, preferable Fette <br />

compressing machine. <br />

• Performs low level programming and reprogramming of <br />

automated manufacturing systems. <br />

• Controls and adjusts systems under normal and emergency <br />

situations. Execute manufacturing operations such as: weighing, <br />

granulation, compression, capsules filling and other <br />

manufacturing operations in a manufacturing environmen <br />

OFICINISTA DE CONTABILIDAD (PLAZA TEMPORERA POR AUDITORÍA <br />

ANUAL) <br />

Requisitos: <br />

• Mínimo dos años Experiencia en Ciclo Completo de Contabilidad <br />

• Experiencia en Peachtree y Programas de Nómina Electrónica <br />

• Proficiente en Excel, Word y Outlook <br />

• Fully bilingual

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!