NR01-022023 Validation Specialist� (Packaging)

Veg Group; Paraná; Presencial; BRL 80.000 - 100.000; Tempo integral

Resumo da oferta

A leading services supplier for the pharmaceutical industry is seeking a Validation Specialist in Brazil. Ideal candidates should have a Bachelor's degree in Science or Engineering, at least 5 years of experience in the pharmaceutical, medical device, or biotechnology sectors, and be fully bilingual in English and Spanish. The role demands strong skills in MS Windows and Microsoft Office, along with a deep understanding of cGxP and regulatory guidelines. Candidates will work in a dynamic environment dedicated to quality and compliance.

Qualificações

• 5+ years of experience in direct pharmaceutical, medical device, or biotechnology industries.
• Strong knowledge in cGxP and regulatory guidance, GAMP 5.
• Experience in System Development Life Cycle Documentation.

Conhecimentos

Bilingual (English / Spanish)

MS Windows proficiency

Microsoft Office applications

Knowledge in cGxP

Regulatory guidance (GAMP 5)

Formação académica

Bachelor's Degree in Science or Engineering

Descrição da oferta de emprego

Career Opportunities with Validation & Engineering Group

A great place to work.

Current job opportunities are posted here as they become available.

NR01-022023 Validation Specialist (Packaging)

Validation & Engineering Group, Inc.(V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

• Validation Specialist (Packaging)

Qualifications

• Bachelor's Degree in Science orEngineering.
• 5+years of experience in direct pharmaceutical, medical device. or biotechnology industries.
• Must be fully bilingual (English / Spanish) with excellent oral skills.
• Must be proficient using MS Windows and Microsoft Office applications.
• Strong knowledge in cGxP and regulatory guidance,GAMP 5.
• Experience in System Development Life Cycle Documentation i.e. URS, VP, DS, TM;RA, DI, IQ, OQ, PQ.
• Qualificationprotocols development and execution, deviations and reports generation.