NR01-061322 Engineer

Veg Group; Paraná; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading services provider is seeking qualified individuals in Brazil to support drug substance operations related to manufacturing and quality systems. Ideal candidates will have a background in engineering and experience in bio-processes. Responsibilities include organizing and analyzing operational projects while adhering to the highest ethical standards. This is a great opportunity to contribute to the pharmaceutical and biotech industries.

Qualificações

• Education background in Engineering.
• Experience in the development and/or manufacturing of bio-processes.
• Working knowledge of pharmaceutical/biotech processes.

Responsabilidades

• Support Drug Substance operations and manufacturing systems.
• Organize and analyze operational issues or projects.

Conhecimentos

Engineering background

Experience in bio-processes

Knowledge of pharmaceutical processes

GMP production operations

Regulatory interactions

Technical writing

Project management

Control charting

Formação académica

Degree in 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.

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

We are seeking talented, dedicated individuals who are committed to work under the highest standards of ethics and possess expertise in the following areas:

Support Drug Substance operations and applicable execution of manufacturing/quality systems such as design of operations and system requirements, procedures, deviation investigations, process monitoring, training, and new product introductions. Organizes, analyzes and presents interpretation of results for operational issues or projects.

Qualifications

• Education background in Engineering
• Experience in the development and/or manufacturing of bio-processes
• Working knowledge of pharmaceutical/biotech processes
• Skilled in performance of GMP production operations
• Regulatory knowledge and interactions
• Organizational, technical writing and presentation skills
• Project management skills
• Knowledge of control charting and basic statistics