Ingeniero De Control De Calidad

Jero Management Group Inc

Lugar de Empleo: Ceiba Norte Industrial Park, Juncos
Número de Vacantes: 1
Sector: Ingeniería / Tecnicatura
Rango de Edad: Entre 30 y 50
Género: Indistinto
Nivel de Educación: Universitario (Graduado)
Idioma Requerido para el Empleo: Inglés
Años de Experiencia: 7
Tipo de Puesto: Contrato

Descripción del Empleo:
Quality Engineer (QE) - The candidate will be able to adapt quickly to changing priorities and manage multiple projects simultaneously while ensuring that every product and service we supply conforms to FDA and Quality Systems Regulation (QSR). The QE will work as part of a core team supporting production and new product introduction activities. The QE will create processes and process improvements to ensure consistent implementation of internal requirements and external regulations and standards. The QE will liaise with customers to align product specifications, manufacturing procedures, test methods, and acceptance criteria. The QE will also ensure that products satisfy customer needs through design control activities, process validation, risk management, and the use of statistical methods. Essential Duties and Responsibilities include, but are not limited to, the following: • Participate as a key member of new product development to ensure quality plans, specifications, manufacturing/test procedures, risk and validation documentation are established. • Participate in design control activities, including design reviews • Evaluate processes and technologies for reliability, capability, consistency and cost effectiveness • Design and develop instructions and forms for recording, evaluating, and reporting quality data • Independently design and execute experiments. • Develop validation protocols for manufacturing equipment and processes; evaluate data and write reports • Assist in design transfer activities of new products • Interface with suppliers to improve or resolve quality issues • Identify and implement improvements to promote product quality and manufacturability Education, Experience and Qualifications: • Requires a BS in Engineering with at least 7 years of experience in the Pharmaceutical Industry, preferable on Medical Devices. • Candidates must have excellent verbal communication and technical writing skills on both: English and Spanish. • Proficient in Microsoft Word, Excel and Power Point. • Ability to plan and manage own work.

Fecha de Publicación: 02 de Mayo de 2014

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