Validation Quality Engineer

JobCourier; Mezzovico-Vira; Vor Ort; CHF 80’000 - 100’000; Vollzeit

Zusammenfassung

A leading staffing agency is seeking a Validation Quality Engineer for a temporary position based in Mezzovico, Switzerland. The ideal candidate should have a Bachelor's Degree and at least 3 years of experience in a manufacturing environment, preferably in medical devices or pharmaceuticals. Responsibilities include supporting new product introductions and validating processes to meet regulatory standards. Fluency in Italian and English is required, with German as a plus. This role is expected to last approximately 10 months.

Qualifikationen

• Minimum 3 years of analogous working experience in a manufacturing environment.
• Experience in a highly regulated environment (e.g., ISO13485, MDR).
• Knowledge of Six Sigma and/or Process Validation techniques is preferred.

Aufgaben

• Support New Product introduction.
• Define Process Validation Strategy and oversight validation activities.
• Collaborate on projects for process improvement.

Kenntnisse

Strong organization skills

Self-motivated

Proactive

Strong communication skills

Creative problem-solving

Ausbildung

Bachelor's Degree in technical matter

Jobbeschreibung

Overview

Randstad Svizzera SA

Randstad Inhouse Services (RIS) is an idea created to support companies with a high demand for flexible staffing. It aims to optimize labor flexibility, productivity and efficiency.

For our client, Jabil Switzerland Manufacturing GmbH, we are looking for temporary staff, such as: Validation Quality Engineer

Responsibilities

• Support the team that is dedicated to New Product introduction
• Support Engineering Studies development and execution, define tests strategy and data analysis
• Define Process Validation Strategy and oversight validation activities
• Define Test Method Validation (TMV) Strategy, oversight and document release
• Approval of Process Validation deliverables: Validation Assessment, IQ, OQ, PQ, Validation Plan etc.
• Collaborate to projects for process improvement and automation implementation
• Evaluate process changes as part of Change Management Process and define impact on Process Validation
• Produce reports and presentation to internal and external stakeholders

Your Profile

• Minimum Bachelor Degree in technical matter (Biomedical/Mechanical/Automation engineering)
• Minimum of 3 years of analogous working experience in a manufacturing environment (Medical Device, pharmaceutical, automotive preferred) or an equivalent combination of education and experience
• Experience in a highly regulated environment (knowledge of standards such as ISO13485, CFR 21 part 820, MDR)
• Knowledge of Six Sigma and/or Process Validation techniques in MedTech is preferred
• Fluent to communicate in Italian and English, German is considered as a plus

Your Skills

• Strong organization skills - Rigorous & Disciplined
• Self-motivated/Driven, Capable of working with limited supervision
• Ability to utilize oral communication and technical writing skills to accomplish departmental goals and objectives
• Proactive, Persistent & Resilient
• Strong communication skills at multiple levels of the organization
• Creative: Ability to translate complex situations into simple solutions

Details

The role is based in Mezzovico and could require occasional availability to work on the RARON site. Position will be limited to approx. 10 months.

If you are interested in working for a global company that empowers the brands contributing to global empowerment, please send us your application in English.

Branche: Anderes

Funktion: Anderes