This job offer is not available in your country.

Manufacturing Risk Control (Contract)

Bayer (Schweiz) AGCimanggis, Jawa Barat, Indonesia

3 days ago

Job description

Overview

PURPOSE

This position is responsible for supporting GMP compliance and digital operational excellence in the Manufacturing Business Unit by executing core manufacturing operations and documentation activities. The key role is to drive value realization from Manufacturing Execution System with a risk-based approach, to ensure consistent and rigorous application across end-to-end process.

Responsibilities

Act as Subject Matter Expert (SME) of MES processes and from a computerized system point of view.
Ensure implementation and documentation of MES-related activities.
Continuously improve MES based on business needs which includes defining requirements, app builders and equipment connectivity, leading User Acceptance Tests, and contributing in CSV.
Manage collaboration and alignment with multiple stakeholders regarding MES requirement definitions with relevant stakeholders.
Maintain MES-related documents, including Functional Specification, Configuration Specification, and MES rollout Playbook.

Qualifications

Education : Bachelor’s degree in Computer Science, Engineering, or Pharmacy.

Experience : Minimum 2 years of experience in a manufacturing environment, with at least 1 year in application or IT infrastructure projects.

Experience in leading projects and project management.

Strong knowledge of pharmaceutical manufacturing processes in a GxP-regulated environment.

Experience with Tulip and Inmation platforms is an advantage.

Skills & Competencies

Strong analytical thinking.

Self-motivated and driven.

Good communication skills.

Ability to work independently and in a team.

Experience / knowledge in managing multiple stakeholders.

Communication

Fluent in English, both verbal and written.

#J-18808-Ljbffr

Create a job alert for this search

Manufacturing • Cimanggis, Jawa Barat, Indonesia