Batch Record Reviewer (7145)

Role Overview

Join a global market leader in the production and process support of active pharmaceutical ingredients across the chemical and biotechnology sectors. This on-site position is located in the Valais area of Switzerland and is offered as a seven-month contract with the option for extension.

Key Responsibilities

• Perform timely and independent reviews of executed electronic batch records (eBRs) within the MES Syncade system.
• Ensure that operations batch records are accurately executed, complete, and ready for QA review.
• Collaborate with Manufacturing and Quality teams to clarify and resolve documentation issues.
• Initiate and support the management of Quality Records, including CAPAs and Deviations, related to Batch Record review observations.
• Support the preparation of documentation packages to enable fast release by QA.

Qualifications and Experience

• Relevant working or residency permit, or Swiss/EU citizenship, is required.
• Previous experience in the GDP and GMP regulated pharmaceutical or API industry.
• Required experience in batch record review (preferred in eBR) or manufacturing.
• Ability to identify non-compliance and gaps from quality standards.
• Very good communication skills and the ability to interact effectively with various interfaces within the organization, demonstrating strong team orientation.
• A structured, focused, and well-organized working attitude.
• Open-mindedness toward new ideas and suggestions, with a solution-oriented approach.
• Agile, highly motivated, and dynamic drive.
• Ability to produce reliable results under stress.