Our client, a major player in the pharmaceutical sector, is looking for an expert to drive the digital transformation of their laboratory environments. The role focuses on developing and integrating electronic laboratory notebooks to automate data flows between bioreactors, chromatography systems, and central databases.
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Our client, a leading pharmaceutical organization, is seeking a senior professional to lead validation and planning efforts for major capital projects. This role focuses on ensuring rigorous compliance with international quality standards while managing project lifecycles, product introductions, and technical coordination between departments.
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Our client, a leading pharmaceutical and medical device organization, is seeking a Project Engineer to provide technical, scientific, and project-driven support for manufacturing operations. The role focuses on leading technical improvements and sustaining on-market products through product change management and risk assessment activities.
Design, implement, and validate digital systems that support GMP manufacturing, ensure data integrity, and enable efficient, compliant operations across life sciences environments.
MES Consultant – Implement and optimize MES to support efficient, compliant manufacturing.
CSV Consultant – Validate GxP systems and ensure regulatory-compliant digital solutions.
MES Specialist – Configure and maintain MES to support production operations.
MBR Editor – Create and update accurate electronic batch records.
MBR Designer – Design structured, compliant electronic batch workflows.
MBR Reviewer – Review and approve electronic batch records for accuracy.
Master Batch Editor – Maintain and update Master Batch documentation.
Master Batch Reviewer – Ensure GMP-compliant batch record quality.
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