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  • Job title:

    USP Master Production Scheduler

  • Sector:

    Biotechnology, Pharmaceutical

  • Job ref:


  • Start Date:


The Company

Our client is the leader in the field of biomedicines. Through the dynamic science of biotechnology, they continue to seek innovative ways to treat cancer, infectious diseases, cardiovascular and metabolic diseases, and immune-mediated inflammatory disorders.


Role Description

In this position you will be responsible for representing Operations on New Product Introduction Tech Transfer, ensuring manufacturing readiness for the NPI, and monitoring process and equipment issues.



- Monitoring and troubleshooting the manufacturing process, equipment issues and process optimization

- Investigating and resolving issues raised within the Manufacturing department

- Leading/supporting Commissioning and Qualification activities

- Preparation of Batch Records, Procedures, and Work Instructions

- Supporting validation activities



- BSc/MSc in a relevant field (Microbiology, Biochemistry, Pharmacy, Engineering)

- Min. of 2 years of working experience in a GMP environment

- Experience in cell culturing or purification process is a must

- NPI experience is a big plus

- Process Engineering/commissioning and qualification is an advantage


Other information

Are you interested and do you want to apply for this role, please fill out your application via the apply button below and contact Camila Castro.