This training provides an overview of the operational standards and quality requirements of the biopharmaceutical industry. During the training, you will learn to understand the significance of industrial logic from the perspective of product safety and the quality of commercial laboratory services, and how these requirements can be applied in practice when transitioning into professional roles.

Notice that the training is a pilot and exclusively for Loimu members only. It can be further developed according to the observations from the feedback. 

Learning methods and practices

Hybrid Short-Course (2 x Live Online Masterclasses + 1 Practical Assignment)

Target Audience

Loimu members (recent graduates or transitioning professionals) struggling to bypass Applicant Tracking Systems (ATS) and secure interviews in the European pharma/biotech sector. Maximum number of participants is 30.

Price

40 € (discount price 20 € for students, unemployed, on family leave, on grant)

Trainer 

Swarnendu Ghosh, MSc (biomedicine, University of Eastern Finland) is an active industry expert specializing in commercial Good Manufacturing Practice (GMP) and Quality Assurance within the European gene therapy and biotechnology sector. See further details from Trainer.

Schedule: See further details from Program

• Tue May 12th at 3.00-5.30 pm Module 1: The Cleanroom Reality & Industry Mindset (Live 2.5-Hour Digital Masterclass via Teams)
• Tue May 19th at 3.00-5.30 pm Module 2: Practical Application & The ATS CV Pivot (Live 2.5-Hour Digital Masterclass)
• Module 3: The "Industry-Ready" Assignment (Independent Work)

Location: Teams. There will be an AI translation of speech and slides available, so the language can be translated e.g. to Finnish. AI translation is provided to make sure an easier understanding for all participants. 

Loimun GDPR statement for trainings: https://www.loimu.fi/en/privacy-policy/privacy-policy-for-events-and-training/