Accessibility links Skip to main content

Just graduated! Ready for a career in the pharmaceutical industry?

A year ago, I graduated from KU Leuven with a Master’s degree in Biomedical Sciences. I’d always been told it was “very valuable” and that “it would open up many opportunities for you later on!” One of the options mentioned was a job in the pharmaceutical industry, but what exactly would that entail, and how well did my degree prepare me for it?

Contact us

Fill out the form and we will contact you shortly.

Naam
Privacy Policy 
Continue reading

After a message from Inge on LinkedIn, a few pleasant conversations followed, and I decided to join Farma Consulting & Partners as a consultant in the pharmaceutical and medical devices industry. I was welcomed with open arms, and within a few weeks, I started my first project with a smaller distributor of medical devices. I now work for one of the major players in the pharmaceutical industry, which shows that Farma Consulting gives you the opportunity to explore various fields and further develop your interests.

After working there for a few months, I can summarize …

…what you do learn in college:

  • Broad background knowledge, including the basics of quality management, the steps drugs go through before they reach the market, what pharmacovigilance entails, research techniques, biochemistry, etc.;
  • Critical thinking;
  • Collaboration;
  • Planning and meeting deadlines;
  • Presenting;
  • Processing large amounts of material and, therefore, quickly acquiring new knowledge.

…what your degree doesn’t prepare you for:

  • Knowledge of the organizational structures of pharmaceutical companies, e.g., which departments and roles are involved;
  • What a quality system actually entails;
  • What a quality system might look like, e.g., what software is used to manage documents;
  • Industry-specific terms and abbreviations;
  • Project planning in collaboration with a client.

Of course, a degree can never fully prepare you for the real-world work environment; it’s more of a ticket to get you started. When you begin your career, you’ll always need to keep learning and familiarize yourself with specific areas of work.

Fortunately, Farma Consulting & Partners is a company where this is possible! In my third week, I already had the opportunity to take Allanta’s ISO 13485:2016 training, focused on quality management systems in the medical device industry. But you can also always turn to your colleagues and Olivier for explanations or examples, which allows you to learn even more on the job.

So, if you’d also like to work in the pharmaceutical or medical device sector, at a growing company where you’ll have plenty of opportunities, don’t hesitate any longer—get in touch with someone on our team!

About the author:


Sofie holds a Master’s degree in Biomedical Sciences and supports our clients in the medical device and pharmaceutical sectors.

Your partner in quality, safety, and compliance

The life sciences sector requires specialized knowledge and reliable guidance. Thanks to our extensive expertise, we help organizations comply with laws and regulations, ensure quality, and continue to innovate with confidence.

Related Services

Medical Team Performing Surgical Operation in Bright Modern Operating Room

Quality Management System (QMS)

Program and Project Management

Related Articles

10 Jul 2026

Project Management

In the complex and highly regulated world of the pharmaceutical industry, project management plays a pivotal role to bring life-saving medications and treatments to the market. From drug discovery to clinical trials and regulatory approval, effective project management is essential for managing timelines, resources, and compliance. Let’s dive in some practical tips and tricks specifically for navigating the complexities of project management in the pharmaceutical sector.

10 Jul 2026

Potential Pitfalls in an MES Project

Just as every project has its pitfalls, the same is true for a Manufacturing Execution System (MES) implementation project. Implementing electronic batch records is no easy task. That’s why, in the blog below, we’ll share a few pitfalls so you can prepare for a successful implementation within your company.

10 Jul 2026

Streamlining Post-Marketing Surveillance with IMDRF Coding

Since the implementation of the Medical Device Regulation (MDR) in Europe, companies have had to maintain and execute a post-marketing surveillance (PMS) procedure. This systematic process involves collecting and analysing data on the performance and safety of medical devices after they have been released to the market. The primary goal is to help manufacturers identify and address potential issues that may arise during actual use, monitor the market for known risks, and identify new risks.

10 Jul 2026

ISO 9001:2015 in Life Sciences Industry

In the life sciences industry, maintaining high quality standards is critical not only to the success and sustainability of organizations but also to patient safety and compliance. ISO 9001:2015, part of the ISO 9000 family, provides a robust framework for quality management systems (QMS) that can be used in organizations in the life sciences, including pharmaceutical, natural technology, including medical devices. This article examines the key features of ISO 9001:2015, its benefits, implementation methods, potential pitfalls, and impact in the life sciences.

10 Jul 2026

The Role of a CQV Expert in the Cold Chain Division of a Pharmaceutical Company

In the pharmaceutical industry, product quality is of vital importance. This is particularly true for medicinal products that are sensitive to temperature fluctuations, such as vaccines, biologics, and certain medications that must be stored and transported in a controlled environment. Within this process, the CQV (Commissioning, Qualification, and Validation) expert plays a crucial role, especially within the cold chain division, which is responsible for monitoring product quality during the transport and storage of these temperature-sensitive products. This blog outlines the various aspects a CQV expert must consider in this context.

10 Jul 2026

Radiopharmaceutical & Selective Internal Radiation Treatments: Overcoming Challenges and Embracing Future Opportunities

Radiopharmaceutical and selective internal radiation treatments have emerged as a transformative force in the pharmaceutical industry, offering precision, personalized therapies for patients with conditions such as cancer and other serious diseases.

10 Jul 2026

Implementation of the European Clinical Trial Regulation (EU-CTR)

By the end of this month (31st of January 2025), the final deadline is reached in the transition period for the implementation of the European Clinical Trial Regulation (EU-CTR). What is it and what is the difference with the previous European Clinical Trial Directive (EU-CTD)?