Welcome aboard!

Christian Mayer-Lusti and his team have been responsible for compliance with GMP guidelines at FRIKE PHARMA AG since January 2023. In this interview, he tells us what GMP means and what the tasks of the person with technical responsibility are.

Share article

What is the role of the person with technical responsibility?

«Medicines are regulated by the authorities, so they are subject to high quality requirements and must be safe for patients. The person with technical responsibility has a bridging function between the regulatory requirements in the manufacture of medicinal products and the internal implementation of these regulations. This ensures that regulatory requirements are also applied in the company and that all products meet the high quality requirements. In this context, the person with technical responsibility also acts as an interface between the authorities and the company.»

What tasks does this person typically perform?

The most important requirement – ensuring high product quality – is set out in the GMP guideline. People often assume that these letters must relate to large tomes of information or the endless quantities of documents out there. In fact, the letters stand for Good Manufacturing Practice and describe what this means for medicinal products. GMP is mandatory for the pharmaceutical industry worldwide and must therefore also be integrated into our own processes.

Success with teamwork

A typical task for a person with technical responsibility is to monitor the implementation of this quality standard in the company. Of course, this can only be achieved with the support of a highly qualified and motivated team that actively evaluates, implements and finally archives the large quantities of paper. Another typical task relates to the release of medicinal products. Since the responsibility for correct production lies with the person with technical responsibility, they are in charge of releasing products and thus confirming that production has been carried out according to GMP.

Why did you choose the FRIKE GROUP as your new employer?

«With around 300 employees, the FRIKE GROUP is one of the largest contract manufacturers in Switzerland. I appreciate being part of the set-up of a large manufacturer with a broad product range and lots of interesting products, as it means exciting projects and challenging tasks. At the same time, I like the informal working environment of FRIKE PHARMA AG, as a small company. Thanks to the manageable size of the company, my tasks are very varied and range from team management to the implementation of the GMP guidelines and the release of medicinal products as the person with technical responsibility. That won me over, and I’m looking forward to taking on many new challenges.»

Share article

More Articles


The new Becolab Mini – a small mixer with big ambitions

A 2.5-litre Becolab Mini has been at Glaropharm AG in Mitlödi since February. The new mixer heralds a new era at FRIKE, because from now on a wide range of options are available for bulk development.

Results of the FRIKE customer survey and what FRIKE donated money for

We asked our customers for feedback at the beginning of 2024 and would like to thank them once again for the fantastic response rate of almost 25%. What came out of it and who benefited from the money donated.

Information on the new cosmetics law in the USA

In the USA, President Biden passed a new law for cosmetic products at the end of 2022: MoCRA (Modernisation of Cosmetics Regulation Act). Read here what this means for us and our customers.

The new FRIKE website is finally live

We are very pleased to announce that our new website is finally live! With a fresh, modern design and improved usability, we offer you an optimised online experience.

Unforgettable flight: our employees at the Swiss Ballooning Championships

This year, we were able to take part in a special company tour organised by Blaser Swisslube. Six people from the FRIKE GROUP were able to take part in the balloon flights around the Swiss Ballooning Championship in Gossau (https://www.smhl.ch/de) from 8 to 12 May 2024.

Annex 3 extended allergen declaration

In the Annex 3 Allergen Declaration, Annex 3 is extended from 26 to over 80 declarable allergens in accordance with SCCS/1459/11 and Regulation (EU) 2023/1545.

Whats up at the Cosmetic Business 2024

The FRIKE Cosmetic team once again had a stand at this year's Cosmetic Business. Find out more about the popular cosmetics trade fair here.

Your expert in aerosol products

Our passion and 60 years of aerosol experience make us the go-to full-service partner for the development, production and filling of aerosols as foams, sprays or gels. Our portfolio includes cosmetics, medical and household products.

FRIKE GROUP Academy: Improved occupational safety

Find out how the newly launched FRIKE Academy offers bulk production specialists the highest standards in occupational health and safety.