Intern MSAT Bio DP (M/F)

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Career Programs

Job Sub Function:
Non-LDP Intern/Co-Op

Job Category:
Career Program

All Job Posting Locations:
Schaffhausen, Switzerland

Job Description:

Join us in creating a future where diseases are no longer a concern! Johnson & Johnson Innovative Medicine in Schaffhausen (Cilag AG) specializes in the production of pharmaceuticals and active ingredients.

The Schaffhausen site plays a strategic role in launching and growing some of Johnson & Johnson's key pharmaceutical products.

Utilizing advanced technologies and processes, this site manufactures a variety of pharmaceutical dosage forms and chemical active ingredients.

We are currently looking for a Senior Cleaning Validation Engineer in MSAT (Manufacturing, Science & Technology) Biotherapeutics to enhance our team.

POSITION SUMMARY:
 

As an MSAT Cleaning Validation Intern, you will support other team members in developing, maintaining, and preparing reliable cleaning processes for product- and indirect-product contact parts to meet future requirements.

This involves support of colleagues in collaborating in cross-functional teams within the site and exchanging knowledge with other locations worldwide.
 

KEY RESPONSIBILITIES:


* Support the development and validation of cleaning processes for new products.


* Support the development and validation of improved cleaning processes for existing products.


* Support the development and implementation of new strategies for cleaning validation.


* Support the creation of documents for cleaning validation activities (protocols, reports, risk assessments, SOPs).


* Coordinate cleaning validation activities with other departments.


* Support calculations for permissible limits for cleaning validation.


* Support investigations and change controls.


* Support the preparation of technical assessments for investigations and change controls.


* Contribute to the digital transformation of MSAT (e.g., digitization and automation of reports, data management, visualization, evaluation of new technologies)

Qualifications:

As an ideal candidate, you have:


* Completed academic high school and are planning to or currently in the course of obtaining a Bachelor’s or Master’s degree in Life Sciences or Engineering.


* A keen interest in gaining insights into the pharmaceutical industry.


* A keen interest in gaining insights into the topic of cleaning vali...