Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers

General Information:

Start Date: 21.09.2026
End Date: 28.02.2027

• Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents.
• Ensuring compliance to cGMP as well as maintaining equipment and facilities.
• The Manufacturing Associate is detail-oriented with strong documentation skills. Maintain training level to the required level and support other functions on site.
• Assist with daily manufacturing operations in manufacturing facility. Typically requires 3-5 years of experience.
• The employee will be responsible for executing manufacturing related work within Solothurn as per procedures and policies.
• The employee will be accountable for maintaining and complying with the environmental, health and safety regulations.
• The employee will be responsible for maintaining his/hers training curriculum and not perform tasks that the employee is not trained to perform.
• Be able to work independently and with minimal direction. Has moderate responsibility.
• The employee will be responsible for maintaining equipment and perform manufacturing activities. Erroneous work can impact product integrity result in batch failures and consequently harm patients.
• The employee must be able to demonstrate the ability to independently document and record information related to their job functions.
• The employee must at all times make sure that if the employee is in doubt that the employee’s supervisor or manager is consulted. Good verbal and written skills are required to ensure proper description of any issues.
• Employee must collaborate well with supporting functions and seek to define best outcomes for patients and the facility.
• A basic knowledge of biopharmaceutical technology and processes. The employee must be able to follow and comply with procedures and protocols.
• The employee should occasionally be able to make routine decisions based on gained experience. The employee must have a solid understanding of the requirements within correct and timely documentation within a cGMP environment.
• The employee must be trained and skilled in all operational and regulatory procedures of manufacturing department.
• Employee understands importance of safety and can teach saftey principles to less experienced colleagues.

If you are interested, please reply with a copy of your CV.