Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Ensures compliance to cGMP as well as maintaining equipment and facilities. The manufacturing associate is detail-oriented with strong understanding of automated systems and process controls. Individual will maintain training to the required level and support other functions in site. 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 and for maintaining equipment and perform manufacturing activities.
- Bau / Gewerbe / Immobilien
Within the Pharmaceutical Industry globally & successfully operating company.
A dynamic working environment focusing on career opportunities where multi-cultural teams from all over the world strive the best results.
Relevant education from chemical industry, food industry, pharmaceutical or biotech industry.
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.
Client reference number BIOBJP00002761, please integrate in your application.