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Manufacturing Associate (M/F/D)
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 MA is detail-oriented with strong documentation skills. Maintain training level to the required level and support other functions on site.
Tasks:
Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation (90%)
Actively participates in training activities, managing their individual training plan. Trains other associates as required. (5%)
Executes validation protocols (3%)
And other job duties that may be assigned from time to time. (2%)
Qualification:
"• High school diploma or equivalent experience and typically 3-5 years relevant experience in related or non-related industry or 2-3 years experience in Pharma/Biotech industry
OR
Bachelor degree in related filed with 1-2 years professional experience
OR
Bachelor degree in not related field and typically 3-4 years experience
Languages: English B1, German and/or French an asset
must have basic understanding of the Biotech process
must have a solid understanding of the requirements within correct and timely documentation within a cGMP environment
must be trained and skilled in all operational and regulatory procedures of at least one manufacturing department
must have basic Automation understanding or must be at ease with technology platforms.
Requirements:
Start: 01.02.2025
Duration: 12 months
Capacity: 5 days per week
Location: Solothurn, Switzerland
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