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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 hands-on experience in Upstream Processing within Pharma/Biotech production
* Experience with aseptic techniques and a solid understanding of aseptic knowledge is preferred
* Must have a 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: asap
Duration: 12 months
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Full-time
Job function
* Job function
Manufacturing
* Industries
Pharmaceutical Manufacturing
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