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Manufacturing Associate Iv
Vor 4 Tagen
**Summary**:
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.
**Minimum Education Requirements**
- Minimum educational level necessary to perform the job (High School diploma, Associate's Degree, Bachelor's Degree, Masters, PhD)
- Principal Accountabilities
- Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation
- Perform troubleshooting/investigation of equipment and process issues
- Revises documents as instructed, Capable of equipment and/or process changes
- Actively participates in training activities, managing their individual training plan. Trains other associates as required.
- Executes validation protocols
- Capable of leading shift when supervisor is absent, and actively leads or participates in shift exchanges. Coordinates activities and daily schedules with cross-functional areas.
- And other job duties that may be assigned from time to time.
**Must haves**:
- High school diploma or equivalent experience and typically 9-11 years relevant experience in Pharma/Biotech industry
OR
- Bachelor degree in related filed with 5-6 years Pharma/Biotech professional experience
OR
- Bachelor degree in not related field and typically 7-9 Pharma/Biotech years experience
- Good understanding of Delta V or Syncade or similar automated systems
- Understanding of full Biotech process
- Languages: English B1, German and/or French an asset
- A solid knowledge of biopharmaceutical technology and processes.
Kontakt: +41 61 282 22 13 (Alba Jansa)
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