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Senior Recruiter at Hays AG | Life Sciences | Occupational Psychologist
Summary:
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 on site.
Responsibilities:
* Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation (USP & DSP in a cGMP environment)
* 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.
Profile:
* High school diploma, Bachelor Degree and several years of experience in DSP and/or USP in Pharma/Biotech industry
* Good understanding of Delta V or Syncade or similar automated systems
* Understanding of full Biotech process
* Languages: English B2, German and/or French an asset
General information:
* 12 months contract - Good chances of internalisation or extension
* Shiftwork (with or without nightshift)
Seniority level
* Associate
Employment type
* Full-time
Job function
* Manufacturing
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