Your mission:
- Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation
- Ensure compliance to cGMP as well as maintaining equipment and facilities
- Maintain training to the required level and support other functions on site
- Execute manufacturing related work as per procedures and policies
Your profile:
- High school diploma or equivalent experience and typiically 4-5 years in related industry or 5-6 years Pharma/Biotech industry OR Bachelor degree in related filed with 3-4 years Pharma/Biotech professional experience
- Exposure to Delta V or Syncade or similar automated systems
- Experience in highly regulated industry
- Languages: Conversational English (minimum B1 level)
- Detail-oriented with strong understanding of automated systems and process controls
To apply or for any further information, please do not hesitate to contact Alina Peeva, senior recruiter: