Archiviertes Projekt - Biotech Engineer (m/f/d)
Firmenname für PREMIUM-Mitglieder sichtbar
Projektbeschreibung
Ihre Aufgaben:
• Run and support the day to day operations of manufacturing processes
• Operate equipment according to batch records, sampling plans and standard operating procedures
• Work with Facility Management / internal team members in the in the maintaining of GMP status of responsible equipment devices in routine monitoring, calibration, maintenance, and certifications
• Support weekend or on-call duty on select time frames to support manufacturing
• Capital Requests and Sourcing
• Qualification of Devices / Equipment
• Authoring of batch records, sampling plans, and standard operating procedures.
• Act as SME for implemented new technologies, guiding the implementation into routine production
• Author Protocols and Prepare Design of Experiments to show comparability of new technologies versus legacy
• Support the area’s implementation of risk assessments, complex changes, and complex investigations
• Support development of a culture of continuous improvement across the site
• Embody Safe by Choice – know and follow the Safety, Health and Environment guidelines and work towards company safety and environment goals
Ihre Qualifikationen:
• Bachelor’s degree in Biotechnology, Chemistry, Biology, Pharmacy, or Process engineering
• Familiarity with Unit Operations for mAb manufacturing
• Competent in analyzing complex situations and show practical problem-solving capabilities
• Verbal or spoken communication skills in German and/or English
• Ability to work independently and within a cross-functional team
• Proficiency in German of B1 or Higher
Ihre Vorteile:
• You will work in an international environment
• 25 days of holidays by year
• A fixed monthly salary
Projektdauer: 12 MM++
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
• Run and support the day to day operations of manufacturing processes
• Operate equipment according to batch records, sampling plans and standard operating procedures
• Work with Facility Management / internal team members in the in the maintaining of GMP status of responsible equipment devices in routine monitoring, calibration, maintenance, and certifications
• Support weekend or on-call duty on select time frames to support manufacturing
• Capital Requests and Sourcing
• Qualification of Devices / Equipment
• Authoring of batch records, sampling plans, and standard operating procedures.
• Act as SME for implemented new technologies, guiding the implementation into routine production
• Author Protocols and Prepare Design of Experiments to show comparability of new technologies versus legacy
• Support the area’s implementation of risk assessments, complex changes, and complex investigations
• Support development of a culture of continuous improvement across the site
• Embody Safe by Choice – know and follow the Safety, Health and Environment guidelines and work towards company safety and environment goals
Ihre Qualifikationen:
• Bachelor’s degree in Biotechnology, Chemistry, Biology, Pharmacy, or Process engineering
• Familiarity with Unit Operations for mAb manufacturing
• Competent in analyzing complex situations and show practical problem-solving capabilities
• Verbal or spoken communication skills in German and/or English
• Ability to work independently and within a cross-functional team
• Proficiency in German of B1 or Higher
Ihre Vorteile:
• You will work in an international environment
• 25 days of holidays by year
• A fixed monthly salary
Projektdauer: 12 MM++
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
Kontaktdaten
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