Vaccine Production Engineer (m/f/d)
Vaccine Production Engineer (m/f/d)
Vaccine Production Engineer (m/f/d)
Vaccine Production Engineer (m/f/d)
persona service AG & Co. KG
Pharma, Medizintechnik
Singen
- Art der Beschäftigung: Vollzeit
- 53.000 € – 61.000 € (von XING geschätzt)
- Vor Ort
- Zu den Ersten gehören
Vaccine Production Engineer (m/f/d)
Über diesen Job
Vaccine Production Engineer (m/f/d)
Full-time
Do you want to contribute your expertise in a new working environment? Then you've come to the right place! We are more than just recruiters - we are your personal career counsellor. Our focus: Your next professional step, where you really feel comfortable.
Our client, a successful pharmaceutical company, is looking for you as an engineer (m/f/d) in vaccine production or cGMP validation in temporary employment .
Our client, a successful pharmaceutical company, is looking for you as an engineer (m/f/d) in vaccine production or cGMP validation in temporary employment .
What we offer
- Attractive remuneration, hybrid working model and 30 days' holiday
- Company pension scheme
- Subsidised health and sports programmes and a subsidised canteen
- Long-term account with various possible uses
- Share programme
- Invalidity insurance and group accident insurance
What you can always rely on at persona service:
- Intensive preparation for the interview with our client
- €50 per month as a gift for your mobility, depending on the position, e.g. for the Germany ticket and the travel expenses. e.g. for the Germany ticket and much more
- Bonuses as well as holiday and Christmas bonuses and attractive industry bonuses
- Free tutoring for your children on the Ubimaster learning & tutoring platform
- Numerous shopping discounts with well-known brands via our corporate benefits programme
- Excellent personal support and regular feedback meetings
- Multiple further training opportunities
Job description
- You will perform change controls, investigations and deviations, oversee CAPAs and drive continuous process improvements during validation and manufacturing activities
- While managing work packages for capital projects and maintaining timelines, guidelines and procedures
- You support the qualification of new vaccine manufacturing facilities and equipment and adhere to cGMP requirements and global regulatory requirements
- In addition, you plan, conduct and report validation activities and analyse data, determine results and draw conclusions
- You will work closely with QA, Quality Control and other support functions, to ensure a smooth flow of technology transfer and validation
- In addition, you coordinate technology transfer as a representative of the Receiving Unit and are responsible for troubleshooting and improvements in technology transfer
- You also create and maintain bills of materials (BOM) for raw materials and single-use materials
- You support the set-up of the practical production process
Requirements
- You have a university degree in biotechnology or a related field
- In addition, you have at least 3 - 5 years of experience in supporting start-up, technology transfer and/or the maintenance of cGMP-compliant biopharmaceutical manufacturing processes
- You also have a sound knowledge of GMP and ideally experience with live viruses as well as technical knowledge in biologics manufacturing
- In addition, you are fluent in German and English and have experience in writing technical documents, including validation documents, protocols and reports
- You are proficient in the use of statistical analysis tools and Design of Experiments (DoE)
- Last but not least, you enjoy interdisciplinary and cross-functional teamwork and have goal-oriented organisational skills