Vaccine Production Engineer (m/f/d)
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
Apply now via WhatsApp
Click here!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
Apply to us now!
Shape your professional life according to your ideas - with us at your side! At persona service you will find the job with freedom that you need right now.
With locations throughout Germany and more than 55 years of experience in the context of people and work, persona service is one of the most successful personnel service providers in Germany.
We have lots of jobs and therefore lots of opportunities and scope for development.
Simply book your appointment online
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Do you still have questions?
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Call us on 02351 7893111.
