Job
- Level
- Junior
- Job Field
- Application
- Employment Type
- Full Time
- Contract Type
- Temporary employment
- Location
- Dresden
- Working Model
- Onsite
Job Summary
In this role, you actively contribute to the digital transformation of manufacturing processes in a pharmaceutical environment, qualify automated inspection systems, and optimize defect detection using AI.
Job Technologies
Your role in the team
- In this position, you will actively contribute to the digital transformation of our manufacturing processes and drive the structured expansion as well as the sustainable use of innovative process technologies, including AI, in a highly regulated pharmaceutical environment.
- You work in our Manufacturing Science & Technology (MSAT) unit at the interface between new production facilities, manufacturing areas, and compliance. Together with experienced project engineers and production staff, you qualify automated systems for visual inspection of vaccines, thereby significantly contributing to the safe, efficient, and practical integration of new technologies into production.
- Support in the implementation and qualification of equipment and processes for visual inspection of filled vaccine syringes, taking into account regulatory requirements in the pharmaceutical GMP environment.
- Optimization of defect detection and characterization through automatic camera systems as well as determination of detection probabilities.
- Implementation and validation of an additional microscopy characterization of spray defects in a GMP production environment.
- Support in the creation of process and validation documents, presentations, and decision-making materials for specialist departments and management.
- Participation in training and educational measures for the introduction of process plants in operational departments.
- Close collaboration with business units as well as, if applicable, external and global GSK partners.
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Our expectations of you
Qualifications
- Enrollment in the field of Engineering, Engineering Sciences, Natural Sciences, or a related discipline.
- Basic understanding of pharmaceutical process equipment, GMP-compliant documentation and validation, as well as artificial intelligence or automation.
- Proficient in MS Office, especially PowerPoint and Excel.
- Analytical thinking skills, structured working approach, and a high degree of initiative as well as willingness to learn.
- Ability to present complex technical content in an understandable manner.
- Strong communication skills and enjoyment in collaborating with different departments.
- Sense of responsibility and high sensitivity to compliance and data management.
- Very good German and good English skills, both written and spoken.
Experience
- Strong interest in the application of new technologies in regulated industries (e.g., pharma, medtech, chemistry) and ideally initial experience with digital tools, data analysis, or AI applications.
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What we offer
- This is a temporary development measure focused on professional development.
- Any refunds, allowances, or other financial support will be provided in accordance with applicable local laws, regulations, and GSK policies.
- More detailed information about the compensation will be provided during the hiring process.
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Benefits
Work-Life-Integration
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Topics that you deal with on the job
Job Locations
This is your employer
GlaxoSmithKline GmbH & Co. KG
A science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.
Description
- Founding year
- 1830
- Company Type
- Established Company
- Working Model
- Hybrid, Onsite
- Industry
- Pharmaceutical Sector, Chemical Industry, Biotech