Delivering project - based Microsoft 365 services in a Professional Services team. Responsible for customer engagement and technical deployment throughout projects.
About the role
- GMP-Consultant managing quality assurance systems in life sciences industry. Developing SOPs, conducting risk analyses, and ensuring compliance in various pharmaceutical processes.
Responsibilities
- Drafting GMP-compliant SOPs and risk analyses in German and English
- Participating in the qualification of pharmaceutical equipment and systems and preparing related documentation
- Reviewing equipment and processes for GMP compliance
- Coordinating and organizing maintenance, calibration and qualification activities
- Checking technical documentation for changes and deviations
- Supporting change control and deviation management
Requirements
- Degree in Process Engineering, Pharmaceutical Engineering, Biotechnology, Chemical Engineering, Life Sciences Engineering, Mechanical Engineering or a comparable engineering or natural science program
- Basic knowledge of the GMP environment or quality assurance is an advantage but not required
- Willingness to travel occasionally; valid driving licence (Class B) required
- Very good German skills and good English skills
Benefits
- Entry into the GMP field with a comprehensive training program
- Onboarding with premium hardware and a buddy/mentor model
- Modern, dynamic working environment with a first-name culture from day one
- Flexible working hours within a flexitime model, 30 days' annual leave and a permanent employment contract
- Social benefits such as a company pension scheme, capital-forming benefits and supplementary health insurance
- Bike leasing and company events
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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