Software Consultant managing clinical IT systems and supporting users in healthcare. Collaborating with teams to optimize workflows and implement new software solutions.
About the role
- GMP-Consultant creating GMP-compliant SOPs and risk analyses for pharmaceutical equipment. Collaborating with teams and supporting quality assurance measures in Life Sciences.
Responsibilities
- Creation of GMP-compliant SOPs and risk analyses in German and English
- Support in the qualification of pharmaceutical equipment and systems and their documentation
- Review of systems and processes for GMP compliance
- Coordination and organization of maintenance, calibration and qualification activities
- Review of technical documentation for changes and deviations
- Support with change control and deviations
Requirements
- Degree in process engineering, pharmaceutical engineering, biotechnology, chemical engineering, life sciences engineering, mechanical engineering or a comparable engineering or natural sciences degree
- Basic knowledge of the GMP environment or quality assurance is advantageous but not required
- Willingness to undertake longer customer assignments (Class B driving licence required) and eagerness to learn on the job
- Very good German and good English language skills
Benefits
- Entry into the GMP field with a comprehensive training program
- Onboarding with top-tier hardware and a mentoring (buddy) scheme
- Modern, dynamic working environment with an informal first-name culture from day one
- Flexible working hours with a flexitime model
- 30 days' vacation and a permanent employment contract
- Social benefits such as a company pension scheme, capital-forming payments 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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