Required skills
- GMP Qualification
- CSV
- Pharmaceutical
- Documentation
- Packaging Lines
- Inspection Systems
- Control Systems
- German
- English
Languages: German
Job description
Experienced freelancer sought for Qualification and Computerized System Validation (CSV) support in a pharmaceutical GMP environment, starting January 2027 in Northern Germany.
Project overview
Freelancer Qualification / CSV Specialist (gn) – GMP / Pharma
For a company in the pharmaceutical sector, we are looking for an experienced freelancer in the field of Qualification and Computerized System Validation (CSV) starting January 2027.
The goal of the project assignment is to provide operational support to the internal team in carrying out qualification activities and in creating and maintaining the associated documentation in a GMP-regulated environment.
The technical responsibility and overall ownership remain with the internal team.
Responsibilities
Operational support in carrying out qualification activities in a GMP environment
Creation, processing, and maintenance of associated qualification documentation
Support in activities related to Computerized System Validation (CSV)
Participation in the qualification of packaging lines and associated inspection and control systems
Support in on-site qualification execution
Requirements
Sound professional experience in a GMP-regulated pharmaceutical environment
Practical experience in Qualification and Computerized System Validation (CSV)
Very good German and English language skills
Ideally, experience with packaging lines, especially labeling and cartoning machines
Experience with integrated inspection and control systems, such as Laetus systems, is an advantage
Willingness for flexible on-site assignments, especially during qualification execution
Project information
Project details
January 2027 (CW 2)
Northern Germany
Project type: Freelance / Contracting
On-site presence: As required by the project
January 2027, from CW 2
Region: Northern Germany
Contract type: Freelance / Contracting
By agreement
On-site presence: As needed, especially during qualification phases
Interested?
Do you have sound experience in GMP qualification and CSV and will be available for a new project from January 2027?
Then we look forward to hearing from you with the following information:
Brief profile with relevant project experience
Earliest possible availability
Desired workload
Hourly rate or daily rate
Willingness for on-site assignments in Northern Germany
We look forward to connecting!
- Start: ab sofort
- Duration: 12 Monate
- Remote: onsite
- Location: Bremen, Deutschland, DE
- Rate: 100-100 EUR/h
- Languages: German
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