- Position: Process Engineer
- Location: Stockholm/Uppsala/Södertälje
- Start date: Immediately
- Type: Permanent contract
Lead the process qualification through the different phases of the projects (design, procurement, implementation and completion)
- Develop the project according to GMP requirements
- Create validation protocols / plans
- Equipments & tools qualifications
- Risk analysis / assessment
- Protocol writing (DQ, IQ, OQ, PQ, FAT, SAT) and testing
- Create quality reports
- Communication with suppliers
- You have a MSc, PhD degree in pharmacology, medical technology, biotechnology or chemistry.
- At least 2 years work experience in qualification and validation.
- You speak Swedish and English.
- As a person, you are committed, responsible, solution oriented and have good communication skills.
You are looking for a new challenge? Do not hesitate contact us :