Employee (m/f/d) for our department - Capulin, NM, United States - Phoenix Industries
Description
Your Responsibilities
- Creation of qualification documentation in the GMP environment (DQ, IQ, OQ, PQ)
- Planning and execution of qualifications for production equipment, laboratory equipment, and clean rooms
- Planning and execution of requalifications, computer system validations, and sterilization validations
- Creation of risk analyses (FMEA)
- Calibration of testing equipment
- Creation or revision of work instructions, documents, and forms for the quality management system
- Participation in the tracking of change control requests
Your Profile
- Ideally, you have a degree, preferably in the field of natural sciences, or a completed technical education.
- Previous experience in qualification and validation activities in a pharmaceutical company would be desirable.
- You have a strong interest in technical issues.
- In addition, you have a strong sense of thoroughness and reliability, and you demonstrate a high level of responsibility.
- Open and respectful communication with departments and suppliers is natural for you.
- You are proficient in using common MS Office applications.
- Excellent German language skills are a prerequisite, and fluent English language skills are desirable.
- Occasional travel readiness (e.g. accompanying FAT) is not a problem for you.
Our Offer
- Permanent employment and a secure job in a growing industry, where you can bring in your motivation and personality
- Familylike company culture with flat hierarchies, a respectful working environment, and open communication across all levels
- Varied field of activity characterized by personal
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