Employee (m/f/d) for our department - Capulin, NM, United States - Phoenix Industries

James Miller

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James Miller

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Freelance
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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