Lead Qualification Specialist

vor 1 Woche


Puch bei Hallein, Österreich Bilfinger Vollzeit

As a key member of our team at Bilfinger Life Science, you will play a crucial role in designing and building process plants and systems worldwide that contribute to improving the quality of our daily lives and sustainably conserving resources.

Our core skills cover the multifaceted requirements of our customers in the pharmaceutical, environmental, and nutrition market segments. Based on professional project management, we meet the requirements of planning, process engineering, automation, assembly, qualification, and service.

Our Offer

  • We work on exciting international projects that offer a unique opportunity to grow and develop individually into experts or managers.
  • We value a first-class working atmosphere and our social benefits, making us an attractive employer in the industry.
  • We are committed to sustainability and resource conservation, aligning with our customers' values and goals.
  • We prioritize flexibility and work-life balance, with up to 50% travel opportunities for international projects.

Your Tasks

  • You will create and check qualification documents, including DQ, FAT, IQ, and OQ test plans and reports, ensuring compliance with regulatory requirements.
  • You will plan and carry out plant qualifications on site at our customers, working closely with process engineering, project management, automation, and assembly departments.
  • You will be responsible for coordinating qualification activities with the customer and internal departments, ensuring seamless project execution.
  • You will be familiar with SOPs and technical standards of our customers, applying your knowledge to ensure compliance and quality.
  • You will significantly contribute to the preparation of GMP risk analyses, identifying and mitigating potential risks.
  • You will serve as the deputy of the team leader, supporting leadership and decision-making.

Your Profile

  • You have good knowledge of regulations for pharmaceutical plant engineering, including cGMP, GEP, GAMP, and other relevant standards.
  • You are business fluent in written and spoken English, with excellent communication and interpersonal skills.
  • You are a responsible, structured, and assertive personality, with a strong work ethic and commitment to quality.
  • You appreciate international business trips and are flexible in terms of time, with up to 50% travel opportunities.

Collectively agreed annual gross salary starting at €55,000. The actual salary is higher and will be agreed individually depending on qualifications.



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