Validation and Qualification Engineer (m/w/d) Pharmaceutical Production Systems in Mannheim (1667)

Your career in machine and equipment qualification in the pharmaceutical industry.

In this position, you will ensure the technical availability of high-modern systems, support the introduction of new technologies, and actively contribute to ensuring the highest quality and GMP standards. An ideal task for technically inclined engineers who want to take responsibility in the pharmaceutical environment.

Tasks

• Equipment Qualification: Development of qualification and validation strategies as well as execution, testing, evaluation, and release of qualifications and validations of new and existing production systems according to GMP.
• Change Control: Management of change control processes for technical systems, manufacturing processes, and documents, as well as implementation and follow-up of CAPAs
• Conceptual Development: Evaluation of new guidelines and standards, derivation of improvement measures, and implementation under efficiency aspects.
• Dokumentation: Creation, maintenance, and further development of GMP-relevant documents such as SOPs, validation master plans, or QRM assessments.

Qualification

• Qualification: Completed studies in mechanical engineering, pharmaceutical technology, process engineering, or a comparable natural science and technical study program.
• Professional Experience: Experience in the qualification & validation of pharmaceutical production systems or in pharmaceutical manufacturing/quality assurance.
• Regulatory Knowledge: Very good knowledge of GMP guidelines as well as experience in dealing with QA-relevant processes.
• Work Style: Solution-oriented, structured, and secure in the handling of Lean and agile methods.
• Soft Skills: Excellent communication skills, high analytical thinking, and a process-oriented working style with understanding for technical and regulatory contexts.
• Languages: Very good German and English language skills.

Benefits

• Attractive Conditions: Look forward to an unlimited full-time position at BRÜGGEN ENGINEERING, with a salary that reflects your expertise.
• Innovation Leadership: Drive the qualification, validation, and introduction of new pharmaceutical production systems as well as digital technologies actively forward – and ensure the highest GMP standards throughout the entire manufacturing process.
• Dynamic Environment: Become part of an engaged and cooperative team that fosters your professional development.

We look forward to your comprehensive application documents with
specification of your earliest start date and salary expectations.

Your contact person for your application is:
Mr. Dipl.-W.-Ing. Thorsten Schermann

Find Jobs in Germany on Arbeitnow