Quality Partner GMP (m/w/d)

Connecting people and technologies to make the Perfect Match for our customers is always the right expert: finding them for the respective challenge - this is our claim at FERCHAU and looking for you: as an expert for our customers. We implement exciting projects for well-known customers in the fields of Pharma and Life Science and convince with expertise and professional know-how every day.

Quality Partner (m/w/d) Mannheim Create and maintain risk assessments for internal processes Close cooperation with internal and external interfaces, e.g. requests from suppliers, customers and authorities Examination and creation of documents in accordance with the GMP guidelines and support in the implementation of audits Proactive participation in improving the quality management system and quality planning Ensuring the regulatory operation of qualified plants (e.g. cooling rooms, clean rooms, RLT systems and cleansing media plants) according to internal and external specifications Creation and coordination of technical changes after consultation and according to change management requirements Creation and tracking of deviation reports and assessment of risks and support in the qualification of systems Creation and archiving of lifecycle documents by default in SAP DVS Your advantages with us unlimited contract Occupational pension Satte discounts with shopping discounts, for example when traveling, electronics or cars Special holiday for important private occasions, e.g. wedding, move, birth Attractive offices and a workplace with modern hardware Flexibility through the ability to work mobile (depending on the customer company) Come and feel comfortable with our onboarding program Premium programme for recommendations from new Members:

Your profile Successfully completed studies in the fields of process engineering, mechanical engineering, natural sciences, packaging technology, medical technology or a comparable qualification; as an alternative technician: with many years of experience in the regulated environment (GxP) or a completed vocational training with corresponding further training in the field of quality management Experience in working with clean rooms, cooling storage and/or cleansing media Experience in creating documentation according to GxP Experience in change management and quality assurance in the pharmaceutical or medical technology industry Very good computer skills (especially SAP knowledge, for example in the SAP DVS document management tool) Good knowledge of regulatory and legal, national and international requirements in the area 13485 and GMP guidelines Self-employed and careful working, strong communication strength, especially with stakeholders German and English knowledge in word and writing