
Rottendorf Pharma is a contract development and manufacturing organization (CDMO) with over 95 years of experience in producing solid oral dosage forms for global pharmaceutical companies. Specializing in bulk manufacturing, packaging, development, analytics, and Total Process Ownership (TPO), the company leverages its expertise to optimize production without competing with clients. Rottendorf Pharma focuses on delivering high-quality products through its commitment to Total Technological Mastering (TTM) and operates as an extension of clients' organizations.
As a Qualified Person (m/w/d) at Rottendorf Pharma, you'll be responsible for the release of manufactured products in accordance with legal requirements. You will assess and approve GMP-relevant documents, serve as the contact person for GMP and regulatory compliance, collaborate with various departments, participate in project teams, and communicate with customers and authorities during inspections. The role demands independent and structured work with a strong sense of responsibility.
Rottendorf Pharma is a contract development and manufacturing organization (CDMO) with over 95 years of experience in producing solid oral dosage forms for global pharmaceutical companies. Specializing in bulk manufacturing, packaging, development, analytics, and Total Process Ownership (TPO), the company leverages its expertise to optimize production without competing with clients. Rottendorf Pharma focuses on delivering high-quality products through its commitment to Total Technological Mastering (TTM) and operates as an extension of clients' organizations.