As a global leading service provider for the development and production of biopharmaceuticals, Rentschler Biopharma makes an essential contribution to the worldwide availability of life-saving therapeutics. We are a family-owned company with approximately 1000 employees. Going forward, we are expanding our team to ensure our consistent growth.
What unites us at Rentschler Biopharma, is the passion for what we do. Every individual member of our team contributes actively to project success with his/her knowledge and skills. Come join our team! We offer you an exciting work environment with excellent career development opportunities.
Process Manager Downstream Development (m/w/d)
As part of our group Process Science DSP, we are seeking a Process Manager. The Process Manager will be in charge of the upstream/downstream processes of our customers’ APIs throughout the complete product lifecycle. This comprises the following key responsibilities:
Design and development of scalable downstream processes from bench to commercial scale for a wide range of biopharmaceuticals
Transfer of customer downstream processes to the Rentschler process format.
Design of late stage process optimization and process characterization / robustness studies by risk based strategies in preparation of process validation at manufacturing scale
These responsibilities will be assumed by actively carrying out and managing the following tasks:
Direct communication and representation towards our customers in “face-to-face meetings”, conference calls, etc.
Consulting our customers in subject matter-specific project strategy within the product lifecycle
Ensure compliance with international technological and regulatory standards
Responsible for compliance of timelines and milestones according to overall project plans
Technical supervision of lab technicians and engineers in DSP development
Scientific advice for manufacturing science and technology team (scale up to internal and external production sites, deviations, changes, process validation)
Subject matter expert in an interdisciplinary and cross-functional team with colleagues from production, USP, quality control, QA/RA and Innovation
Compile and review protocols and reports in a timely manner
Review relevant chapters of CMC dossiers (IND/IMPD and BLA/MAA)
Participate in customer audits and authority inspections
Participate in innovation and internal projects for driving progress of the group / Company
PhD or relevant experience in biotechnology, biochemistry or comparable scientific/technical field
Several years of active experience in the field of DSP development preferably using scalable technologies in context of industrial pharmaceutical manufacturing
Deep knowledge and understanding of chromatographic processes, filtration techniques, protein chemistry and analytical methods
Significant knowledge in upstream processing
Fluent in German and English
Basic knowledge in project management
High level of initiative and excellent organizing ability
Entrepreneurial mindset, economic and analytical thinking
Strong and collaborative communication skills, team spirit, flexibility and outcome-oriented working
Willingness to work at Weekends
Variod working environment in a future-proof industry
Flexible work time
Occupational Health Management and retirement provision