Rentschler Biopharma is a leading global contract development and manufacturing organization (CDMO) for biopharmaceuticals. From our headquarters in Laupheim, Germany, and our site in Milford, MA, USA, we offer end-to-end solutions, including bioprocess development and manufacturing, as well as related consulting activities such as project management and regulatory support. In Stevenage, UK, we have launched Rentschler ATMP Ltd. dedicated to cell and gene therapies.
We are a family-owned company with approximately 1.400 employees from 25 nationalities. What unites us at Rentschler Biopharma, is the passion for what we do. We empower our clients to help patients with serious or rare diseases. With our dedication and expertise, we convert medical research into outstanding biopharmaceuticals. Thus, we provide an important contribution to the global availability of essential therapies. Going forward, we are expanding our team to ensure our long-term sustainable growth. Join us and be part of a unique journey, shaping the future of biopharmaceutical manufacturing together.
Duties and Responsibilities
- Perform routine high-throughput platform testing of in-process samples for process development activities of proteins
- Assist in optimization and troubleshooting of analytical methods.
- Identify, evaluate, and implement new and existing technologies to improve process efficiency, control and understanding
- Serve as PD representative and participate in cross functional meetings
- Author high-quality documents, including technical reports, SOP's and experimental protocols
- Ability to interpret analytical data and understand relation to manufacturing process steps
- Review data packages and compile slides for client presentations
- Provide technical support (e.g., method and instrument troubleshooting) to QC group
- Ability to work in a team environment
- Ability to work in a fast paced, rapidly changing CDMO environment
- Contribute to the overall operations of the process sciences lab and infrastructure improvements
Qualifications
- Minimum required experience:
- A university degree and 2-3+ years of related experience
- A Masters degree and 0-1+ years of related experience
- Basic understanding of theoretical knowledge and hands-on experience with analytical technique such as: HPLC/UPLC, cGE/iCIEF, bioassay, activity assay, and microbial testing
- Basic understanding of method development, qualification, and validation is a bonus
- Knowledge and understanding of protein manufacturing process (upstream/downstream) is a bonus
- Proficient in Microsoft Office (Word, Excel, Power Point, SharePoint).
- Demonstrates ability to work both independently and as a member of local / global teams
- Excellent customer service skills and ability to meet client project deadlines
- Flexibility to switch between projects
- The candidate should be self-motivated, accountable, inquisitive, and have excellent organization and communication skills
Working Conditions
- Laboratory environment working with chemical reagents and analytical equipment
- Personal Protective Equipment must be worn as required
- Normal office working conditions: computer, phone, files, fax, copier
- Will interact with other people
- Pace may be fast and job completion demands may be high
Physical Requirements
- Frequent lifting up to 10lbs
- Frequent standing/walking to work in lab environment for extended periods
- Frequent sitting for extended periods to use computer