Associate Scientist I, Process Development Analytics (Separations)
Rentschler Biopharma
Summary
We are recruiting for a proactive and "hands-on" Associate Scientist I, Process Development Analytics. They will demonstrate flexibility, adaptability, and can work in a fast paced, rapidly changing CDMO environment. They are self-motivated, accountable, inquisitive, and have excellent organizational and communication skills. They can multi-task while delivering service excellence to internal stakeholders.
Job description
Duties And Responsibilities
- Routine testing of in-process samples for process development activities of proteins with a focus on separation-based assays, such as SEC, RP-HPLC, CIEX, HIC, icIEF, CE-SDS, Titer
- Optimization and troubleshooting of analytical assays by learning assay principles and equipment capabilities
- Decrease routine in-process assay turnaround times by increasing lab efficiencies and employing high-throughput methodologies
- Interpret analytical data and understand relation to manufacturing process steps
- Provide complete data packages for review and compile slides for client presentations
- Be proficient in LIMS and enter / review all LIMS results prior to release
- Author high-quality documents, including technical reports, SOPs and experimental protocols as needed
- Provide technical support (e.g., method and instrument troubleshooting) to QC group
Qualifications
- Bachelor's degree in STEM with 1+ year(s) of relevant experience
- The candidate should be self-motivated, accountable, inquisitive, and have excellent organization and communication skills
- Proficient in Microsoft Office (Word, Excel, Power Point, SharePoint)
Preferred Qualifications
- Experience with monoclonal antibodies, bispecific, fusion proteins, and enzymes
- Experience with method development, qualification, and validation
- Hands-on experience with analytical technique such as: HPLC/UPLC, cGE/iCIEF, CE-SDS
- Knowledge and understanding of protein manufacturing process (upstream/downstream)
Requirements
- Bachelor's degree in STEM with 1+ year(s) of relevant experience
- Self-motivated, accountable, inquisitive, and have excellent organization and communication skills
- Proficient in Microsoft Office (Word, Excel, Power Point, SharePoint)
Benefits
- Annual Discretionary Bonus
- Medical Insurance
- 401(k)
Company overview
Rentschler Biopharma is a leading global Contract Development and Manufacturing Organization (CDMO) specializing in biopharmaceutical services. Founded in 1872 and now in its fifth generation as a family-owned company, Rentschler Biopharma has over 50 years of experience in biopharmaceutical manufacturing. The company operates from two main sites: its headquarters in Laupheim, Germany, and a facility in Milford, Massachusetts, USA. With approximately 1,400 employees, Rentschler Biopharma offers comprehensive full-service solutions for bioprocess development and manufacturing of complex biopharmaceuticals, including analytical development, process development, formulation development, cGMP manufacturing, and regulatory affairs consulting. The company has an impressive track record, having contributed to nearly 25% of FDA-approved biopharmaceuticals in 2023 and serving over 180 clients worldwide since 1997. Rentschler Biopharma specializes in complex molecules, with more than 50% of their modalities being complex proteins including advanced antibody formats and recombinant enzymes. The company is known for its reliability, quality management systems, and operational excellence philosophy that ensures product quality and productivity at every development and manufacturing stage.