About this opportunity
Rentschler Biopharma Inc. lists this Associate Scientist I, Process Development Analytics (Separations) opportunity in milford, Connecticut. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases. Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family‑owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best‑in‑class solutions – together with our clients. Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability. As an independent family‑owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.
Role Overview
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.
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)
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
Base Pay Range
Base Pay Range $70,000 - $90,000
Disclosure Statement
Rentschler Biopharma, Inc is committed to fair and equitable compensation practices. The base pay range listed for this position is the anticipated annual base salary range the organization reasonably, and in good faith, expects to pay for this position at this time. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law. The annual base salary is just one component of our Total Rewards package, which also includes our annual discretionary bonus program, medical insurance, our generous 401K program, plus a host of other benefits to aligned to support our employees’ personal and professional wellness. The salary pay range is subject to change and may be modified at any time.
annual discretionary bonus program
medical insurance
our generous 401K program
plus a host of other benefits to aligned to support our employees’ personal and professional wellness
Additional Company Information
Rentschler Biopharma is a contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family‑owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best‑in‑class solutions – together with our clients. 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. We live by the motto: Many hands, many minds - one team! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents, we pursue one vision together: advancing medicine to save lives.
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Worksite address
milford, CT, 06466, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.