Rentschler Biopharma
Scientist, Process Development Analytics
Rentschler Biopharma, Milford, Massachusetts, us, 01757
Scientist, Process Development Analytics
Join to apply for the
Scientist, Process Development Analytics
role at
Rentschler Biopharma
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.
Duties And Responsibilities
Routine high‑throughput testing of in‑process samples for process development activities of proteins
Lead optimization and troubleshooting of analytical methods
Process, review, compile data into slide decks, and present results of in‑process samples for process development work packages
Author high‑quality documents, including technical reports, SOPs, and experimental protocols for use in both development and quality control laboratories
Support onsite lab activities by overseeing ordering and tracking of routine and client‑billable consumables; and coordinating work orders
Provide alignment between development and quality control laboratories for upcoming sample transfer and testing requests
Coordinate technical transfer of established methods to quality control and clients
Present data at client project team meetings and written reports
Serve as PD representative and participate in cross functional meetings
Ability to interpret analytical data and understand relation to manufacturing process steps
Review data packages and compile slides to present at client project presentations
Provide technical and strategic planning support to business development activities with respect to new client projects and new business initiatives
Contribute to the overall operations of process sciences lab and infrastructure improvements
Ability to work in a team environment and drive the success of the team
Training and lead of associate scientists
Qualifications
Minimum required experience:
A university degree and 5+ years of related experience
A Masters degree and 3+ years of experience
A PhD and 1+ years of experience
Hands‑on experience with analytical technique such as: HPLC/UPLC, cGE/iCIEF, bioassay, activity assay, and microbial testing
Experience with monoclonal antibodies, bispecific, fusion proteins, and enzymes is preferred
Experience with method development, qualification, and validation
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 10 lbs
Frequent standing/walking to work in lab environment for extended periods
Frequent sitting for extended periods to use computer
Seniority level:
Mid‑Senior level
Employment type:
Full‑time
Job function:
Analyst, Science, and Manufacturing
Industries:
Biotechnology Research and Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Rentschler Biopharma by 2x
Get notified about new Process Development Scientist jobs in
Milford, MA .
#J-18808-Ljbffr
Scientist, Process Development Analytics
role at
Rentschler Biopharma
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.
Duties And Responsibilities
Routine high‑throughput testing of in‑process samples for process development activities of proteins
Lead optimization and troubleshooting of analytical methods
Process, review, compile data into slide decks, and present results of in‑process samples for process development work packages
Author high‑quality documents, including technical reports, SOPs, and experimental protocols for use in both development and quality control laboratories
Support onsite lab activities by overseeing ordering and tracking of routine and client‑billable consumables; and coordinating work orders
Provide alignment between development and quality control laboratories for upcoming sample transfer and testing requests
Coordinate technical transfer of established methods to quality control and clients
Present data at client project team meetings and written reports
Serve as PD representative and participate in cross functional meetings
Ability to interpret analytical data and understand relation to manufacturing process steps
Review data packages and compile slides to present at client project presentations
Provide technical and strategic planning support to business development activities with respect to new client projects and new business initiatives
Contribute to the overall operations of process sciences lab and infrastructure improvements
Ability to work in a team environment and drive the success of the team
Training and lead of associate scientists
Qualifications
Minimum required experience:
A university degree and 5+ years of related experience
A Masters degree and 3+ years of experience
A PhD and 1+ years of experience
Hands‑on experience with analytical technique such as: HPLC/UPLC, cGE/iCIEF, bioassay, activity assay, and microbial testing
Experience with monoclonal antibodies, bispecific, fusion proteins, and enzymes is preferred
Experience with method development, qualification, and validation
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 10 lbs
Frequent standing/walking to work in lab environment for extended periods
Frequent sitting for extended periods to use computer
Seniority level:
Mid‑Senior level
Employment type:
Full‑time
Job function:
Analyst, Science, and Manufacturing
Industries:
Biotechnology Research and Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Rentschler Biopharma by 2x
Get notified about new Process Development Scientist jobs in
Milford, MA .
#J-18808-Ljbffr