locations
Milford, MA, United States
time type
Vollzeit
posted on
Vor 2 Tagen ausgeschrieben
job requisition id
JR2353
Medizin vorantreiben, um Leben zu schützen. Gemeinsam.
Dank vieler Jahrzehnte Erfahrung und unserer Leidenschaft für das, was wir tun, leisten wir einen essenziellen Beitrag zur weltweiten Verfügbarkeit von Biopharmazeutika, auch und gerade für Patienten mit seltenen und schweren Erkrankungen.
Rentschler Biopharma SE ist ein führendes Auftragsentwicklungs- und Produktionsunternehmen (CDMO) und ausschließlich auf Kundenprojekte fokussiert. Wir bieten maßgeschneiderte Full-Service-Lösungen für die Bioprozessentwicklung und die Herstellung komplexer Biopharmazeutika. Als deutsches Familienunternehmen mit internationalem Footprint und globaler Reichweite verbinden wir Experten, Expertise und langjährige Erfahrung, um zusammen mit unseren Kunden beste Lösungen zu entwickeln.
Rentschler Biopharma beschäftigt rund 1.400 Mitarbeiter und hat den Hauptsitz in Laupheim, Deutschland, sowie einen Standort in Milford, MA, USA. Im Jahr 2024 haben wir uns dem Global Compact der Vereinten Nationen angeschlossen und unterstreichen damit unser Engagement für Nachhaltigkeit.
Als unabhängiges Familienunternehmen leben wir nach dem Motto: Many hands, many minds – ONE TEAM! Ein offenes, respektvolles Miteinander prägt unsere Arbeitswelt, in der Qualitätsbewusstsein, Sorgfalt und Verantwortung an erster Stelle stehen. Denn bei aller Vielfalt unserer Talente im Rentschler Team verfolgen wir gemeinsam einen Zweck: Medizin voranzutreiben, um Leben zu schützen.

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

Brauchen Sie Hilfe?
Wenn Sie Unterstützung beim Hochladen Ihrer Bewerbung brauchen, wenden Sie sich bitte an unser Recruiting-Team:
welcome@rentschler-biopharma.co

• 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 scientist