Senior Scientist, Process Development Analytics

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Milford, MA, USA
In-Office
120K-150K Annually
Senior level
Biotech
The Role
The Senior Scientist will lead method development, analytical characterization, and support quality control processes for biopharmaceuticals. Responsibilities include designing experiments, mentoring staff, and collaborating with clients to ensure timely project delivery.
Summary Generated by Built In

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. 

The Senior Scientist, Process Development Analytics, is a proactive, strategic, and “hands-on” technical lead who will drive and execute on team objectives in the client-facing role. They will demonstrate flexibility and adaptability while working 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 excellent customer service.
The Senior Scientist, Process Development Analytics, will support the development of protein biologics through analytical characterization of process development intermediates and establishment of analytical methods.

Duties and Responsibilities 

 

  • Design, lead, and execute method development in support of internal and external partners for use within quality control departments for clinical and commercial manufacturing

  • Lead, execute, review, and present high-throughput testing of in-process sample for process development work packages

  • Provide technical and strategic planning support to business development activities with respect to new client projects and new business initiatives

  • Coordinate with management for the day-to-day execution of experiments in lab to ensure proper personnel coverage for timely completion

  • Author high-quality documents, including technical reports, SOPs, and experimental protocols

  • Identify, evaluate, and implement new and existing technologies to improve testing efficiency, control and understanding

  • 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

  • Provide technical support Quality Control and Manufacturing floor activities

  • Serve as PD representative and participate in cross functional meetings

  • Oversee ordering and tracking of routine and client-billable consumables

  • Lead, train, and mentor junior lab staff  

  • Interpret analytical data and understand relation to manufacturing process steps

  • Review data packages and compile slides to present at client project presentations

  • Contribute to the overall operations of process science lab and infrastructure improvements

  • Ability to work in a team environment and drive the success of the projects 

 

Qualifications 

 

  • Minimum required experience:  

  • A university degree and 8 + years of related experience 
  • A Master’s degree and 5+ years  
  • A PhD and 2+ years of experience 
  • Hands-on experience with analytical technique such as: HPLC/UPLC, cGE/iCIEF, bioassay, activity assay, ELISA, qPCR, 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 is preferred

  • 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

  • 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

____________________________________________________________________________
Base Pay Range
$120,000 - $150,000
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.

Skills Required

  • Minimum 8 years of related experience or Master's degree with 5+ years, or PhD with 2+ years
  • Hands-on experience with analytical techniques
  • Experience with monoclonal antibodies, bispecific, fusion proteins, and enzymes
  • Experience with method development, qualification, and validation
  • Proficient in Microsoft Office (Word, Excel, Power Point, SharePoint)
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The Company
Baden-Württemberg
813 Employees
Year Founded: 1927

What We Do

Rentschler Biopharma is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. The company offers process development and manufacturing of biopharmaceuticals, including advanced therapies, as well as related consulting activities, project management and regulatory support. Rentschler Biopharma's high quality is proven by its long-standing experience and excellence as a solution partner for its clients. A high-level quality management system, a well-established operational excellence philosophy and advanced technologies ensure product quality and productivity at each development and manufacturing step. Rentschler Biopharma is a family-owned company with about 1,400 employees, headquartered in Laupheim, Germany, with operations in Milford, MA, USA and Stevenage, UK. In 2024, the company joined the United Nations Global Compact, emphasizing Rentschler Biopharma’s focus on sustainability

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