Accelerate biotechnology

Scientist Downstream Process Development in US (Woburn MA)

To report to the Team leader of viral vaccine development team, US, we are looking for a Scientist Downstream Process Development for our R&D department in Woburn, MA -USA. We are seeking for a highly motivated expert in development of viral vaccines and viral vectors purification processes.

Most of the projects are related to viral vaccines and viral vectors development and are funded by biopharmaceutical companies or NGO’s, such as the Bill and Melinda Gates Foundation, CEPI or IAVI. The DSP team collaborates closely with the upstream processing and assay teams in a number of large process development projects which are executed according to aggressive timelines.

In our startup culture, the ideal candidate will show entrepreneurial spirit, independence and ability to take strategic, calculated risks to guarantee efficient progression of the projects and build the team and the US operations. This innovator will be motivated by assessing and implementing new manufacturing technologies to keep Batavia ahead of the competition. Agility, flexibility and will to contribute to projects that have a strong impact on global health are key components of the culture of Batavia Biosciences.

RESPONSIBILITIES:

  • Guide technical strategies for purification process development to support pre-clinical and clinical programs at all development stages, including process development, optimization, technology transfer, and process characterization of cGMP viral vaccines and viral vectors processes;
  • Take responsibility for the design and execution of purification process development studies;
  • Independently design, execute and interpret purification experiments including clarification, tangential flow filtration, column packing, and chromatography;
  • Demonstrate experience with viral process validation and scale down models for biopharmaceutical processes, including review and interpretation of results;
  • Demonstrate expert knowledge of scale up principles with respect to virus purification;
  • Work on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors;
  • Author Standard Operating Procedures, technical reports, process descriptions, including data interpretation and procedures suitable for inclusion in pre-IND, IND, or equivalent regulatory submission;
  • Must be familiar with BSL-II lab safety requirements;
  • Lead technology transfer and technical oversight of processes to Batavia’s cGMP facility;
  • Participate in multi-disciplinary projects with multi-cultural teams, and guide project and business strategies;
  • Facilitate collaboration with both internal and external drug substance analytical, quality control, quality assurance, and manufacturing teams;
  • Exercise judgment in selecting methods, techniques and evaluation criteria to obtain high quality results on time and on budget;
  • Manage, train, guide and coordinate activities of junior staff members;
  • Update group members on background and status of projects by giving oral updates or internal presentations;
  • Actively seek opportunities for continuous improvement;
  • Assist other departments and performs all other duties as assigned.

EDUCATION AND EXPERIENCE:

  • B.S. or M.S. in life sciences, chemical engineering, biochemistry or related fields
  • 10+ years  of experience working in a biopharmaceutical laboratory focusing on viral vaccines and viral vectors purification process development
  • Demonstrated understanding of cGMP process development and production
  • Experience operating in early stage clinical to commercial environments, as well as contract development and manufacturing
  • Demonstrated history of strong hands-on ability, problem solving, and independent experimental design and execution
  • Demonstrated technical proficiency and knowledge of scientific concepts
  • Ability to adapt to change and effectively deliver under pressure and time constraints, while maintaining a high level of work quality

Please send applications to Mrs. Ingrid van Aarle, HR Manager, by e-mail recruitment@bataviabiosciences.com.

 

Batavia Biosciences is committed to providing every applicant equal consideration for employment without regard to disability, race, color, sex, sexual orientation, gender identity, religion, national origin or veteran status. We pride ourselves for our diversified and inclusive culture that helps us leverage the best talents to create growth opportunities for our people and our business.