MEDVACON Life Sciences is seeking an AD for Biopharma down-stream process in Indianapolis for our direct Biotech client.

Downstream Process Development (DSP) Associate Director/Director to join a Biotech CDMO in Indianapolis, IN. This individual should display strong technical knowledge and scientific understanding of protein purification as well as having experience in process development at both small and large process scales. The person in this scientific role is expected to work collaboratively with the team to establish and implement best laboratory practices and lead the execution of complex experiments.

• Manage the DSP team, including hiring, training, career and goal development and assessment
• Lead and support downstream process development for purification and concentration of viral vectors or biologics
• Evaluate transferred downstream process for feasibility, quality and scalability
• Collaborate with analytical and upstream functional areas to determine appropriate method for viral vector/protein purification
• Use DoE and QbD approach for process design to guide decisions and/or assess impact to product or process
• Collaborate on technical transfer and scale-up as needed across departments
• Apply technical, functional and industry knowledge to design and evaluate upstream process, review and analyze data, and frame early and late phase needs
• Communicate with clients and internal quality and regulatory groups to transfer processes
• Communicate with internal teams for internal technology transfer process
• Maintain high quality deliverables and open communication, creating a collaborative working environment
• Execute research timelines to meet program and corporate objectives
• Serve as a subject matter expert for all areas of downstream processing

• BS in Engineering, Biotechnology, Biology or similar discipline + 10 years of industry experience
  • OR A minimum of 5 years of experience with a MS OR 3 years of experience with a PhD

• Experience in downstream process development, deep knowledge of viral vectors or biologics downstream process development strategies and familiar with current industry best practices
• Demonstrated problem solving skills and written/verbal communication skills
• Ability to work independently within a team environment
• Demonstrated interpersonal skills to build relationships, act as change agent, and adapt to rapidly changing organizational and business needs
• Ability to thrive in a quickly changing, CDMO environment where flexibility and teamwork is essential

US work eligibility required

Please attach a WORD resume to your submission

All of your information will be kept confidential according to EEO guidelines.