Director of Drug Substance Manufacturing

Found in: Appcast Linkedin GBL C2 - 2 weeks ago

Cambridge, United States QurAlis Full time

ABOUT THE COMPANY 

QurAlis is a clinical-stage biotechnology company developing breakthrough precision medicines for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with genetically validated targets. 

 

QurAlis is trailblazing the path to conquering amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with genetically validated targets with next-generation precision medicines. QurAlis’ proprietary platforms and unique biomarkers enable the design and development of drugs that act directly on disease-causing genetic alterations. Founded by an internationally recognized team of neurodegenerative biologists from Harvard Medical School and Harvard University, QurAlis is advancing a deep pipeline of antisense oligonucleotides and small molecule programs including addressing sub-forms of ALS that account for the majority of ALS patients. 

 

SUMMARY OF POSITION 


The Director of Drug Substance Manufacturing at QurAlis plays a pivotal role in developing and optimizing chemical processes for Oligonucleotides production and overseeing the refinement of external manufacturing processes. This leader is tasked with steering a team through process development, scale-up, analytical, and technology transfer to manufacturing sites, including managing operations and coordinating with Contract Manufacturing Organizations. His responsibilities are critical to ensuring the consistent delivery of high-quality drug substances for clinical and commercial use, adhering to stringent regulatory standards. By optimizing manufacturing strategies and fostering collaboration with cross-functional teams, the Director plays an instrumental role in enhancing efficiency, quality, and safety, driving innovation, and ensuring that manufacturing practices are in sync with QurAlis' core values. 

 

Primary Job Responsibilities:  

 

  • Oversee the operation of drug substance manufacturing at our Contract Manufacturing Partners, ensuring compliance with all regulatory, safety, and quality standards. 
  • Develop and optimize scalable chemical processes for the synthesis of drug substances, focusing on efficiency, yield, and purity. 
  • Direct the planning and implementation of process development, scale-up, technology transfer, and validation efforts in drug substance manufacturing, ensuring strategic alignment and operational excellence. 
  • Collaborate with cross-functional teams, including analytical development, formulation development, quality assurance, and regulatory affairs, to ensure seamless project progression. 
  • Manage relationships with contract manufacturing organizations and ensure they meet our quality and production requirements. Oversee technology transfer of drug substance processes to CMOs. 
  • Prepare technical reports and presentations to communicate results and progress to internal and external stakeholders. Contribute to the preparation and filing of IMPD, IND, and NDA documentation. 
  • Develop and manage the DS budget, ensuring efficient use of resources and cost-effective processes. 
  • Implement continuous improvement initiatives to enhance manufacturing efficiency, reduce costs, and improve product quality. 
  • Collaborate with regulatory affairs to support regulatory submissions and inspections. 
  • Stay informed about industry trends, technological advancements, and regulatory changes to ensure our manufacturing processes are competitive and compliant. 

 

Primary Job Requirements:     

 

  • Advanced degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or equivalent, with significant experience in Oligo chemistry. 
  • Proven track record in Active Pharmaceutical Ingredient process development, including scale-up and technology transfer, coupled with a deep understanding of synthetic organic chemistry. Proficient in synthesizer operation, chromatography, and principles of process optimization and scale-up. 
  • Deep understanding of regulatory requirements and quality standards in pharmaceutical manufacturing. 
  • Experience in working with CMOs and managing external partnerships. 
  • Excellent communication, organizational, and project management skills. 
  • Ability to think strategically and solve problems effectively. 
  • Commitment to fostering a collaborative and inclusive work environment. 

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    2 weeks ago

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