Kailera Therapeutics is a biotech company developing advanced therapies for obesity and related conditions. Their lead product, KAI-9531 (HRS9531), an injectable GLP-1/GIP receptor dual agonist, has shown positive results in Phase 2 trials. The company also advances a diversified pipeline with oral administration options. Kailera's mission is to provide transformative weight management solutions that enhance overall health.
Open Positions
Director, Corporate Communications
10+ years of experience in corporate communications, strong writing and project management skills, and ability to work cross-functionally
Senior Manager, GMP Quality Assurance
8+ years of experience in an FDA regulated Pharmaceutical Industry with GMP experience, extensive knowledge of cGMP and quality systems
Director, Clinical Scientist
8+ years of experience, advanced degree in life sciences, strong understanding of clinical trial conduct and cross-functional trial workflows
Associate Director, Device Quality Engineering (Drug Device Combination Products)
10+ years of experience in medical device quality engineering, proven experience with pre-filled syringes and autoinjectors, and deep understanding of design controls and statistical analysis tools
Director, Global Regulatory Affairs (Submission Project Management)
10+ years of experience in regulatory affairs and/or project management, strong project management skills, and excellent communication, organizational, and leadership abilities
Associate Director, Device Engineering
10+ years of experience in medical device development, 3+ years in a team leadership role, and a deep understanding of design controls and regulatory standards
Associate Director, Clinical Quality Assurance
10+ years of experience in FDA regulated industry, Bachelor’s degree required, and previous hands-on experience with Veeva Quality Docs, Veeva Training, and Veeva QMS
Director, Drug Product Manufacturing and Development
10+ years of experience in the pharmaceutical/biotech industry, technical expertise in aseptic manufacture of sterile drug products, and strong problem-solving skills
Associate Director, Program Management
10+ years of experience in project management, Bachelor's degree in science, engineering, or a related field
Senior Director, Toxicology
12+ years of relevant experience or advanced degree with 10+ years of experience
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