Senior Specialist, GMP Quality Assurance

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera’s mission to advance novel therapies for obesity and related conditions. We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team. What You’ll Do: The Senior Specialist, GMP Quality Assurance will collaborate internally with QA, RA, and CMC departments. As needed, work with external Approved Service Providers to ensure oversight and compliance. The Senior Specialist will perform review of drug substance/drug product manufacturing records and associated documents (i.e. deviations) for product that will be released for use in Kailera phase I-III clinical programs. The Senior Specialist will help continuously improve Quality System Procedures related to GMP activities related to their function and will collaborate closely with internal cross-functional teams. Required location: Waltham, MA (hub-based, onsite 3-4 days per week) Responsibilities: Review and approve Service Provider GMP documentation Review and approve master batch/packaging records Review executed batch/packaging records for Intermediates, Drug Substance, and Drug Product Prepare batch file for final batch disposition for Kailera’s Phase I-III clinical programs Review GMP Quality Events, change controls, CAPA’s, and other GMP documentation as needed Identify and escalate issues effectively Compile data for Quality System Reviews Evaluate GMP activities for continuous improvement opportunities Support creation and continuous improvement of Kailera procedures Other Quality Assurance responsibilities as assigned Required Qualifications: 6+ years of experience in an FDA regulated Pharmaceutical Industry with GMP experience Understanding and knowledge of industry standards, concepts, current cGMP (21 CFR Parts 210 & 211 & Part 11 and EudraLex), and other agency standards and guidance as they relate to quality systems/quality assurance Experience with review of GMP manufacturing/packing records (Master/Executed Batch Records, Deviations, Change Controls, etc.) associated with Phase I-III clinical studies Proficient in Veeva QualityDocs and Veeva QMS a plus Demonstrates proven track record of communication with internal and external Service providers Ability to identify quality issues requiring escalation Clear, concise writing skills and good verbal presentation skills Self-motivated, detail oriented, well organized, and able to manage multiple projects Ability to interact constructively and efficiently with co-workers within and across departments and Management, as well as with Service providers in a professional and collaborative manner Preferred Qualifications: Biotech experience preferred Education: BA or BS degree in a scientific discipline or supplemental Quality education Salary Range $122,000 — $150,000 USD For Full Time Roles: This range represents the company’s good-faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year-end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grants—because your well-being and future matter to us. EQUAL EMPLOYMENT OPPORTUNITY INFORMATION: Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hair