Associate Director, Biologics Drug Substance

Associate Director, Biologics Drug Substance About Servier With commercial stage products and a promising pipeline, Servier Group is a unique global organization headquartered in France. Operating in more than 150 countries and governed by a non‑profit foundation, we have multiple approved medicines worldwide. We are primarily focused on oncology and other disease states, serving patients with high unmet needs. Role Summary Reporting to the Director of Drug Substance (Biologics), MSAT, this individual‑contributor position serves as a subject‑matter expert in upstream and downstream processes for outsourced drug‑substance manufacturing, technology transfer, life‑cycle management, and global regulatory submissions of complex biopharmaceuticals. Primary Responsibilities Technical Oversight & Manufacturing Support Serve as primary technical interface with global CMOs supporting Drug Substance manufacturing. Lead investigations for technical deviations, root‑cause analyses, and CAPA implementation. Supervise campaign readiness, change management, and process development discussions. Lead internal technical meetings and contribute to Virtual Plant Teams to manage timelines, supply impact, risks, and budget. Oversee process scale‑up, technology transfer, PPQ readiness, and validations across CMO sites. Author and review validation protocols, reports, and technical documentation. Drive continuous improvement initiatives across upstream and downstream processes. Drive standardization and knowledge‑sharing practices across sites and the global network. Lifecycle Management & CPV Own lifecycle management strategies for assigned commercial products across manufacturing sites. Establish and maintain robust process monitoring and Continuous Process Verification strategies. Perform statistical analysis on campaign data to create and analyze process trends and control charts. CMC & Regulatory Support Author and review CMC sections for global regulatory submissions (NDA, BLA, MAA, ND, IPMD). Support filing in new markets and post‑approval changes impact assessment. Support responses to health authority questions related to manufacturing processes and controls. Ensure manufacturing and validation strategies align with GMP, ICH, and global regulatory expectations. Technical Leadership & SME Role Lead process risk and criticality assessments to identify gaps and define improvements. Support business development and technical due diligence activities as needed. Stay current with scientific literature, evolving technologies, and MSAT best practices. Education and Required Skills Academic Background Ph.D. with 5 years of experience or M.S. with 8 years of experience preferred; B.S. with 10 years of experience required in Chemical Engineering, Biochemistry, Biotechnology, Synthetic Organic Chemistry or Pharmaceutical Sciences. Technical Expertise Extensive hands‑on experience in upstream (microbial fermentation & mammalian cell culture) and chromatography, UF/DF, viral clearance, depth filtration techniques in protein purifications. Proven experience with bioconjugation techniques, linker‑payload development, HPAPIs for clinical/commercial ADC manufacturing is desirable. Experience in synthesis, purification, and characterization of antibody drug conjugates and enzymes is preferred. Deep understanding of single‑use technologies, microbiology, extractables and leachables, scale‑down models, DoE, QbD, regulations, and process control strategy. Regulatory and Compliance Proven track record in drafting and reviewing regulatory filings (MAA/NDA/BLA and variations) and responding to health authority queries. Experience in authoring/reviewing dossier sections & reports. Strong understanding of cGMP & ICH guidelines. Data Analysis and Problem Solving Expertise in data management, statistical, and visualization tools such as JMP or Minitab. Advanced proficiency in problem‑solving frameworks (Ishikawa, Kepner‑Tregoe, 5‑Whys). Proven experience collaborating with CMOs and external partners. Proficient in strategic planning and managing multiple complex projects simultaneously. Strong negotiation and influencing skills with the ability to work effectively in interdisciplinary teams. Excellent skills in drafting development reports, summaries, and technical presentations. Excellent verbal and written English skills, including active listening, attention to detail, and the ability to draft technical reports and presentations. Ability to thrive in dynamic environments that embrace change, risk, and flexibility. Travel and Location Preferred location is Boston, US but will consider remote applicants. Domestic and international travel up to 20%. Candidate Profile Servier’s Commitment Servier is committed to modeling diversity, equity, and inclusion within the industry. We are dedicated to fostering an environment that maintains equitable treatment for all and we welcome applicants who are passionate, committed, and innovative. We encourage candidates to apply to our open roles as we are always willing to consider experiences and skills beyond what is listed in the job description. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Salary Range The salary range for this role is $150,000 – $211,000. A pay position within the range will be based on education, qualifications, certifications, experience, skills, geographic location, performance, and business needs. Employees in this position may be eligible for short‑term and long‑term incentive programs. Servier also offers a competitive and comprehensive benefits package that includes medical, dental, vision, flexible time off, 401(k), life and disability insurance, recognition programs, and other benefits subject to eligibility requirements. #J-18808-Ljbffr Servier Group