Group Leader - Analytical Development

Group Leader - Analytical Development   Catalent is seeking   Group Leaders   to join our growing   Analytical Development   team in Madison, Wisconsin.   This is an exciting opportunity for those who are passionate about analytical method development,   people   leadership, and client collaboration. In this role, you will lead a team of scientists responsible for developing,   optimizing , characterizing, and transferring analytical methods that support a diverse portfolio of biologics programs, including proteins, monoclonal antibodies ( mAbs ), and emerging modalities such as mRNA therapeutics.   As a Group Leader, you will combine technical   expertise , leadership, and cross-functional collaboration to help advance client programs from development through GMP manufacturing while ensuring the highest standards of quality, compliance, and scientific excellence.   About Catalent Madison   Catalent's Madison, Wisconsin facility is   a state-of-the-art   biologics   development and manufacturing site supporting customers from research through early- and mid-stage clinical production. Located at 726 Heartland Trail, the 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance manufacturing, and biopharmaceutical process development.   The site is home to Catalent's proprietary   GPEx ® and   GPEx ® Lightning technologies, enabling the generation of high-producing mammalian cell lines for biologic therapies. With production capabilities ranging from 50L to 4,000L and a recent $45 million expansion, the Madison campus continues to play a critical role in Catalent's global   biologics   network while supporting Wisconsin's growing life sciences industry.   Location:   100% Onsite at our facility in Madison, Wisconsin   Shift:   Monday – Friday, First Shift    Key Responsibilities   Lead, mentor, and develop   a team of 5–10 scientists by   providing   technical guidance, coaching, performance feedback, and career development support.   Manage team priorities, workloads, and resources   to ensure analytical development projects are executed successfully and delivered on schedule.   Oversee analytical method development, optimization, characterization, and technology transfer activities   supporting biologics development programs.   Review and approve scientific data, technical reports, and GMP documentation   to ensure quality, compliance, and data integrity.   Serve as a primary client-facing representative   for Analytical Development by   participating   in meetings, communicating project updates, and addressing technical questions.   Collaborate cross-functionally   with Project Management, Quality, Manufacturing, Process Development, Cell Line Development, and other stakeholders to achieve program milestones and drive continuous improvement.   Other responsibilities as needed.   Required Qualifications   PhD   in Biotechnology, Biochemistry, Molecular Biology, Analytical Chemistry, or related scientific discipline with a   minimum   of   2 years of laboratory leadership experience,   or   master's degree   in a related scientific discipline with a   minimum   of   5 years of laboratory leadership experience, or   bachelor's degree   in a related scientific discipline with a   minimum   of   8 years of laboratory leadership experience   Analytical method development experience within a biologics or biopharmaceutical environment   Previous   laboratory leadership experience   Experience managing multiple priorities, projects, and timelines   Strong written and verbal communication skills   Ability to effectively engage with clients and cross-functional stakeholders   Experience   operating   within a GMP-regulated environment   Preferred Qualifications   Experience with the following analytical techniques: ELISA (highly preferred), Western Blot, SDS-PAGE. Agarose Gel Electrophoresis, HPLC/UHPLC, Capillary Electrophoresis (CE),   cIEF, Product Binding and Potency Assays, LC-MS, qPCR, Sanger Sequencing   Experience in biologics, protein, monoclonal antibody ( mAb ), and/or mRNA analytical development   highly preferred   CDMO, CRO, or biopharmaceutical industry experience   Why you should join Catalent     Opportunity to play a key role in driving growth within a global CDMO leader.    Competitive compensation package, including incentive opportunity.    Day-one medical, dental, and vision coverage.    401(k) with company   match .    Tuition reimbursement and professional development opportunities.    Generous paid time off and holiday schedule (152 hours   + 8 holidays)    Collaborative, mission-driven culture focused on improving patient outcomes worldwide.   ​ Catalent offers rewarding opportunities to further your career!   Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.  personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [email protected] . This option is reserved for individuals who require accommodation due to a disability. Information received w