Manufacturing Technician (Contract/Fixed Term)

Job Description ABOUT ELEKTROFI Elektrofi is revolutionizing the delivery of biologic therapies by giving patients the ability to control how they want to receive and benefit from life-changing medicines. Our breakthrough ultra-high concentration microparticle technology platform resolves the limitations associated with intravenously administered biologic therapies by enabling convenient at-home subcutaneous self-administration. With a focus on monoclonal antibodies, therapeutic proteins, and other biologics, we partner with companies to develop and commercialize our novel Hypercon formulations. We believe a patient-centered healthcare approach can lead to a healthier world. We are headquartered in Boston and innovate globally. We are Formulating the Future of Biologics. POSITION SUMMARY Elektrofi is seeking a talented, enthusiastic, and experienced Manufacturing Technician to operate lab and pilot plant scale unit operations. Reporting to the Associate Director, Manufacturing Sciences & Technology, this role supports the manufacturing of biologically active microparticle suspensions and collaborates with scientists and engineers in a multidisciplinary team. This individual will support technology transfer efforts, execute processes for monoclonal antibody drug substance and drug product manufacturing, and assist in continuous process improvement initiatives. The technician will coordinate material requests and transportation for pilot-scale and laboratory manufacturing campaigns, working cross-functionally with various teams. The candidate should contribute to safety, quality, delivery, and operational excellence, thriving in a fast-paced, team-oriented environment with attention to detail and adaptability. KEY RESPONSIBILITIES Execute pilot-scale manufacturing processes for IND-enabling studies in accordance with cGxP and SOPs. Support technology transfer and scale-up of clinical manufacturing processes. Complete batch records and documentation accurately. Participate in team meetings and cross-functional discussions. Partner with Process Development, Analytical Development, Quality, Supply Chain, and Laboratory Operations. Perform cleaning, sanitization, and sterilization of equipment and areas. Contribute to automation, digital systems, and operational efficiency improvements. Develop and implement innovative approaches to meet business challenges. Author and execute SOPs and batch records for IND-enabling studies. Maintain compliance with cGXP and ensure training and qualifications are up-to-date. REQUIREMENTS Bachelor’s degree in a scientific discipline. At least two years of hands-on experience in biopharmaceutical or pharmaceutical manufacturing, including pilot plant or clinical manufacturing. Knowledge of cGMP and/or cGLP. Experience supporting aseptic or bulk biologics manufacturing. Strong documentation and communication skills. Basic calculation skills for solutions and process documentation. Familiarity with bioprocess lab equipment (centrifuges, pumps, filtration systems, pipettes). Ability to work independently and in teams. Proficiency with Microsoft Office and familiarity with digital documentation tools; experience with automation is a plus. Attention to detail and organizational skills focused on data integrity and compliance. Experience with monoclonal antibody processing, solvent handling, or tech transfer is a plus. Our strength lies in transforming pioneering ideas into life-changing solutions. We prefer in-office work to support our collaborative culture. Please apply at

elektrofi.com/careers . EEOC Statement: Elektrofi provides equal employment opportunities and prohibits discrimination and harassment of any kind. Note: No phone calls or emails to employees about this requisition. Resumes sent outside our engagement process are property of Elektrofi. Candidates must be authorized to work in the US. #LI-Onsite

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