Manufacturing Technician

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™.

Elektrofi is seeking a talented, enthusiastic, and experienced Manufacturing Technician who will be responsible for operating lab and pilot plant scale unit operations s role reports to the Associate Director, Manufacturing Sciences & Technology and will support the manufacturing of biologically active microparticle suspensions. This individual will join a growing, multidisciplinary team of scientists/engineers to contribute to a variety of manufacturing activities in a highly collaborative environment.

This role supports technology transfer efforts to introduce new drug substances into the pilot plant for manufacturing. The Manufacturing Technician will assist in executing robust processes for monoclonal antibody drug substance and drug product manufacturing to support IND-enabling studies. This includes supporting pilot-scale operations at the Elektrofi site and contributing to continuous improvement initiatives in process optimization and digital manufacturing, aligned with the company’s IT strategic roadmap.

This technician will work cross-functionally, serving as a key link between the MS&T, Quality, Supply Chain, Operations, Process Development, and Analytical Development teams. Responsibilities include coordinating material requests, handling, and transportation for pilot-scale and laboratory manufacturing campaigns.

The ideal candidate will contribute to discussions around safety, quality, delivery, cost, engagement, and drive operational excellence through performance monitoring and process improvement. Success in this role requires adaptability, attention to detail, and the ability to thrive in a fast-paced, team-oriented environment.

• Execute pilot-scale manufacturing processes for IND-enabling studies in accordance with cGxP requirements and company SOPs.
• Adhere to applicable regulations, safety policies, and company core values in daily operations.
• Support technology transfer and scale-up of clinical manufacturing processes.
• Accurately complete batch records and associated documentation
• Actively participate in team meetings and cross-functional discussions.
• Partner closely with Process Development, Analytical Development, Quality, Supply Chain, and Laboratory Operations.
• Perform cleaning, sanitization, and sterilization of manufacturing equipment and controlled areas.
• Contribute to ongoing improvement efforts in automation, digital systems, and operational efficiency.
• As a member of the Technical Operations Team, be a change leader to develop and implement innovative approaches to meet the challenges of a rapidly growing business.
• Accountable for authoring and executing SOPs & manufacturing batch records in support of IND-enabling studies.
• Adhere to cGXP requirements while maintaining sufficient agility to adapt to dynamic and evolving business needs.
• Ensure training and qualifications are maintained to deliver safe, right-first-time execution.

• Bachelor’s degree in scientific discipline is preferred.
• Minimum of two years of hands‑on experience in biopharmaceutical or pharmaceutical manufacturing; pilot plant or clinical manufacturing experience preferred.
• Working knowledge of current Good Manufacturing Practices (cGMP) and/or Good Laboratory Practices (cGLP).
• Experience supporting aseptic or bulk manufacturing processes for biologics strongly preferred.
• Strong communication…