Manufacturing Technician (Contract/Fixed Term)

Job DescriptionJob DescriptionDescription:

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 who will be responsible for operating lab and pilot plant scale unit operations at Elektrofi. This 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.

KEY RESPONSIBILITIES

• 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.

Requirements:

MINIMUM QUALIFICATIONS

• Bachelor’s degree in scientific discipline is .
• Minimum of two years of hands-on experience in biopharmaceutical or pharmaceutical manufacturing; pilot plant or clinical manufacturing experience .
• Working knowledge of current Good Manufacturing Practices (cGMP) and/or Good Laboratory Practices (cGLP).
• Experience supporting aseptic or bulk manufacturing processes for biologics strongly .
• Strong communication skills, with the ability to clearly document activities and deviations in batch records and logbooks.
• Comfortable performing basic calculations required for solution prep, buffer/media calculations, and process documentation.
• Familiarity with standard bioprocess lab equipment (e.g. centrifuges, pumps, filtration systems, pipettes).
• Proven ability to work effectively both independently and as part of a cross-functional team.
• Proficiency with Microsoft Office and familiarity with digital documentation tools; experience with automation or data capture systems is a plus.
• Strong attention to detail and organizational skills with a focus on data integrity and compliance.
• Prior experience with monoclonal antibody processing, solvent handling, and/or tech transfer is a plus.

Our unique strength lies in transforming pioneering ideas into concrete, life-transforming solutions. To realize this ambitious vision, we are dedicated to nurturing an in-office work ethos. While remote work has its merits, it does not constitute a fundamental aspect of our working approach. Please apply at elektrofi.com/careers.

EEOC Statement:

Elektrofi provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to , , , , , origin, status, genetics, protected veteran status, , or expression, or any other characteristic protected by federal, state, or local laws.

To all agencies, please, no phone calls or emails to any employee of Elektrofi about this requisition. All resumes submitted by search firms/employment agencies to any employee at Elektrofi via email, the internet, or in any form and method will be deemed the sole property of Elektrofi unless such search firms/employment agencies were engaged by Elektrofi for this requisition and a valid agreement with Elektrofi is in place. If a candidate submitted outside of the Elektrofi agency engagement process is hired, no or payment of any kind will be paid

All candidates must be legally authorized to work in the US

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