Elektrofi
Overview
Manufacturing Technician (Contract/Fixed Term)
at Elektrofi. Elektrofi is revolutionizing the delivery of biologic therapies by giving patients the ability to control how they receive and benefit from life-changing medicines. Our ultra-high concentration microparticle technology enables convenient at-home subcutaneous self-administration of monoclonal antibodies and other biologics. We partner with companies to develop and commercialize Hypercon formulations. We are headquartered in Boston and innovate globally.
Position Summary Elektrofi is seeking a talented, enthusiastic, and experienced Manufacturing Technician who will operate lab and pilot plant scale unit operations and support manufacturing of biologically active microparticle suspensions. Reports to the Associate Director, Manufacturing Sciences & Technology and collaborates with cross-functional teams (MS&T, Quality, Supply Chain, Operations, Process Development, Analytical Development). This role includes supporting technology transfer to pilot plant, assisting in executing robust processes for monoclonal antibody drug substance and drug product manufacturing to support IND-enabling studies, and contributing to process optimization and digital manufacturing aligned with the IT roadmap.
The technician will work cross-functionally, coordinating material requests, handling and transport for pilot-scale and lab campaigns, and contribute to safety, quality, delivery, and cost objectives with a focus on operational excellence. Adaptability and attention to detail are essential 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.
Support technology transfer and scale-up of clinical manufacturing processes.
Accurately complete batch records and associated documentation.
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 manufacturing equipment and controlled areas.
Contribute to ongoing improvement in automation, digital systems, and operational efficiency.
As a member of the Technical Operations Team, contribute to innovative approaches to meet the challenges of a rapidly growing business.
Author and execute SOPs and manufacturing batch records in support of IND-enabling studies.
Adhere to cGXP requirements while maintaining agility to adapt to business needs.
Ensure training and qualifications are maintained to deliver safe, right-first-time execution.
Minimum Qualifications
Bachelor’s degree in a scientific discipline (preferred).
Minimum of two years of hands-on experience in biopharmaceutical or pharmaceutical manufacturing; pilot plant or clinical manufacturing experience preferred.
Working knowledge of cGMP and/or cGLP.
Experience supporting aseptic or bulk manufacturing processes for biologics preferred.
Strong communication skills with ability to 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 independently and in cross-functional teams.
Proficiency with Microsoft Office; familiarity with digital documentation tools; automation or data capture systems a plus.
Strong attention to detail and 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 life-changing solutions. We value an in-office work ethos. Remote work is not a fundamental aspect of our 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 race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity 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 fee or payment of any kind will be paid.
All candidates must be legally authorized to work in the US.
Job Details
Seniority level: Entry level
Employment type: Contract
Job function: Management and Manufacturing
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at Elektrofi. Elektrofi is revolutionizing the delivery of biologic therapies by giving patients the ability to control how they receive and benefit from life-changing medicines. Our ultra-high concentration microparticle technology enables convenient at-home subcutaneous self-administration of monoclonal antibodies and other biologics. We partner with companies to develop and commercialize Hypercon formulations. We are headquartered in Boston and innovate globally.
Position Summary Elektrofi is seeking a talented, enthusiastic, and experienced Manufacturing Technician who will operate lab and pilot plant scale unit operations and support manufacturing of biologically active microparticle suspensions. Reports to the Associate Director, Manufacturing Sciences & Technology and collaborates with cross-functional teams (MS&T, Quality, Supply Chain, Operations, Process Development, Analytical Development). This role includes supporting technology transfer to pilot plant, assisting in executing robust processes for monoclonal antibody drug substance and drug product manufacturing to support IND-enabling studies, and contributing to process optimization and digital manufacturing aligned with the IT roadmap.
The technician will work cross-functionally, coordinating material requests, handling and transport for pilot-scale and lab campaigns, and contribute to safety, quality, delivery, and cost objectives with a focus on operational excellence. Adaptability and attention to detail are essential 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.
Support technology transfer and scale-up of clinical manufacturing processes.
Accurately complete batch records and associated documentation.
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 manufacturing equipment and controlled areas.
Contribute to ongoing improvement in automation, digital systems, and operational efficiency.
As a member of the Technical Operations Team, contribute to innovative approaches to meet the challenges of a rapidly growing business.
Author and execute SOPs and manufacturing batch records in support of IND-enabling studies.
Adhere to cGXP requirements while maintaining agility to adapt to business needs.
Ensure training and qualifications are maintained to deliver safe, right-first-time execution.
Minimum Qualifications
Bachelor’s degree in a scientific discipline (preferred).
Minimum of two years of hands-on experience in biopharmaceutical or pharmaceutical manufacturing; pilot plant or clinical manufacturing experience preferred.
Working knowledge of cGMP and/or cGLP.
Experience supporting aseptic or bulk manufacturing processes for biologics preferred.
Strong communication skills with ability to 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 independently and in cross-functional teams.
Proficiency with Microsoft Office; familiarity with digital documentation tools; automation or data capture systems a plus.
Strong attention to detail and 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 life-changing solutions. We value an in-office work ethos. Remote work is not a fundamental aspect of our 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 race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity 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 fee or payment of any kind will be paid.
All candidates must be legally authorized to work in the US.
Job Details
Seniority level: Entry level
Employment type: Contract
Job function: Management and Manufacturing
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