Metagenomi is a gene editing company committed to developing potentially curative therapeutics by leveraging a proprietary toolbox of next-generation gene editing systems to accurately edit DNA where current technologies cannot. Our metagenomics-powered discovery platform and analytical expertise reveal novel cellular machinery sourced from otherwise unknown organisms. We adapt and forge these naturally evolved systems into powerful gene editing systems that are ultra-small, extremely efficient, highly specific and have a decreased risk of immune response. These systems fuel our pipeline of novel medicines and can be leveraged by partners. Our goal is to revolutionize gene editing for the benefit of patients around the world.
Whether it's the biological diversity of our gene editing systems or the people that help discover them, Metagenomi celebrates the diversity of life. This is achieved through a compassionate culture that acknowledges the dimensions of our diversity. We know that when people feel a sense of inclusion and belonging in the workplace, they have a safe space to bring creativity and innovation to everything they do. We are intentional about building and maintaining a culture where people are valued and respected, there is equity in opportunities, and our respective opinions and differences matter.
Contract Senior Manufacturing Associate
We are seeking an experienced Contract Senior Manufacturing Associate to join our gene-editing reagents and therapeutics manufacturing team. This role combines hands-on manufacturing with project management duties to ensure the successful execution of production projects. The ideal candidate will have a strong background in gene therapy production processes, excellent organizational skills, and the ability to manage projects from inception to completion. This role will be based in Emeryville, California.
How you’ll contribute:
Gene Therapy Production:
- Perform daily gene therapy production processes, including vector production, purification, and formulation.
- Follow established protocols and standard operating procedures (SOPs) to ensure consistent and high-quality product output.
- Conduct in-process testing and sampling to monitor production quality and process parameters.
Quality Assurance and Compliance:
- Ensure all manufacturing activities comply with Good Manufacturing Practices (GMP) and relevant regulatory requirements.
- Actively engage with quality systems (deviations, CAPA, change controls, root cause analysis).
- Maintain accurate and thorough documentation of production activities and project progress.
- Participate in internal and external audits, providing necessary documentation and support.
- Equipment and Facility Maintenance:
- Operate, maintain, and troubleshoot manufacturing equipment and systems, ensuring optimal performance and minimal downtime.
- Coordinate with maintenance teams to schedule and perform routine equipment calibrations and preventive maintenance.
- Ensure the manufacturing facility remains clean, organized, and compliant with safety and regulatory standards.
Process Optimization:
- Identify opportunities for process improvements and implement strategies to enhance production efficiency and product quality.
- Collaborate with cross-functional teams to develop and refine manufacturing processes and protocols.
- Utilize data-driven approaches to analyze production metrics and drive continuous improvement initiatives.
- Support and actively contribute to initiatives to foster a Continuous Improvement culture.
- Work closely with other departments to support production goals and timelines.
- Communicate effectively with team members and supervisors regarding production status, challenges, and opportunities for improvement.
- Prepare and present project updates and reports to management and stakeholders.
What you bring - Knowledge, Skills, and Abilities
- Bachelor’s degree in Biology, Molecular Biology, Biochemistry, Biotechnology
- A minimum of five years of experience in gene therapy or biopharmaceutical manufacturing.
- Proficiency in aseptic techniques and closed system processing. Strong understanding of GMP, FDA, and other regulatory requirements related to gene therapy manufacturing.
- Experience with production equipment, including bioreactors, chromatography systems, and filtration units.
- Strong analytical and problem-solving abilities, with a focus on troubleshooting and optimizing production processes.
- Ability to make data-driven decisions and implement effective solutions in a fast-paced environment.
- Excellent verbal and written communication skills, with the ability to interact effectively with team members and other departments.
- Strong interpersonal skills and the ability to collaborate effectively in a team-oriented environment.
California Pay Transparency Disclosure:
Under the Federal Labor Standards Act, this position is classified as non-exempt. The anticipated hourly rate for this position will be $46.00 to 63.00. Depending on the position offered, you will also be eligible to receive equity, bonuses, and a full range of benefits. Please note that individual total compensation for this position will be determined at the Company’s sole discretion and may vary based on location, skill level, years and depth of relevant experience, and education.
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What makes Metagenomi a unique place to work?
- We are passionate about developing technologies derived from microbial-rich ecosystems that have the power to enable therapeutic development and the potential to cure devastating diseases.
- We have cultivated an amazing culture that values teamwork, curiosity, scientific rigor, and fun. We have a strong commitment to work/life balance, host a weekly employee happy hour and events, provide catered lunches and endless snacks, and more!
- We offer competitive compensation, including a market-benchmarked salary, annual target bonus potential, equity, comprehensive benefits plan, 401(k) with company matching, retirement safe harbor plan, and other perks.
At Metagenomi, we know that our people drive our success. We are an equal opportunity employer and believe in and value diversity and inclusion. Metagenomi provides an open, collegial, and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. Metagenomi does not discriminate on the basis of race, color, religion, sexual orientation, gender, age, physical or mental disability, or any other status protected under federal, state, or local law.
Applicants/Employees have rights under various State and Federal Employment Laws, including without limitation:
- Family & Medical Leave Act
- Equal Employment Opportunity Commission
- Employee Polygraph Protection Act
- California Family Rights Act
- California Fair Employment and Housing Act
Notice to agencies: Our in-house Talent Acquisition Team manages all employment opportunities at Metagenomi. Agencies and independent recruiters must be approved as a vendor by Metagenomi’s Talent Acquisition team. To protect the interests of all parties, Metagenomi will not accept unsolicited resumes, profiles, or biographies. Any unsolicited resumes sent to Metagenomi will be considered referrals and the property of Metagenomi.