Manufacturing Associate II, Oligo

Maravai Life Sciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.

At Maravai, we believe that diverse perspectives are the foundation of innovation.

Through an inclusive andequitableculture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together,providing differentiated value to our customers, and enabling the miracles of science.

For over 35 years,Maravai’sport folio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market.

Your next role as a Miracle Maker

Maravai Life Sciences is seeking a #Miracle Maker to join our Oligo Manufacturing team as an Manufacturing Associate II, Oligo . The Manufacturing Associate II, Oligo is responsible for executing daily manufacturing operations to produce research- and clinical-grade oligonucleotide products in accordance with established procedures and quality standards. This role supports production activities within ISO-classified environments, including equipment setup, operation, cleaning, maintenance, and troubleshooting.

The Manufacturing Associate II collaborates with cross-functional teams to ensure efficient production, adherence to cGMP requirements, and timely completion of manufacturing schedules. Additionally, this position provides technical guidance and training to junior manufacturing personnel while supporting continuous improvement initiatives.

How you will make an impact:

• Review production schedules, interpret manufacturing specifications, calculate material requirements, and coordinate resources to ensure timely execution of production activities.
• Prepare manufacturing areas, equipment, and materials for cGMP production activities, including project initiation and changeovers.
• Execute manufacturing processes in accordance with approved standard operating procedures (SOPs), batch records, and cGMP requirements.
• Accurately complete batch records, production logs, equipment records, and other required documentation in compliance with Good Documentation Practices (GDP).
• Operate, maintain, and troubleshoot manufacturing equipment, perform routine preventive maintenance, and coordinate repairs as needed.
• Author, review, revise, and execute batch records, SOPs, and other controlled manufacturing documents.
• Train, mentor, and provide technical guidance to manufacturing personnel, ensuring adherence to established procedures, quality standards, and production timelines.
• Support onboarding, qualification, and implementation of new manufacturing equipment and processes with minimal supervision.
• Identify and troubleshoot manufacturing process issues, evaluate production bottlenecks, and implement continuous improvement initiatives to enhance operational efficiency and product quality.
• Collaborate with Process Development, Quality, Engineering, and other cross-functional teams to support production requirements, process transfers, and manufacturing improvements.
• Provide timely written and verbal updates to supervisors and cross-functional stakeholders regarding production progress, technical challenges, and operational priorities.
• Maintain a safe, clean, and compliant manufacturing environment in accordance with established SOPs, safety requirements, and cGMP standards.
• Complete…