Process Development Specialist I

Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Process Development team as a Process Development Specialist I. The Process Development Specialist I supports the production of research- and clinical-grade components and products by executing established laboratory and manufacturing procedures. This role contributes to process development, equipment readiness, process characterization, and manufacturing activities while maintaining quality, documentation, and safety standards. Working under general supervision, the Specialist I supports process improvements, routine troubleshooting, and technology transfer activities within CDMO manufacturing operations.

How you will make an impact: 

• Produces research and clinical-grade components and products by following established manufacturing procedures and quality standards.
• Prepares for production by reviewing production schedules, following specifications, calculating material requirements, and assembling necessary materials and supplies.
• Maintains a safe and clean work environment by adhering to standard operating procedures (SOPs), safety guidelines, and applicable quality requirements.
• Executes batch records and maintains accurate manufacturing documentation in accordance with established procedures and Good Documentation Practices (GDP).
• Operates and maintains manufacturing equipment, performs routine troubleshooting, and escalates equipment issues as needed.
• Accurately completes production forms, reports, logs, and equipment records to ensure proper documentation and traceability.
• Assists with the setup and qualification of new equipment and provides input on associated operating procedures.
• Collects, records, and summarizes production and process data to identify routine trends or deviations and support manufacturing activities.
• Identifies potential process inefficiencies and supports the implementation of improvements under guidance.
• Assists with process characterization activities and developmental experiments to support manufacturing improvements.
• Supports the transfer of process improvements into manufacturing by participating in training and technical transfer activities in accordance with established procedures and under guidance.
• Performs other functions and duties as assigned.

 The skills and experience that you will bring: 

• High school diploma or GED and 2+ years of relevant laboratory or manufacturing experience; or an Associate's or Bachelor's degree in a related scientific discipline; or an equivalent combination of education and experience.
• Hands on laboratory experience in areas such as HPLC purification and/or small molecule synthesis, cGMP clean room, oligonucleotide synthesis, mRNA.
• Experience with drafting, editing, implementing and executing Standard Operating Procedures.
• Strong written and verbal skills.
• Self-motivated and able to organize and prioritize multiple tasks.
• Ability to mentor other team members on processes they have become proficient at executing.

The anticipated hourly rate for this position is $28.00 - $30.00 per hour. The offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role. 

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