Temporary Process Development & Manufacturing Specialist II, CDMO

The role

You will produce research and clinical grade components and products. This involves setting up and maintaining equipment, performing wet chemistry reactions, and utilizing purification systems.

What you will do

• Produces research and clinical grade components and products
• Prepares for production by reviewing schedule, clarifying specifications, and assembling materials
• Maintains safe and clean work environment by following SOPs
• Writes and executes batch records, authors and reviews SOPs, and maintains quality documents
• Keeps equipment operating and troubleshoots breakdowns
• Documents production following good documentation practices
• Trains and mentors new team members
• Onboards and authors procedures for new equipment
• Collects, records and analyzes data
• Implements process improvements to minimize bottlenecks

Required qualifications

• High school diploma or GED
• 5+ years of industry 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

Nice to have

• Associate or Bachelor’s degree (Science)

Before you apply

• Benefits do not apply to temporary employees or contractors

About the company

Maravai LifeSciences provides products and services within the fields of nucleic acid production and biologics safety testing. They serve biotech, biopharma, and life sciences companies.