Process Development & Manufacturing Specialist II, CDMO

Our talented employees drive our mission and share core values that both stem from and define our culture, which plays an invaluable role in our execution at all levels in our organization. Our culture is based on shared core values which we believe contribute to our success and continued growth.

Maravai promotes a safe and healthy work environment while celebrating and recognizing accomplishments both individually and collectively.

We offer a highly competitive total rewards program to attract and retain top talent: stock plans, healthcare, bonuses, work-life balance, and career development.

Be part of our growing team. Explore our job opportunities .

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 customer development team as a Process Development & Manufacturing Specialist II . As a Process Development & Manufacturing Specialist II, you will produce research and clinical grade components and products by setting up, cleaning, operating , and maintaining equipment; performing wet chemistry reactions; utilizing pilot grade purification systems, authoring and implementing SOPs, and documenting actions in batch records.

Must document all actions using Good Documentation Practices. This role is the subject matter expert and provides leadership/mentoring/training in the laboratory.

How you will make an impact:

• Produces research and clinical grade components and products
• Prepares for production by reviewing production schedule; studying and clarifying specifications; calculating requirements; assembling materials and supplies
• Maintains safe and clean work environment by following standard operating procedures
• Writes and executes batch records, author and review SOPs, and maintain quality documents associated with manufacturing
• Keeps equipment operating by following operating instructions; troubleshooting breakdowns; calling all repairs
• Documents production by accurately completing forms, reports, logs, and records of equipment and batches following good documentation practices
• Trains and mentors new team members
• Onboards and authors procedures for new equipment
• May collect, records and analyze data
• Interprets key process bottlenecks and implements process improvements to minimize bottleneck
• Performs characterization assays centered around developmental improvements
• Transfers developmental improvements to manufacturing team through training/technical transfer
• Perform other functions and duties as required

The skills and experience that you will bring:

• High school diploma or GED required , Associate or Bachelor’s degree preferred (Science)
• 5+ years of industry experience
• Hand…