Temporary Process Development & Manufacturing Specialist II, CDMO

Maravai LifeSciences•San Diego, CA
•Onsite

About The Position

Maravai LifeSciences is seeking a Temporary Process Development & Manufacturing Specialist II to join its customer development team. The role produces research- and clinical-grade components and products by setting up, cleaning, operating, and maintaining equipment; performing wet chemistry reactions; and using pilot-grade purification systems. The specialist authors and implements SOPs and documents work in batch records using Good Documentation Practices. The position serves as a subject matter expert and provides leadership, mentoring, and training in the laboratory. It also supports process development, characterization assays, equipment onboarding, and transfer of improvements to the manufacturing team.

Requirements

  • High school diploma or GED.
  • At least 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, or mRNA.
  • Experience drafting, editing, implementing, and executing Standard Operating Procedures.
  • Strong written and verbal communication skills.
  • Self-motivated, with the ability to organize and prioritize multiple tasks.
  • Ability to mentor team members in processes they have become proficient at executing.

Nice To Haves

  • Associate or bachelor's degree, preferably in science.

Responsibilities

  • Produce research- and clinical-grade components and products.
  • Prepare for production by reviewing schedules, clarifying specifications, calculating requirements, and assembling materials and supplies.
  • Maintain a safe and clean work environment by following standard operating procedures.
  • Write and execute batch records; author and review SOPs; and maintain manufacturing quality documents.
  • Keep equipment operating by following instructions, troubleshooting breakdowns, and arranging repairs.
  • Accurately document production, equipment, and batches using forms, reports, logs, and records in accordance with Good Documentation Practices.
  • Train and mentor new team members.
  • Onboard and author procedures for new equipment.
  • Collect, record, and analyze data as needed.
  • Interpret key process bottlenecks and implement improvements to minimize them.
  • Perform characterization assays focused on developmental improvements.
  • Transfer developmental improvements to the manufacturing team through training and technical transfer.
  • Perform other functions and duties as assigned.

Benefits

  • Potential to become a part owner in Maravai through RSU grants and optional employee stock purchase plans.
  • Comprehensive medical plans and HSA/FSA options.
  • Fertility and family planning assistance.
  • Optional benefits and insurance options, including pet insurance.
  • Retirement contributions.
  • Holidays and paid time off.
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