Temporary Process Development & Manufacturing Specialist II, CDMO

Maravai LifeSciences • San Diego, CA

26d • $38 - $40 • 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 through laboratory and manufacturing activities, including wet chemistry reactions and the use of pilot-grade purification systems. Responsibilities include setting up, cleaning, operating, and maintaining equipment; preparing and documenting production; and writing, reviewing, and implementing standard operating procedures and batch records in accordance with Good Documentation Practices. The position serves as a subject matter expert and provides leadership, mentoring, and training in the laboratory. The anticipated hourly rate is $38–$40, depending on factors that may include the successful candidate’s skills, experience, qualifications, and role location. Benefits described in the posting do not apply to temporary employees or contractors.

Requirements

• High school diploma or GED.
• At least 5 years of industry experience.
• Hands-on laboratory experience in areas such as HPLC purification, 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-motivation and ability to organize and prioritize multiple tasks.
• Ability to mentor team members on processes the candidate is proficient in.

Nice To Haves

• Associate or bachelor’s degree in a science field.

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 in forms, reports, logs, and equipment and batch records in accordance with Good Documentation Practices.
• Train and mentor new team members.
• Onboard new equipment and author procedures for it.
• 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 required.

Benefits

• Potential to become a part owner 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.

What This Job Offers

• Career Level: Mid Level
• Education Level: High school or GED