Help us bring the miracles of science to life 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.
Process Development & Manufacturing Specialist II, CDMO Maravai LifeSciences 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, providingdifferentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai’sportfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since itsinception, we are now leading the way in the rapidly expanding mRNA market.
Your next role as a Miracle Maker
Maravai LifeSciences is seeking a #MiracleMaker 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
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 salary range for this position is $80,000 - $85,000. In addition, highly competitive long-term incentives in the form of company equity, bonus participation and company sponsored benefits are provided as part of the total compensation package. The salary 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.
#LI-Onsite
The benefits of being a #MiracleMaker:
You have the potential to change, improve, and save lives around the world.
You have the opportunity to be a partowner inMaravai through RSU grants andoptionalemployee stock purchase plans.
Weoffer comprehensivemedical plansandHSA/FSAoptions.
Fertility &family planningassistance.
A variety ofadditionaloptional benefitsand insurance options, includingpet insurance.
Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexualorientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
Voluntary Self-Identification For government reporting purposes, we ask candidates to respond to the below self-identification survey. Completion of the form is entirely voluntary. Whatever your decision, it will not be considered in the hiringprocess or thereafter. Any information that you do provide will be recorded and maintained in aconfidential file.
As set forth in TriLink BioTechnologies’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
If you believe you belong to any of the categories of protected veterans listed below, please indicate by making the appropriate selection. As a government contractor subject to the Vietnam Era Veterans Readjustment Assistance Act (VEVRAA), we request this information in order to measurethe effectiveness of the outreach and positive recruitment efforts we undertake pursuant to VEVRAA. Classification of protected categoriesis as follows:
A "disabled veteran" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service-connected disability.
A "recently separated veteran" means any veteran during the three-year period beginning on the date of such veteran's discharge or release from active duty in the U.S. military, ground, naval, or air service.
An "active duty wartime or campaign badge veteran" means a veteran who served on active duty in the U.S. military, ground, naval or air service during a war, or in a campaign or expedition for which a campaign badge has been authorized under the laws administered by the Department of Defense.
An "Armed forces service medal veteran" means a veteran who, while serving on active duty in the U.S. military, ground, naval or air service, participated in a United States military operation for which an Armed Forces service medal was awarded pursuant to Executive Order 12985.
