Engineer II, MS&T

Posted 14 Days Ago
Be an Early Applicant
San Diego, CA
85K-92K
Junior
Biotech
The Role
As an Engineer II, MS&T, you will support project execution, process development, and provide technical expertise to ensure compliant manufacturing. Responsibilities include efficiency improvements, technology transfers, and collaboration across teams to support product processes.
Summary Generated by Built In

Who we are: 

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 and equitable culture 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’s portfolio 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 LifeSciences is seeking a #MiracleMaker to join our Engineering team as an Engineer II, MS&T. As an Engineer II, MS&T you will be able to support execution of projects and establish expertise in new manufacturing processes and business sustainment. Job responsibilities will include process development and characterization and providing technical support and expertise to production operations to ensure compliant and seamless manufacturing throughout TriLink facilities. 

The MS&T Engineer II will contribute to diverse projects, requiring careful generation and analysis of data and at times creative solutions. They will support critical decisions that impact project success. They will collaborate with cross-functional teams such as Research & Development, Manufacturing, Supply Chain, Legal, IT, Supply Chain, Maintenance, Validation, and Quality Assurance in support of new and current manufacturing processes. 

How you will make an impact: 

  • Support sustainment of processes across TriLink facilities by identifying and implementing efficiency and safety improvements to existing processes 
  • Support process and technology transfers of NPIs from R&D to manufacturing as well as site to site transfers for existing processes. 
  • Provide support for tech transfer for commercialization of pharmaceutical and biotech products 
  • Collaborate on a cross functional team to define technical requirements for new products and processes  
  • Develop SOPs and support recipe development 
  • Design and execute experimental protocols, interpreting data from different sources/formats, using statistical analysis, and preparing scientific/operations development reports 
  • Support resolution of process deviations and investigations 
  • Review and develop technical information for the process such as but not limited to Hazard Information/data, P&IDs, Material of Const. Compatibility, PFDs (Process Flow Diagrams), Unit operation Sequence, Material (including consumables) & Energy Balances, and Equipment operating procedures. 
  • Develop and support implementation of process learning and qualification 
  • Support projects that impact company’s revenue and business strategy 
  • Stay current with industry trends on modern manufacturing technologies (process automation, novel processing equipment, and disposable technologies) 
  • Perform other functions and duties as required 

 The skills and experience that you will bring: 

  • BS in Chemistry, Chemical Engineering, or related field with at least 2 years of experience in a cGMP industrial setting, or MS / PhD in Chemistry, Chemical Engineering, or related field with 0 or more years of experience in cGMP industrial setting. 
  • Verbal and communication skills, including ability to present complex information clearly and concisely, required. 
  • Experience in small and large molecule scale-up in pharmaceutical development is preferred. 
  • Experience with a variety of process equipment (e.g. equipment for reactions, crystallization, Tangential Flow Filtration (TFF), chromatography) is preferred. 
  • Strong understanding of Statistical Process Control (SPC) and statistical knowledge (DOEs, statistical analysis, statistical software, etc.) is strongly preferred. 
  • Experience with cGMP, ICH & PDA guidelines, process validation, project management, and control strategy development preferred.  
  • Experience with automated equipment control systems (DCS / SCADA) is a plus. 
  • Familiarity with nucleoside/nucleotide chemistry, Oligo synthesis is strongly preferred. 
  • Experience working in a self-driven, performance/results oriented, fast paced environment, preferred. 
  • Experience working collaboratively within department and interdepartmentally 
  • Proficiency in Excel, Word, PowerPoint is preferred. 
  • Experience with root-cause analysis tools such as DMAIC and leading process FMEA and risk management exercises is preferred and six sigma certified is preferred. 
  • Experience with 21 CFR 820, ICH Q7, ISO 9001, and/or ISO 13485 requirements a plus. 

The anticipated salary range for this position is $85,342 - $92,088.  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 part owner in Maravai through RSU grants and optional employee stock purchase plans. 
  • We offer comprehensive medical plans and HSA/FSA options. 
  • Fertility & family planning assistance. 
  • A variety of additional optional benefits and insurance options, including pet insurance. 
  • Retirement contributions. 
  • Holidays & Paid Time Off. 

Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at https://www.maravai.com/careers/benefits-and-growth/ 

To view more opportunities to become a #MiracleMaker, visit our career site at https://www.maravai.com/careers/  

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 sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

Click here to view Maravai LifeSciences Privacy Notice 


HIRING SCAM ALERT 

Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: 

  • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.) 
  • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment. 
  • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. 


If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at [email protected]. If you believe you have been a victim of fraud, you can report this activity at: www.iC3.gov or www.stopfraud.gov. 

Top Skills

Chromatography
Dcs
Does
Excel
Nucleoside/Nucleotide Chemistry
PowerPoint
Process Automation
Scada
Statistical Process Control
Tangential Flow Filtration
Word
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The Company
HQ: San Diego, California
114 Employees
On-site Workplace
Year Founded: 2014

What We Do

Maravai brands set the standard in nucleic acid products and services, enzyme development, and biologics safety testing. From producing revolutionary mRNA technologies that drive infectious disease vaccines, cancer vaccines, and other cell and gene therapies to delivering gold-standard bioprocess impurity detection solutions, Maravai is helping life sciences companies overcome their biggest development and manufacturing challenges to streamline and scale from research through clinical trials to commercialization.

For over 35 years, Maravai’s brands have served as proven catalysts for innovative, lifesaving technology for humanity. Across our portfolio of brands, we hold numerous patents and offer more than 1,500 innovative products and services, including CleanCap® technology, CleanAmp® hot start PCR, Antibody Affinity Extraction™, EndonucleaseGTP®, PROTEIN A MIX-N-GO™, MockV®, Sterling™, Glen Pak™, Glen Gel-Pak™.

Each of our brands are ISO-9001:2015 certified and have earned hundreds of thousands of citations in peer-reviewed scientific publications.

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