Full-Time

Engineer – Manufacturing Sciences & Technology

Confirmed live in the last 24 hours

Moderna

Moderna

5,001-10,000 employees

Develops mRNA-based medicines and therapies

Biotechnology
Healthcare

Mid

Norwood, MA, USA

May telecommute up to 2 days per week.

Category
Manufacturing Engineering
Mechanical Engineering
Required Skills
Minitab
SAP Products
Data Analysis
Requirements
  • Requires a Bachelor’s degree in Chemical Engineering or related field and 4 years of progressive post-baccalaureate experience in the position offered or as Process Engineer, Equipment Engineer, Validation Engineer, or related position in the pharmaceutical or biotechnology industry.
  • Alternatively, employer will accept a Master’s degree in the stated fields and 2 years of experience in the stated occupations.
  • Must have 2 years of experience with: Executing Technology Transfers, Process Scale-ups and Process Validations in a GMP environment; Supporting Unit Operations, including Mixing, Filling and Filtration, Chromatography test methods and providing person-in-plant support to troubleshoot incidents; Supporting health agency audits and authoring responses/reports to health agency inquiries; Risk Assessments including FMEA, Failure Mode, FMECA, FTA, HAZOP, and Alarm Rationalization; Incident Investigations, including RCA by using TapRooT methodology, Ishikawa diagrams, Scatterplots, and Pareto Charts; and Data analysis with MiniTab and JMP.
Responsibilities
  • Lead the technology transfer of Small Molecules (SM) products and nucleotide production processes from development to GMP manufacturing.
  • Apply knowledge of unit operations, including Tangential Flow Filtration, Anion Exchange Chromatography, Small Molecule Synthesis Reaction, Inline Filtration, Bottling/Filling, Lipid Encapsulation, Mixing, Clean-in-Place (CIP) and Clean-out-of-Place (COP) to determine process, equipment, and quality control strategy requirements and perform facility fit assessments.
  • Develop User Requirement Specifications (URS’s), Process Flow Diagrams (PFD’s), and technology transfer documents, including process descriptions, bill of materials, bill of parameters, bill of equipment, study protocols, monitoring protocols, study reports, qualification summary reports, sensor risk assessments, standard operating procedures, and master batch records (step-by-step instructions to manufacture product batches).
  • Drive or support Failure Mode and Effects Analysis (FMEA), Failure Mode, Effects and Criticality Analysis (FMECA), Fault Tree Analysis (FTA), Hazard and Operability Analysis (HAZOP), and Alarm Rationalization assessment to quantify risk and recommend risk mitigation strategies.
  • Support Process Characterization with a Quality by Design approach to determine Design of Experiment (DoE) strategy tailored to each specific process and product.
  • Determine Critical Process Parameters, Proven Acceptable Range and Normal Operating Range, as well as Critical Quality Attributes.
  • Support incident investigations through Root Cause Analysis (RCA) and other TapRooT methodologies including Ishikawa diagrams, Scatterplots, and Pareto Charts.
  • Troubleshoot instruments such as Filter Integrity Testers, pH meter and probes, temperature control units, conductivity meter and probes, temperature meter and probes, sensor flowrate meters, single use mixers, chromatography skids, jacketed mixing glass reactors, peristaltic pumps, quaternary diaphragm pumps, biosafety cabinets and fume hoods.
  • Utilize quality documentation management tool (Veeva Vault QMS), laboratory database (LabVantage), equipment database (BlueMountain), and software such as OSI PI Historian, Spotfire, JMP, SAP, Microsoft Office (Excel, Visio, OneNote, PowerPoint, Word, etc) in performance of job duties.
  • Ensure operations are in compliance with all Regulatory, Environmental, Health and Safety (EH&S), and cGMP (current Good Manufacturing Practices) quality systems that assure proper design, monitoring, and control of manufacturing processes and facilities.
  • Author Biologics License Application (BLA) Filing documentation and support Regulatory/Health Agency audits.
  • Lead optimization activities and provide technical expertise for process improvements using DMAIC methodology (Define, Measure, Analyze, Improve and Control) and tools such as Process Mapping, Control Charts, and Pareto Charts.
  • Ensure high degree of performance consistency at the required quality standard.

Moderna focuses on developing medicines using messenger RNA (mRNA), which is a molecule that provides instructions for cells to produce proteins essential for various biological functions. Their approach involves creating a new class of medicines that leverage mRNA to potentially enhance the discovery, development, and manufacturing of drugs. Unlike traditional methods, which often rely on proteins or other biological materials, Moderna's use of mRNA allows for a more versatile and efficient way to create treatments. The company's goal is to improve patient outcomes by harnessing the power of mRNA to address a wide range of health issues.

Company Stage

Grant

Total Funding

$5.9B

Headquarters

Cambridge, Massachusetts

Founded

N/A

Growth & Insights
Headcount

6 month growth

3%

1 year growth

12%

2 year growth

54%
Simplify Jobs

Simplify's Take

What believers are saying

  • Moderna's expansion into combination vaccines and autoimmune therapies showcases its potential for diversified revenue streams and market leadership.
  • The company's continuous innovation and FDA approvals for updated COVID-19 vaccines highlight its resilience and adaptability in a rapidly changing market.
  • Moderna's educational initiatives, like the free mRNA course, position it as a thought leader and advocate for mRNA technology.

What critics are saying

  • The collapse in demand for COVID-19 vaccines could significantly impact Moderna's revenue and growth prospects.
  • Ongoing class action lawsuits alleging securities fraud could damage Moderna's reputation and financial stability.

What makes Moderna unique

  • Moderna is pioneering the use of mRNA technology to create a new class of medicines, setting it apart from traditional pharmaceutical companies.
  • The company's focus on mRNA as the 'software of life' allows for rapid development and manufacturing of vaccines and therapies, unlike conventional methods.
  • Moderna's ability to secure regulatory approvals for mRNA vaccines beyond COVID-19, such as for RSV, demonstrates its leadership in mRNA technology.

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