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Mrna Quality Control Jobs (NOW HIRING)

Alphazyme

Manager, QA Operations

Jupiter, FL · On-site

... expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a ... Support Quality Control with customer complaints and Out of Specification (OOS) investigations

CAMRIS

Quality Assurance Manager

Silver Spring, MD · On-site

$128K - $173K/yr

... mRNA, and monoclonal antibodies).Requires a minimum of at least four years of experience in QA management/supervision in the areas of documentation control, raw material management, instrument ...

CAMRIS

Quality Assurance Manager

Silver Spring, MD · On-site

$128K - $173K/yr

... mRNA, and monoclonal antibodies). * Requires a minimum of at least four years of experience in QA management/supervision in the areas of documentation control, raw material management, instrument ...

GT Bio

Research Assistant

Cambridge, MA · On-site

$21 - $29/hr

Perform formulation characterization and quality control measurements (e.g., particle size, PDI ... Experience handling RNA, including mRNA, siRNA, or other oligonucleotides. * Experience with DLS ...

AleloPharma INC.

Research Scientist

Detroit, MI · On-site

Manufacturing will include preparation of synthetic mRNA fusion transcripts, primers/probes sets ... The quality control will be conducted by RT-qPCR experiments using ultra-pure chimeric transcript ...

AleloPharma INC.

Research Scientist

Detroit, MI · On-site

Manufacturing will include preparation of synthetic mRNA fusion transcripts, primers/probes sets ... The quality control will be conducted by RT-qPCR experiments using ultra-pure chimeric transcript ...

GenScript/ProBio

LNP Lab Technician

Redmond, WA · On-site

$55K - $65K/yr

In process QC for LNP size, zeta, PDI, encapsulation efficiency measure and others, make sure ... Prior experience working with mRNA or Lipid Nanoparticles (LNP) is a definite plus. * Technical ...

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Mrna Quality Control information

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How much do mrna quality control jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for mrna quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What is an mRNA Quality Control job?

mRNA Quality Control jobs involve monitoring and testing the quality of messenger RNA (mRNA) products during their manufacturing process. Professionals in these roles ensure that mRNA used in vaccines or therapies meets strict regulatory and safety standards by performing various laboratory tests, analyzing data, and documenting results. They work closely with research scientists, production teams, and regulatory bodies to identify and resolve any issues that could affect the purity, potency, or stability of the mRNA. Their work is critical to ensuring that final products are safe and effective for use in medical treatments.

What are some common challenges faced by mRNA Quality Control professionals, and how can they be addressed?

mRNA Quality Control professionals often encounter challenges such as maintaining consistency in sample analysis, troubleshooting assay variability, and keeping up with evolving regulatory requirements. Addressing these challenges typically involves rigorous adherence to standard operating procedures, ongoing training in new analytical technologies, and close collaboration with R&D and manufacturing teams. Effective communication and a proactive approach to process optimization are key to ensuring high-quality results and compliance in this rapidly advancing field.

What are the key skills and qualifications needed to thrive as an mRNA Quality Control specialist, and why are they important?

To excel as an mRNA Quality Control specialist, you need a background in molecular biology, biochemistry, or a related field, often supported by a relevant degree and laboratory experience. Familiarity with analytical techniques such as qPCR, HPLC, and the use of laboratory information management systems (LIMS) is typically required. Attention to detail, problem-solving, and strong organizational skills help ensure accuracy and reliability in testing processes. These competencies are vital for maintaining product safety, regulatory compliance, and the overall quality of mRNA therapeutics.

What is the difference between Mrna Quality Control vs Mrna Manufacturing Associate?

AspectMrna Quality ControlMrna Manufacturing Associate
Primary RoleInspect and test mRNA products for quality and complianceAssist in the production and assembly of mRNA vaccines or therapeutics
Required SkillsLaboratory testing, quality assurance, attention to detailManufacturing processes, equipment operation, teamwork
Work EnvironmentLaboratories, quality control labsManufacturing floors, cleanrooms
CertificationsQuality assurance certifications, laboratory trainingManufacturing and safety certifications

While both roles are essential in mRNA production, Mrna Quality Control focuses on testing and ensuring product quality, whereas Mrna Manufacturing Associate handles the production process. Understanding these differences helps in choosing the right career path or job search focus within the biotech industry.

What are popular job titles related to Mrna Quality Control jobs?

For Mrna Quality Control jobs, the most frequently searched job titles are:

Infographic showing various Mrna Quality Control job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

LNP Production Intern (Full time)

Redmond, WA • On-site

GenScript/ProBio
See more jobs at GenScript/ProBioexternal

$22 - $24/hr

Full-time, Internship

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 days ago

Job description

About GenScript

Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.

Role Description:

The LNP Production Intern supports the manufacturing and quality control activities associated with mRNA-LNP formulations and related nanoparticle products. This role is responsible for assisting with LNP formulation, purification, concentration, in-process quality testing, inventory management, documentation, and preparation of final products for shipment. The ideal candidate is detail-oriented, highly organized, and able to thrive in a fast-paced production environment while following established SOPs and quality standards. The responsibilities are aligned with existing LNP production workflows used by the team.

Key Responsibilities:

Production Operations:

  • Assist with preparation of buffers, reagents, lipids, and payload materials.
  • Support mRNA-LNP formulation and downstream processing activities.
  • Perform purification and concentration processes following approved SOPs.
  • Operate laboratory equipment including centrifuges, filtration devices, TFF systems, and other production equipment.
  • Assist in antibody-decorated LNP preparation and purification processes following established procedures.

In-Process Quality Control

  • Perform routine QC measurements including: Particle size, PDI, Zeta potential, Encapsulation efficiency and others
  • Accurately record and review production and QC data.
  • Ensure all activities comply with GDP (Good Documentation Practices).

Sample Handling & Shipment

  • Prepare final products for customer delivery.
  • Conduct sterile filtration, aliquoting, tube labeling, and packaging.
  • Maintain sample traceability throughout production and shipping processes.

Inventory & Materials Management

  •  Follow all production SOPs, work instructions, and safety procedures.
  •  Complete batch records and laboratory documentation accurately.
  •  Maintain compliance with ISO and internal quality systems.
  •  Participate in training and continuous improvement initiatives.

Qualifications:

  • Associate's degree or Bachelor's degree in Biology, Biotechnology, Biochemistry, Chemical Engineering, Chemistry, or related field.
  • 0-2 years of laboratory, manufacturing, or biotechnology experience.
  • Strong attention to detail and documentation skills.
  • Basic understanding of laboratory techniques and equipment.
  • Ability to follow SOPs and work independently after training.
  • Ability to lift up to 25 lbs and stand for extended periods
  • Preferred having experience with mRNA production, LNP technology, sterile techniques, centrifugal filtration or TFF, DLS and experience in GMP, ISO regulated environment.

Please note that this is a full-time role based onsite in Redmond, WA with lunch provided daily. The hourly pay-rate is $22-$24 per hour.

Please note that we are not looking for candidates that are unable to commit to a full-time schedule of 40 hours per week. 

Benefits:

Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.