2

Entry Level Mrna Jobs (NOW HIRING)

Post Doc Res Assoc

Campus, IL

$65.60K - $73.14K/yr

... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Microprotein or peptide biology; therapeutic peptide, mRNA, or gene therapy development related to ...

Post Doc Res Assoc

Campus, IL

$65.60K - $73.14K/yr

... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Microprotein or peptide biology; therapeutic peptide, mRNA, or gene therapy development related to ...

Post Doc Res Assoc

Campus, IL · On-site

$65.60K - $73.14K/yr

... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Microprotein or peptide biology; therapeutic peptide, mRNA, or gene therapy development related to ...

... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Microprotein or peptide biology; therapeutic peptide, mRNA, or gene therapy development related to ...

Post Doc Res Assoc

Salt Lake City, UT · On-site

$65.60K - $73.14K/yr

... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Microprotein or peptide biology; therapeutic peptide, mRNA, or gene therapy development related to ...

Post Doc Res Assoc

Salt Lake City, UT · On-site

$65.60K - $73.14K/yr

... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Microprotein or peptide biology; therapeutic peptide, mRNA, or gene therapy development related to ...

Entry Level Mrna information

See salary details

$12

$16

$22

How much do entry level mrna jobs pay per hour?

As of May 30, 2026, the average hourly pay for entry level mrna in the United States is $16.94, according to ZipRecruiter salary data. Most workers in this role earn between $15.62 and $18.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Entry Level mRNA Scientist, and why are they important?

To thrive as an Entry Level mRNA Scientist, you generally need a bachelor’s or master’s degree in molecular biology, biochemistry, or a related field, with a strong understanding of nucleic acid technologies. Familiarity with laboratory techniques such as PCR, RNA extraction, gel electrophoresis, and experience using lab management software are typically required. Strong attention to detail, problem-solving abilities, and effective teamwork and communication skills help individuals excel in this role. These skills and qualities are crucial for ensuring accurate experimental results, maintaining lab safety, and contributing to successful research outcomes.

What are some common challenges entry-level mRNA professionals face when transitioning from academia to the biotech industry?

Entry-level mRNA professionals often find the shift from academic research to industry challenging due to the fast-paced, results-driven environment and the need to adapt to strict regulatory standards. Unlike academia, where projects may be more exploratory, industry roles require adherence to protocols and tight timelines, with a strong focus on teamwork and communication across multidisciplinary teams. Additionally, new hires may need to quickly learn specialized equipment, documentation practices, and industry-specific software, which can be a steep learning curve but offers valuable professional growth.

What does an entry-level mRNA job involve?

An entry-level mRNA job typically involves assisting in laboratory research, production, or quality control related to messenger RNA (mRNA) technologies. Responsibilities may include preparing samples, operating laboratory equipment, documenting data, and supporting senior scientists or technicians in the development or manufacturing of mRNA-based products, such as vaccines or therapeutics. These roles are usually found in biotechnology or pharmaceutical companies, and provide valuable hands-on experience in a rapidly growing field.

What is the difference between Entry Level Mrna vs Entry Level rRNA?

AspectEntry Level MrnaEntry Level rRNA
Required CredentialsBiology degree, lab experienceBiology degree, lab experience
Work EnvironmentResearch labs, biotech companiesResearch labs, biotech companies
Industry UsageGene expression studies, biotech researchRibosome structure, protein synthesis research
Common Search IntentEntry level mRNA roles, mRNA technicianEntry level rRNA roles, rRNA technician

Entry Level Mrna and Entry Level rRNA roles both require a biology background and lab experience. While they share similar work environments in research labs and biotech companies, they focus on different aspects of molecular biology. Entry Level Mrna positions typically involve gene expression analysis, whereas Entry Level rRNA roles focus on ribosomal RNA and protein synthesis. Candidates should choose based on their specific interests in molecular biology research areas.

More about Entry Level Mrna jobs
What are the most commonly searched types of Mrna jobs? The most popular types of Mrna jobs are:
Infographic showing various Entry Level Mrna job openings in the United States as of May 2026, with employment types broken down into 33% As Needed, and 67% Temporary. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $35,227 per year, or $16.9 per hour.
Technician - Biomanufacturing, Downstream/mRNA

Technician - Biomanufacturing, Downstream/mRNA

Catalent Pharma Solutions

Madison, WI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago


Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

45th of 70 rated pharmaceutical


Job description

Technician - Biomanufacturing, Downstream/mRNA

Position Summary:

  • Work Schedule: 2pm-12am (Sunday-Wednesday or Wednesday-Saturday shift availability)
  • 100% on-site

Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.

This is an entry level position in the Manufacturing team and is the starting point to acquiring skills and training required for a cGMP biomanufacturing environment. The Technician is responsible for the manufacture of biopharmaceutical products within a clean room environment. The position is expected to follow detailed instructions and established procedures with frequent supervision.

The Role:

  • Perform basic Downstream purification and mRNA production activities, such as in-vitro transcription (IVT) reactions, chromatography, tangential flow filtration (TFF), viral filtration, and column packing and qualification
  • Accurately follows manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) and with a focus on "right first time" execution
  • Documents all activities in accordance with Good Documentation Practices (GDPs) in BPRs, Forms, and other quality documentation
  • Recognizes deviations from the intended procedure and raises awareness through the Rapid Response process
  • Proactively identifies safety, quality, and efficiency improvements; Actively participates in the Catalent Way (Continuous Improvement Culture)
  • May lead "Just Do It" (JDI) Continuous Improvement (CI) activities and engage in implementation of CI projects
  • May coach more junior team members on basic execution activities and act as an "onboarding buddy" to facilitate bringing new team members quickly up to speed on culture and basic workplace expectations
  • Performs general cleanroom housekeeping, including room and equipment cleaning, disposal of waste, and maintenance of 5S standards
  • Other duties as assigned

The Candidate:

  • Must have High School Diploma or equivalent plus at least two (2) years of relevant experience. We will also accept a Bachelors or Associates Degree in a scientific, engineering, or biomanufacturing discipline without any formal experience
  • GMP manufacturing experience preferred
  • Ability to use Microsoft Word and Excel, and other Office systems
  • GMP manufacturing experience preferred
  • Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, Chromatography software
  • Physical requirements: This position requires frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities for the position. Working conditions will be Heating Ventilation and Air Conditioned controlled. Ability to operate within a clean room environment as needed.

Why you should join Catalent:

  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • 152 hours of PTO + 8 paid holidays
  • Generous 401K match
  • Medical, dental and vision benefits
  • Tuition Reimbursement- Let us help you finish your degree or start a new degree!

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Catalent logo

About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

Social media