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Entry Level Pharmaceutical Quality Control Jobs (NOW HIRING)

QC Scientist I

Cincinnati, OH · On-site

$18 - $24/hr

We are hiring for an Entry-Level Pharmaceutical Scientist here in the Cincinnati, Ohio area! This ... the QC Chemistry Laboratory of a large pharmaceutical company in the area. This role supports ...

Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through ... Experience in pharmaceutical/regulated environment preferred but not required Knowledge, Skills ...

Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...

QC Chemist

San Diego, CA · On-site

$24 - $28/hr

Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences , or a related scientific discipline. * Minimum of 2 years of experience in a Quality Control or analytical laboratory ...

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QC Chemist

San Diego, CA · On-site

$24 - $28/hr

Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences , or a related scientific discipline. * Minimum of 2 years of experience in a Quality Control or analytical laboratory ...

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QC Analyst II

Fremont, CA · On-site

$41/hr

Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading ... This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe ...

Microbiologist This role focuses on supporting a growing animal health pharmaceutical facility by performing microbiology quality control activities in a QC laboratory. The microbiologist develops ...

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Entry Level Pharmaceutical Quality Control information

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$12

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How much do entry level pharmaceutical quality control jobs pay per hour?

As of Jul 23, 2026, the average hourly pay for entry level pharmaceutical quality control in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Pharmaceutical Quality Control vs Entry Level Pharmaceutical Quality Assurance?

AspectEntry Level Pharmaceutical Quality ControlEntry Level Pharmaceutical Quality Assurance
Primary FocusTesting and analyzing raw materials, in-process, and finished products to ensure qualityDeveloping, implementing, and maintaining quality systems and procedures
Work EnvironmentLaboratory settings with emphasis on testing and analysisOffice and laboratory settings focusing on documentation and compliance
Required CredentialsTypically a bachelor's in science or related field; certifications like GMP are commonSimilar educational background; GMP knowledge and certifications are also valued

Entry Level Pharmaceutical Quality Control focuses on testing and analyzing products to ensure they meet quality standards, while Entry Level Pharmaceutical Quality Assurance emphasizes establishing and maintaining quality systems and compliance. Both roles require similar educational backgrounds and certifications, but their daily tasks and focus areas differ within the pharmaceutical industry.

What cities are hiring for Entry Level Pharmaceutical Quality Control jobs? Cities with the most Entry Level Pharmaceutical Quality Control job openings:
What are the most commonly searched types of Pharmaceutical Quality Control jobs? The most popular types of Pharmaceutical Quality Control jobs are:
What states have the most Entry Level Pharmaceutical Quality Control jobs? States with the most job openings for Entry Level Pharmaceutical Quality Control jobs include:
QC Scientist I

Full-time

Posted 5 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 418 frontline employees who took The Breakroom Quiz

200th of 535 rated manufacturers


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
How will you make an impact?
Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of pharmaceutical products. You will perform chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP). Working with advanced analytical instruments, you'll conduct testing of raw materials, in-process samples, finished products, and stability samples. Our collaborative environment provides opportunities for continuous learning and career growth as you help deliver vital therapies to patients.
 

How will you get there?

  • Bachelor's degree required, no prior experience required
    • Preferred Fields of Study: Chemistry, Biology, Biochemistry or related scientific field
  • Proficiency with analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods
  • Experience with microbiological testing, environmental monitoring, and aseptic techniques
  • Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards
  • Strong attention to detail with ability to follow standard procedures and maintain data integrity
  • Excellent problem-solving skills and logical approach to scientific challenges
  • Proficient computer skills including Microsoft Office and laboratory information systems
  • Strong written and verbal communication abilities
  • Ability to work both independently and collaboratively in a dynamic environment
  • Physical requirements include standing/walking for extended periods, lifting up to 50 lbs, and manual dexterity
  • Must be able to work in cleanroom environments wearing required PPE
  • Ability to work various shifts including nights, weekends, and holidays as needed
  • Experience in pharmaceutical/regulated environment preferred but not required

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