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Entry Level Pharmaceutical Quality Control Jobs (NOW HIRING)

Noven Pharmaceuticals

QC Analyst

Miami, FL

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on ...

Noven Pharmaceuticals

QC Analyst

Miami, FL · On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on ...

Noven Pharmaceuticals

QC Analyst

Miami, FL · On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on ...

Noven Pharmaceuticals

QC Analyst

Miami, FL · On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on ...

Colorcon

QC Technician

West Point, PA · On-site

$18.25 - $23.25/hr

... pharmaceutical, nutritional, and animal health industries. Our best-in-class products and ... Position Summary The QualityControl Technician is an entry level technician located in the Quality ...

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Entry Level Pharmaceutical Quality Control information

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

As of Jun 9, 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:
Entry Level Pharmaceutical Quality Control jobs near you
QC Analyst

QC Analyst

Noven Pharmaceuticals

Miami, FL

$23 - $30.75/hr

Full-time

Posted 13 days ago

Job description

Performs professional, technical laboratory functions.


  • The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents.
  • Performs physical and chemical analysis of raw materials, components, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs).
  • Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and other analytical techniques as applicable in compliance with cGMP and current safety regulations.
  • Creates and maintains laboratory record documentation in compliance with regulatory requirements.
  • Actively participates in investigation of laboratory results, when required.
  • Prepares volumetric test solutions following USP or in-house methods for wet chemical tests, standardizes such solutions as required, standardizes API for use as in-house reference standard as assigned.

Competencies:

 

Education / Experience:

  • Bachelor’s Degree (BA/BS) in Chemistry or related field – Required.
  • Less than one year testing of chemicals/pharmaceutical products – Required.
  • Must be able to read and understand analytical procedures – Required.
  • Must be able to effectively communicate results, problems, or issues, in English verbally as well as in writing – Required.
  • Must be computer literate.
  • Must be precise and consistent in day-to-day analysis, easily trainable, and ready to learn.
  • Must be able to work in a team environment and be flexible to easily adapt to changes in assignments.
  • Must follow safe practices as identified in appropriate SDS while working with chemicals and must follow applicable state and federal regulations.
  • Must possess a working knowledge of analytical chemistry techniques, such as analytical weighing, quantitative transfer, preparation of quantitative solutions, analytical dilutions, spectrophotometric analytical techniques, dissolution and drug release, disintegration, moisture determination (Karl Fischer, Coulometric, LOD), thin-layer chromatographic technique, gas chromatographic techniques, HPLC, and measuring physical parameters (bulk and tapped densities, and particle size by sieve analysis).
  • Must be able to follow compendial (USP/EP/BP/JP) procedures for wet chemical tests.
  • Must understand and apply cGMP requirements applicable to quality control laboratory.

 

Judgment / Decision Making:

Duties are performed within framework of departmental or functional guidelines, requiring interpretation and original thinking.

 

Work Environment:

A laboratory environment with exposure to chemicals, caustics, fumes, heat and electrical current.

 

Physical Demands:         

Visual acuity and manual dexterity required to operate computer, analytical instrumentation, sample preparation. Majority of time spent standing. Often required to lift objects weighing up to 20 pounds.

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