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Quality Control Pharmacist 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

$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

$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 ...

Precigen, Inc

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

Advanced experience with QC testing in pharmaceutical or biopharmaceutical laboratories * Familiarity with analytical testing procedures: qPCR, HPLC, ELISA, Cell-based Assays, etc. DESIRED KEY ...

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 ...

ANI Pharmaceuticals

QC Chemist

Baudette, MN · On-site

$48K - $52K/yr

About Us Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients ... Quality Control Chemists must successfully complete the following training: Policy and Standard ...

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

$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 ...

TekWissen LLC

Quality Control Specialist

Vacaville, CA · On-site

$20 - $26/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Job Title: QC Specialist II Location: Vacaville, CA, 95688 Duration: 6 Months Job Type: Temporary ...

Artius Solutions

QC Chemist

Central Islip, NY · On-site

$65K - $90K/wk

Pharmaceutical Experience Required: 2 to 15 years Compensation: *,000 - *,000 Visa Sponsorship: Not available Remote Option: No Job Overview: We are looking for a dedicated Quality Control Chemist to ...

Thermo Fisher Scientific

QC supervisor

Florence, SC · On-site

Other science degrees, with experience in a pharmaceutical analytical laboratory, will be ... Knowledge of QC analytical techniques is required (for example, HPLC, GC, KF, IR, optical rotation ...

Thermo Fisher Scientific

QC supervisor

Florence, KY

Other science degrees, with experience in a pharmaceutical analytical laboratory, will be ... Knowledge of QC analytical techniques is required (for example, HPLC, GC, KF, IR, optical rotation ...

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All JobsQuality Control Pharmacist Jobs

Quality Control Pharmacist information

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$27

$60

$74

How much do quality control pharmacist jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for quality control pharmacist in the United States is $60.91, according to ZipRecruiter salary data. Most workers in this role earn between $56.01 and $67.31 per hour, depending on experience, location, and employer.

What are Quality Control Pharmacists?

Quality Control Pharmacists are professionals responsible for ensuring that pharmaceutical products meet established quality standards before they reach consumers. They conduct a variety of tests and analyses to verify the identity, purity, strength, and composition of medications. Their role is crucial in maintaining compliance with regulatory guidelines and ensuring patient safety. They often work in laboratories within pharmaceutical manufacturing companies, collaborating with production and regulatory teams. Quality Control Pharmacists also document their findings and help implement corrective actions when necessary.

Is QC a high paying job?

Quality Control Pharmacists typically earn competitive salaries that vary by experience, location, and employer. In the pharmaceutical industry, they often receive higher pay compared to entry-level roles, especially with specialized certifications and skills in laboratory testing and compliance. Overall, QC roles can be considered well-paying within the healthcare and manufacturing sectors.

What is the difference between Quality Control Pharmacist vs Quality Assurance Specialist?

AspectQuality Control PharmacistQuality Assurance Specialist
CredentialsPharmacy license, often with GMP or QA certificationsRelevant certifications like CQE or ISO auditor
Work EnvironmentLaboratories, manufacturing plants, pharmaceutical companiesQuality management departments, regulatory agencies
Industry UsageEnsures product quality through testing and analysisDevelops and maintains quality systems and processes

The main difference is that a Quality Control Pharmacist focuses on testing and verifying pharmaceutical products to meet quality standards, while a Quality Assurance Specialist develops and oversees quality systems to prevent issues. Both roles are essential in pharmaceutical manufacturing but serve different functions within the quality management process.

What is the highest paid pharmacist job?

The highest paid pharmacist roles are often in specialized areas such as clinical pharmacy, nuclear pharmacy, or pharmaceutical consulting, with salaries exceeding $150,000 annually. Pharmacists with advanced certifications, extensive experience, or leadership positions in healthcare organizations tend to earn the highest compensation.

What is a QC pharmacist?

A QC pharmacist is a quality control pharmacist responsible for reviewing and ensuring the quality, safety, and compliance of pharmaceutical products. They perform testing, review data, and collaborate with manufacturing teams to meet regulatory standards, often using laboratory tools and documentation systems. Certification in pharmacy and knowledge of Good Manufacturing Practices (GMP) are typically required.

What are the key skills and qualifications needed to thrive as a Quality Control Pharmacist, and why are they important?

To thrive as a Quality Control Pharmacist, you need a strong background in pharmaceutical sciences, analytical chemistry, and regulatory compliance, typically supported by a pharmacy degree and relevant licensure. Familiarity with laboratory equipment, chromatographic techniques (like HPLC or GC), and quality management systems (such as GMP) is essential. Attention to detail, problem-solving abilities, and clear communication are crucial soft skills for ensuring accuracy and effective teamwork. These skills and qualifications are vital to maintain product safety, uphold regulatory standards, and ensure the integrity of pharmaceutical products.

What is the role of a quality control pharmacist?

A quality control pharmacist is responsible for reviewing and testing pharmaceutical products to ensure they meet safety, quality, and regulatory standards. They analyze raw materials, in-process samples, and finished products, often using laboratory tools and adhering to Good Manufacturing Practices (GMP). Their work helps ensure that medications are safe and effective for patient use.

What are some common challenges faced by a Quality Control Pharmacist when working with cross-functional teams?

Quality Control Pharmacists often collaborate closely with production, research and development, and regulatory affairs teams. A common challenge is ensuring clear communication regarding testing protocols and results, especially when timelines are tight and multiple departments are involved. Balancing strict regulatory compliance with practical production needs can also create tension, requiring strong problem-solving and negotiation skills. Building strong working relationships and maintaining thorough documentation help navigate these challenges and ensure product quality and safety.
More about Quality Control Pharmacist jobs
What states have the most Quality Control Pharmacist jobs? States with the most job openings for Quality Control Pharmacist jobs include:
What job categories do people searching Quality Control Pharmacist jobs look for? The top searched job categories for Quality Control Pharmacist jobs are:
Quality Control Pharmacist jobs near you
Infographic showing various Quality Control Pharmacist job openings in the United States as of June 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $126,701 per year, or $60.9 per hour.
QC Analyst

QC Analyst

Noven Pharmaceuticals

Miami, FL

$23 - $30.75/hr

Full-time

Posted 16 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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