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Quality Control Pharmacist Jobs (NOW HIRING)

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 ...

QC Chemist

North Salt Lake, UT · On-site

$30 - $36/hr

... pharmaceuticals, nutraceuticals, or food and beverage industries. This is a contract position ... Responsibilities Of The QC Chemist * Prepare, collect, and analyze samples using standard ...

Minimum of 4 years of relevant laboratory experience in a GMP pharmaceutical or biopharmaceutical manufacturing environment. * Strong background in analytical testing within a QC chemistry setting.

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QC Specialist

El Paso, TX · On-site

$26/hr

Minimum 2 years of experience in a Chemistry lab in a Pharmaceutical environment. If you think this QC Specialist position is a good fit for you, please reach out to me - feel free to call, e-mail ...

QC Chemist

Pearl River, NY · On-site

$55K - $95K/yr

RK Pharma Inc, a vertically integrated pharmaceutical company with our main manufacturing site in Pearl River, NY, is seeking a Quality Control Chemist to work with our growing Quality Teams as we ...

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Company Overview Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility ... other Quality Control duties, as needed Has the decision-making authority for the following : · ...

Previous QA/QC experience in a manufacturing setting, preferably in the food, personal care, pharmaceutical, or related industry. * Strong attention to detail with the ability to find mistakes and ...

Quality Control Analyst

Houston, TX

$23 - $30.75/hr

Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...

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On-Site Required: * 5 to 10 years of experience in Quality Control within pharmaceutical, biotech, or CDMO environments. * Previous experience as QC Manager, QC Supervisor, QC Lead, or senior QC ...

Quality Control Analyst

Houston, TX · On-site

$23 - $30.75/hr

Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...

Quality Control Analyst

Houston, TX

$23 - $30.75/hr

Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...

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Quality Control Pharmacist information

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$27

$60

$74

How much do quality control pharmacist jobs pay per hour?

As of Jun 16, 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:
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 supervisor

Full-time

This job post has expired today. Applications are no longer accepted.


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 398 frontline employees who took The Breakroom Quiz

188th of 518 rated manufacturers


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Summary: 

This position will oversee a team responsible for one of three functions: Day shift, Chromatography group, or Wet chemistry group.  These groups support raw material release, API (drug substance) release, in-process reaction completion testing and intermediate release, and stability testing in order to support the site’s fast-paced manufacturing needs.  A key opportunity in this role will be the development of staff to grow into future roles within the site. 

Essential Functions:   

  • Provide day to day leadership to a team of approximately 3-8 analysts by performing the following: leading organizational change; developing and empowering staff; cultivating relationships; putting staff in a position to succeed, meeting their personal career goals while also achieving organizational goals; building effective teams that apply their diverse skills and perspectives to achieve common goals; driving engagement and creating a climate where staff are motivated to do their best. 

  • Revise/review specifications, SOPs, and other documents regarding QC and assay execution. 

  • Train and supervise staff in order to perform QC tasks by ensuring completion of technique-related training, SOPs, OJT, and knowledge assessments, as well as ensuring on-going compliance to training and site SOPs. 

  • Participate in the discrepancy management process. 

  • Drive closure of deviations/ investigations/ CAPA. 

  • Interact with auditors/clients during visits and tours. 

  • Oversee daily activity for the group to ensure quality results 

  • Performance management for direct reports. 

  • Prepare and Assist in the Writing of Procedures (Standard Operating Procedures, Equipment Operating Procedures, Department Procedures, and Laboratory Investigations) accordance with established standard lead times. 

  • Effectively communicate with peers, manufacturing, AD and QC staff, to resolve technical issues and direct activities. 

  • Provide support to site Safety initiatives. 

  • Other job duties as assigned. 

Education: 

Bachelor’s degree in physical science, preferably in Chemistry. Other science degrees, with experience in a pharmaceutical analytical laboratory, will be considered. 

Experience:  

Requires a minimum of 5 years’ experience in quality/analytical/pharmaceutical industry or similar experience with a minimum of one year supervisory/ team lead experience within the pharmaceutical industry in a QA/QC leadership role, preferably with a plant manufacturing focus preferred.  Knowledge of QC analytical techniques is required (for example, HPLC, GC, KF, IR, optical rotation, etc.), Empower 3 experience for IPC and Chromatography group roles is preferred. 

Competencies:   

Excellent knowledge and understanding of chemistry and analytical instrumental technologies. Excellent knowledge of qualitative and quantitative chemical analysis. Excellent understanding of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs and descriptive organic chemistry. Excellent problem solving skills and logical approach to solving scientific problems. Excellent proficiency with HPLC, GC, LC/MS KF, FTIR, and other wet chemistry methodology. Excellent interpersonal and communication skills (both oral and written). Good presentation skills to present information to customers, clients, and other employees. Good leadership skills. Ability to read, analyze, and interpret technical procedures and governmental regulations. Ability to write standard operating procedures and policy manuals. Ability to apply mathematical operations, to such tasks as determination of test reliability, analysis of variance, and correlation techniques.       

Physical Requirements: 

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, organic respirator occasionally. 


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