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Entry Level Pharmaceutical Quality Control Jobs (NOW HIRING)

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ · On-site

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

Astrix Inc

QC Analyst II (Chemistry)

Rensselaer, NY · On-site

$30 - $47/hr

Candidates with strong analytical chemistry, chromatography, and pharmaceutical QC laboratory experience are highly encouraged to apply. Key Responsibilities * Perform analytical testing for incoming ...

Cipla

Quality Control (QC) Chemist

Fall River, MA

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One Holdings, LLC

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

Cipla

$65K - $105K/yr

What You'll Do Analytical Testing & Expertise Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) Evaluate critical ...

Alexza Pharmaceuticals

QC Analyst II

Fremont, CA

$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 ...

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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 Jul 22, 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 Supervisor

QC Supervisor

Garonit Pharmaceutical

Fairfield, NJ • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

QC Supervisor

Onsite in Fairfield, NJ

We're looking for a QC Supervisor who's both a hands-on technical expert and a strong leader. This role manages the daily operations of our QC Laboratory - leading testing, method development, and data review while ensuring full cGMP compliance.

 What You'll Do

  • Supervise and lead a team of QC chemists and analysts.
  • Oversee all analytical testing for manufacturing, release, and stability.
  • Review and interpret HPLC, GC, and wet chemistry data in compliance with cGMP.
  • Author and review SOPs, analytical methods, and validation protocols.
  • Conduct and support laboratory investigations, CAPA, and change controls.
  • Manage and schedule lab workloads to meet production timelines.
  • Ensure lab safety, data integrity, and adherence to FDA and ICH guidelines.
  • Collaborate cross-functionally to resolve quality-related issues quickly.
  • Develop and mentor QC staff through training and performance development.
  • Support continuous improvement initiatives to enhance compliance and efficiency.

 What You'll Bring

  • Bachelor's degree in Chemistry or a related scientific field.
  • 2+ years in a supervisory or management role in a pharmaceutical QC lab.
  • Strong experience with Empower 3, HPLC, GC, and wet chemistry.
  • Deep understanding of cGMP, ICH, CFR, and USP testing requirements.
  • Experience in method development, validation, and stability testing.
  • Proven leadership, training, and coaching skills.
  • Excellent problem-solving, documentation, and communication abilities.
  • High attention to detail, strong work ethic, and commitment to quality.

 Why Garonit Pharma

  • Work with cutting-edge equipment in a collaborative, growth-oriented environment.
  • Play a key role in ensuring product quality and regulatory success.
  • Competitive compensation and career growth opportunities.

Apply