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Entry Level Pharmaceutical Quality Control Jobs (NOW HIRING)

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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Pharmaceutical Quality Assurance

Sylmar, CA · On-site

$25 - $30/hr

A pharmaceutical Quality Assurance (QA) professional ensures that drug products are safe, effective ... Document Control: Author, review, and manage Standard Operating Procedures (SOPs), protocols, and ...

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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 Analyst II (Chemistry)

QC Analyst II (Chemistry)

Astrix Inc

Rensselaer, NY • On-site

$30 - $47/hr

Contractor

Re-posted 3 days ago

Job description

QC Analyst II
Albany, NY
Pay Range: $30-47/hr
Available Shifts:
• 1st Shift - 6am-6:30p on a 2-2-3 rotating schedule (every other weekend)
• 3rd Shift - 6pm-6:30am on a 2-2-3 rotating schedule (every other weekend)
Starts out on a 6 month contract with strong potential of extension and/or conversion!
About the Role
We are seeking experienced QC Analyst II professionals to support analytical testing and laboratory operations within a GMP-regulated pharmaceutical/manufacturing environment. This role is responsible for performing analytical testing, supporting laboratory instrumentation, assisting with investigations, and ensuring compliance with quality and regulatory standards.
Candidates with strong analytical chemistry, chromatography, and pharmaceutical QC laboratory experience are highly encouraged to apply.
Key Responsibilities
  • Perform analytical testing for incoming raw materials, in-process samples, finished products, and stability samples
  • Utilize laboratory instrumentation including balances, pipettes, pH meters, UV/Visible spectrophotometers, TOC analyzers, HPLC, UPLC, GC, IR, and other analytical equipment
  • Perform chromatography and wet chemistry assays with minimal supervision and training
  • Conduct raw material testing and/or sampling activities
  • Support analytical instrument calibration, maintenance, and troubleshooting activities
  • Maintain laboratory cleanliness, organization, and audit readiness
  • Assist with QC method qualifications, method transfers, validations, and method development activities
  • Support cleaning validation studies and evaluation of new laboratory equipment and processes
  • Review analytical data and provide summaries and documentation support to QC management
  • Assist with investigations related to OOS results, deviations, CAPAs, and quality events
  • Support analytical sample receipt, processing, shipment coordination, tracking, documentation, and result distribution activities
  • Ensure compliance with GMP, SOP, safety, and data integrity requirements

Qualifications
  • Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or related scientific discipline preferred
  • Previous QC analytical laboratory experience within pharmaceutical, biotech, medical device, or regulated manufacturing environments required
  • Hands-on experience with HPLC, UPLC, GC, wet chemistry, UV, IR, and analytical instrumentation strongly preferred
  • Knowledge of GMP, laboratory documentation, and quality systems required
  • Experience supporting investigations, deviations, CAPAs, and method validation activities preferred
  • Strong attention to detail, analytical thinking, and documentation skills
  • Ability to work independently within fast-paced laboratory environments

Additional Information
• Multiple openings available across all shifts
• Position begins as a contract opportunity with potential for long-term growth
• Candidates with strong chromatography and pharmaceutical QC backgrounds are highly preferred
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