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Contract Pharmaceutical Quality Control Jobs (NOW HIRING)

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ

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 ...

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 ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One Holdings, LLC

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

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 ...

ANI Pharmaceuticals

Quality Control Technician

Baudette, MN

$17.25 - $22/hr

Position Summary Responsible for supporting Quality Control testing operations through laboratory ... Zero to two years of experience in a laboratory or pharmaceutical environment preferred. * Ability ...

ANI Pharmaceuticals

Quality Control Technician

Baudette, MN · On-site

$17.25 - $22/hr

Position Summary Responsible for supporting Quality Control testing operations through laboratory ... Zero to two years of experience in a laboratory or pharmaceutical environment preferred. * Ability ...

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 ...

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All JobsContract Pharmaceutical Quality Control Jobs

Contract Pharmaceutical Quality Control information

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

To thrive as a Contract Pharmaceutical Quality Control specialist, you need a strong background in chemistry, biology, or a related field, with experience in laboratory testing and quality assurance processes. Familiarity with analytical instruments such as HPLC, GC, and LIMS, as well as knowledge of regulatory standards like GMP and relevant certifications, is typically required. Attention to detail, problem-solving abilities, and strong communication skills are essential for accurate testing and effective collaboration. These skills and qualities ensure product safety, regulatory compliance, and the reliability of pharmaceutical products in a highly regulated industry.

What is the difference between Contract Pharmaceutical Quality Control vs Contract Pharmaceutical Quality Assurance?

AspectContract Pharmaceutical Quality ControlContract Pharmaceutical Quality Assurance
Primary FocusTesting and analyzing drug samples to ensure quality and complianceDeveloping, implementing, and maintaining quality systems and procedures
Work EnvironmentLaboratories, testing facilities, manufacturing sitesOffice settings, quality management departments, regulatory agencies
Required CredentialsDegree in pharmacy, chemistry, or related field; certifications in lab testingDegree in pharmacy, chemistry, or related field; certifications in quality systems
Industry UsageUsed by pharmaceutical companies during product testing phasesUsed for ensuring overall quality compliance and regulatory adherence

Contract Pharmaceutical Quality Control focuses on testing and analyzing pharmaceutical products to verify quality, while Contract Pharmaceutical Quality Assurance emphasizes establishing and maintaining quality systems to ensure compliance. Both roles are essential in the pharmaceutical industry but serve different functions within the quality management process.

What is Contract Pharmaceutical Quality Control?

Contract Pharmaceutical Quality Control refers to the process where pharmaceutical companies outsource the testing and analysis of their products to third-party laboratories or service providers. These contract labs ensure that drug products meet regulatory standards for safety, efficacy, and quality before they reach the market. Services often include analytical testing, microbiological testing, method development, and stability studies. By outsourcing this work, companies can access specialized expertise and equipment, streamline operations, and maintain compliance with global regulations.

What are some common challenges faced in a Contract Pharmaceutical Quality Control role and how can they be effectively managed?

In a Contract Pharmaceutical Quality Control role, professionals often navigate challenges such as tight project deadlines, varying client expectations, and strict regulatory requirements. Managing these challenges effectively involves clear communication with clients, thorough documentation, and staying updated with industry standards like GMP and FDA guidelines. Team collaboration is key, as projects typically involve coordination with analytical chemists, quality assurance specialists, and production staff. Adaptability and attention to detail are essential for ensuring both compliance and client satisfaction in a fast-paced, contract-based environment.
More about Contract Pharmaceutical Quality Control jobs
What cities are hiring for Contract Pharmaceutical Quality Control jobs? Cities with the most Contract 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 Contract Pharmaceutical Quality Control jobs? States with the most job openings for Contract Pharmaceutical Quality Control jobs include:
What job categories do people searching Contract Pharmaceutical Quality Control jobs look for? The top searched job categories for Contract Pharmaceutical Quality Control jobs are:
Contract Pharmaceutical Quality Control jobs near you
Infographic showing various Contract Pharmaceutical Quality Control job openings in the United States as of July 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution.
QC Analyst II (Chemistry)

QC Analyst II (Chemistry)

Astrix Inc

Rensselaer, NY • On-site

$30 - $47/hr

Contractor

Posted 25 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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