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Qc Control Jobs in New York (NOW HIRING)

Ardena

Scientist - Quality Control (QC)

Somerset, NJ · On-site

Quality Control Location: Somerset, New Jersey FLSA Status: Exempt Employment Type: Full-Time Ardena is seeking a Scientist - Quality Control (QC) to join our Quality Control team in Somerset, NJ.

FullSteam

Quality Control

East Rutherford, NJ · On-site

$17 - $18/hr

Quality Control Technician - East Rutherford, NJ We are seeking a Quality Control Technician to join our team in East Rutherford, NJ . If you have experience in quality control and a strong attention ...

613 Originals

Quality Control

Mahwah, NJ

613 Originals, a leading heat transfer printing company is looking to fill several Quality control roles for 2nd shift (3pm to 11pm) Candidates should have the following skills:Keen eye for detail ...

613 Originals

Quality Control

Mahwah, NJ · On-site

613 Originals, a leading heat transfer printing company is looking to fill several Quality control roles for 2nd shift (3pm to 11pm) Candidates should have the following skills:Keen eye for detail ...

Icon plc

Manager, Quality Control

New York, NY · On-site

$100K - $125K/yr

Manager, Quality Control (QC), Bioanalytical Clinical Research Labs, Whitesboro, New York (NY) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring ...

New

CookUnity

Quality Control Supervisor

New York, NY

The Role The Quality Control Supervisor is responsible for overseeing the performance of the QC area, ensuring compliance with operational procedures, and driving continuous improvement across all ...

Actalent

QC Investigator

Orangeburg, NY

$45 - $50/hr

QC Investigator book here for more information:  The QC Investigator is responsible for the oversight and execution of complex and critical Phase I and Phase II investigations related to quality ...

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Qc Control information

What is the difference between Qc Control vs Quality Assurance Technician?

AspectQc ControlQuality Assurance Technician
CertificationsOften requires quality control certifications (e.g., CQE)May require similar certifications, with additional focus on QA processes
Work EnvironmentPrimarily in manufacturing or production settings, inspecting productsInvolved in both manufacturing and office settings, focusing on process compliance
Employer & Industry UsageUsed in industries like automotive, electronics, and food productionCommon in manufacturing, pharmaceuticals, and consumer goods industries
Search & Comparison IntentOften compared for roles focused on product inspectionCompared for roles emphasizing process improvement and compliance

While both Qc Control and Quality Assurance Technician roles focus on maintaining product quality, Qc Control primarily involves inspecting and testing products during manufacturing. Quality Assurance Technicians often have a broader scope, including process audits and compliance checks. Understanding these differences helps in selecting the right career path or job role.

What is the job of quality control?

The job of quality control involves inspecting products or services to ensure they meet specified standards and requirements. Quality control professionals use testing, measurements, and documentation to identify defects and prevent faulty items from reaching customers, often working with tools like checklists and quality management systems. Attention to detail and adherence to safety and quality protocols are essential in this role.

What cities in New York are hiring for Qc Control jobs?

Cities in New York with the most Qc Control job openings:

Qc Control jobs near you
Infographic showing various Qc Control job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Scientist - Quality Control (QC)

Somerset, NJ • On-site

Ardena
See more jobs at Ardenaexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago

Job description

About Ardena
Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development. Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to market.
The Ardena Group operates from five sites across Europe and the United States, employing more than 750 professionals. Ardena's European sites are located in Oss and Assen (the Netherlands), Ghent (Belgium), and Pamplona (Spain). Ardena's U.S. facility is based in Somerset, New Jersey.
For our Somerset, New Jersey site, we are looking for a Scientist - Quality Control (QC) to join our Quality Assurance Division.
Ardena provides integrated services spanning drug substance development, drug product formulation, GMP manufacturing, bioanalytical services, clinical logistics, fill and finish, and CMC regulatory support.
Job Overview
Position: Scientist - Quality Control (QC)
Division: Quality Assurance
Department: Quality Control
Location: Somerset, New Jersey
FLSA Status: Exempt
Employment Type: Full-Time
Ardena is seeking a Scientist - Quality Control (QC) to join our Quality Control team in Somerset, NJ. This role supports pharmaceutical development and commercial manufacturing by performing analytical testing of raw materials, in-process materials, finished products, and stability samples within a GMP-regulated laboratory environment.
The successful candidate will perform laboratory testing using a variety of analytical techniques while ensuring compliance with cGMP, data integrity, and regulatory requirements. This position offers the opportunity to contribute directly to the quality, safety, and timely release of pharmaceutical products supporting patients worldwide.
Role Description
As a Scientist - Quality Control (QC) at Ardena, you will independently perform analytical testing and support quality control activities for clinical and commercial pharmaceutical products. You will analyze laboratory data, interpret results, investigate deviations, and communicate findings through technical reports and documentation.
Working in a GMP-regulated laboratory, you will collaborate closely with cross-functional teams including Quality Assurance, Manufacturing, Regulatory Affairs, Project Management, and other technical departments to ensure projects are completed on schedule while maintaining the highest standards of quality and compliance.
Key Responsibilities
  • Perform analytical testing of raw materials, in-process materials, finished products, and stability samples to support pharmaceutical development and commercial manufacturing.
  • Independently execute laboratory testing with accuracy while maintaining complete and compliant documentation.
  • Analyze laboratory data, evaluate results for accuracy and integrity, and communicate findings through technical reports and presentations.
  • Perform Quality Control activities required to meet project timelines and customer deliverables.
  • Utilize analytical techniques including, but not limited to:
    • High Performance Liquid Chromatography (HPLC/LC)
    • Gas Chromatography (GC)
    • Dissolution Testing
    • Standard Wet Chemistry
  • Operate laboratory instrumentation and electronic systems including CDMS, LIMS, ELN, and other laboratory software.
  • Review analytical data for completeness, accuracy, and compliance with regulatory and data integrity requirements.
  • Conduct and document laboratory investigations, deviations, and change management activities.
  • Author and review analytical methods, protocols, reports, specifications, and Standard Operating Procedures (SOPs).
  • Collaborate with cross-functional teams to ensure project objectives and customer timelines are achieved.
  • Support Quality Systems and laboratory infrastructure initiatives.
  • Maintain compliance with cGMP, Health, Safety, Environmental, and Data Integrity requirements.
  • Perform additional technical and administrative duties as assigned.
Profile & Qualifications
Required Qualifications
  • Associate's degree in Chemistry or Analytical Chemistry with 5+ years of experience supporting pharmaceutical product development and manufacturing,

OR
  • Bachelor's degree in Chemistry or Analytical Chemistry with 3+ years of experience supporting pharmaceutical product development and manufacturing.
  • Experience working within a GMP-regulated pharmaceutical laboratory.
  • Strong understanding of analytical chemistry principles and pharmaceutical Quality Control practices.
  • Experience performing analytical testing using chromatographic and wet chemistry techniques.
  • Proficiency with analytical instrumentation, including LC (HPLC), GC, and Dissolution systems.
  • Experience using laboratory electronic systems such as CDMS, LIMS, and Electronic Laboratory Notebooks (ELN).
  • Strong organizational, analytical, and problem-solving skills.
  • Excellent verbal and written communication skills.
  • Ability to effectively manage multiple priorities while meeting project deadlines.
  • Fluent in English, both written and spoken
Preferred Qualifications
  • Experience supporting pharmaceutical development and commercial manufacturing environments.
  • Working knowledge of cGMP, FDA regulations, and data integrity requirements.
  • Experience authoring or reviewing SOPs, analytical methods, laboratory investigations, deviations, and technical reports.
  • Proficiency with Microsoft Office applications, including Teams, Word, Excel, and PowerPoint.
  • Experience working collaboratively with cross-functional technical teams.
  • Alignment with Ardena's CARE values:
    • Communicative
    • Accountable
    • Reliable
    • Excellent
Physical Requirements
  • Ability to occasionally lift up to 15 pounds.
  • Ability to work within laboratory, manufacturing, and office environments.
  • Frequent use of computers and laboratory instrumentation.
  • Ability to read and interpret technical documentation.
  • Must be capable of wearing required Personal Protective Equipment (PPE), including safety glasses, respirators (when required), and safety shoes.
  • Must successfully complete required safety and OSHA training, including respirator fit testing.
  • Ability to work in temperature- and humidity-controlled laboratory environments.
What Ardena Offers
Ardena is a science-driven and people-focused employer. Working at Ardena means contributing to pharmaceutical projects that support the availability, safety, and quality of medicines for patients worldwide.
Ardena offers an international working environment where employees are encouraged to develop their expertise, take ownership, and grow their careers across functions and locations.
Benefits and perks at Ardena include:
  • Competitive salary and comprehensive benefits package.
  • Paid time off and company-recognized holidays.
  • Medical, dental, vision, life, and disability insurance.
  • 401(k) retirement savings plan with company match.
  • Professional development and training opportunities.
  • Collaborative international work environment across Europe and the United States.
  • Opportunities to contribute to innovative pharmaceutical development projects that improve patient health.
  • A values-driven culture guided by Ardena's CARE principles: Communicative, Accountable, Reliable, and Excellent.
How to Apply
Ready to advance your career in pharmaceutical Quality Control?
Apply today through the Ardena Careers website at careers.ardena.com and become part of a team dedicated to advancing pharmaceutical innovation and improving patient lives worldwide.
Department Quality Assurance Locations Somerset (New Jersey, US)

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