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Quality Control Lab Intern Jobs in New Jersey (NOW HIRING)

Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our training, your responsibilities will include managing daily activities, performance, and coaching ...

Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our training, your responsibilities will include managing daily activities, performance, and coaching ...

QC Lab Technician

Moorestown, NJ · On-site

$20 - $21/hr

Requirements Essential Duties of the QC Lac Tech: PRIORITY - Product sample testing as required ... Monitor lab consumables and order as needed * Maintain clean lab * Monitor calibration status of ...

QC Lab Technician

Moorestown, NJ · On-site

$20 - $21/hr

Requirements Essential Duties of the QC Lac Tech: PRIORITY - Product sample testing as required ... Monitor lab consumables and order as needed * Maintain clean lab * Monitor calibration status of ...

Manufacturing QC Lab Technician-

Thorofare, NJ · On-site

$19.25 - $24.25/hr

Temporary Tecnoflon QC Lab Technician Position Summary Perform controlled testing of Tecnoflon products produced at the West Deptford site to ensure they meet customer requirements before release for ...

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

Support QC lab inventory management, including but not limited to QC lab inventory ordering, receiving, storage,distribution, inventory tracking by using either paper-based forms or LIMS inventory ...

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

Support QC lab inventory management, including but not limited to QC lab inventory ordering, receiving, storage,distribution, inventory tracking by using either paper-based forms or LIMS inventory ...

Associate Scientist, QC

Cranbury, NJ · On-site

$49K - $79K/yr

Support QC lab inventory management, including but not limited to QC lab inventory ordering, receiving, storage, distribution, inventory tracking by using either paper-based forms or LIMS inventory ...

Maintains QC laboratory in accordance with standard lab practices for cleanliness and organization. * Maintains computer files containing QC information in an organized. * Accurately record and ...

New

Maintains QC laboratory in accordance with standard lab practices for cleanliness and organization. * Maintains computer files containing QC information in an organized. * Accurately record and ...

New

Quality Control Technician

Norwood, NJ · On-site

$60K - $68K/yr

Maintains QC laboratory in accordance with standard lab practices for cleanliness and organization. * Maintains computer files containing QC information in an organized. * Accurately record and ...

New

Quality Control Technician

Norwood, NJ · On-site

$60K - $68K/yr

Maintains QC laboratory in accordance with standard lab practices for cleanliness and organization. * Maintains computer files containing QC information in an organized. * Accurately record and ...

New

Ensure the quality control lab is held to GxP standards and safety standards * Create/Review and approve Certificate of Analysis * Conduct investigation regarding out of specifications (OOS) results ...

Ensure the quality control lab is held to GxP standards and safety standards * Create/Review and approve Certificate of Analysis * Conduct investigation regarding out of specifications (OOS) results ...

QC Analytical Chemist I -Bachelor's Degree in Chemistry or related science field and minimum 1-5 years lab experience in a cGMP related industry. * Hands-on experience with analytical instrumentation ...

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Showing results 1-20

Quality Control Lab Intern information

What is the difference between Quality Control Lab Intern vs Quality Control Technician?

AspectQuality Control Lab InternQuality Control Technician
CredentialsTypically pursuing or recently completed a degree in science or related fieldUsually requires relevant certifications or experience in quality control
Work EnvironmentLaboratory setting, supervised, learning-focusedOperational lab environment, more independent work
Employer & Industry UsageInternships offered by pharmaceutical, food, or manufacturing companiesFull-time role in similar industries, responsible for testing and quality assurance

The main difference is that a Quality Control Lab Intern is a learning position often held by students or recent graduates gaining hands-on experience, while a Quality Control Technician is a full-time role requiring more experience and responsibility in testing and quality assurance processes.

What is a quality control lab intern?

Quality Control Lab Interns are entry-level professionals who support laboratory teams by conducting tests and inspections to ensure products meet quality standards. They assist with sample preparation, data collection, and analysis under the supervision of experienced lab staff. This role provides hands-on experience in quality assurance procedures, laboratory equipment operation, and documentation practices. Interns gain valuable insight into regulatory compliance and industry best practices, often serving as a stepping stone for future careers in quality control or laboratory science.

What skills and qualifications are needed to thrive as a quality control lab intern?

To thrive as a Quality Control Lab Intern, you need a solid understanding of laboratory procedures, basic chemistry or biology, and attention to detail, typically supported by coursework in a related scientific field. Familiarity with laboratory equipment, safety protocols, and data analysis software such as LIMS or Excel is often required. Strong organizational skills, effective communication, and a willingness to learn help interns excel in collaborative and fast-paced lab environments. These skills and qualities are crucial to ensure accurate testing, maintain safety standards, and support the overall quality assurance process.

What types of projects or tasks can a quality control lab intern expect to work on during their internship?

As a Quality Control Lab Intern, you can expect to assist with daily sample testing, data analysis, and documentation to ensure products meet company and regulatory standards. Interns often help prepare and conduct laboratory experiments under supervision, perform equipment calibration, and maintain accurate records of test results. You may also participate in team meetings to discuss findings and collaborate with other departments, such as production and R&D, to resolve quality-related issues. This hands-on experience provides valuable insight into quality assurance processes and teamwork in a laboratory environment.
What are the most commonly searched types of Quality Control Lab jobs in New Jersey? The most popular types of Quality Control Lab jobs in New Jersey are:

Manager, Quality Control Lab

QuVa Pharma

Bloomsbury, NJ

$98K - $135K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 days ago


QuVa Pharma rating

7.7

Company rating: 7.7 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

55th of 86 rated pharmaceutical


Job description

Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our training, your responsibilities will include managing daily activities, performance, and coaching and developing staff.  Coordinate analytical activities including method transfers and stability testing. Perform release testing for analytical studies. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

 What the Manager Quality Control -Lab Does Each Day:

  • Test and Release Finished Product routinely for Commercial lots for Potency, Endotoxin, and Sterility
  • Maintain accurate and complete notebook records for all method validation and investigational studies in accordance with SOPs, cGMP, and current GdP
  • Implement improvements to analytical test methods or to instrumentation
  • Write investigation report for OOS for Sterility results
  • Provide quality oversight of Laboratory
  • Responsible for assigned testing and work from beginning to end with minimal supervision
  • Write SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements
  • Communicate with Operation for Scheduling the QC Samples
  • Ensure that analytical methods are validated as efficiently as possible to ensure business milestones are met
  • Provide technical support on an as-needed basis as directed by Director of the Laboratories
  • Manage the budget for the Labs
  • Ensure testing is conducted in a safe manner including but not limited to the proper PPE and ventilation; Any safety issue must be brought to the attention of the Director immediately

Our Most Successful Manager Quality Control- Lab:

  • Has a sense of urgency, accountability and resourcefulness (e.g., work in changing environment)
  • Is a self-starter and independent learner
  • Promotes active listening with team members; Contributes appropriately to conversations; Has strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization
  • Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform

Minimum Requirements for this Role:

  • BS. or M.S. degree in chemistry, biology or related field required
  • 5 years prior experience in Quality Assurance /Laboratory/ cGMP / FDA regulated industry
  • 3 years of supervisory or management experience required
  • 18+ years of age
  • Able to successfully complete a drug and background check
  • Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas

Any of the Following Will Give You an Edge: 

  • Prior experience in Quality Assurance /Laboratory/ cGMP / FDA regulated industry

Benefits of Working at Quva:

  • Set, full-time, consistent work schedule
  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 5 paid  PLP and 17 PTO days off plus 8 paid holidays per year
  • Occasional weekend and overtime opportunities with advance notice
  • National, industry-leading high growth company with future career advancement opportunities
  • The base compensation for this role is estimated to be within the range described below.  The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions
  • Range: $98,891 - $135,975  Annually
  • This role is also eligible for an annual incentive bonus, subject to program terms and guidelines

About Quva: 

Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma’s multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva’s overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.

Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.”

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