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Overnight Biotech Quality Control Jobs (NOW HIRING)

Kashiv BioSciences, LLC

QC Analyst II

Piscataway, NJ

$24 - $32.25/hr

Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in ...

Kashiv Biosciences LLC

QC Analyst III

Piscataway, NJ · On-site

$24 - $32.25/hr

... in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 years of ... QC laboratory. Alternatively, master's degree in above areas with 8 years of experience in a ...

Kashiv Biosciences LLC

QC Analyst II

Piscataway, NJ · On-site

$24 - $32.25/hr

... biotech QC laboratory. Experience: • Previous experience in a cGMP laboratory. • Strong ... background in small molecule and protein chemistry and experience troubleshooting analytical ...

Kashiv BioSciences, LLC

QC Analyst III

Piscataway, NJ

$24 - $32.25/hr

Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, master's degree in ...

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Overnight Biotech Quality Control information

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How much do overnight biotech quality control jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for overnight biotech 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 Overnight Biotech Quality Control vs Microbiologist?

AspectOvernight Biotech Quality ControlMicrobiologist
CredentialsBachelor's in biology, microbiology, or related field; GMP trainingBachelor's or higher in microbiology, biology, or related field; lab certifications
Work EnvironmentLaboratory setting, often overnight shifts, regulated biotech facilitiesLaboratory, research, or clinical settings; may include overnight or day shifts
Industry UsageBiotech, pharmaceutical manufacturing, quality assuranceHealthcare, research institutions, biotech, pharmaceuticals

Overnight Biotech Quality Control specialists focus on testing and ensuring product quality in biotech manufacturing, often working overnight shifts. Microbiologists conduct research, analyze microorganisms, and may work in various settings, including clinical labs. While both roles require microbiology knowledge and lab skills, Quality Control roles emphasize compliance and product safety in biotech environments, whereas Microbiologists may have broader research responsibilities.

What are some common challenges faced by overnight Biotech Quality Control professionals, and how can they be managed?

Overnight Biotech Quality Control professionals often encounter challenges such as working with limited onsite support, maintaining focus during late hours, and responding quickly to unexpected results or equipment issues. Effective communication with day-shift teams and thorough documentation are essential to ensure continuity and avoid errors. Establishing a consistent routine, prioritizing tasks, and utilizing available digital resources can help manage the unique demands of this role and ensure the accuracy and reliability of quality control results.

What are Overnight Biotech Quality Control jobs?

Overnight Biotech Quality Control jobs involve performing laboratory tests and inspections on biotechnology products during nighttime or overnight shifts. These professionals ensure that products such as pharmaceuticals, biologics, or laboratory samples meet quality and safety standards before they reach the market. Responsibilities often include running assays, documenting results, maintaining equipment, and following strict protocols and Good Manufacturing Practices (GMP). Working overnight helps maintain round-the-clock quality assurance in fast-paced biotech environments. Candidates typically need a background in biology, chemistry, or related fields and attention to detail.

What are the key skills and qualifications needed to thrive as an Overnight Biotech Quality Control professional, and why are they important?

To thrive as an Overnight Biotech Quality Control professional, you need a strong background in biology or chemistry, attention to detail, and familiarity with quality assurance practices, often supported by a relevant bachelor's degree. Proficiency in laboratory equipment, data analysis software, and compliance with regulatory standards like GMP or ISO is typically required. Strong problem-solving skills, reliability, and effective communication are important soft skills for this role. These skills are crucial to ensure consistent product quality, regulatory compliance, and effective issue resolution during overnight operations.
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Overnight Biotech Quality Control jobs near you
Infographic showing various Overnight Biotech Quality Control job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 83% Full Time, and 16% Part Time. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

QC Analyst II

Kashiv BioSciences, LLC

Piscataway, NJ

$24 - $32.25/hr

Other

Posted 15 days ago

Job description

Description

 Position Summary


The QC Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial small molecule and biosimilar products in cGMP-compliant laboratories. A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required.


Essential Duties & Responsibilities


  • Analytical testing to support product in-process, release, Raw materials and stability programs.
  • Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance.
  • Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans.
  • Work with cross-functional teams to advance projects, maintain equipment, and authoring of documents and reports.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards
  • Perform the investigation analysis during the non-conformance.
  • Conduct the investigation process as a part of Quality Event and work with supervisor to close the investigation.

Requirements

 Position Requirements and Qualifications


Education:


Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in above areas with 6 years of experience in a pharmaceutical/biotech QC laboratory.


Experience:  


Previous experience in a cGMP laboratory.

Strong background in small molecule and protein chemistry and experience troubleshooting analytical results.

Demonstrated success at writing, revising, and complying with SOPs, policies, and QC methods.


Specialized Knowledge and Skills: 


Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. 

Knowledge of and experience with Empower and/or Shimadzu software

Previous experience supporting regulatory inspections (e.g. PAI).

Familiarity with preparing regulatory dossiers and data packages for interactions between Kashiv and regulatory agencies.


Work Environment & Physical Demands:


General Working Environment:


Some time spent in an office doing office work (reading, writing, reviewing, and editing documents).

Significant amount of time spent in the laboratory.

Must be able to work extended hours or weekend hours, as may be required.

Noise:

No extraordinary noise levels.

Standing/Lifting:

Must be able to lift at least 25 lbs.

Visual:

No extraordinary requirements.

Stress:

High-paced demanding environment to meet ambitious project goals.

Travel:

No travel required.


Supervisory Responsibility, if any: No


This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.

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