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Day Biotech Quality Control Jobs (NOW HIRING)

Kashiv BioSciences, LLC

QC Analyst II

Piscataway, NJ · On-site

$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

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 ...

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 ...

Krystal Biotech, Inc.

Quality Control Analyst I

Pittsburgh, PA · On-site

$22.50 - $30.25/hr

Quality Control Analyst / Specialist At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization ...

Legend Biotech US

Sr. QC Analyst

Somerville, NJ · On-site

$24.50 - $33/hr

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life ... Role Overview The Sr. QC Analyst is an exempt level position with responsibilities for performing Q ...

Legend Biotech US

Sr. QC Analyst

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life ... Role Overview The Sr. QC Analyst is an exempt level position with responsibilities for performing Q ...

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

As of Jun 6, 2026, the average hourly pay for day 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 Day Biotech Quality Control vs Day Biotech Quality Assurance?

AspectDay Biotech Quality ControlDay Biotech Quality Assurance
Primary FocusTesting and inspecting products to ensure quality standards are met
ResponsibilitiesConducting lab tests, analyzing samples, documenting results
Work EnvironmentLaboratories, manufacturing facilities
CertificationsRelevant lab certifications, GMP training

Day Biotech Quality Control professionals focus on testing products to verify quality, while Day Biotech Quality Assurance staff develop and maintain processes to prevent defects. Both roles are essential in biotech manufacturing, often working closely but with distinct responsibilities.

What cities are hiring for Day Biotech Quality Control jobs? Cities with the most Day Biotech Quality Control job openings:
What are the most commonly searched types of Biotech Quality Control jobs? The most popular types of Biotech Quality Control jobs are:
What states have the most Day Biotech Quality Control jobs? States with the most job openings for Day Biotech Quality Control jobs include:
Day Biotech Quality Control jobs near you

QC Analyst II

Kashiv BioSciences, LLC

Piscataway, NJ • On-site

$24 - $32.25/hr

Other

Posted 2 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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