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Master In Biotechnology Jobs in Lisle, IL (NOW HIRING)

Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ... Master File (TMF) and the Investigator Site File (ISF). A central part of this role involves ...

Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ... Master File (TMF) and the Investigator Site File (ISF). A central part of this role involves ...

Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ... Master File (TMF) and the Investigator Site File (ISF). A central part of this role involves ...

Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ... Master File (TMF) and the Investigator Site File (ISF). A central part of this role involves ...

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Master In Biotechnology information

What is the difference between Master In Biotechnology vs Biotechnology Research Associate?

CriteriaMaster In BiotechnologyBiotechnology Research Associate
Required CredentialsMaster's degree in Biotechnology or related fieldBachelor's or Master's degree in Biotechnology or related field
Work EnvironmentLaboratories, research facilities, academic institutionsLaboratories, biotech companies, research organizations
Employer & Industry UsageAcademic, research, biotech industryBiotech companies, research labs, pharmaceutical firms
Common Search & ComparisonYesYes

The Master In Biotechnology typically prepares individuals for advanced roles in research, development, and academia, requiring a master's degree. A Biotechnology Research Associate usually holds a bachelor's or master's degree and works directly in research projects within biotech companies or labs. While both roles involve laboratory work and research, the Master's degree often leads to more senior or specialized positions.

What can I do with a master of biotechnology?

A Master in Biotechnology prepares graduates for roles such as research scientist, bioprocess engineer, quality control analyst, or laboratory manager in industries like pharmaceuticals, agriculture, and healthcare. It often involves skills in laboratory techniques, data analysis, and regulatory compliance, with opportunities in research and development, manufacturing, or clinical settings.

What jobs can I get after an MSc in biotechnology?

An MSc in biotechnology qualifies graduates for roles such as research scientist, quality control analyst, bioprocess engineer, clinical research associate, and laboratory technician. These positions often require knowledge of laboratory techniques, data analysis, and familiarity with biotech tools and regulations.

What are the key skills and qualifications needed to thrive as a Master in Biotechnology, and why are they important?

To thrive as a Master in Biotechnology, you need advanced knowledge in molecular biology, genetics, and laboratory techniques, typically supported by a master's degree in biotechnology or a related field. Familiarity with bioinformatics tools, PCR, and laboratory information management systems (LIMS) is essential, and certifications in laboratory safety can be advantageous. Strong problem-solving, critical thinking, and teamwork skills distinguish top professionals in this field. These competencies enable effective research, innovation, and collaboration in the rapidly evolving biotech industry.

What is a Master in Biotechnology?

A Master in Biotechnology is a graduate-level degree program focused on the advanced study of biological processes and the use of technology to manipulate living organisms for applications in medicine, agriculture, and industry. Students learn about molecular biology, genetics, bioinformatics, and laboratory techniques, as well as how to apply these skills to develop new products and solutions. This degree prepares graduates for careers in research, pharmaceuticals, healthcare, environmental management, and biotechnology companies, or for further study at the doctoral level.

What careers can I get with a masters in biotechnology?

A master's in biotechnology prepares individuals for careers such as research scientist, bioprocess engineer, quality control analyst, or regulatory affairs specialist. These roles often require knowledge of laboratory techniques, data analysis, and familiarity with biotech tools and regulations.

What are 5 careers in biotechnology?

Five common careers in biotechnology include research scientist, bioprocess engineer, quality control analyst, clinical research associate, and regulatory affairs specialist. These roles often require knowledge of laboratory techniques, data analysis, and familiarity with industry regulations. Biotechnology professionals work in labs, manufacturing facilities, and regulatory agencies to develop and improve products like medicines, vaccines, and agricultural solutions.

What are some typical career paths for professionals with a Master in Biotechnology, and how can they progress within the industry?

Graduates with a Master in Biotechnology can pursue diverse career paths, such as research scientist, quality control analyst, regulatory affairs specialist, or roles in product development and project management. Advancement often involves taking on leadership responsibilities, such as managing teams or projects, or specializing further in areas like bioinformatics or clinical research. Many professionals also transition into roles in biotech startups, pharmaceuticals, or government agencies, and may further their expertise through certifications or a doctoral degree. Networking, continuous skill development, and staying updated with industry trends are key to progressing within the biotechnology sector.
What cities near Lisle, IL are hiring for Master In Biotechnology jobs? Cities near Lisle, IL with the most Master In Biotechnology job openings:
Infographic showing various Master In Biotechnology job openings in Lisle, IL as of July 2026, with employment types broken down into 41% Locum Tenens, 2% Internship, 42% Full Time, 9% Part Time, 1% Contract, and 5% Summer. Highlights an 74% Physical, 3% Hybrid, and 23% Remote job distribution.
Quality Control (QC) Analyst II

$24.75 - $33.25/hr

Other

Posted 22 days ago


Job description

Description

Position Summary


The Quality Control Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial biosimilar products in cGMP-compliant laboratories and will also be expected to be engaged in continuous improvement initiatives to drive efficiency and effectiveness of Kashiv's Quality Systems. 


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, 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.
  • Train other analysts to perform laboratory procedures and assays. Participate in internal assessments and audits as and when required.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards

Requirements

Minimum Qualifications:


Education:

  • Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 5 years of experience in a pharmaceutical/biotech QC laboratory. 
  • Alternatively, Master's degree in above areas with 3 years of experience in a pharmaceutical/biotech QC laboratory or PhD in above areas with a minimum of 2 years of experience. 

Preferred Qualifications: 


Experience:

  • Previous experience in a cGMP laboratory.
  • Strong background in protein chemistry and experience troubleshooting analytical results.
  • Demonstrated success at writing, revising, and complying with SOPs, protocols/reports, and QC methods.

Special Skills:

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

  • 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 requested.
  • Must be able to lift at least 25 lbs.
  • Ability to work under pressure and meet deadlines. 
  • High-paced environment structured to meet ambitious project goals
  • Some travel may be required

Supervisory Responsibility, if any: No


This position description is not a complete list of all responsibilities, duties, or skills 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.


Kashiv BioSciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Kashiv BioSciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.