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Biotech Quality Control Jobs in Tennessee (NOW HIRING)

Integrated Resources, Inc

QC Bioassay Analyst

Memphis, TN · On-site

$23.25 - $31.25/hr

Job Title: QC Bioassay Analyst Job Location: Memphis, TN Job Duration: 6 months+ Possible Extension ... Minimum 1-2 years of applicable experience in laboratory, biotech, cell therapy, or related ...

New

Maxonic

Be Seen First

QC Analyst I-BioAssay

Memphis, TN · On-site

$21/hr

Job Title: QC Analyst I-BioAssay Job Type: Contract Job Location: Memphis, TN Work Schedule: On ... Minimum 1-2 years of applicable experience in laboratory, biotech, cell therapy, or related ...

New

LabConnect

Senior Quality Specialist

Johnson City, TN · On-site +1

$79K - $109K/yr

Overview LabConnect improves lives by partnering with pharmaceutical and biotech companies, and ... Leads and project manages QMS activities including document control, change control, non ...

LabConnect

Medical Writer

Johnson City, TN · On-site +1

Overview LabConnect improves lives by partnering with pharmaceutical and biotech companies, and ... Coordinate quality control of clinical trial and regulatory documents. * Engage with cross ...

LabConnect

Clinical Sample Specialist

Johnson City, TN · On-site

Overview LabConnect improves lives by partnering with pharmaceutical and biotech companies, and ... Specimen labeling * Assist with quality control (QC) of specimens for courier pick-ups, scheduled ...

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All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Tennessee

Biotech Quality Control information

See Tennessee salary details

$27.7K

$73.8K

$117.5K

How much do biotech quality control jobs pay per year?

As of Jul 30, 2026, the average yearly pay for biotech quality control in Tennessee is $73,811.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,900.00 and $90,800.00 per year, depending on experience, location, and employer.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
What are the most commonly searched types of Biotech Quality Control jobs in Tennessee? The most popular types of Biotech Quality Control jobs in Tennessee are:
What are popular job titles related to Biotech Quality Control jobs in Tennessee? For Biotech Quality Control jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Tennessee look for? The top searched job categories for Biotech Quality Control jobs in Tennessee are:
What cities in Tennessee are hiring for Biotech Quality Control jobs? Cities in Tennessee with the most Biotech Quality Control job openings:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Tennessee as of July 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $73,811 per year, or $35.5 per hour.

QC Bioassay Analyst

Integrated Resources, Inc

Memphis, TN • On-site

$23.25 - $31.25/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: QC Bioassay Analyst
Job Location: Memphis, TN
Job Duration: 6 months+ Possible Extension
Shift: Monday through Friday 8:00am to 4:30pm (overtime as needed)
Job summary:
QC Analyst II requires the utmost attention to detail, very strong organizational skills, computer proficiency, and a basic understanding of laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment are essential for success.
Essential duties and responsibilities:
  • Strong background and experience with cell-based immunological in vitro methods (e.g. MLR, cytotoxicity, HLA-restriction, CTLp, cell proliferation, etc.) and instrumentation.
  • An understanding of cGMP/GLP regulations as well as excellent documentation skills in order to complete paperwork dealing in all aspects of Quality Control Reviews test results of other QC analysts for accuracy and precision and maintains efficient workflow of an required testing documentation ensuring timely submission relative to product release dates
  • Study design, data/statistical analysis, reporting results in both written and oral format (presentation)
  • Enters observations and results into the appropriate trending databases for periodic analysis and trending
  • Previous experience working with aseptic techniques and culturing of mammalian cells and familiarity with cell culturing basics
  • Assists the QC Team with maintaining proper overall operation of department (inventories, logs, documentation, filing, etc.)
  • Assists with implementation of quality improvement initiatives for QC laboratory operations Participates in laboratory, OOS, CAPA, or other investigations, as required
  • Adheres to Standard Operating Procedures (SOPs) and good documentation practices to ensure data integrity and traceability
  • Perform all other related duties as assigned.
Qualifications:
  • Bachelor’s degree in the biological sciences or related field preferred
  • Minimum 1-2 years of applicable experience in laboratory, biotech, cell therapy, or related industry or a combination of 1-2 years of education and related work experience required.
  • Previous experience working with aseptic technique and culturing of mammalian cells
  • Familiarity with cGMP as defined in 21CFR210 and 211.
  • Detail-oriented with strong written and verbal communication skills
  • Experience in cell-based assays and molecular biology-based assays
  • Ability to work independently and as part of a team.
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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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