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Biotech Quality Control Jobs in Tennessee (NOW HIRING)

WMS Workflow Architect

Memphis, TN

$61.25 - $80.75/hr

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... Lot/batch/serial control * Quarantine/QA/hold/release * Temperature-controlled workflows

WMS Workflow Architect

Memphis, TN · On-site +1

$61.25 - $80.75/hr

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... Lot/batch/serial control * Quarantine/QA/hold/release * Temperature-controlled workflows

WMS Workflow Architect

Memphis, TN

$61.25 - $80.75/hr

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... Lot/batch/serial control * Quarantine/QA/hold/release * Temperature-controlled workflows

Reliability Engineer

Nashville, TN · On-site

$99K - $124K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... The role partners closely with Manufacturing Engineering, Maintenance, Operations, Quality ...

Reliability Engineer

Nashville, TN · On-site

$99K - $124K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... The role partners closely with Manufacturing Engineering, Maintenance, Operations, Quality ...

Reliability Engineer

Nashville, TN

$99K - $124K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... The role partners closely with Manufacturing Engineering, Maintenance, Operations, Quality ...

Drive results by owning and completing the subsequent projects including high quality technical ... Control Units, Clean in Place Skids, etc.) * Excellent interpersonal and communication skills ...

Reliability Engineer

Nashville, TN · On-site

$110 - $170/hr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... Provide technical support to investigations, deviations, CAPAs, audit responses, and quality or ...

New

Drive results by owning and completing the subsequent projects including high quality technical ... Control Units, Clean in Place Skids, etc.) * Excellent interpersonal and communication skills ...

Drive results by owning and completing the subsequent projects including high quality technical ... Control Units, Clean in Place Skids, etc.) * Excellent interpersonal and communication skills ...

Structural Design Engineer

Tullahoma, TN · On-site

$109K - $170K/yr

Establish, control and report on material key quantities; provide analysis and forecasts. * Provide ... Manufacturing, pharmaceutical or biotechnology Business Profile: Cimarron is a global solutions ...

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... quality assurance, or training. * Experience in aseptic manufacturing and contamination control ...

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... quality assurance, or training. * Experience in aseptic manufacturing and contamination control ...

Showing results 41-60

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 Aug 7, 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.

What does a biotech quality control do?

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.

What is a biotech quality control?

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 biotech quality control?

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 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:
Infographic showing various Biotech Quality Control job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $73,811 per year, or $35.5 per hour.

Supervisor, Microbiology

August Bioservices

Nashville, TN • On-site

Full-time

Posted 4 days ago


Job description

Headquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project - including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!
The Supervisor Microbiology reports to the Director of Quality Control. They provide leadership to the microbiology laboratory through all phases of development. They are responsible for managing the microbiological evaluation of raw materials, components, drug product intermediate, finished drug product and stability samples. They are also responsible for managing the environmental monitoring and aseptic process simulation programs. They are required to work in development and regulated environments, including adherence to cGMPs, regional and country specific regulations, as well as internal SOPs.
ESSENTIAL DUTIES & RESPONSIBILITIES
  • Oversee microbiological testing activities for several of the following functions but not limited to raw material, component, drug product, stability, validation, investigational, in-process testing, etc.
  • Oversee environmental monitoring, aseptic process simulation and gowning qualification programs.
  • Serve as a subject matter expert for microbiology.
  • Lead, guide, and mentor analysts
  • Foster a culture of continuous improvement.
  • Ensure the laboratories are clean, organized, compliant, and audit ready always.
  • Support formulation, process development, and scale-up activities
  • Review and approve laboratory data for accuracy and completeness.
  • Lead and serve on cross-functional project teams.
  • Prepare protocols, technical reports, and other documentation for CMC related activities.
  • Identify and resolve project-related issues that have the potential to impact project deliverables.
  • Ensure compliance of laboratory personnel and equipment
  • Prepare annual laboratory budgeting.
  • Perform annual performance assessments of direct reports.

QUALIFICATIONS
  • Bachelor's degree in biology, or related science and 8-10 years of experience in a pharmaceutical laboratory management role.

KNOWLEDGE, SKILLS, & ABILITIES
  • Must possess strong knowledge of SOPs, laboratory procedures, FDA and ICH guidance, USP regulations, microbiological testing techniques, and cGMP.
  • Strong track record of leadership skills and influence
  • Strong interpersonal skills. Ability to build effective and constructive relationships.
  • Ability to work cross-functionally both internally and externally
  • Must be a leader, mentor, and self-motivated to develop a high performing team
  • Must possess excellent written and verbal communication skills, interpersonal skills, management skills, strong work ethic, and organizational skills
  • Demonstrated analytical and problem-solving skills

PHYSICAL REQUIREMENTS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Prolonged periods sitting at a desk and working on a computer.
  • Must be able to lift up to 15 pounds at times.

August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.
At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule - from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment.
We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team!
August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.