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Quality Control Pharma Jobs in Tennessee (NOW HIRING)

Sky Mavis

WMS Workflow Architect

Memphis, TN · On-site

$100 - $125/hr

Lot/batch/serial control * Quarantine/QA/hold/release * Temperature‑controlled workflows * Controlled substances handling * Multi‑client 3PL billing * VAS/kitting/custom pharma processes

EVERSANA

WMS Workflow Architect

Memphis, TN · On-site +1

$61.25 - $80.75/hr

Lot/batch/serial control * Quarantine/QA/hold/release * Temperature-controlled workflows * Controlled substances handling * Multi-client 3PL billing * VAS/kitting/custom pharma processes * Optimize ...

Eversana

WMS Workflow Architect

Memphis, TN · On-site

$61.25 - $80.75/hr

Lot/batch/serial control * Quarantine/QA/hold/release * Temperature-controlled workflows * Controlled substances handling * Multi-client 3PL billing * VAS/kitting/custom pharma processes * Optimize ...

August Bioservices

Production Scheduler

Nashville, TN · On-site

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... Adjust schedules in real time in response to deviations, equipment downtime, material delays, QC ...

August Bioservices

Production Scheduler

Nashville, TN · On-site

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... Adjust schedules in real time in response to deviations, equipment downtime, material delays, QC ...

Zifo

GxP Lab Computing Analyst

Sparta, TN

Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team ...

Zifo

GxP Lab Computing Analyst

Sparta, TN · On-site

$80 - $100/hr

Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team ...

Zifo

GxP Lab Computing Analyst

Sparta, TN · On-site

Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team ...

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Showing results 21-40

All JobsQuality Control Pharma JobsQuality Control Pharma Jobs in Tennessee

Quality Control Pharma information

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

Is Quality Control Pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It requires attention to detail, knowledge of laboratory techniques, and often involves certifications such as GMP training. The role offers stable employment opportunities in the pharmaceutical industry with potential for career advancement.

What are popular job titles related to Quality Control Pharma jobs in Tennessee?

For Quality Control Pharma jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Quality Control Pharma jobs in Tennessee look for?

The top searched job categories for Quality Control Pharma jobs in Tennessee are:

What cities in Tennessee are hiring for Quality Control Pharma jobs?

Cities in Tennessee with the most Quality Control Pharma job openings:

Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 10% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

QA Specialist - On the Floor Support (3rd Shift)

August Bioservices

Nashville, TN

Full-time

Re-posted 15 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!

We are seeking a proactive QA Specialist to provide real-time quality oversight across manufacturing, packaging, inspection, and warehouse operations. The role ensures cGMP compliance, supports production activities, and promotes a strong quality culture. The ideal candidate is detail-oriented, hands-on, and able to provide guidance to operators while maintaining inspection readiness.
Responsibilities
  • Maintain a daily presence on the production floor to provide real-time QA support and guidance.
  • Ensure adherence to batch records, SOPs, and validated procedures during manufacturing, packaging, and inspection activities.
  • Perform QA line clearances, in-process checks, and AQL inspections, and support visual inspection and automated inspection processes.
  • Act as a Designated Observer for controlled substance handling, ensuring compliance with internal and regulatory requirements.
  • Routinely walk through production, lab, and warehouse areas to assess GMP compliance and escalate issues as needed.
  • Verify labeling issuance, reconciliation, and documentation to ensure proper handling of materials and finished products.
  • Provide on-the-floor coaching and guidance to operators, reinforcing GMP compliance and best practices.
  • Collaborate with Manufacturing and Planning teams to prioritize lot disposition, minimize downtime, and support operational flow.
  • Monitor cleaning, sanitization, and environmental controls prior to critical operations.
  • Promote a quality-focused culture by sharing lessons learned and encouraging proactive issue identification.
  • Maintain knowledge of deviation, OOS/OOT, and CAPA processes to support investigations if required.
  • Assist in gathering facts, reviewing documentation, and providing QA input when deviations occur on the floor.
  • Understand root cause analysis tools (5 Whys, Fishbone, FMEA) to support quality discussions.
  • Review, revise, and proofread GMP documentation, including batch records, SOPs, and logbooks.
  • Support document control processes and ensure training documentation is correctly linked to controlled systems.
  • Ensure compliance with regulatory standards (FDA, ICH, DEA) and Good Documentation Practices.
  • Conduct routine walk-throughs to maintain inspection readiness.
  • Support internal audits and regulatory inspections by providing floor-level guidance and documentation as needed.
Qualifications
  • Bachelor’s degree in a scientific discipline or equivalent experience.
  • 2–5 years in a GMP-regulated environment, with experience in on-the-floor QA support.
  • Knowledge of cGMPs, FDA/ICH regulations, and QA documentation practices.
  • Familiarity with Master Control or electronic quality systems preferred.
  • Strong communication, problem-solving, and interpersonal skills.
  • Regular presence in GMP manufacturing and cleanroom environments with proper gowning.
  • Occasional off-shift, weekend, or extended coverage may be necessary.
Preferred Qualifications:
  • Experience with automated visual inspection processes.
  • Knowledge of controlled substance handling.
  • Prior involvement in regulatory inspections.
Work Environment & Physical Demands
ADA Accommodation Notice
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.
 
Physical Requirements
  • Ability to safely wear and work in a PAPR hood and associated equipment weighing approximately 2 to 3 pounds during assigned tasks.
  • Ability to perform sustained physical activities, including standing, walking, bending, reaching, lifting, and handling manufacturing equipment while wearing required respiratory protection and personal protective equipment (PPE).
  • Ability to wear and operate a Powered Air-Purifying Respirator (PAPR) for extended periods, up to 4 to 6 hours per shift, while performing manufacturing, equipment cleaning, and sanitization activities.
  • Ability to wear required PPE, including pharmaceutical gowning, respiratory protection, safety glasses, chemical-resistant gloves, and additional protective equipment as required by operational and safety procedures
Shifts

2nd shift: 3:00pm - 11:30pm , Monday - Friday 

3rd shift: 11:00pm - 7:30am , Sunday - Thursday 

Weekend Day shift: 7:00 am - 7:00 pm, Friday - Sunday

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.