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Plant QA Specialist

Tjoapack -
Clinton, TN

Quick Apply

Job Details

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Raw material quality management
Document control experience within pharmaceutical industry
Pharmaceutical regulatory compliance
Manufacturing facility experience
Manufacturing process inspections
Continuous improvement
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Quality improvement
Compliance documentation
Collaboration with manufacturing teams
Quality control experience within pharmaceutical industry
Operational excellence initiatives
Productivity software
Production batch record review
Quality control communication
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

Plant QA Specialist

Clinton, TN | 11:00pm-7:30am Sunday-Friday
Vacancies: 1 on 3rd, 1 on 4th

Experience working within a Pharmaceutical cGMP Environment is required for consideration.

About Tjoapack

Tjoapack is a global contract packaging organization (CPO) specializing in primary and secondary pharmaceutical packaging and supply chain solutions. With more than 35 years of industry experience, we support pharmaceutical and healthcare customers in over 46 countries by ensuring millions of medication packages each year are available when patients need them.

Originally founded in Europe in1989 and operating in Clinton, Tennessee since 2021, Tjoapack is committed to delivering safe, compliant, and reliable packaging services with patients always at the center of everything we do.

In 2026, Tjoapack became part of Alcami Corporation, expanding our capabilities across the pharmaceutical supply chain and strengthening our ability to support customers from development through final packaging and distribution

Summary of the Role:

The Plant QA Specialist is a hands-on quality role that serves as the primary quality representative on the production floor, ensuring packaging operations comply with SOPs, GMP requirements, and quality standards. The position is responsible for conducting inspections, reviewing batch records, supporting material release activities, managing deviation documentation, and assisting with investigations, CAPAs, risk assessments, and change controls. This role partners closely with production teams to provide real-time quality guidance, improve deviation reporting, and support continuous improvement initiatives. Ideal candidates have a bachelor's degree in a relevant scientific field, experience in quality or manufacturing environments, strong documentation and problem-solving skills, and familiarity with batch record review, controlled documents, and compliance processes.

✅Your Expectations:

Shop Floor Quality & Production Support

Perform daily quality inspections during packaging operations to ensure compliance with SOPs, work instructions, and quality standards.
Serve as the first point of contact for production teams on quality-related questions and issues.
Provide real-time guidance and coaching to operators on GMP requirements and proper documentation practices.
Conduct finished product checks and monitor production activities to ensure products meet release requirements.

Documentation, Batch Records & Material Control

Review batch records and production documentation for accuracy, completeness, and compliance.
Support inspection, approval, and release of packaging materials and bulk products.
Maintain retain sample programs and support Right First Time (RFT) performance reporting.
Create, review, and update SOPs, work instructions, forms, and training documentation.
️ Deviations, Investigations & Compliance

Review and approve minor deviations while ensuring timely and accurate documentation.
Support investigations of major deviations through data gathering and root cause analysis.
Assist with CAPAs, risk assessments, change controls, and other quality system activities.
Guide production staff on deviation reporting processes and compliance expectations.

Training & Continuous Improvement

Assist in developing and delivering GMP and quality-related training programs.
Support implementation of process improvements to enhance quality, compliance, and efficiency.
Participate in quality projects and help execute operational changes on the production floor.
Collaborate with cross-functional teams to identify opportunities for improving procedures and reducing errors.

Requirements:

Bachelor's degree in Life Sciences, Food Science/Hygiene, Process Engineering, or a related scientific discipline preferred.
1–2 years of experience in a Quality Assurance, Quality Control, or quality-focused support role within pharmaceutical, healthcare, food, or other regulated manufacturing environments.
Experience performing shop-floor quality inspections and supporting production teams in a fast-paced manufacturing setting.
Experience working within a Pharmaceutical cGMP Environment is required for consideration.
Ability to review batch records, production documentation, and quality records for accuracy, completeness, and compliance.
Familiarity with deviation management, investigations, CAPAs, root cause analysis, risk assessments, and change control processes preferred.
Experience supporting material inspection, product release activities, and finished product quality checks.
Strong attention to detail with the ability to identify issues, maintain accurate records, and ensure compliance with established procedures.
Experience creating, reviewing, or updating SOPs, work instructions, forms, training materials, or other controlled documents is preferred.
Ability to provide real-time quality guidance to production personnel and effectively communicate quality expectations across teams.
Strong analytical, problem-solving, organizational, and time-management skills.
Demonstrated ability to support continuous improvement initiatives and drive quality-focused process enhancements.
Proficiency with Microsoft Office and electronic or paper-based document management systems.
Excellent verbal and written communication skills, with the ability to collaborate effectively across Quality, Operations, and Production teams.

Why Choose Tjoapack?

At Tjoapack, we believe our employees are at the center of our success. We are committed to creating a supportive, employee-focused culture that encourages teamwork, growth, curiosity, and continuous learning. Our teams work collaboratively every day to help ensure life-changing medications reach patients around the world safely and on time.

We offer competitive compensation and a comprehensive total rewards package designed to support both your personal and professional wellbeing.

Competitive pay with regular overtime opportunities
Three weeks of PTO Annually
9 paid holidays each year
Medical, dental, and vision insurance
401(k) with company matching
Short-term disability, long-term disability, and life insurance coverage

At Tjoapack, you’ll find opportunities to learn, take on new challenges, and make a direct impact. We are a team that supports one another, works hard together, and moves toward success together. Apply to work with us today!

All Offers are conditional pending successful completion of Tjoapack’s Pre-Employment Drug Screening, Physical Examination, and Background Check.

#TJO123

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quality assurance specialist jobs in clinton tn

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