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Process Engineer

Tjoapack
Posted 2 months ago, valid for 18 days
Location

Clinton, TN 37716, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Tjoapack is seeking a Process Engineer in Clinton, TN, offering a full-time position with a focus on optimizing manufacturing performance in pharmaceutical packaging.
  • Candidates must possess a Bachelor's degree in Engineering and have a minimum of 4 years of engineering project planning or management experience, along with at least 1 year in a GMP manufacturing environment.
  • The role involves coordinating production trials, validating process changes, and utilizing Lean and Six Sigma methodologies to drive continuous improvement initiatives.
  • Strong analytical skills and proficiency in Microsoft Office applications are required, with a preference for candidates who have experience in sterile manufacturing environments.
  • Compensation is competitive, reflecting the importance of the role in ensuring life-changing medications reach patients safely and on time.

Process Engineer

Clinton, TN Ā | Full-time
Ā 
Vacancies: 1


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 distributionĀ 


At least one year of working in a Pharmaceutical cGMP evironment is required for consideration.


Ā Summary of the Role:

This role is responsible for optimizing manufacturing performance by coordinating production trials, validating process changes, and ensuring improvements are effective, sustainable, and aligned across the entire production process. Acting as a technical expert, this individual evaluates how equipment, systems, and technologies interact, identifying opportunities and resolving obstacles to keep production lines running smoothly, efficiently, and in harmony. The position develops and maintains technical documentation, standardizes best practices, and supports Continuous Improvement initiatives through the application of Lean and Six Sigma methodologies. Additionally, the role analyzes production metrics such as OEE, downtime, and waste using tools like Excel, Power BI, and MES systems to drive data-based decisions, performance reporting, and visual management practices.


Ā āœ…Your Expectations:

āš™ļø Process Validation & Production Optimization

  • Coordinate and execute production trials, machine tests, and process improvement initiatives.
  • Validate process changes to ensure improvements are effective, sustainable, and meet performance objectives.
  • Analyze production workflows to identify inefficiencies, bottlenecks, and opportunities for optimization.
  • Troubleshoot technical issues and support solutions that improve line efficiency, reliability, and throughput.

Technical Systems Integration & Manufacturing Support

  • Evaluate how production equipment, automation, and technologies interact across the manufacturing process.
  • Optimize machine settings and process parameters to ensure equipment operates efficiently and in harmony.
  • Identify and resolve obstacles between interconnected systems that impact production performance.
  • Support the implementation of new equipment, technologies, and process enhancements.

Continuous Improvement & Performance Management

  • Lead and support Continuous Improvement initiatives using Lean Manufacturing and Six Sigma methodologies.
  • Collect and analyze production metrics, including OEE, downtime, waste, and efficiency data.
  • Utilize tools such as Excel, Power BI, and MES systems to monitor trends and drive data-based decisions.
  • Support visual management practices through KPI tracking, reporting, and daily performance reviews.

Documentation & Standardization

  • Create, maintain, and update technical documentation, including process parameters, changeover procedures, and technical standards.
  • Develop standardized processes and best practices to improve consistency and operational performance.
  • Ensure technical knowledge and process improvements are effectively documented and shared across teams.
  • Support compliance with established manufacturing standards and continuous improvement objectives.


Ā Requirements:

  • Bachelor's degree in Engineering required, with a minimum of 4 years of engineering project planning and/or project management experience.Ā 
  • At least one year of working in a Pharmaceutical cGMP evironment is required for consideration.
  • Demonstrated ability to evaluate complex manufacturing processes, solve technical problems, and make data-driven decisions in dynamic production environments.Ā 
  • Strong analytical skills, including the ability to perform complex mathematical calculations, analyze data trends, and interpret graphs, charts, and technical information.Ā 
  • Excellent verbal, written, and presentation skills, with the ability to communicate effectively and collaborate across all levels of the organization.Ā 
  • Proficiency in Microsoft Office applications, including Word, Excel, and PowerPoint.Ā 
  • Previous experience in a sterile manufacturing environment is preferred.Ā 
  • Ability to interpret written, verbal, diagrammatic, and schedule-based instructions while consistently executing work in accordance with established procedures and timelines.Ā 
  • Demonstrated commitment to maintaining a safe, clean, and organized work environment while adhering to all company policies, regulatory requirements, and quality standards.Ā 
  • Proven ability to work collaboratively across functions, build strong working relationships, and leverage the expertise of others to achieve business objectives.Ā 
  • Strong leadership capabilities, including strategic thinking, decisive decision-making, performance accountability, continuous learning, and a passion for delivering value to customers.Ā 
  • High level of integrity and professionalism, with a commitment to ethical conduct, customer focus, operational excellence, and a "first-time-right" mindset.



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. Ā 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.Ā 




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