Careers | Accupac

Careers

Validation Associate

Job Title
Validation Associate
Job ID
27747353
Location
Mainland, PA, 19451 
Other Location
Description

Job Title: Validation Associate I & II 
Location: Mainland, PA 19451 

Join Our Team: 
At Accupac, we are Makers. From formulation to manufacturing, we serve the most trusted brands in the beauty and personal care industries with a wide range of cosmetics, over-the-counter and medical devices across skincare, haircare, oral care, and healthcare products. 

But beyond that, we make a difference. We make a difference in the lives of our people, we make a difference in the community around us, we make a difference in the health of our planet for a better, brighter, more beautiful future for all. 

We value detail-driven professionals who thrive on accuracy and compliance. As a Validation Associate, you’ll ensure our processes and equipment meet rigorous quality standards and regulatory requirements, keeping products safe and effective for the people who rely on them. 

 

What We Offer: 

  • Competitive Pay  

  • Salary Range: $44,000.00 - $60,000.00 

  • Bonus: Exempt employees are eligible for a bonus in accordance with Accupac’s Bonus Plan. 

  • The posted job may span more than one career level. The final offer, including level and pay, will be determined based on a variety of factors such as the candidate’s relevant job and industry experience, education, knowledge, skills, geographic location, and abilities. Internal equity and alignment with market data will also be considered. We are committed to providing fair and competitive compensation based on each candidate’s qualifications and fit for the role. 

  • Employees are eligible for the following benefits: 

  • Medical, Dental, and Vision insurance 

  • Health Savings Account 

  • Life Insurance with Optional Supplemental Plan 

  • Pet Insurance 

  • Short-Term Paid Disability 

  • 401(k) Retirement Plan with Vested Company Match Contribution 

  • Paid Time Off (PTO) 

  • 10 Paid Holidays 

  • Health Advocacy Programs 

Career Growth 

 

What You’ll Do: 

  • Review customer documentation to assess required validation activities 

  • Write and execute protocols, perform IQ/OQ testing, and maintain validation reports 

  • Collaborate with Quality Systems, Project Management, and Operations teams 

  • Manage validation documentation in compliance with SOPs and GMP standards 

  • Support calibration and preventative maintenance tracking 

  • Maintain the Calibration Management database and ensure timely PMs and calibrations 

  • Investigate and resolve validation deviations and errors with QA and departmental managers 

What We’re Looking For: 

  • Bachelor’s degree preferred or 1–4 years of experience in a cGMP-regulated environment 

  • Strong organizational and documentation skills 

  • Experience with IQ/OQ/PQ validation protocols 

  • Familiarity with manufacturing, packaging, and cleaning processes 

  • Ability to read, write, and communicate effectively in English 

  • Strong attention to detail and ability to work independently 

  • Proficiency in Microsoft Word, Excel, and PowerPoint 

Ready to Apply? 
Join us at Accupac and become part of a company that values your skills and dedication. Click below to apply today! 

 

Required Skills

Essential Functions of the Job:
• Maintain the Company’s compliance with established Accupac, LLC. Standard Operating Procedures, FDA Current Good Manufacturing Practices, and the Customer’s specifications.
• Establish performance and quality criteria. Create and run quality tests based on appropriate protocols.
• Ensure compliance with safety and quality standards.
• Strong understanding of manufacturing, packaging, and cleaning processes and safety regulations.
• Ensure products meet company requirements by writing protocols and creating a documented trail of results for both manufacturing and packaging processes.
• Strong documentation bias – managing and documenting the entire validation process. The protocols produced must comply with both internal SOPs and external regulations.
• Perform Equipment IQ/OQ and Gap analysis.
• Review all questions, errors, and deviations with the respective departmental Management and QA and resolve issues.
• Maintain the completed validation documentation and all associated data.
• Maintain open communication with Project Management and Operations for validation requirements.
• Maintain Calibration Management database including entering, changing, and updating equipment status in the Calibration Manager database.
• Provide PM and Calibration documentation to either internal or external personnel.
• Provide oversight on the timely completion of PMs and Calibrations.
• Review completed validation, PM, calibration documentation for accuracy and GMP compliance.
• Performs other related duties as required and assigned.

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