Document Control Specialist
Tri-Pac IncSouth Bend, Indiana, United States
Posted October 15, 2025
Full Time
About the Company
Tri Pac, Inc. is a Contract Development & Manufacturing Organization (CDMO) specializing in compounding, manufacturing, and filling of topicals, orals, skincare, and haircare products for various formats. With extensive certifications including ISO 13485, UL Health Canada OTC, and FDA registration, Tri Pac offers a comprehensive range of services from turn-key product development to regulatory compliance and quality assurance. The company's focus on innovation, supply chain management, and environmental sustainability positions it as a reliable partner for the OTC, consumer healthcare, cosmetic, and medical device industries.
Job Description
Tri-Pac, Inc. is seeking an experienced Document Control Specialist for immediate addition to their growing team. The role involves maintaining document control systems, coordinating document issuance and revisions, reviewing and approving documentation, and ensuring adherence to Quality Management System requirements. This position requires excellent communication skills and a high degree of organization.
Requirements
- Maintain document and record control systems according to Quality Management System requirements.
- Coordinate issuance, revision, review, and approval of SOP’s and other documents.
- Monitor document status and prepare documentation for QA and product release.
- Review and archival documents and support continuous improvement efforts.
- Manage new equipment, asset lists, and vendor documentation.
- Assist in internal audits and quality system validation.
Benefits
- Competitive Salary
- Vacations
- Insurance
- Life Insurance
- Disability (Long term/ Short term)
- Continuous Training
- Work where you are HAPPY!
