Document Controller

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets : United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.

Responsibilities

• Author, revise, and maintain SOPs and related controlled documents in accordance with regulatory and company standards.
• Collaborate with cross-functional teams (e.g., QA, QC, Manufacturing, R&D, Regulatory) to gather process information and ensure SOPs reflect current practices.
• Ensure SOPs are clear, concise, and user-friendly , enabling consistent execution by staff.
• Manage document lifecycle using electronic document management systems (EDMS), including version control, approvals, and archival.
• Support internal and external audits by ensuring documentation is inspection-ready.
• Train staff on new or revised SOPs and maintain training records.
• Continuously improve documentation practices to enhance clarity, compliance, and usability.

Qualifications Requirements / Knowledge / Education / Skills

Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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