Regulated Pharma Document Control Specialist

MENTOR Technical Group Corporation; Carolina (PR); On-site; USD 40,000 - 55,000; Full time

Job summary

A leading technical support provider is seeking a Document Clerk to manage and maintain essential documents in compliance with FDA and ISO standards. This role involves organizing electronic and physical documents, supporting audits, and ensuring accuracy in record-keeping. The ideal candidate will have an associate's degree and 2–5 years of relevant experience, along with a strong attention to detail in a fast-paced environment. Join a team where you can contribute to quality and operational processes.

Qualifications

• 2–5 years of experience in document control or clerical support in a regulated pharmaceutical or biotech environment.
• Knowledge of cGMP, FDA, and ISO documentation standards.
• Strong attention to detail and ability to manage multiple priorities.

Responsibilities

• Partner with Quality Assurance and Regulatory Affairs teams to manage controlled documents.
• Maintain electronic and physical document control systems.
• Prepare, review, and distribute controlled documents.

Skills

Document control

Organizational skills

Communication skills

Proficiency with Microsoft Office

Problem-solving

Education

Associate's degree in Life Sciences

Tools

Electronic Document Management Systems

Veeva Vault

MasterControl

Job description

A leading technical support provider is seeking a Document Clerk to manage and maintain essential documents in compliance with FDA and ISO standards. This role involves organizing electronic and physical documents, supporting audits, and ensuring accuracy in record-keeping. The ideal candidate will have an associate's degree and 2–5 years of relevant experience, along with a strong attention to detail in a fast-paced environment. Join a team where you can contribute to quality and operational processes.