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Job summary
A leading technical solutions provider is seeking an experienced Document Clerk to support pharmaceutical and biotechnology clients by managing documentation in compliance with FDA and ISO standards. Responsibilities include maintaining document control systems and ensuring regulatory compliance. Candidates should have an Associate’s degree and 2–5 years of relevant experience. Strong organizational and communication skills are essential for success. This position offers the opportunity to contribute to quality assurance processes in a fast-paced environment.
Qualifications
2-5 years of experience in document control or clerical support in a regulated environment.
Knowledge of cGMP, FDA, and ISO documentation standards.
Ability to manage multiple priorities in a fast-paced, regulated environment.
Responsibilities
Manage controlled documents with Quality Assurance and Regulatory Affairs teams.
Maintain document control systems ensuring proper versioning and security.
Prepare and distribute controlled documents including SOPs and batch records.
Skills
Document control
Attention to detail
Communication skills
Problem-solving
Organizational skills
Education
Associate’s degree or higher in Life Sciences or Business Administration
Tools
Electronic Document Management Systems (eDMS)
Microsoft Office Suite
Job description
A leading technical solutions provider is seeking an experienced Document Clerk to support pharmaceutical and biotechnology clients by managing documentation in compliance with FDA and ISO standards. Responsibilities include maintaining document control systems and ensuring regulatory compliance. Candidates should have an Associate’s degree and 2–5 years of relevant experience. Strong organizational and communication skills are essential for success. This position offers the opportunity to contribute to quality assurance processes in a fast-paced environment.