Documentation Specialist

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test1242
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Documentation Specialist

Stratatech Corporation, a regenerative medicine company focused on the commercialization of unique, proprietary skin substitute products for therapeutic and research uses, is seeking a highly-motivated and organized individual to join our Quality Assurance team.

Responsibilities of this position include:

• Coordinate the review and revision of procedures, specifications and forms.
• Assist with preparation, formatting, distribution, routing, and maintenance of Standard Operating Procedures (SOP) and other version controlled documents.
• Assemble regulatory filing documents and maintain computerized files to support all documentation systems.
• Review and release raw materials, intermediate products and finished products.
• Create and maintain various filing systems.
• Update QA logbooks, databases and document manuals.
• Remain cognizant of regulatory compliance requirements, guidelines, and trends.
• Perform internal and external audits as needed.

Qualifications:
Associate’s or Bachelor’s degree or equivalent required. Minimum of 1 to 2 years related experience desirable. Familiarity with documentation control systems (manual and/or computerized) required. Excellent writing and proofreading skills required. Must have excellent verbal communication skills. Basic knowledge of current Good Manufacturing Practices (cGMP) and/or relevant Quality Assurance/Compliance experience desirable.

For more information please visit our website at: www.stratatechcorp.com. Interested applicants please send introductory letter, resume or CV including salary requirements to: eval(unescape('%64%6f%63%75%6d%65%6e%74%2e%77%72%69%74%65%28%27%3c%61%20%68%72%65%66%3d%22%6d%61%69%6c%74%6f%3a%6a%6f%62%73%40%73%74%72%61%74%61%74%65%63%68%63%6f%72%70%2e%63%6f%6d%22%3e%6a%6f%62%73%40%73%74%72%61%74%61%74%65%63%68%63%6f%72%70%2e%63%6f%6d%3c%2f%61%3e%27%29%3b')).

Stratatech Corporation is an Equal Opportunity Employer

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