PSG Global Solutions Careers
Documentation Specialist
PSG Global Solutions Careers, Boston, Massachusetts, us, 02298
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The Opportunity
Description
We're looking for a
Documentation Specialist , working in
Pharmaceuticals and Medical Products
industry in
Boston, Massachusetts, United States .
Assists with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
High school diploma/GED and 4 years of experience working in a GMP regulated environment with experience working in a Document Control or similar function 2 years of experience in document and/or records management Knowledge of MS Office software (Word, Excel and PowerPoint) Very strong organizational skills Ability to work independently and multi-task in a fast-paced, deadline-driven organization Experience authoring standard operating procedures, training materials and other controlled documents Knowledge and technical competencies using document and/or records management software solution and other business tools including Sharepoint and Adobe Acrobat Familiarity with validation lifecycle documentation Experience with deviation, CAPA and change management quality processes Team and customer service oriented Ability to multi-task in a fast-paced, deadline-driven organization
What Do You Think? Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?
Documentation Specialist , working in
Pharmaceuticals and Medical Products
industry in
Boston, Massachusetts, United States .
Assists with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
High school diploma/GED and 4 years of experience working in a GMP regulated environment with experience working in a Document Control or similar function 2 years of experience in document and/or records management Knowledge of MS Office software (Word, Excel and PowerPoint) Very strong organizational skills Ability to work independently and multi-task in a fast-paced, deadline-driven organization Experience authoring standard operating procedures, training materials and other controlled documents Knowledge and technical competencies using document and/or records management software solution and other business tools including Sharepoint and Adobe Acrobat Familiarity with validation lifecycle documentation Experience with deviation, CAPA and change management quality processes Team and customer service oriented Ability to multi-task in a fast-paced, deadline-driven organization
What Do You Think? Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?