PSG Global Solutions
Documentation Specialist
PSG Global Solutions, Boston, Massachusetts, us, 02298
Job Industry:
Pharmaceuticals and Medical ProductsSalary:
The pay we're offering is$20-$22per hourApply now and our proprietary system will quickly have you in front of a live recruiter.The Opportunity
DescriptionWe're looking for a
Apply now and our proprietary system will quickly have you in front of a live recruiter.The Opportunity
DescriptionWe'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 regulatoryrequirements.Our ClientOur 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 SuccessHigh school diploma/GED and 4 years of experience working in a GMPregulated environment with experience working in a Document Control orsimilar function2 years of experience in document and/or records managementKnowledge of MS Office software (Word, Excel andPowerPoint)Very strong organizational skillsAbility to workindependently and multi-task in a fast-paced, deadline-drivenorganizationExperienceauthoring standard operating procedures, training materials and othercontrolled documentsKnowledge and technical competencies using documentand/or records management software solution and other business toolsincluding Sharepoint and Adobe AcrobatFamiliarity with validationlifecycle documentationExperience with deviation, CAPA and changemanagement quality processesTeam and customer service orientedAbilityto multi-task in a fast-paced, deadline-driven organizationWhat 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?Apply Now
When people and technology come together, you get exceptional results. We combine our dedicated global workforce of 3000+ recruiting resources with a best-of-breed tech stack and next-gen processes to deliver the best talent possible to our portfolio of global clients.
#J-18808-Ljbffr
Pharmaceuticals and Medical ProductsSalary:
The pay we're offering is$20-$22per hourApply now and our proprietary system will quickly have you in front of a live recruiter.The Opportunity
DescriptionWe're looking for a
Apply now and our proprietary system will quickly have you in front of a live recruiter.The Opportunity
DescriptionWe'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 regulatoryrequirements.Our ClientOur 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 SuccessHigh school diploma/GED and 4 years of experience working in a GMPregulated environment with experience working in a Document Control orsimilar function2 years of experience in document and/or records managementKnowledge of MS Office software (Word, Excel andPowerPoint)Very strong organizational skillsAbility to workindependently and multi-task in a fast-paced, deadline-drivenorganizationExperienceauthoring standard operating procedures, training materials and othercontrolled documentsKnowledge and technical competencies using documentand/or records management software solution and other business toolsincluding Sharepoint and Adobe AcrobatFamiliarity with validationlifecycle documentationExperience with deviation, CAPA and changemanagement quality processesTeam and customer service orientedAbilityto multi-task in a fast-paced, deadline-driven organizationWhat 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?Apply Now
When people and technology come together, you get exceptional results. We combine our dedicated global workforce of 3000+ recruiting resources with a best-of-breed tech stack and next-gen processes to deliver the best talent possible to our portfolio of global clients.
#J-18808-Ljbffr