Regulatory Affairs Specialist V (5608050)
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Job description
Company Description Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Job Description: Candidate to author technical documents in Client's internal documentum system.
Must have working knowledge of bacterial biologics and regulations pertaining to early and late phase pre-licensure activities. Must have working knowledge of GMPs and application to preparing clinical materials. Must be well-organized, work with minimal management and meet aggressive timelines.
Utilizes knowledge of word processing software, strong writing and analytical skills to document software capabilities and functionality. Job
Responsibilities
**This position is working in the CMC area. Relevant experience is required
- Experience: 3 to 6 years
- Experience with drug/biologics licensure Prior regulatory experience Technical writing experience (CMC experience ) Scientific background, Required Skills: CMC/ Regulatory writing experience Scientific background, vaccines preferred Microsoft Office (word, excel, powerpoint) Documentum Applications Trackwise Applications ICH Guidelines GMP experience
- Experience with drug/biologics licensure Prior regulatory experience Education:
- BS in Biology/Chemistry or related field
Qualifications
BS Additional Information For more information, Please contact Akriti Gupta Office: 973.967.3409 | Fax: 973.998.2599