Validation Engineer III

Company DescriptionArtech 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 DescriptionThis position is responsible for documenting Laboratory Equipment Qualification / Validation studies, specifically pertaining to Quality Control. Prepare drafts of the protocol and technical report documentation for review with subject matter experts, project staff and/or customers. Edit, standardize, or revise material prepared by other writers or subject matter experts. Create and revise protocols and technical reports for Laboratory Equipment Qualification (IQ, OQ, and PQ) with input from subject matter experts and according to company policies. Assist multiple teams of technical experts in the technical writing of Laboratory Equipment Qualification Prepare binders containing all relevant documentation. Organize documentation and cross-reference documents as necessary. Route final documents for the appropriate approvals. Revisions of Laboratory Equipment Qualification documentation must be done utilizing defined content and formatting requirements. Ensure cGXP compliance in all documentation. Investigate and document non-conformances in a timely manner. Able train on and follow company SOP documentation standards, templates and practices. Work in compliance with cGMPs. Additional Responsibilities Incorporate new material or information while understanding its implications. Work independently under minimal supervision and direction. Work effectively across organizational and functional boundaries Skills:. Excellent writing and editing skills and must write in a concise and easy-to-read manner Proficient with MS Office Applications Experience with HPLC, Dionex, GC, LCMS, UVVis Spectroscopy and empower software Familiarity with 21CFR part 11 validation automation systems is required. QualificationsBachelor's degree with 6-9 years in biopharmaceuticals or Life Sciences OR Master s degree with 4-7 years in biopharmaceuticals or Life Sciences 2 years experience working in cGMP environmentAdditional InformationRegards,Akriti GuptaAssociate RecruiterArtech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: View phone number on us.fitly.work | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: EngineeringExperience level: Mid-Senior LevelIndustry: Pharmaceuticals