Document Control Specialist # 26-27029

Duration: 03 Months ContractSchedule: 1st Shift - 8AM to 5PM - Wednesday to SundayJob Description:Review and approve GMP/GLP Manufacturing and related documentation to support timely product and system release. Responsibilities:Conduct internal audit of SOPs, training records, and other document types on an as needed basis. Assist and guide engineering in the preparation of product documentation, product configuration and document change request package development. Responsible for activities related to providing required documentation and implementing related documentation systems. Assist in providing training on documentation and labeling processes and systems. Participate on project teams as needed. The incumbent will perform other duties assigned. Document configuration and product data managementAid in the execution of user acceptance testingAid in the creation/writing of training materialsAssist in training internal and external personnel on documentation and labeling related processes and systemsMaintain and own internal documentsReview documentation for accuracy and compliance to procedures. Route, release or reject as appropriate. Ensure all document and system elements are identified, accurate and assembled for review and approval. Maintain, proofread, and change as needed Standard Operating Procedures To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Experience:3-5 years related experienceSkillsets:Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Product/document configuration. Intermediate level and document management (e.g. Word) software skillsProject Management SkillsMust have excellent conceptual, analytical, written and verbal configuration skillsComprehension of design methodology, product configuration and complex manufacturing processesAbility to work under strict deadlines and changing priorities with minimal supervisionStrong interpersonal skills and great attention to detail are necessaryMust be a strong team player with good problem solving, and good verbal and written communications skillsMust be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations, Applications of Good laboratory Practices, and Application of Good Manufacturing Practices Include the education and experience that is necessary to perform the job satisfactorilyAbility to discuss normally encountered technical or project management issues, both verbally and in written form. Knowledge of product/document configuration management. Working knowledge of related business systems. Education:B.A. or B.S. and 3-5 years related experience (in-house or acquired outside). About US Tech Solutions:US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.