Artech Information System LLC
Technical Writer I (5625794)
Artech Information System LLC, Northborough, Massachusetts, us, 01532
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.
Please read the following job description thoroughly to ensure you are the right fit for this role before applying.Job Description
Ensure timely and efficient creation/review of Label & Pack documents: standard operating procedures, batch records, technical protocols and reports, etc.Contribute understanding of Good Documentation Practices (GDP) and Current Good Manufacturing Practices (CGMP), analytical skills, and interpretation of the information to be captured on the document.Ensure a consistent style of presentation of Label and Pack documents to maintain quality and ease of review.Coordinate with Engineering on tasks for validation qualification, preventative maintenance and re-qualification program processes.Act as subject matter expert (SME) for documentation with Development and Training (D&T), and provide input in cross-functional teams, including during Quality Assurance (QA) and Quality Control (QC).Help develop OJT's for proficiency of L&P staff with respect to process knowledge and critical parameters; ensure understanding and interpretation of results from tools deployed in the process.Support readiness for regulatory inspections and compliance audits.Assess current documentations for Error Reduction updates and ensure timely revision and review of periodic review.Support development of junior analysts through mentoring.Coordinate CAPA tasks with document changes for timely closure of compliance events with deviations investigators.Revise standard operating procedures as needed.Practice safe work habits and adhere to Sanofi's safety procedures and guidelines.Skills
Minimum of 5 years of experience in a regulated environment.Previous experience with technical writing for manufacturing in a regulated environment.Use of documentation controls systems to manage workflow.Qualifications Education: Bachelor's degree in a related discipline.
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Please read the following job description thoroughly to ensure you are the right fit for this role before applying.Job Description
Ensure timely and efficient creation/review of Label & Pack documents: standard operating procedures, batch records, technical protocols and reports, etc.Contribute understanding of Good Documentation Practices (GDP) and Current Good Manufacturing Practices (CGMP), analytical skills, and interpretation of the information to be captured on the document.Ensure a consistent style of presentation of Label and Pack documents to maintain quality and ease of review.Coordinate with Engineering on tasks for validation qualification, preventative maintenance and re-qualification program processes.Act as subject matter expert (SME) for documentation with Development and Training (D&T), and provide input in cross-functional teams, including during Quality Assurance (QA) and Quality Control (QC).Help develop OJT's for proficiency of L&P staff with respect to process knowledge and critical parameters; ensure understanding and interpretation of results from tools deployed in the process.Support readiness for regulatory inspections and compliance audits.Assess current documentations for Error Reduction updates and ensure timely revision and review of periodic review.Support development of junior analysts through mentoring.Coordinate CAPA tasks with document changes for timely closure of compliance events with deviations investigators.Revise standard operating procedures as needed.Practice safe work habits and adhere to Sanofi's safety procedures and guidelines.Skills
Minimum of 5 years of experience in a regulated environment.Previous experience with technical writing for manufacturing in a regulated environment.Use of documentation controls systems to manage workflow.Qualifications Education: Bachelor's degree in a related discipline.
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