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 This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment in the Upstream group. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations. ESSENTIAL FUNCTIONS: • Executes manufacturing processes according to Technical Operations and Operational Services standard operating procedures • Verifies and enters production parameters per SOP and Batch Record on trained procedures • Retrieves and analyze trend charts and process data on trained procedures • Accurately completes documentation in SOP's, logbooks and other GMP documents • Demonstrate training progression through assigned curriculum • Accountable for adherence to compliance policies and regulations • Wear the appropriate PPE when working in manufacturing and other hazardous working environments • Takes necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors ADDITIONAL RESPONSIBILITIES/DUTIES: • Carries out duties in compliance with all state and federal regulations and guidelines including FDA, EPA and OSHA. • Adheres to the Safety Code of Conduct and attend all required EHS training • Support the ongoing production schedule by: • Report to work on-time and according to the shift schedule • Be available for other duties as assigned • Attend departmental and other scheduled meetings • Good interpersonal and communication skills • Demonstrates positive team-oriented attitude in the daily execution of procedures • Promote and work within a team environment • Continue professional development through learning new skills, procedures, processes • and seminars Qualifications • College degree or HS Diploma with +5 years biopharmaceutical industry experience • Experience must be Biotech/Pharmaceutical industry or relevant experience working with Standard Operating Procedures (SOP's) where formal documentation is required • Previous experience with Manufacturing Execution System (MES) would be an advantage • Mechanical aptitude for assembling and disassembling process equipment would be an advantage • Process flow aptitude to recognize and understand process pathways • Knowledge of routine and non-routine testing and sampling methods, techniques and related equipment would be an advantage Additional Information Regards, Sneha Shrivastava 9739673348