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.

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 

• 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 

Regards,

Sneha Shrivastava

9739673348