Manufacturing Technician

New Brunswick, NJ 08901

Post Date: 05/03/2018 Job ID: 8199 Industry: Industry Pay Rate: $25.00 - $30.00

SUMMARY

The Manufacturing Technician is responsible for the production of commercial, clinical and/ or development batches by setting-up, cleaning, and maintaining equipment, following procedures and documenting actions.



RESPONSIBILITIES

  • Prepares for production by reviewing production schedule; reviewing and clarifying specifications; calculating requirements; assembling and weighing materials and supplies.



  • Prepares equipment by performing sterile cleaning-in-place (CIP); Cleaning out-of-place (COP); conducting operator set-up/ inspections, and routine preventive maintenance



  • Responsible to operate mixing tanks, glassware washers, autoclaves, filtration equipment, UF/ DF systems as per Standard Operating Procedures



  • Executes SOPs for unit operations (Daily and Long Term) for different equipment and systems which includes but not limited to routine monitoring and preventive maintenance



  • Production activities include operating and monitoring equipment; observing varying conditions; adjusting equipment controls; calculating concentrations, dilutions, and yields, adhering to current good manufacturing practices (cGMP)



  • Maintains safe and clean work environment by following current good manufacturing practices (cGMP), and standard operating procedures



  • Keeps equipment operating by following operating instructions. Assist in maintenance scheduling by initiate work orders to perform equipment repairs/ maintenance and troubleshooting breakdowns.



  • Documents production activities by completing forms, reports, logs, and records of equipment and batches



  • Maintain inventory of manufacturing supplies by inventory tracking and ordering of manufacturing supplies



  • Provides support during audits and with audit observation closure.





QUALIFICATIONS

  • Be able to lift 50 lbs.



  • Minimum High School diploma is required.



  • 1 to 3 years of relevant experience is required.



  • Experience of working in a GMP manufacturing environment is desired.



  • The ability to execute against the SOPs and document entries in a cGMP compliant manner.



  • Ability to interpret and prioritize workflow to maintain the production schedule.



  • Effective verbal and written communication skills.







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