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GMP Manufacturing Operations Technician

Company: NetSource, Inc.
Location: Raritan
Posted on: January 16, 2022

Job Description:

Please note that this is a 1 year contract position. Minimum of 2-4 Years MD&D/Pharmaceutical experience or equivalent industry experience requiredPOSITION SUMMARY:This position is responsible for performing manufacturing procedures and executing diverse tasks in various manufacturing areas related to Filling, Labeling and Line Tending according to detailed operational specifications and execution of scheduled tasks within a cGMP environment. Ensure materials are available to meet production schedule. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations. Accountable for adhering to all EHS guidelines.*ESSENTIAL FUNCTIONS: Execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum. Support schedule adjustments to meet production, material receipt and shipping requirements. Work with Shift Leader//Team Leader to review departmental production schedules, work orders and related information to ensure materials are available for production. Maintain working knowledge of cGMP requirements to ensure adherence to compliance policies and regulations Sets up and operates production equipment to produce work in process and finished goods Perform in-process testing as required by processes and procedures utilizing equipment such as: (Fillers, Labelers, autoclave, oven, torque testers, scales and printers) list is not all inclusive Check products on line to confirm proper assembly and remove defective products Take samples for further downstream testing and perform tests during processing according to standard procedures Use of ERP system for performing material transactions/moves/quantities/cycle counts Cleans , maintains, and performs basic repairs on equipment as needed Operate and troubleshoot equipment in clean room and non-clean room environment Assure manufacturing facility and equipment meets all requirements prior to production on all shifts. Accurately complete documentation in batch records, logbooks, forms and other GMP documents. Verify and enter production parameters per SOP and Batch Records. Monitor environmental conditions inside and outside classified rooms Wear the appropriate PPE when working in manufacturing and other working environments. Demonstrate training progression, train designated personnel in all levels of responsibility Understand Lean principles as it relates to work Understand Value Stream maps and relevancy Actively participates in Kaizen, problem solving and asset care Proactively maintain a clean and safe work environment by performing sanitizing and housekeeping duties and looks for opportunities to improve. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors*ADDITIONAL RESPONSIBILITIES/DUTIES: Offer suggestions and follow up on process improvements related to safety, compliance, cost, yield and productivity. Carry out duties in compliance with all state and federal regulations and guidelines including FDA, TUV, EPA and OSHA. Adhere to the safety code of Conduct & EHS policies and attend all required EHS training. Follow Global Leadership Profile (GLP) competencies based on their leadership level within the organization (individual leader)Support the ongoing production schedule by:o Report to work on-time and according to the shift schedule.o Perform other duties as assigned.o Attend departmental and other scheduled meetings.o Practice good interpersonal and communication skills.o Demonstrate positive team-oriented approach in the daily execution of procedures.o Promote and work within a team environmento Learn new skills, procedures and processes as assigned by management and continue to develop professionally.o Assist with validation activities in the area Responsible for audit preparation and participation*This is not an exhaustive or comprehensive listing of job functions. May perform other duties as assigned.AUTONOMY and COMPLEXITY: Needs some direction to perform manufacturing daily tasks within functional area. Performs and has good understanding of processes and procedures. Assist with validation activities within the area. Notifies Shift Leader or Supervisor of maintenance and/or repairs needed on manufacturing equipment or processesMay assist in troubleshooting of routine manufacturing equipment/ processesNATURE OF TASKS: Good mechanical and troubleshooting knowledge within functional area Demonstrate a good understanding of the process in order to properly perform the assigned manufacturing tasks Identify discrepancies or trends that might need additional attention and notifies supervisionCOMPUTER ABILITY: Good working knowledge and understanding of systems as required. Utilizes tools within MS Office and other systems to improve business effectiveness. Accurate Data Entry skills in ERP systemEDUCATION AND EXPERIENCE: Minimum of 2-4 Years MD&D/Pharmaceutical experience or equivalent industry experience HS Diploma or Equivalent required.LANGUAGE SKILLS: Ability to read, write and speak English Read and interpret documents such as safety rules, operating instructions and logbooks Review and provide feedback for SOP and Batch Record Revisions Good communication and written skillsREASONING ABILITY: Follow a variety of instructions furnished in written, oral, diagram or schedule form. Follow instructions, strong understanding of processes and interpretation of results Solve practical problems and troubleshoot routine manufacturing equipment and processes MATHEMATICAL SKILLS: Add, subtract, multiply and divide in all units of measure, using whole numbers, common factions, and decimals.OTHER SKILLS, ABILITIES OR QUALIFICATIONS: Understand Lean principles as it relates to work Understand Value Stream maps and relevancy Actively participates in Kaizen, problem solving and asset care PHYSICAL DEMANDS:While performing the duties of this job, the employee: Needs to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position. Is frequently required to communicate with coworkers. While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; climb, bend and stoop; and reach with hands and arms for extended periods of time. Must pass vision acuity test for inspection of work in process and finished goods Ability to lift up to 40 lbs. Needs to perform gowning procedures to work in manufacturing core or classified rooms. Work with blood, blood products and chemicals Work in a cGMP area and/or clean room environment Overtime is required, as necessary Shift work may be required, as necessaryApplicants must provide their phone number. Reference job number A1052. - provided by Dice

Keywords: NetSource, Inc., Trenton , GMP Manufacturing Operations Technician, Professions , Raritan, New Jersey

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