Manufacturing Operator
3.
6 Raritan, NJ Raritan, NJ Contract Contract $20 - $22 an hour $20 - $22 an hour Title:
Manufacturing Operator 2 Location:
Raritan NJ Duration:
12 Months Job ID 4774 POSITION
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:
oExecute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum.
oSupport schedule adjustments to meet production, material receipt and shipping requirements.
oWork with Shift Leader//Team Leader to review departmental production schedules, work orders and related information to ensure materials are available for production.
oMaintain working knowledge of cGMP requirements to ensure adherence to compliance policies and regulations oSets up and operates production equipment to produce work in process and finished goods oPerform 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 oCheck products on line to confirm proper assembly and remove defective products oTake samples for further downstream testing and perform tests during processing according to standard procedures oUse of ERP system for performing material transactions/moves/quantities/cycle counts oCleans , maintains, and performs basic repairs on equipment as needed oOperate and troubleshoot equipment in clean room and non-clean room environment oAssure manufacturing facility and equipment meets all requirements prior to production on all shifts.
oAccurately complete documentation in batch records, logbooks, forms and other GMP documents.
oVerify and enter production parameters per SOP and Batch Records.
oMonitor environmental conditions inside and outside classified rooms oWear the appropriate PPE when working in manufacturing and other working environments.
oDemonstrate training progression, train designated personnel in all levels of responsibility oUnderstand Lean principles as it relates to work oUnderstand Value Stream maps and relevancy oActively participates in Kaizen, problem solving and asset care oProactively 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:
oOffer suggestions and follow up on process improvements related to safety, compliance, cost, yield and productivity.
oCarry out duties in compliance with all state and federal regulations and guidelines including FDA, TUV, EPA and OSHA.
oAdhere to the safety code of Conduct & J&J EHS policies and attend all required EHS training.
oFollow Global Leadership Profile (GLP) competencies based on their leadership level within the organization (individual leader) Support the ongoing production schedule by:
oReport to work on-time and according to the shift schedule.
oPerform other duties as assigned.
oAttend departmental and other scheduled meetings.
oPractice good interpersonal and communication skills.
oDemonstrate positive team-oriented approach in the daily execution of procedures.
oPromote and work within a team environment oLearn new skills, procedures and processes as assigned by management and continue to develop professionally.
oAssist with validation activities in the area oResponsible 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:
oNeeds some direction to perform manufacturing daily tasks within functional area.
oPerforms and has good understanding of processes and procedures.
oAssist with validation activities within the area.
oNotifies Shift Leader or Supervisor of maintenance and/or repairs needed on manufacturing equipment or processes May assist in troubleshooting of routine manufacturing equipment/ processes NATURE OF TASKS:
oGood mechanical and troubleshooting knowledge within functional area oDemonstrate a good understanding of the process in order to properly perform the assigned manufacturing tasks oIdentify discrepancies or trends that might need additional attention and notifies supervision COMPUTER ABILITY:
oGood working knowledge and understanding of systems as required.
oUtilizes tools within MS Office and other systems to improve business effectiveness.
oAccurate Data Entry skills in ERP system EDUCATION AND
Experience:
oMinimum of 2-4 Years MD&D/Pharmaceutical experience or equivalent industry experience oHS Diploma or Equivalent required.
LANGUAGE SKILLS:
oAbility to read, write and speak English oRead and interpret documents such as safety rules, operating instructions and logbooks oReview and provide feedback for SOP and Batch Record Revisions oGood communication and written skills REASONING ABILITY:
oFollow a variety of instructions furnished in written, oral, diagram or schedule form.
oFollow instructions, strong understanding of processes and interpretation of results oSolve practical problems and troubleshoot routine manufacturing equipment and processes MATHEMATICAL SKILLS:
oAdd, subtract, multiply and divide in all units of measure, using whole numbers, common factions, and decimals.
OTHER SKILLS, ABILITIES OR
Qualifications:
oUnderstand Lean principles as it relates to work oUnderstand Value Stream maps and relevancy oActively participates in Kaizen, problem solving and asset care PHYSICAL DEMANDS:
While performing the duties of this job, the employee:
oNeeds to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position.
oIs frequently required to communicate with coworkers.
oWhile 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.
oMust pass vision acuity test for inspection of work in process and finished goods oAbility to lift up to 40 lbs.
oNeeds to perform gowning procedures to work in manufacturing core or classified rooms.
oWork with blood, blood products and chemicals oWork in a cGMP area and/or clean room environment oOvertime is required, as necessary oShift work may be required, as necessary Job Type:
Contract Salary:
$20.
00 - $22.
00 per hour Schedule:
8 hour shift Monday to Friday Work Location:
In person 8 hour shift Monday to Friday.
Estimated Salary: $20 to $28 per hour based on qualifications.
6 Raritan, NJ Raritan, NJ Contract Contract $20 - $22 an hour $20 - $22 an hour Title:
Manufacturing Operator 2 Location:
Raritan NJ Duration:
12 Months Job ID 4774 POSITION
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:
oExecute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum.
oSupport schedule adjustments to meet production, material receipt and shipping requirements.
oWork with Shift Leader//Team Leader to review departmental production schedules, work orders and related information to ensure materials are available for production.
oMaintain working knowledge of cGMP requirements to ensure adherence to compliance policies and regulations oSets up and operates production equipment to produce work in process and finished goods oPerform 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 oCheck products on line to confirm proper assembly and remove defective products oTake samples for further downstream testing and perform tests during processing according to standard procedures oUse of ERP system for performing material transactions/moves/quantities/cycle counts oCleans , maintains, and performs basic repairs on equipment as needed oOperate and troubleshoot equipment in clean room and non-clean room environment oAssure manufacturing facility and equipment meets all requirements prior to production on all shifts.
oAccurately complete documentation in batch records, logbooks, forms and other GMP documents.
oVerify and enter production parameters per SOP and Batch Records.
oMonitor environmental conditions inside and outside classified rooms oWear the appropriate PPE when working in manufacturing and other working environments.
oDemonstrate training progression, train designated personnel in all levels of responsibility oUnderstand Lean principles as it relates to work oUnderstand Value Stream maps and relevancy oActively participates in Kaizen, problem solving and asset care oProactively 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:
oOffer suggestions and follow up on process improvements related to safety, compliance, cost, yield and productivity.
oCarry out duties in compliance with all state and federal regulations and guidelines including FDA, TUV, EPA and OSHA.
oAdhere to the safety code of Conduct & J&J EHS policies and attend all required EHS training.
oFollow Global Leadership Profile (GLP) competencies based on their leadership level within the organization (individual leader) Support the ongoing production schedule by:
oReport to work on-time and according to the shift schedule.
oPerform other duties as assigned.
oAttend departmental and other scheduled meetings.
oPractice good interpersonal and communication skills.
oDemonstrate positive team-oriented approach in the daily execution of procedures.
oPromote and work within a team environment oLearn new skills, procedures and processes as assigned by management and continue to develop professionally.
oAssist with validation activities in the area oResponsible 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:
oNeeds some direction to perform manufacturing daily tasks within functional area.
oPerforms and has good understanding of processes and procedures.
oAssist with validation activities within the area.
oNotifies Shift Leader or Supervisor of maintenance and/or repairs needed on manufacturing equipment or processes May assist in troubleshooting of routine manufacturing equipment/ processes NATURE OF TASKS:
oGood mechanical and troubleshooting knowledge within functional area oDemonstrate a good understanding of the process in order to properly perform the assigned manufacturing tasks oIdentify discrepancies or trends that might need additional attention and notifies supervision COMPUTER ABILITY:
oGood working knowledge and understanding of systems as required.
oUtilizes tools within MS Office and other systems to improve business effectiveness.
oAccurate Data Entry skills in ERP system EDUCATION AND
Experience:
oMinimum of 2-4 Years MD&D/Pharmaceutical experience or equivalent industry experience oHS Diploma or Equivalent required.
LANGUAGE SKILLS:
oAbility to read, write and speak English oRead and interpret documents such as safety rules, operating instructions and logbooks oReview and provide feedback for SOP and Batch Record Revisions oGood communication and written skills REASONING ABILITY:
oFollow a variety of instructions furnished in written, oral, diagram or schedule form.
oFollow instructions, strong understanding of processes and interpretation of results oSolve practical problems and troubleshoot routine manufacturing equipment and processes MATHEMATICAL SKILLS:
oAdd, subtract, multiply and divide in all units of measure, using whole numbers, common factions, and decimals.
OTHER SKILLS, ABILITIES OR
Qualifications:
oUnderstand Lean principles as it relates to work oUnderstand Value Stream maps and relevancy oActively participates in Kaizen, problem solving and asset care PHYSICAL DEMANDS:
While performing the duties of this job, the employee:
oNeeds to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position.
oIs frequently required to communicate with coworkers.
oWhile 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.
oMust pass vision acuity test for inspection of work in process and finished goods oAbility to lift up to 40 lbs.
oNeeds to perform gowning procedures to work in manufacturing core or classified rooms.
oWork with blood, blood products and chemicals oWork in a cGMP area and/or clean room environment oOvertime is required, as necessary oShift work may be required, as necessary Job Type:
Contract Salary:
$20.
00 - $22.
00 per hour Schedule:
8 hour shift Monday to Friday Work Location:
In person 8 hour shift Monday to Friday.
Estimated Salary: $20 to $28 per hour based on qualifications.
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