Manufacturing Operator
Manufacturing Operator
Posted on :
03-11-2024
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Job Description
Title: Manufacturing Operator
Duration: 12 Months
Location: Raritan NJ
Duration: 12 Months
Location: Raritan NJ
Responsibilities:
Inspect products on line to confirm proper assembly and remove defective products
Accurately complete documentation in batch records logbooks forms and other GMP documents.
Verify and enter production parameters per SOP and Batch Records
Use of ERP system for performing material transactions/moves/quantities/cycle counts
Maintain working knowledge of cGMP requirements to ensure adherence to compliance policies and regulations
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.
Inspect products on line to confirm proper assembly and remove defective products
Accurately complete documentation in batch records logbooks forms and other GMP documents.
Verify and enter production parameters per SOP and Batch Records
Use of ERP system for performing material transactions/moves/quantities/cycle counts
Maintain working knowledge of cGMP requirements to ensure adherence to compliance policies and regulations
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.
Supervisory Responsibilities:
Trains employees
Plans Work of others
Reviews work quality and quantity of others
Sets up and operates production equipment to produce work in process and finished goods.
Assure manufacturing facility and equipment meets all requirements prior to production on all shifts
Trains employees
Plans Work of others
Reviews work quality and quantity of others
Sets up and operates production equipment to produce work in process and finished goods.
Assure manufacturing facility and equipment meets all requirements prior to production on all shifts
Skills Required:
This position is responsible for performing manufacturing procedures and executing diverse tasks in manufacturing related to Donor Screening
Antisera and Red Cell processes in the Packaging manufacturing lines according to detailed operational specifications and execution of scheduled tasks within a cGMP environment.
This position is responsible for quality and maintaining the highest standards in compliance within company policies procedures and all applicable regulations.
This position is responsible for performing manufacturing procedures and executing diverse tasks in manufacturing related to Donor Screening
Antisera and Red Cell processes in the Packaging manufacturing lines according to detailed operational specifications and execution of scheduled tasks within a cGMP environment.
This position is responsible for quality and maintaining the highest standards in compliance within company policies procedures and all applicable regulations.
Ensure materials are available to meet production schedule.
Accountable for adhering to all EHS guidelines
Minimum of 24 Years MD&D/Pharmaceutical experience or equivalent industry experience
High School diploma required.
QC inspectors Fill/Label Planning Quality engineers Engineering Facilities
Accountable for adhering to all EHS guidelines
Minimum of 24 Years MD&D/Pharmaceutical experience or equivalent industry experience
High School diploma required.
QC inspectors Fill/Label Planning Quality engineers Engineering Facilities
Employment Type
Full Time
Key Skills
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