Supervisor I, Manufacturing
Company Name:
Baxter
## Description
Job Description:
The supervisor position is responsible for implementing and supervising daily activities in a specific production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (GMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. May monitor and control labor.
Total compliance with all applicable specifications, SOPs, FDA regulations (GMPs) and new drug applications.
Technical expertise and direction are provided to all quality and manufacturing operations in order to facilitate successful completion of routine tasks, as well as, product/process improvements and problem solving.
Must interface with various support departments such as QM, Engineering, Maintenance, Scheduling, Accounting, and Human Resources.
Responsible for adequacy of Specifications and SOPs to assure all products meet the requirements for quality, safety, and integrity.
Improve quality and reduce customer complaints through a proactive program that includes interaction with internal and external suppliers to improve quality of incoming materials and utilize collective data from customers to enhance quality of the product, as perceived by the customer.
Plan, develop and manage shift teams that monitor, predict or regulate all steps of manufacturing. These activities are accomplished through statistical sampling, product auditing and process control.
Assist in the validation of new equipment, process, systems, and changes that impact product quality.
Represent the company during FDA inspections. Provide information as necessary to FDA that established creditability and demonstrated compliance with GMPs.
Review, approve, and manage documentation for batch and system records. Assist in the release for distribution. Assist in meeting product release time goals.
Create an environment that stresses and encourages teamwork.
Support and encourage all plant activities, i.e., VIPs, QLP, CIs, TPM, Business Process teams and plant growth and development.
Responsible for Quality, Production and overall operating performance of all shifts.
Must have knowledge of both plant and department environmental health and safety regulations and comply with said regulations accordingly.
Must perform all other duties and responsibilities as determined by supervision/management.
## Qualifications
Bachelors Degree in a scientific or engineering discipline with 0-3 years of manufacturing experience or equivalent manufacturing experience.
Plastics experience preferred.
Experience with liquid silicone rubber and injection molding is preferred.
Demonstrated interpersonal and leadership skills with ability to interface well with other departments, and lead effectively and efficiently in a team environment.
Ability to manage multiple priorities in a manufacturing plant setting.
Strong professional writing skills and ability to prepare technical reports.
Ability to understand GMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.
Strong assessment and troubleshooting skills.
Basic computer skills.
Must be willing/able to come in on any shift as needs may dictate.
Candidates must meet visual acuity requirements as documented in Baxter Cleveland Visual Acuity Procedure CL-01-01-037.
Job: Manufacturing
Primary Location: United States-Mississippi-Cleveland
Organization: Manufacturing
Schedule: Full-time
Job Posting: Apr 18, 2014, 11:59:00 AM
Unposting Date: Ongoing
Req ID: 66392BREstimated Salary: $20 to $28 per hour based on qualifications.
Baxter
## Description
Job Description:
The supervisor position is responsible for implementing and supervising daily activities in a specific production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (GMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. May monitor and control labor.
Total compliance with all applicable specifications, SOPs, FDA regulations (GMPs) and new drug applications.
Technical expertise and direction are provided to all quality and manufacturing operations in order to facilitate successful completion of routine tasks, as well as, product/process improvements and problem solving.
Must interface with various support departments such as QM, Engineering, Maintenance, Scheduling, Accounting, and Human Resources.
Responsible for adequacy of Specifications and SOPs to assure all products meet the requirements for quality, safety, and integrity.
Improve quality and reduce customer complaints through a proactive program that includes interaction with internal and external suppliers to improve quality of incoming materials and utilize collective data from customers to enhance quality of the product, as perceived by the customer.
Plan, develop and manage shift teams that monitor, predict or regulate all steps of manufacturing. These activities are accomplished through statistical sampling, product auditing and process control.
Assist in the validation of new equipment, process, systems, and changes that impact product quality.
Represent the company during FDA inspections. Provide information as necessary to FDA that established creditability and demonstrated compliance with GMPs.
Review, approve, and manage documentation for batch and system records. Assist in the release for distribution. Assist in meeting product release time goals.
Create an environment that stresses and encourages teamwork.
Support and encourage all plant activities, i.e., VIPs, QLP, CIs, TPM, Business Process teams and plant growth and development.
Responsible for Quality, Production and overall operating performance of all shifts.
Must have knowledge of both plant and department environmental health and safety regulations and comply with said regulations accordingly.
Must perform all other duties and responsibilities as determined by supervision/management.
## Qualifications
Bachelors Degree in a scientific or engineering discipline with 0-3 years of manufacturing experience or equivalent manufacturing experience.
Plastics experience preferred.
Experience with liquid silicone rubber and injection molding is preferred.
Demonstrated interpersonal and leadership skills with ability to interface well with other departments, and lead effectively and efficiently in a team environment.
Ability to manage multiple priorities in a manufacturing plant setting.
Strong professional writing skills and ability to prepare technical reports.
Ability to understand GMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.
Strong assessment and troubleshooting skills.
Basic computer skills.
Must be willing/able to come in on any shift as needs may dictate.
Candidates must meet visual acuity requirements as documented in Baxter Cleveland Visual Acuity Procedure CL-01-01-037.
Job: Manufacturing
Primary Location: United States-Mississippi-Cleveland
Organization: Manufacturing
Schedule: Full-time
Job Posting: Apr 18, 2014, 11:59:00 AM
Unposting Date: Ongoing
Req ID: 66392BREstimated Salary: $20 to $28 per hour based on qualifications.
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