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Shift Supervisor MS Open (J#26508)
Education: High School
Experience: 1 - 3 years

Baxter International Inc. develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide.

Our Cleveland facility is a global leader in the manufacturing medical devices and we ship products to many of our customers worldwide.

Job Description: Manufacturing Supervisor - 3rd Shift

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.

Responsible for on-going self-audit program of the Injection Molding operation.

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.

Manage Injection Molding.

Must perform all other duties and responsibilities as determined by supervision/management.

Job Requirements:

Plastics experience preferred

High school graduate.

Substantial interpersonal skills for interaction with plant management and subordinates.

Must have knowledge of both plant and department environmental health and safety regulations and comply with said regulations accordingly.

Candidates must meet visual acuity requirements as documented in Baxter Cleveland Visual Acuity procedure CL-01-01-037.

Baxter provides its employees with comprehensive compensation and benefits. Our total compensation package includes base salary (dependent on experience), market-competitive benefits to help employees meet their healthcare needs, and 401K.

For more information about Baxter and to apply for this position, please visit our Baxter website. Reference: #62742BR.
Baxter is an Equal Opportunity Employer
For more information contact:

Company: Baxter Healthcare

Contact: Linda Arthur
Phone: (828) 756-6519
Fax: (828) 756-4821
Reference: 62742BR
 
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