We have a contract opportunity for a Manufacturing Production Coordinator with a possibility of being hired directly by the customer. This position is located in Salt Lake City Utah. The client is a world class manufacturer of Diagnostic Medical Devices.
2 shifts available:
Thursday - Saturday 6:00AM to 6PM and every other Wednesday.
Thursday – Saturday 5:50PM to 6:20AM and every other Wednesday. (7% differential for night shift)
Pay Rate: $21.00 to $26.00/Hr. (depending on experience)
Principal Job Duties and Responsibilities:
1. Perform work in compliance with company policy and guidelines of the Quality System.
2. Responsible for assisting Team Leads, Supervisors, & Managers with technical issues such as troubleshooting production issues, organization workflow, scheduling and batch records issues, and ensuring correct raw materials are being consumed.
3. Assist teams with technical support issues such as manufacturing specialized orders and coordinating the delivery and consumption of special R&D materials.
4. Assists as directed by management with resolving process/product related issues using tools such as Temporary Deviations, rework procedures, NCR’s, etc.
5. Generate and maintain records as required by the Quality System.
6. Evaluates the master production schedule and issues production batch records.
7. Works with Materials Management, QA, R&D and within production departments to ensure necessary materials are available and inspections are performed in preparation for scheduled manufacture events.
8. Ensures digital and paper records are properly maintained, providing general support and assistance with documentation issues and corrections.
9. Interfaces with databases and spreadsheets to compile and maintain reports concerning progress of work and failures through the production process and to track production units.
10. Responsible for ordering Kanban items and maintaining stocks of critical raw materials and sub-assemblies, including monitoring of expiration dates.
11. Responsible for coordinating the testing of critical raw materials and subassemblies.
12. Must be able to perform duties wearing a Powered Air Purifying Respirator (PAPR).
Qualifications
High School Diploma required. Bachelor’s degree in a Biology/Chemistry or Supply Chain a plus.
Experience:
Prior cGMP/FDA/ISO manufacturing experience is required. Prior experience in manufacturing reagents is preferred. Demonstrated working knowledge of PCR is preferred.
Skills:
Demonstrated understanding of inventory control and electronic MRP systems and intermediate proficiency using Excel and other Microsoft applications. Must be able to assign and transcribe numerical data associated with assigning and tracking lot numbers. Able to use mathematical skills to assess materials availability and assignment to job orders and assess inventory, throughput and yield performance.
Physical Requirements: Able to perform duties wearing a Powered Air Purifying Respirator (PAPR).
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit https://www.yoh.com/applicants-with-disabilities [1]to contact us if you are an individual with a disability and require accommodation in the application process.
Links:
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[1] https://www.yoh.com/applicants-with-disabilities
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