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QA Issue & Release Coordinator

Multi-Pack Solutions Greenville, SC

  • Expired: over a month ago. Applications are no longer accepted.
Job Description
Summary:

Manages the final product review and release of product to customers in compliance with Span’s

policies and procedures and cGMP’s.

Primary Responsibilities:

· Issues both Manufacturing Records and Packaging Batch Records

· Complies and audit batch records.

· Oversees final product review and release of product to customer in compliance with

Multi Pack's Policy & Procedures and cGMP’s.

· Follows established departmental policies in compliance with GMP’s as well as all safety

and environmental standards.

· Stays current with all policy and procedures. Makes recommendation for improvement in

written procedure as indicated based on information gathered from issues generated on

line, during production, or in finished product release procedure.

· Acts a liaison with Sales Support Coordinator (s) to ensure that product is shipped in

accordance with customer specifications (under quarantine or fully released).

· Maintains appropriate documentation of status of current and past shipped products.

· Maintains and archives all batch record documentation until destruction.

· Represents the company in a positive and professional manner during regular customer

and vendor site visits.

· Communicates problems, situations, opportunities and progress to management.

· Performs other duties as assigned.

· Responsible for Pest control program at both locations (escorts contractors during

inspection)

Education Requirements:
Associates Degree in a technical science background strongly preferred and a minimum of 3 years experience in a FDA regulated facility.
Company Description
Our Greenville, South Carolina facility is our corporate headquarters and has over 25 packaging lines in an over 100,000 square feet of contract manufacturing and packaging space with production seven days a week. Serving the personal care, OTC and medical device markets, we are registered with and compliant to current, applicable EPA regulations and current FDA regulations for Drugs and Medical Devices, as well as certified to ISO13485 for Medical Devices. We offer turnkey solutions, with blending, in-house microbiology and chemistry labs.

Multi-Pack Solutions

Our Greenville, South Carolina facility is our corporate headquarters and has over 25 packaging lines in an over 100,000 square feet of contract manufacturing and packaging space with production seven days a week. Serving the personal care, OTC and medical device markets, we are registered with and compliant to current, applicable EPA regulations and current FDA regulations for Drugs and Medical Devices, as well as certified to ISO13485 for Medical Devices. We offer turnkey solutions, with blending, in-house microbiology and chemistry labs. In January 2020, MPS relocated to a new, custom-built facility located in the Donaldson Center to support our long-term, rapid growth strategy.

Address

1301 Perimeter Road

Greenville, SC
29605 USA

Industry

Technology

View all jobs at Multi-Pack Solutions