
Quality Operations Material Management Specialist
Nephron Pharmaceuticals Corporation
- West Columbia, SC
- $23.00 per hour
- Permanent
- Full-time
- Receives, samples, inspects and releases production components along with raw materials, within Nephron's electronic inventory system and process corresponding documentation necessary in manufacturing operations
- Send reports requesting timeframes of all raw materials sampled weekly
- Delegate task in regards to receiving, inspecting, and sampling of all raw materials and components
- Work with other departments to ensure receipts, sampling, and releases are within compliance and completed in a timely manner
- Work with other departments to ensure raw materials and components are reviewed and closed in a timely manner
- Assists with additional work duties or responsibilities as evident or required
- Performs other duties as assigned or apparent
- Documents, reviews and completes all required paperwork to release or reject the raw materials and components, related corresponding documentation based on inspection results
- Processes R&D production components; reviews, approves and dispositions material
- Responsible for notifying Quality Assurance management of any deviation, product failure or any issues or concerns that might arise
- Receives, inspects, samples, and assigns a disposition for raw materials and components for all business operations
- Processes, documents, reviews, and completes all corresponding paperwork and documentation for raw materials and components to determine disposition
- Processes production components corresponding documentation provided by warehouse
- Collects samples for incoming inspection based on MIL-STD 105E/ANSI/ASQ Z1.4
- Performs the incoming inspection, as necessary, using current procedures, measurement equipment, drawings, and other elements
- Documents, reviews and completes all required paperwork (for Production Components) to release or reject the production components, related corresponding documentation based on inspection results
- Processes R&D production components; reviews, approves and dispositions material
- Responsible for notifying Quality Assurance management of any deviation, product failure or any issues or concerns that might arise
- Transfers and samples raw materials in the cleanroom in compliance with associated standard operating procedures
- Bachelor's degree preferred; High School Diploma or GED required.
- Minimum of 2 years in the pharmaceutical industry preferred.
- Must be able to be Clean Room Certified.
- Detail-oriented.
- Strong computer skills (Microsoft Office Suite)
- Strong writing and oral communication skills.
- Specific expertise, skills and knowledge within quality assurance gained through education and experience.
- A well-developed knowledge of the consumer/customer demonstrated through continuous efforts to exceed their expectations.
- The ability to take strategic objectives and accept accountability to drive results through effective actions.
- The ability and willingness to change direction and focus to meet shifting organizational and business demands.
- The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals.
- Ability to pass required medical screenings to ensure safe handling of pharmaceutical raw materials used within the manufacturing process and participate in any periodic medical screenings as defined by company
- Position requires bending (desk to floor), lifting (up to 15lbs.), vision (20/20) corrected with glasses or contacts, standing (5%), sitting (90%), typing and walking.
- Salary range: Based on experience.
- Hours of work: Monday thru Friday on an 8-hour shift, or as needed based on company demand.