Quality Operations Material Management Specialist chez Nephron Pharmaceuticals

Description

  Position Summary: 

• 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

Primary Accountabilities: 

NOTE: The primary accountabilities and the knowledge, skills and abilities listed below, are intended to describe the general content of and requirements for this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed. Specific tasks or responsibilities will be documented in the incumbents’ performance objectives as outlined by the incumbents’ immediate supervisor or manager 

• 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

Knowledge, Skills & Abilities: 

• 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.