[**Quality Assurance Visual Inspector- Tier 1

[**ALL ENTRY LEVEL POSITIONS STARTING AT $23.00 PER HOUR MINIMUM!

OPEN INTERVIEWS WILL BE HELD AT SC WORKS LEXINGTON (671 Main St, West Columbia, SC in South Congaree next to Food Lion) ON 3/14/24 FROM 9 AM TO 4 PM!**

[Corporate Statement [Nephron Pharmaceuticals Corporation is a privately-owned global leader in the manufacturing of generic drug products, over-the-counter (OTC) drug products and medical devices. Nephron's products are sterile, preservative and additive free and proudly made in the USA! We are headquartered in West Columbia, South Carolina. Our location provides the ability to develop new devices and medications including respiratory therapies, ophthalmic, and injectables, for in-house or contract manufacturing opportunities. The facility utilizes completely automated manufacturing, packaging, and distribution systems, in addition to high volume and redundant utility systems, to ensure production system availability. Nephron specializes in Blow-Fill-Seal (BFS) manufacturing, a niche technology that allows a vial of medication to be formed, filled and sealed in a continuous process, in a sterile, enclosed environment and without human intervention. [ [As an industry leader in product safety and quality, Nephron produces a variety of inhalation solutions, and has distributed over 1 billion doses of respiratory medication per year since 2009. Nephron is currently working on research and development projects that include over 50 new products. The company's longstanding relationships with major drug wholesalers allow us to distribute our products to retail pharmacies, mail order pharmacies, hospitals, home care companies, and long-term care facilities. Nephron has a sales force that covers all fifty states and Puerto Rico, with additional sales channels throughout South America, the Middle East, and Europe. *Nephron exists to provide top-quality, affordable medications to everyone. [ [Position Summary: *]{new="" roman="" times=""}]{new="" roman="" times=""}]{new="" roman="" times=""}]{new="" roman="" times=""}]{new="" roman="" times=""}]{new="" roman="" times=""}]{new="" roman="" times=""}**]{new="" roman="" times=""}

• Perform visual inspection of injectable products in compliance with company policies/procedures, FDA and cGMP regulations
• Maintains quality assurance documentation by ensuring the accuracy and completeness of batch records.
• Promotes teamwork both within the QA Team and other departments.
• Monitor all packaging areas and personnel for adherence to all cGMP, SOP's and safety regulations.
• Keep line and work station clean and orderly.
• Perform line clearance including equipment, components and label verification.
• Communicate quality- related observations, issues, problems, discrepancies and any violations of company policies or procedures to the Supervisor.
• Specific expertise, skills and knowledge within quality assurance gained through education and experience.
• The ability and willingness to change direction and focus to meet shifting organizational and business demands.
• Able to handle diversity of projects.
• The ability to create and contribute environment that values people, encourages trust, teamwork, and open communication, and provides participation, learning, feedback and recognition.
• The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals.

[*Primary Accountabilities: *]{new="" roman="" times=""}

• Monitors and performs finished product attribute inspections.
• Performs visual inspections of Outsourcing products if deemed necessary or required.
• Supports secondary packaging operations by performing QA verifications of packaging, label verifications, etc.
• Maintains quality documentation and review to ensure completion and compliance.
• Promotes teamwork both within the QA T am and other departments.
• Keep line and work station clean and orderly.
• Ensure that there is no cross contamination.
• Perform line clearances.
• Support validation and manufacturing studies including special sampling and testing.
• Organize workload during lot changeovers for efficient execution.

[Shop Floor QA Accountabilities:]{new="" roman="" times=""}

Assists with monitoring all production areas and personnel for adherence to all cGMP, SOPs, and safety regulations.

[]{new="" roman="" style="font-famil

"}