BFS Line Technician

Nephron Pharmaceuticals 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. 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 some international territories.

Nephron exists to provide top‑quality, affordable medications to everyone. Our quality first culture is built on:
Transformation
, Execution and Trust
.

The BFS Line Technician I plays a vital role in ensuring the efficient and compliant operation of Blow‑Fill‑Seal machinery used in the production of sterile pharmaceutical products. This position is responsible for operating, monitoring, and maintaining BFS downstream equipment, ensuring product quality, and adhering to all Current Good Manufacturing Practices (CGMP), safety regulations, and company protocols.

• Set up and operate BFS downstream machinery according to established SOPs and Batch Records.
• Monitor machine performance and production output to ensure efficiency and compliance.
• Perform routine adjustments and troubleshoot minor issues to maintain continuous operation.
• Reset equipment alarms and ensure all materials are properly staged for production.

• Accurately complete Batch Records, logbooks, setup sheets, and other documentation in a timely manner.
• Identify and elevate product quality or equipment concerns to supervisors.
• Ensure all work is completed in strict adherence to CGMP standards.
• Support investigations into deviations and assist in implementing corrective actions.
• Review MBRs and log book for accuracy and GMP standard.

• Adhere to all safety protocols and wear proper personal protective equipment (PPE) when needed.
• Maintain cleanroom and production areas to meet internal and regulatory cleanliness standards.
• Perform and document routine housekeeping and participate in facility inspections.

• Collaborate with Quality, Maintenance, Packaging, and other cross‑functional teams to ensure smooth operations.
• Participate in training sessions to build technical and procedural knowledge.
• Provide guidance and training to new or junior operators as needed.

• Complete required training and maintain certifications in alignment with company and regulatory requirements.
• Stay updated on procedural changes and complete retraining within designated time frames.
• Provide mentorship and training to junior machine operators and new team members in equipment operation, safety protocols, and industry best practices.

• Perform additional responsibilities as assigned to support production goals and departmental needs.

• Basic mechanical aptitude and understanding of automated manufacturing equipment.
• Ability to interpret SOPs, technical documents, and Batch Records.
• Strong attention to detail with a focus on accuracy and quality.
• Effective verbal and written communication skills.
• Team‑oriented…