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Engineer, Quality Engineering

Job in Columbia, Lexington County, South Carolina, 29228, USA
Listing for: Nephron Pharmaceuticals Corp
Full Time position
Listed on 2026-03-07
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: Columbia

Description

Job Purpose:

This position will be responsible for ensuring the efficient design, optimization, and maintenance of manufacturing systems and processes to meet quality, safety, and regulatory standards. This role plays a key part in driving continuous improvement in production operations, working closely with cross‑functional teams to enhance production efficiency, reduce costs, and maintain product quality.

Essential Duties and Responsibilities
  • Team member and subject‑matter expert on cross functional team to develop Process Development Studies. Responsible for protocol generation and summary analysis of results for process changes or new products.
  • Team member and subject‑matter expert for the design and implementation of new equipment and equipment modifications to help improve safety, quality, reliability, and throughput.
  • Responsible for implementation of new processes while maintaining cGMP compliance.
  • Team member and subject‑matter expert for the generation of User Requirement Specification documents for new equipment.
  • Manages capital projects from a small to medium scope requiring moderate coordination. Ability to manage several assignments (project & process duties) simultaneously is required.
  • Ensure all equipment is in compliance with established safety standards.
  • Responsible for acquiring and reviewing equipment/materials quotations. Completes or supervises the completion of necessary designs, drawings, calculations and specifications on associated equipment.
  • All other duties as assigned or apparent.
  • Ability to interact with all levels of management.
  • Ability to work in collaboration with machinists and technicians, etc. in the modification, adjustment, removal and installation of new or existing equipment as required.
  • As required within the scope of the project, responsible for associated documentation:
    Operations Procedures, Preventive Maintenance schedules, Engineering Change Notifications, spare parts listings, etc.
  • Leads process improvement activities. Must have ability to design and implement machine modifications.
Supplemental Functions
  • Performs other similar duties as required.
Knowledge & Skills
  • Must have bachelor's degree in engineering. Mechanical, Electrical, Biomedical, or Chemical Engineering preferred.
  • Exceptional technical writing and documentation skills.
  • Advanced proficiency in Microsoft Word for authoring, formatting, and maintaining GMP‑compliant technical documents (protocols, reports, SOPs, specifications).
  • Attention to detail and commitment to data integrity.
  • Working knowledge of Microsoft Excel for data analysis, trending, calculations, tables, and graphical presentation of engineering and development data.
  • Highly organized with the ability to manage multiple projects and changing priorities while under pressure.
  • Work closely with operations, quality control, maintenance, validation, and other departments to ensure smooth coordination and timely completion of projects.
  • Ability to successfully prioritize and manage large projects, deadlines, and tasks while working independently or with a team.
  • Effective verbal and written communication.
  • Ability to work independently while collaborating across teams.
  • Proficiency in mechanical design (AutoCAD and Solid Works) and troubleshooting.
  • Knowledge of PLC, Vision Systems, and equipment troubleshooting preferred.
  • Knowledge of PLC, Vision Systems, and equipment troubleshooting preferred.
  • Experience in manufacturing environment. Pharmaceutical or Medical Device experience highly preferred.
  • Six Sigma certification (green belt or black belt) preferred.
  • Familiarity with the following processes: liquid dispense, sterile pathway, autoclave cycle development, leak detection, pick‑n‑place, printing/labeling.
  • Highly organized with the ability to manage multiple projects and changing priorities while under pressure.
  • Ability to successfully prioritize and manage large projects, deadlines, and tasks while working independently or with a team.
  • Position requires bending (desk to floor), lifting (up to 15 lbs.), corrected vision (20/20), standing, sitting, typing, and walking.
  • MUST have a valid driver’s license or government issued .
  • MUST pass a drug test.
  • Salary…
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