Ecolab - Greensboro, NC

posted 4 months ago

Full-time - Entry Level
Greensboro, NC
Chemical Manufacturing

About the position

The Manufacturing Quality Assurance Engineer will play a crucial role in supporting cGMP-like production activities within the Pharma and Personal Care (PPC) division. This position is responsible for overseeing production activities through a quality lens, ensuring that all processes align with product and customer quality requirements. The engineer will be tasked with making and documenting decisions as manufacturing challenges arise, and will work closely with impacted personnel to determine the best path forward. As the primary delegate for the Quality Manager, the Manufacturing Quality Assurance Engineer will handle critical activities such as batch review and release, non-conformance review and approval, and preparation for management reviews. Given the current growth trajectory of the PPC division, the role will also involve performing project-based work in a timely manner, contributing to the overall success of the division. In this position, the Manufacturing Quality Assurance Engineer will oversee and guide the manufacturing process, collaborating with the Greensboro-based Operations team to evaluate challenges and execute risk-based decision-making in compliance with Quality Management System (QMS) and validation requirements. The engineer will identify areas for improvement or gaps in the division's development based on their previous experience in regulated industries. Responsibilities will include executing batch review and release, non-conformance review and approval, and management review preparation as bandwidth allows. The role requires working under the general supervision of the PPC Quality Manager and collaborating primarily with the Production Team Lead and Quality Team Lead. The engineer will be expected to utilize their previous experience to drive risk-based decision-making and recommend additional improvements or new quality-related projects.

Responsibilities

  • Oversee and guide the manufacturing process with a focus on product and customer quality requirements in collaboration with the Greensboro based Operations team.
  • Evaluate challenges as they arise and execute risk-based decision making in compliance with QMS and validation requirements.
  • Identify areas for improvement or gaps in the division development based on previous experience in regulated industries.
  • Execute batch review and release, non-conformance review and approval, and management review preparation as bandwidth allows.
  • Perform work under general supervision of the PPC Quality Manager and collaborate primarily with the Production Team Lead and Quality Team Lead.
  • Utilize previous experience to drive risk-based decision making in compliance with QMS and validation requirements and identify, recommend, and prioritize additional improvements or new quality related projects.

Requirements

  • Four-year degree in a related field (e.g. microbiology, biology, chemistry, engineering, etc.).
  • Two to five years of experience in a cGMP or ISO environment.
  • Experience in Quality is preferred.

Benefits

  • Comprehensive and market-competitive benefits to meet the needs of associates and their families.
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