Manufacturing Quality Assurance Specialist

Job Summary:

• Manufacturing Quality Assurance Specialist will be responsible for supporting cGMP-like production activities for the Pharma and Personal Care (PPC) division. Duties include overseeing production activities through a quality lens, including making and documenting decisions as manufacturing challenges arise and aligning impacted personnel to the path forward.
• Manufacturing Quality Assurance Engineer will additionally be the primary delegate for the Quality Manager for activities such as batch review and release, non-conformance review and approval, and management review preparation. Due to the current growth trajectory of the PPC division, performing project-based work as specified in a timely manner will also be required.

What's in it For You:

• The opportunity to become part of a growing division in North America dedicated to ensuring our customers can maintain clean and safe cleanroom production environments
• The ability to make an impact and shape your career with a company that is passionate about growth
• The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best

What You Will Do:

• Oversee and guide the manufacturing process with a focus on product and customer quality requirements in collaboration with 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.
• Performs work under general supervision of the PPC Quality Manager and collaborates primarily with the Production Team Lead and Quality Team Lead.
• Executes assigned responsibilities where discretion and initiative are required in resolving problems and making recommendations. Expected to 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.

Education/Work Experience:

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

Benefits

Ecolab strives to provide comprehensive and market-competitive benefits to meet the needs of our associates and their families. Click here to see our benefits.

If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at jobs.ecolab.com/working-here.

Covid-19 Vaccine Notice

Due to local mandates and customer requirements, applicants for certain customer-facing positions must be fully vaccinated (which in some situations requires a booster if eligible), unless a religious or medical accommodation is requested by the applicant and approved by Ecolab.

Americans with Disabilities Act (ADA)

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