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US01 Elanco US Inc. - Clinton, IN

posted 2 months ago

Full-time - Entry Level
Clinton, IN

About the position

As an Associate in Quality Assurance at Elanco, you will support the Clinton Manufacturing Operations by ensuring compliance with Good Manufacturing Practices (GMP). This role involves facilitating quality systems, supporting continuous improvement initiatives, and providing guidance to operational staff to maintain high standards of quality in production processes.

Responsibilities

  • Provide production floor support, including assistance with procedures, master batch records, and quality system monitoring.
  • Maintain GMP compliance in preparation for regulatory inspections.
  • Facilitate continuous improvement through coaching and support for deviation investigations and change control proposals.
  • Collaborate with the area director to drive improvements via self-inspections.
  • Offer coaching and feedback to operational staff.

Requirements

  • Bachelor's Degree or equivalent experience in a science-related field preferred.
  • A minimum of 3 years of experience in cGMP within pharmaceutical manufacturing.
  • Strong proficiency in computer systems (Microsoft Office, Document Management, Maintenance Management, Inventory, Quality Systems).
  • Excellent communication skills.

Nice-to-haves

  • Experience in Quality Assurance, Quality Control, or Manufacturing in a regulated environment.
  • Proven ability to prioritize and manage multiple tasks effectively.
  • Strong problem-solving skills and interpersonal abilities.
  • Experience with deviation investigations and change control processes.
  • Knowledge of industry regulations and compliance standards.

Benefits

  • Multiple relocation packages
  • Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • Flexible work arrangements
  • Up to 6% 401K matching
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