Specialist, Operational Quality & Compliance

Posted 9 Days Ago
Be an Early Applicant
Lincoln, NE, USA
In-Office
Mid level
Biotech • Pharmaceutical
The Role
Support day-to-day operational quality and compliance: manage and review Quality Events, maintain QMS records in Q-Pulse, assist root-cause troubleshooting and CAPA, support ISO/document control and audit prep, train staff on quality processes, and identify process improvements.
Summary Generated by Built In
Come Be Part of a Mission that Matters!

Hybrid Flexibility

ESSENTIAL FUNCTIONS:

  • Carries out day-to-day tasks related to operational quality and compliance to support operational goals and ensure alignment with established company standards.
  • Helps operational teams complete Quality Events by providing support, guidance, and follow-up to ensure timely and thorough documentation and resolution.
  • Reviews Quality Event records on a regular basis to confirm they are complete, accurate, and include appropriate corrective or preventive actions (CAPA).
  • Works with scheduling and planning teams to help align production with quality requirements and ensure products are available to meet customer needs.
  • Participates in troubleshooting efforts to identify root causes and help define clear, timely action steps for resolution.
  • Supports the rollout and improvement of quality-related procedures, workflows, and response timelines, based on departmental priorities.
  • Accurately enters, tracks, and maintains quality records in Q-Pulse and other quality management systems.
  • Ensures quality management systems data is kept current and complete; follows up with responsible team members to close out open items within required timeframes.
  • Assists with basic training to employees on quality processes, documentation procedures, and use of quality systems.
  • Identifies and communicates process improvement opportunities to reduce errors, increase efficiency, and enhance quality and compliance.
  • Works in collaboration with the Quality team to support ISO requirements, including document control, audit preparation, and corrective actions.
  • Other duties as assigned by the manager.

PREFERRED QUALIFICATIONS:

  • Bachelor's degree in genetics, molecular biology, biology, bioinformatics, or a related field; or equivalent experience within the organization.
  • Prior experience in quality assurance, compliance, or operations support, preferably in a laboratory, manufacturing, or regulated environment.
  • Familiarity with electronic quality management systems (EQMS).
  • Working knowledge of ISO standards and quality system documentation practices.
  • Strong attention to detail with effective organizational and recordkeeping skills.
  • Ability to follow established procedures and meet deadlines consistently.
  • Effective communication and interpersonal skills to work across teams and departments.
  • Proficient in Microsoft Office applications (Word, Excel, Outlook).
WHO IS NEOGEN:

Neogen is home to the largest genomic operation in the world! Our worldwide genomics operations deliver innovative, affordable DNA testing for the discovery and commercial application of genomic advances that enhance the safety and abundance of life. Our genomics tools are used by farmers and ranchers, and veterinary practitioners, to provide the best animal care possible, as well as enhance breeding programs.

Neogen’s culture combines stability with a deep belief in providing professional and personal growth. Our Pillars of Trust — the principles that guide our everyday decision-making, include Openness, Honesty, Credibility, Respect, and Service. It’s our belief in these characteristics that provides a consistent, happy and healthy work environment for our employees.

Skills Required

  • Bachelor's degree in genetics, molecular biology, biology, bioinformatics, or related field; or equivalent experience
  • Prior experience in quality assurance, compliance, or operations support, preferably in a laboratory, manufacturing, or regulated environment
  • Familiarity with electronic quality management systems (EQMS)
  • Working knowledge of ISO standards and quality system documentation practices
  • Strong attention to detail with effective organizational and recordkeeping skills
  • Ability to follow established procedures and meet deadlines consistently
  • Effective communication and interpersonal skills to work across teams and departments
  • Proficient in Microsoft Office applications (Word, Excel, Outlook)

Neogen Corporation Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Neogen Corporation and has not been reviewed or approved by Neogen Corporation.

  • Healthcare Strength The benefits suite includes comprehensive medical, dental and vision coverage, plus disability, life insurance, and an Employee Assistance Program. These core coverages are consistently described as a relative bright spot.
  • Retirement Support A defined-contribution 401(k) with company match and immediate vesting is highlighted, alongside standard retirement and savings programs. This structure provides clear baseline retirement support for eligible roles.
  • Equity Value & Accessibility An employee stock purchase plan offers discounted access to company shares. This adds an ownership pathway that complements cash compensation.

Neogen Corporation Insights

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The Company
HQ: Lansing, MI
1,160 Employees
Year Founded: 1982

What We Do

NEOGEN Corporation develops and markets products dedicated to food and animal safety. The company’s Food Safety Division markets dehydrated culture media and diagnostic test kits to detect foodborne bacteria, natural toxins, genetic modifications, food allergens, drug residues, plant diseases and sanitation concerns. NEOGEN’s Animal Safety Division markets a complete line of diagnostics, veterinary instruments, veterinary pharmaceuticals, nutritional supplements, disinfectants and rodenticides.

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