Quality Assurance Auditor - Molecular Bioa

Lauer Kim Laboratory

Greenfield, IN, US
Not specified; not specified; comprehensive benefi...
3 years regulatory environment experience
1 year molecular bioa experience
Knowledge of glp and gcp auditing
The role involves conducting inspections in support of GLP or GCP method validation and study-based data reports

Job Summary

  • The role involves conducting inspections in support of GLP or GCP method validation and study-based data reports.
  • Candidates must have at least 3 years of experience in a regulatory environment with specific expertise in Molecular Bioanalysis.
  • Employees are eligible for comprehensive benefits including medical, dental, vision, life insurance, and a 401(k) plan.

Matching Summary

Match Score: 75

The role involves conducting inspections in support of GLP or GCP method validation and study-based data reports.

Salary

Not specified; Not specified; Comprehensive benefits package including medical, dental, vision, life, STD/LTD, 401(k), PTO, tuition reimbursement, and employee stock purchase plan.

Skills & Requirements

Must-have

  • 3 years regulatory environment experience
  • 1 year Molecular BioA experience
  • Knowledge of GLP and GCP auditing
  • Experience with qPCR and RT-qPCR techniques
  • Ability to lead internal facility inspections

Nice-to-have

  • Strong critical thinking and problem-solving skills
  • Experience influencing QA strategy
  • Clear communication and training delivery abilities
  • Process improvement initiative leadership

Key Requirements

  • Bachelor's Degree in Life Sciences preferred
  • Minimum 3 years in regulatory environment
  • Minimum 1 year in Molecular BioA
  • Knowledge of industry quality systems and standards

Work Rights

Not specified

Tailored Resume

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