Quality Assurance Auditor II: GLP Compliance & Audits

Inotiv, Inc.

Rockville (MD)

Hybrid

USD 61,000 - 80,000

Full time

14 days+

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Benefits offered by this job

Health and dental coverage
Short- and long-term disability
Paid time off
Paid parental leave
401K
more!

Job summary

Inotiv in Rockville, MD is seeking a Quality Assurance Auditor II with a BS in chemistry or life sciences and 2–4 years in GLP environments. The role focuses on conducting audits, reviewing protocols, and ensuring regulatory compliance within a laboratory setting.

The position requires excellent written and verbal communication, strong organizational skills, and the ability to work independently. Inotiv offers competitive pay and comprehensive benefits, with salary commensurate with experience.

Qualifications

  • B.S. in chemistry or life sciences or related field with 2–4 years in GLP or regulated environment.
  • Prefer 1+ year of auditing experience.
  • Equivalent combination of education and regulatory, quality, compliance and/or industry experience.
  • Experience with quality systems management is preferred.

Responsibilities

  • Follow SOPs and maintain confidentiality.
  • Interact with clients, other employees, and the community in a professional manner.
  • Provide assistance or support to other Inotiv QA team members as necessary.
  • Maintain knowledge of facility SOPs, policies, study protocols, etc.
  • Adhere to safety regulations and procedures.
  • Prepare audit reports and submit findings promptly.
  • Conduct quality training for new hires and other employees.
  • Represent the QA team on regulatory topics as requested.

Skills

Excellent written/verbal comms
Interpersonal skills
Organizational skills
Lab procedures awareness
Regulatory knowledge
Independent work
MS Office proficiency
Quality systems knowledge
Auditing experience

Education

Bachelor's degree in chemistry or life sciences or related field

Job description

Inotiv in Rockville, MD is seeking a Quality Assurance Auditor II with a BS in chemistry or life sciences and 2–4 years in GLP environments. The role focuses on conducting audits, reviewing protocols, and ensuring regulatory compliance within a laboratory setting.

The position requires excellent written and verbal communication, strong organizational skills, and the ability to work independently. Inotiv offers competitive pay and comprehensive benefits, with salary commensurate with experience.

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