Remote QA Manager – Life Sciences (Govt)

The Emmes Company, LLC

Rockville (MD)

Remote

USD 125,000 - 180,000

Full time

7 days ago
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Benefits offered by this job

Flexible Approved Time Off
Tuition Reimbursement
401k Retirement Plan
Work From Home Anywhere in the US
Maternal/Paternal Leave
Casual Dress Code & Work Environment

Job summary

Emmes Group is seeking a Quality Assurance Manager for Government programs. The role leads the QA program, oversees staff, and ensures compliance with regulations and project requirements across a remote US footprint.

You will drive internal audits, supplier/vendor audits, and regulatory inspections, while drafting policies and guiding process improvements. Strong leadership, communication, and regulatory experience are essential.

Qualifications

  • Bachelor's Degree in Life Sciences or related field is required.
  • Quality certifications (CQA, RAC, RQAP, Six Sigma) preferred.
  • 7–9 years in a regulated environment (GXP/ISO) required.
  • Management experience required.
  • Strong written and verbal communication skills.

Responsibilities

  • Oversee components of the Quality Management System (internal audits, document control, CAPA).
  • Supervise QA staff as needed and review audit reports.
  • Lead internal and client audits and regulatory inspections.
  • Draft QA policies and procedures and contribute to process improvements.
  • Prepare management reports and review corporate SOPs.

Skills

Leadership
Regulatory knowledge
Prioritization
Negotiation
Communication
Problem solving
Attention to detail

Education

Bachelor's Degree Life Sciences

Tools

Microsoft Office

Job description

Emmes Group is seeking a Quality Assurance Manager for Government programs. The role leads the QA program, oversees staff, and ensures compliance with regulations and project requirements across a remote US footprint.

You will drive internal audits, supplier/vendor audits, and regulatory inspections, while drafting policies and guiding process improvements. Strong leadership, communication, and regulatory experience are essential.

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