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Salary
≈ $78k – $169k per year (Estimated)
Location
In office (United States)
Seniority
Staff · 5+ years exp
Visa
H-1B filings in 12 months: 27 · green card filings: 5
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Confirmed on the employer's own hiring board on Oct 10, 2026. First seen by Alion on Oct 9, 2026. Frontage Laboratories scores B on the Alion truth index.

Overview
Company
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Frontage Laboratories is a contract research organisation that provides integrated, science-driven product development services across drug discovery and development. It runs laboratories in the United States, Canada and China covering drug metabolism, pharmacokinetics, bioanalytical services, safety and toxicology, and its North American facility is in Exton. Its Chinese business, which runs the group's pharmaceutical research base, is based in Shanghai, China.

Title: Manager/Senior Manager/Associate Director/Director, Quality Assurance

Location: Concord, OH

Reports To: Senior Director/VP of Quality Assurance

Company

Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position Summary:

We are seeking a senior GLP quality assurance leader to oversee site quality assurance personnel, manage compliance program, host regulatory and sponsor inspections, and ensure adherence to FDA GLP standards for preclinical safety and toxicology testing.

Roles and Responsibilities:

  • Leadership to build, manage and enable the QA team to have peak performance
  • Drive continuous process improvement and develop a risk-based QA management strategy to achieve quality and productivity goals
  • Manage, schedule, perform, and supervise audits and inspections of critical study phases, equipment, and facilities, protocols, experimental data and reports.
  • Host and organize site inspections and audits by government agencies and sponsors.
  • Assess the GLP compliance level and quality test sites and contractors.
  • Interface with Frontage Laboratories’ Global Quality Assurance.
  • Author or review Standard Operating Procedures.
  • Summarize inspection/audit findings, documents Quality Assurance activities and recommend improvements to the QA program.
  • Administer and conduct GLP training and manage quality compliance across facilities.
  • Complete tasks within time and budget constraint.
  • Demonstrate the ability to contribute to the success of assignments.
  • Perform other duties as assigned by Management.

Education and Requirements:

  • Bachelor’s Degree in Life Sciences or related discipline.
  • Minimum of five years of experience in preclinical safety & toxicology GLP including hands-on interaction with government regulatory agencies.
  • Excellence in strong leadership, communication, multitasking, problem-solving under pressure, and proficiency in standard office software (Microsoft Office, Adobe PDF).

Salary and Benefits:

Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

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