Onsite QA Associate Manager, Laboratory Quality Assurance

ThermoFisher Scientific

Richmond (VA)

On-site

USD 76,000 - 126,000

Full time

14 days+

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Benefits offered by this job

Total Rewards package
Stock Purchase Plan
PTO and holidays
Tuition reimbursement

Job summary

Thermo Fisher Scientific in Richmond, VA is seeking an Associate Manager, Quality Assurance for an onsite role in the BIOA Laboratory. You will lead a QA team, ensure compliance, and support client and regulatory inspections while guiding staff development and project prioritization.

Requirements include a Bachelor’s degree, 0–5 years experience, and at least 1 year in leadership. This role emphasizes accuracy, collaboration, and adherence to global pharmaceutical guidelines in a fast-paced

Qualifications

  • Bachelor's degree or equivalent and relevant formal qualification.
  • 0 to 5 years of relevant experience.
  • 1+ year of leadership responsibility.
  • Relocation assistance not provided; authorized to work in the United States.

Responsibilities

  • Manage day-to-day QA team operations and oversee staff performance.
  • Assess project priority with supervisors and ensure adequate resourcing.
  • Support QA program evaluations to maintain regulatory compliance.
  • Evaluate QA issues, communicate findings to staff and leadership.
  • Participate in client and regulatory inspections and respond.

Skills

Leadership
Regulatory knowledge
Analytical methodologies
Verbal & written communication
Documentation
Prioritization
Molecular Genomics knowledge

Education

Bachelor's degree or equivalent

Job description

Thermo Fisher Scientific in Richmond, VA is seeking an Associate Manager, Quality Assurance for an onsite role in the BIOA Laboratory. You will lead a QA team, ensure compliance, and support client and regulatory inspections while guiding staff development and project prioritization.

Requirements include a Bachelor’s degree, 0–5 years experience, and at least 1 year in leadership. This role emphasizes accuracy, collaboration, and adherence to global pharmaceutical guidelines in a fast-paced

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