Quality Control Specialist

Leidos is seeking a Quality Control Specialist to work full time onsite in Atlanta, GA.

Candidate MUST:

Be local to Atlanta or be willing to relocate

Be a US Citizen with the ability to obtain a Public Trust Clearance.

The Strategic National Stockpile (SNS) at Leidos currently has an opening for a Quality Control Specialist in Atlanta, GA. This is an exciting opportunity to provide quality control support to assist in operating and maintaining the SNS national stockpiled inventory. In this mission, we assist in ensuring the SNS inventory is ready for deployment, providing the ability to respond 24 x 7 in an emergency. The successful candidate will provide quality control support to facilitate and maintain a high level of readiness.

Primary Responsibilities

• Provide quality control program support; QA assessments; controlled document reviews; deviation investigations assist; draft audit plans and deficiency documentation; internal control recommendations; audit/internal control reports; advisory support for regulatory/quality alignment; process improvement recommendations
• Provide technical support to assist the Government in maintaining a comprehensive quality control program to help ensure that cGMP standards and other applicable regulatory guidelines are adhered to during the receipt, storage, handling, transport, and distribution of pharmaceutical products.
• Monitor and assess quality assurance activities and provide recommendations to the Government regarding potential program modifications or revisions, as appropriate.
• Conduct audits and ad hoc assessments of SNS facilities, 3PLs, and partners to support Government oversight of cGMP compliance and to identify potential deficiencies. Provide written findings and recommendations to Government personnel.
• Review facility data and documentation and provide technical assessments to the Government regarding whether quality assurance requirements are in place, controlled and align with cGMP and other applicable regulatory requirements.
• Support Government-led deviation investigations by conducting analyses, identifying potential root causes, and recommending CAPAs, as requested. Provide technical review support for controlled documents, including Deviation Reports, CAPAs, Change Control documentation, and Validation/Qualification records. Final approval authority remains with the Government.
• Coordinate and communicate with Government officials and relevant stakeholders, including ASPR, HHS, other Federal agencies, contract partners, and members of the scientific community, as directed by the Contracting Officer (CO) or Contracting Officer's Representative (COR), to support resolution of quality-related matters.
• Provide technical support to the QC in activities related to ensuring compliance with applicable cGMP requirements for the storage and transportation of finished pharmaceuticals.
• Develop draft audit plans and proposed cGMP audit criteria for Government review and approval.
• Document observed deficiencies and/or discrepancies and provide recommended corrective actions to maintain cGMP and all local, state, and federal compliance regulations. Government personnel will determine and direct the implementation of corrective actions.
• Analyze and evaluate internal cGMP-related controls, policies, and procedures, and provide written recommendations to address non-compliance, control gaps, lack of controls or operational improvement opportunities. Provide drafting support for SOPs and protocols, as requested by the Government.
• Prepare draft audit and internal control reports by collecting, analyzing, and summarizing relevant information and trends for Government review and final approval.
• Support QC in ensuring compliance with established internal cGMP control procedures by examining records, operating practices, and documentation.
• Provide advisory support to assist the Government in maintaining cGMP compliance with applicable regulatory requirements, industry standards, and program Quality System policies. Recommend process improvements to enhance Quality System effectiveness and efficiency. Implementation decisions remain the responsibility of the Government.

Basic Qualifications

Bachelor's and 2 years or High School Diploma and 6 years of experience or Associates and 4 years

• 2 years of experience in related field
• 2 years of experience supporting cGMP compliance
• The ability to work both independently and as a team member
• Strong relationship-building and diplomacy skills
• Must have the ability to work handle request (s) from multiple groups/organizations
• Must be able to identify error (s), problem (s), or non-standard situations and suggest alternative (s).
• Must be proficient in common software, particularly with Microsoft Office: Excel, Word, and PowerPoint.
• Ability to lift up to 50 lbs.
• Most have a privately owned vehicle
• Must possess character traits of being accurate, meticulous, proactive, efficient, self-starter, a team player.

Preferred Qualifications

• Previous experience supporting a government agency.
• Experience supporting the validation or qualification of systems used in pharmaceutical storage and distribution, including reviewing protocols, test results, and validation/qualification records for alignment with cGMP requirements.

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If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo - because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 - and moving faster than anyone else dares.

Original Posting:

October 23, 2026

For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above.

Pay Range:

Pay Range $45,500.00 - $82,250.00

The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.