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Principal QA Specialist

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: KBI Biopharma Inc.
Full Time position
Listed on 2026-02-18
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
*
* Position Summary:

** Individual contributor and special project leader responsible for ensuring compliance with internal quality documents, regulatory requirements, and cGMP. The role will serve as Quality-to-Quality client liaison and sometimes SME for the Quality team reporting cross-QA metrics and status for KBI and clients. The role is client-facing. The role will be responsible for supporting processes required for product release, including deviation investigation guidance and CAPA review and approvals.

Additionally, this will be responsible for compiling, analyzing, and reporting of associated Quality and Client metrics. The completion of the Annual Product Quality Review for commercial programs is also required. The role requires routine interactions with all functions supporting the external network, including interaction with functions across our company’s global network.

The role supports activities to ensure systems and business processes are robust, effective, and efficient to comply with required regulations, policies, and guidelines governing the manufacture and holding of materials for our company.
*
* Position Responsibilities:

*** Provides interface between KBI Quality and client regarding batch status, Quality metrics, and Quality issues impacting batch disposition and disposition timeline.
* Communicates client concerns to KBI teams; facilitates discussions as necessary to resolve client issues. Escalates issues to leadership as needed.
* Routinely interfaces with the PMO team to ensure any Quality topics are addressed.
* Serves as QA facilitator for the Quality aspect of all projects requiring QA support. Serves as the accountable Quality lead, decision maker, and delegate for project teams and in related meetings.
* Supports audit / inspection readiness of the site. Participates in regulatory and other quality and compliance report-outs; reviews client audit outcomes to ensure appropriate corrective actions are implemented as assigned.
* Serves as client liaison and quality representative on behalf of KBI in audits, client and other client facing meetings and those requiring a Quality SME where the job skills and proficiencies allow.
* Supports Deviation Management activities by participating in investigational meetings, activities, writing as needed, and approving investigations. Leads Product and Client Complaint activities in accordance with SOP and established requirements.
* Supports efforts to ensure organization operates within established policies/procedures and complies with all applicable governmental regulations (cGMP, etc.), both domestic and foreign.
* Operates in a safe and efficient manner and in compliance with the safety and health policy.
*
* Minimum Requirements:

*** BS/BA Degree in Science or Engineering relevant to the pharmaceutical / Life Science or related industries AS/AA acceptable with 7-10 years of relevant experience as described below.
* Minimum 5 years prior experience in the Pharmaceutical/Biotechnology industry with a thorough knowledge of Quality Systems, Quality Assurance and Quality Control including solid knowledge of global GMP Quality and Regulatory requirements.
* Minimum of 2 years of previous experience in QA and experience in a Client-Facing QA role. Project Management experience or formal training is a plus.
* Demonstrates solid Body of Knowledge of Quality systems and functions supporting drug or related FDA governed manufacturing obtained from professional Quality roles. Includes a balance of, from such areas as Supplier Quality Assurance, Compliance, Audits/Inspections, Shop Floor Support, Batch / Material release, Quality document control, review and approval, Validation, QC, Deviations, Prior direct regulatory agency, and audit management /r support experience a plus.
* Ability to work effectively with others and communicate in customer-facing forums to progress issues and obtain positive results. Able to navigate conflict to achieve deliverables and drive to targeted outcomes. Ability to resolve differing perspectives with effective negotiation.
* Ability to work professionally and facilitate positive interdepartmental interactions…
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