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Open nowPosted 11 days ago

Senior QA Validation Specialist

KBI Biopharma87 open roles

Where
USA - NC - Durham - National Way
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Your applicationOpen nowSenior QA Validation SpecialistKBI Biopharma · USA - NC - Durham - National Way

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. KBI Biopharma postings stay open a median of 50 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.7%14 days
  5. 35.6%30 days
  6. 58.0%60 days
This job: posted 11 days ago

KBI Biopharma median: 50 days open

The posting

Position Summary

The Senior QA Specialist provides Quality Assurance oversight and support for Facilities, Engineering, Validation, Cleaning Validation, Metrology, computerized systems, and related GMP activities supporting clinical and commercial manufacturing operations.

This position partners with Engineering, Facilities, Validation, Manufacturing, MSAT, IT, and other cross-functional teams to provide science- and risk-based Quality oversight and ensure facilities, utilities, equipment, systems, and validated processes remain compliant and in a state of control throughout their lifecycle.

Key Responsibilities

  • Provide QA oversight for GMP facilities, utilities, equipment, Engineering, Validation, Cleaning Validation, Metrology, and computerized systems.
  • Review and approve GMP documentation including qualification and validation protocols/reports, cleaning validation documentation, risk assessments, deviations, CAPAs, change controls, and return-to-service documentation.
  • Provide QA oversight of commissioning, qualification, and validation activities, including facility/utility and equipment qualification, IQ/OQ/PQ, process validation, cleaning validation, and computerized system validation, as applicable.
  • Support cleaning validation activities including validation strategies, protocols/reports, risk assessments, sampling plans, acceptance criteria, worst-case assessments, hold-time studies, and lifecycle management.
  • Assess qualification and validation impact associated with new products, technology transfers, facility/equipment/process changes, and new client onboarding.
  • Provide QA oversight of change controls and ensure appropriate qualification, validation, cleaning validation, and GMP requirements are identified and addressed.
  • Support facility upgrades, capital projects, shutdowns, equipment modifications, and commercial manufacturing readiness.
  • Review and support investigations and CAPAs associated with facilities, utilities, equipment, validation, cleaning validation, maintenance, calibration, and computerized systems.
  • Support regulatory inspections, client audits, internal audits, and inspection/PAI readiness activities.
  • Identify and escalate Quality and compliance risks and partner with cross-functional teams to drive issues to resolution.
  • Support continuous improvement of Quality, qualification, validation, and change control processes.

Qualifications

  • Bachelor’s degree with 8+ years of relevant experience, or Master’s degree with 5+ years of relevant experience, in a QA role within a cGMP-regulated biopharmaceutical or equivalent environment.
  • Experience reviewing and approving change controls, deviations, investigations, and CAPAs.
  • Knowledge of U.S. and EU cGMP regulations and guidelines is required.
  • Experience supporting clinical and/or commercial biopharmaceutical manufacturing is preferred.
  • Strong technical judgment, problem-solving, communication, and cross-functional collaboration skills.
  • Ability to independently manage multiple priorities and provide pragmatic, risk-based Quality guidance in a fast-paced manufacturing environment.

Preferred Skills

  • Experience supporting cleaning validation, including protocols/reports, risk assessments, sampling strategies, deviations, and lifecycle activities.
  • Experience providing QA oversight of commissioning, qualification, and validation activities for GMP facilities, utilities, equipment, and computerized systems.
  • Strong technical judgment, problem-solving, and risk-based decision-making skills.
  • Strong technical writing, communication, and cross-functional collaboration skills.
  • Ability to independently manage priorities and provide pragmatic Quality solutions in a fast-paced cGMP environment.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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