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Deviation Management Specialist

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: WorkLlama, Inc.
Full Time position
Listed on 2026-06-30
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Deviation Management Specialist

We are seeking a detail-oriented Deviation Management Specialist to provide scientific and technical support within a cGMP-regulated manufacturing environment. This role partners closely with cross-functional teams to investigate process deviations, resolve atypical events, and implement effective corrective and preventative actions (CAPAs). The ideal candidate brings strong analytical thinking, technical writing expertise, and a collaborative approach to supporting pharmaceutical or biotech manufacturing operations.

Responsibilities
  • Provide day-to-day technical support to manufacturing operations, focusing on the resolution and reduction of process deviations.
  • Lead manufacturing and laboratory investigations, including root cause analysis for atypical events and test failures.
  • Develop and implement corrective and preventative actions (CAPAs) to ensure compliance and continuous improvement.
  • Apply sound scientific and engineering principles to investigate process deviations and manufacturing issues.
  • Design and execute laboratory and/or pilot-scale experiments to analyze complex technical problems.
  • Collaborate cross-functionally with teams supporting aseptic manufacturing, testing, planning, and product release.
  • Develop strong working relationships across Manufacturing, Technical Services, Quality, and related departments.
  • Support continuous improvement initiatives utilizing Lean Six Sigma methodologies.
  • Participate in off-shift support activities as required.
Education
  • Bachelor’s (B.S.) or Master’s (M.S.) degree in Engineering, Science, or a related technical field required.
Experience
  • 0–3 years of post-bachelor’s experience in a cGMP-regulated environment within the pharmaceutical or biotechnology industry.
  • Experience in Production, Development, Process Engineering, Technical Services, or a related function preferred.
  • Prior experience writing investigations for atypical events in a manufacturing environment required.
  • Familiarity with Lean Six Sigma methodologies and demonstrated analytical/problem-solving capabilities.
  • Proven ability to work both independently and collaboratively within cross-functional teams.
Additional Information
  • Excellent written and verbal communication skills required.
  • Strong organizational skills and attention to detail are essential.
  • Role may require off-shift support based on manufacturing needs.
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