Vaccine Manufacturing Process Specialist

MSD

North Carolina

On-site

USD 87,000 - 137,000

Full time

5 days ago
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Benefits offered by this job

Annual bonus
Long‑term incentive
Comprehensive benefits

Job summary

The Maurice R. Hilleman Center for Vaccine Manufacturing in Durham, NC, is seeking a PSL Specialist to oversee key projects—laboratory studies, process monitoring, tech transfer, and continuous improvement. You will work cross-functionally with Manufacturing, Quality, and Technical Operations to support vaccine products and pipeline programs.

Strong lab analytics and cGMP documentation are essential. Off‑shift or weekend coverage may be required to support project schedules and vaccine

Qualifications

  • Bachelor’s degree with 2+ years of relevant experience or higher degrees with related study.
  • Experience in vaccine or biologics processing and analytics.
  • Experience authoring technical documentation in a cGMP context.
  • Strong technical communication (written and presentation) skills.
  • Ability to mentor and develop SME teammates.

Responsibilities

  • Lead PSL projects from scope to planning, execution and stakeholder updates.
  • Contribute technically to lab studies supporting investigations and tech transfer.
  • Draft protocols, reports and data summaries aligned with cGMP.
  • Apply vaccine manufacturing knowledge to upstream/downstream processing and analytics.
  • Coordinate use of analytical equipment and troubleshoot methods.
  • Support investigations and continuous improvement for Durham vaccines.

Skills

Lab analytics
cGMP documentation
Project management
Data analysis
Cross-functional collaboration
Cell culture
DOE/OFAT methods

Education

Bachelor's degree in Engineering or Science
Master's or PhD in Engineering or Science

Tools

SoloVPE
Lighthouse
Cedex Bio
ViCell
UPLC
Plate readers

Job description

The Maurice R. Hilleman Center for Vaccine Manufacturing in Durham, NC, is seeking a PSL Specialist to oversee key projects—laboratory studies, process monitoring, tech transfer, and continuous improvement. You will work cross-functionally with Manufacturing, Quality, and Technical Operations to support vaccine products and pipeline programs.

Strong lab analytics and cGMP documentation are essential. Off‑shift or weekend coverage may be required to support project schedules and vaccine

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