Listed on Merck’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role manages documentation systems and quality records for a biological vaccine manufacturing facility, supporting regulatory compliance and continuous improvement through document control and systems administration. It suits candidates with strong organizational skills and attention to detail who thrive in regulated manufacturing environments and want to contribute to product safety and quality.
Our summary, not Merck’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- High school diploma or GED with 5 years relevant work experience
- Ability to work independently with minimal supervision
- Strong organizational skills and attention to detail
- Strong Microsoft Office skills (Word and Excel)
- Good communication and writing skills
- Ability to follow Standard Operating Procedures
- Ability to work in a team-oriented environment
Nice to have
- Associate's or Bachelor's degree
- Experience in document control, quality systems, or regulated manufacturing environments
- Quality, Biology, or Microbiology background or knowledge
- Ability to assume additional responsibilities with minimal supervision