What are the responsibilities and job description for the Document Control Specialist position at Eliassen Group?
CQV Document Control Specialist
CONTEXT (client background / the program)
Our Pharma CDMO Partner is focused on preclinical development through to commercial manufacturing for biologics, advanced therapies, and vaccines. They provide start-to- finish solutions for drug development and manufacturing. Daily activities would include assisting with writing protocols, handling documentation and closing reports, and closing out deviations.
QUALIFICATION SUMMARY
1. Willingness to learn: Individual must be flexible and willing to work closely with a small team
2. Must have 5-10 years of either a Validation or Engineering Background.
3. Candidate must have a strong Pharma GMP Experience
4. Heavy Writing, Executing and Closeout Skillset
NICE TO HAVES
1. Experience with Capital Projects or large-scale fill-line operations.
2. Ability to work and communicate well with others
3. Flexibility to jump from one project to another over the course of the assignment
LOCATION & TRAVEL
40 Hours Onsite Holly Springs, NC
START & TERM
October start date, initial 6-month contract with a high probability of extending out a few years.
