Start Date: ASAP
Duration: 4-6 Months, 40 hours per week
Description: The client is in need of a mid level contractor who is detailed oriented and ready to work in a “start up” environment. This person will serve as the first step towards their goal of being GMP certified by September of 2023. The candidate will be working on reviewing, editing and converting SOPs and QA Documents. Currently there is no SOP template in place and the candidate must ensure compliancy as well as cohesiveness for each SOP. The contractor will also be responsible for uploading the complete SOP’s to their eQMS program using Master Control. The perfect candidate will be able to focus on this task and be able to drive the project without much direction or hand holding.
Skills:
• 5-7 Years in QA Biotech/Pharma GMP Environment
Quality Assurance Background
• QA review with paper documentation
• Must have experience with SOP review, Documentation review, SOP transfer to eQMS
• Master Control experience is a plus
Plus: Local to MA is a plus but NOT required
Quality Documentation Contractor (233185) Waltham, MA
