QA Documentation Specialist Merrimack Pharmaceuticals
THIS JOB HAS EXPIRED Merrimack Pharmaceuticals is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of serious diseases, with an initial focus on cancer. Merrimack applies Network Biology, its proprietary systems biology-based approach to biomedical research, throughout the research and development process. Merrimack currently has six targeted therapeutic oncology candidates in clinical development.
This position will be responsible for supporting GxP operations through control of documentation, including formatting and editing of Microsoft word documents, issuance of hardcopy controlled documents, and maintaining electronic copies of documents (pdf). Additionally, this position will support hardcopy archival efforts for GxP documents through work with an off-site storage vendor.
Edit and process GXP documentation through use of Microsoft Word, Microsoft Excel, and Adobe
File GXP documentation as required and maintain organization of GxP File Room
Perform archival and retrieval of all GxP Documentation
Issue GMP documentation such as batch records
The ideal candidate would have a Bachelor?s degree in Biology, English or Life Sciences or 2+ years of work experience with GMP or GCP documentation systems. Advanced word processing and database skills with good organizational and communication skills are a must. Excellent organizational skills, written and verbal communication skills, are needed to be successful in this role. Experience in a pharmaceutical or biotech manufacturing environment is preferred.
||One Kendall Square |
Building 700, Second Floor
Cambridge, MA 02139
THIS JOB HAS EXPIRED