The QA Documentation Specialist will be responsible for the creation, modification, and evaluation of master batch records and manufacturing documents to ensure adherence to GMP regulations. This role involves partnering with diverse teams to facilitate document approvals, oversee version control, and identify any deficiencies in documentation. Ideal candidates should possess experience in developing or assessing batch records specifically within the pharmaceutical, biotech, or life sciences sectors. A solid grasp of GMP, good documentation practices, and proficiency in technical writing are essential for this position.
Genovice provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
