San Diego, California, 92101
Apply now
Onsite
Job description
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.
STEMHUNTER is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, gender identity, and gender expression), national origin, age, disability, genetic information, veteran status, or any other status protected by applicable federal, state, or local law. We comply with all applicable equal employment opportunity and affirmative action regulations.
