Review photos to ensure they match the bill of materials
Obtain approvals via email
Analyze documents
Document control
Manage Document release process
Qualifications:
3- 5 years of GMP/ ISO13485, quality document control experience within Medical Device field
Excellent written communication
FDA regulation & audit experience
Willing to take on other office tasks- there can be down time in this role, during the down time they are looking for someone to support with office management duties
All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county , to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.